WO2002002081A1

WO2002002081A1 - Rapid-melt semi-solid compositions, methods of making same and methods of using same

Info

Publication number: WO2002002081A1
Application number: PCT/US2001/041272
Authority: WO
Inventors: Subraman Rao Cherukuri
Original assignee: Capricorn Pharma, Inc.
Priority date: 2000-07-05
Filing date: 2001-07-05
Publication date: 2002-01-10
Also published as: US20090304824A1; US20020187188A1; US20080020065A1; AU2001279284A1; US7229641B2

Abstract

A novel rapid-melt, semi-solid molded composition, including methods of making the same, and methods of using the same for the delivery of prophylactic and therapeutic active materials to a mammal wherein the prophylactic or therapeutic active is a psychotropic, a gastrointestinal therapeutic or a migraine therapeutic.

Description

RAPID-MELT SEMI-SOLID COMPOSITIONS, METHODS OF MAKING SAME AND METHODS OF USING SAME

BACKGROUND OF THE INVENTION Field of the Invention

The present invention relates to a rapid-melt, semi- solid composition for delivery of prophylactic and therapeutic active materials to a mammal, methods of making the same, and methods of using the same. Preferably, the prophylactic or therapeutic active is a psychotropic, a gastrointestinal therapeutic or a migraine therapeutic.

Description of the Prior Art

Pharmaceutical compositions may be produced in a variety of dosage forms, depending upon the desired route of administration of the therapeutic material. Oral dosage forms, for example, include such solid compositions as tablets, emulsions, and suspensions. The particular dosage form utilized will depend on such factors as the solubility and chemical reactivity of the pharmaceutical active. Further, the dosage form may be selected so as to optimize delivery of the pharmaceutical active and/or consumer acceptability of the composition.

Tablet compositions offer many advantages, including ease of product handling, chemical and physical stability, portability (in particular, allowing ready availability to the consumer when neede'd) , aesthetic acceptability and dosage precision, i.e., ensuring consistent and accurate dosages of the pharmaceutical active. However, liquid formulations may offer advantages in the treatment of certain disorders, such as disorders of the upper gastrointestinal tract, wherein delivery of an active material dissolved or dispersed in a liquid ensures rapid and complete delivery to the afflicted area. In an effort to obtain the therapeutic advantages associated with liquid formulations as well as the broad advantages associated with solids, many chewable tablet formulations have been developed.

One important factor in formulating chewable tablets is palatability and mouth feel, especially in tablets that include pharmaceutical dosages. Many pharmaceutical and confectionery tablets are designed to be chewed either to provide proper flavor or to increase the surface area of a particular drug to permit rapid activity in the digestive tract or circulatory systems. However, many pharmaceutical ingredients usually have both an unpleasant mouth feel and unpalatable taste due to chalkiness, grittiness, dryness and astringent properties of these materials. Accordingly, the practical value of these materials is substantially diminished since patients finding them objectionable may fail to take them as prescribed. A number of formulations have been investigated to ease the mouth feel and palatability of such compositions. Khankari et al . , U.S. Patent No. 6,024,981, discloses a rapidly dissolving robust dosage form directed to a hard tablet that can be packaged, stored and processed in bulk. The solid tablet dissolves in the mouth of a patient with a minimum of grit. The tablet contains an active ingredient mixed into a matrix of a non-direct compression filler and a relatively high lubricant content.

Amselem, U.S. Patent No. 5,989,583, discloses a dry solid lipid composition suitable as an oral dosage form. The composition contains a lipophilic substance, at least one fat which is a solid at about 25°C and at least one phospholipid present in an amount of about 2 to 40% by weight of the composition. However, the resultant product is a dry solid lipid composition. United Kingdom patent application GB 2 195 892 discloses pharmaceutical chewable tablets with improved palatability. The lipid-containing molded tablets include a lipid material having a melting point from about 26°C to about 37°C, a particulate dispersant material, an emulsifier and a safe and effective amount of a pharmaceutically active material. The tablets of the lipid composition exhibit improved palatability, and effective dispersion in the mouth and stomach.

United Kingdom patent application GB 2 195 891 also discloses pharmaceutical chewable tablets with improved palatability. The lipid-containing molded tablets include a lipid material, a dispersant, a nonionic emulsifier having an HLB of at least 10, and a safe and effective amount of a pharmaceutical active material, wherein the average HLB of all emulsifiers in the composition is at least about 8.

Nakamichi et al . , U.S. Patent No. 5,837,285, discloses fast soluble tablets that can be produced by a simple method. The tablet base is a sugar alcohol. The mixture of the sugar alcohol and a drug is subjected to compressive shaping prior to drying in the process. The dry solid tablet can be produced by modification of conventional tableting technology and possesses physico-chemical stability.

Chavkin et al . , U.S. Patent No. 5,753,255 discloses a chewable medicinal tablet. The tablet contains about 30 to about 95% by weight of a capric triglyceride and a medicinally active ingredient up to 60% by weight. If the medicinally active ingredient is less than about 30% by weight, then the composition also contains up to 10% by weight of a member of the group consisting of glyceryl monostearate, a mixture of glyceryl monostearate and glyceryl monopalmitate, and a mixture of glyceryl monostearate and glyceryl distearate.

Geyer et al . , U.S. Patent No. 5,320,848, discloses a non-aqueous chewable composition for oral delivery of unpalatable drugs. The drug is intimately dispersed or dissolved in a pharmaceutically-acceptable lipid that is solid at room temperatures. The lipid material desirably readily melts with the application of mild temperatures, i.e. about 55 to 95°C. Lapidus, U.S. Patent No. 4,937,076, discloses a chewable aspirin and buffering material tablet in a single dosage form. The buffering materials are integrally dispersed and bound in a fatty material of chocolate, synthetic chocolate or hydrogenated tallow. The fatty material individually coats the aspirin and buffering material .

Valentine, U.S. Patent No. 4,684,534, discloses quick- liquefying, chewable tablets. The tablets have a harder outer shell which inhibits penetration of liquid, and a softer interior which quickly liquefies when the tablet and shell are broken into pieces and contacted by the liquid. The excipient or base material of the tablet is made from carbohydrates held together with small quantities of a carbohydrate binder such as maltodextrin. The tablets can contain active ingredients such as pharmaceuticals, breath sweeteners, vitamins and dietary supplements.

Morris et al . , U.S. Patent No. 4,609,543, discloses a soft homogeneous antacid tablet. The tablet contains solid antacid particles thoroughly coated with a mixture composed of a fatty material or oil, a surfactant, and a flavor. The fat or oil is present in an amount of from about 25% to about 45% of the mixture. The primary particle size of the antacid is less than 100 millimicrons.

Fountaine, U.S. Patent No. 4,446,135, discloses chewable calcium carbonate-containing antacid tablets having good mouth feel properties. The good mouth feel properties of the tablet are obtained by using calcium carbonate of a particular particle size in combination with certain excipients. The calcium carbonate is present in an effective amount and has a size from about 5 to 50 microns in diameter.

Puglia et al., U.S. Patent No. 4,327,077, discloses a compressed chewable antacid tablet which has good flexibility, is breakage resistant and disintegrates immediately upon chewing. The tablet is formed of a recrystallized fatty material, such as chocolate, a bulking material and an active ingredient bound up in the particles of the recrystallized fatty material. The preferred recrystallized fatty material is a chocolate or a synthetic chocolate. Puglia et al., U.S. Patent No. 4,327,076, also discloses a compressed chewable antacid tablet which has good flexibility, is breakage resistant and disintegrates immediately upon chewing. The tablet is formed of particles of the antacid or other active ingredient which are admixed with particles formed of edible fat or oil absorbed on a fat-absorbing material, such as microcrystalline cellulose. Upon chewing, the tablet is quickly converted to a smooth creamy non-gritty palatable emulsion.

However, the prior art compositions contain various disadvantages. For example, tablets may be incompletely chewed due to the poor palatability of the composition. Such compositions may also have a gummy texture, and are subject to "taste fatigue," i.e., the composition is perceived to be less palatable after ingestion of multiple doses. Further, the binders and other materials used in such chewable tablets may prevent rapid and effective delivery of active materials to the stomach.

There is a need for a rapid-melt, semi-solid composition that behaves like a liquid when consumed by a mammal, and yet acts like a solid in many other ways. The need extends for compositions in which no biting or chewing is necessary in order for the composition to melt in the mouth of a mammal. Such compositions are ideal for uses in the fields of pediatric and geriatric care, that is, for use with people or mammals that do not have any teeth.

It has been found that semi-solid product formulations containing one or more certain lipid materials, emulsifiers and particulate materials are highly palatable and effective compositions for the delivery of pharmaceutical active materials. Such compositions afford better taste, mouth feel and storage stability than those compositions known in the art. BRIEF SUMMARY OF THE INVENTION

Applicant has unexpectedly developed a novel rapid- melt, semi-solid molded composition comprising: a) at least one binder in an amount from about 0.01% to about 70% by weight; b) a salivating agent in an amount from about 0.05% to about 15% by weight; c) a diluent/bulking material in an amount from about 10% to about 90% by weight; and d) an active material in an amount from about

0.001% to about 70% by weight; wherein the composition is prepared in the absence of free water.

Applicant has further developed a novel method of preparing a rapid-melt, semi-solid molded composition comprising the steps of: a) melting at least one binder in an amount from about 0.01% to about 70% by weight with a salivating agent in an amount from about 0.05% to about 15% by weight, to form a mixture b) mixing an active material with said mixture to form an active mixture; c) mixing a diluent/bulking material with said active mixture to form a final mixture; and ^• d) molding said final mixture into said semi-solid molded composition. Further, Applicant has unexpected developed a novel rapid-melt, semi-solid molded composition comprising: a) at least one binder in an amount from about 0.01% to about 70% by weight; b) a salivating agent in an amount from about

0.05% to about 15% by weight; c) a diluent/bulking material in an amount from about 10% to about 90% by weight; d) water in an amount less than 2% by weight; and e) an active material in an amount from about

0.001% to about 70% by weight.

In addition, Applicant has developed a rapid melt, semi-solid molded composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; and a therapeutically effective amount of a drug, wherein said drug is selected from the group consisting of psychotropics , gastrointestinal therapeutics, cardiovascular therapeutics, migraine therapeutics, inflammation therapeutics, benign prostatic hypertrophy therapeutics, fungal therapeutics, allergic rhinitis therapeutics, anticonvulsants, and viral therapeutics. Further, Applicant has developed a method of preparing a rapid-melt, semi-solid molded composition comprising the steps of: a) melting at least one binder in an amount from about 0.01% to about 70% by weight with a salivating agent in an amount from about 0.05% to about 15% by weight, to form a mixture; b) mixing a therapeutically effective amount of a drug with said mixture to form an active mixture; said drug selected from the group consisting of psychotropics, gastrointestinal therapeutics, cardiovascular therapeutics, migraine therapeutics, inflammation therapeutics, benign prostatic hypertrophy therapeutics, fungal therapeutics, allergic rhinitis therapeutics, anticonvulsants, and viral therapeutics. c) mixing a diluent/bulking material with said active mixture to form a final mixture; and d) molding said final mixture into said rapid- melt, semi-solid molded composition. Still further, Applicant has developed a method for treating depression, anxiety or insomnia comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an anti- depressant, anti-anxiety therapeutic or an insomnia therapeutic and wherein said composition is prepared in the absence of free water.

Yet still further, Applicant has developed a method for treating diarrhea and nausea comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an gastrointestinal therapeutic, a anti-emetic or an anti- diarrheal therapeutic and wherein said composition is prepared in the absence of free water.

Even yet still further, Applicant has developed a method for treating migraines comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an migraine therapeutic and wherein said composition is prepared in the absence of free water.

The rapid-melt, semi-solid molded compositions of the present inventive subject matter exhibit good resistence to prolonged exposure to heat and the atmosphere. More particularly, the compositions surprisingly maintain their texture and rapid melting properties when exposed to those elements .

DETAILED DESCRIPTION OF THE EMBODIMENTS

The rapid-melt, semi-solid molded compositions of the present inventive subject matter contains at least one binder, a salivating agent, an active material, and a diluent/bulking material. The rapid-melt, semi-solid compositions may also contain a slipping agent to aid in the transport of the composition from the mouth of the mammal to the stomach thereof.

As used herein, the expression "mammal" includes without limitation any mammalian subject, such as mice, rats, guinea pigs, cats, dogs, human beings, cows, horses, sheep or other livestock.

As used herein, the expression "free water" means water that is not found in other ingredients. Many ingredients used in the present inventive compositions may also have water as part of the ingredient, and the term "free water" refers to water that is separate from those ingredients .

The unique novel combination of elements allows for fast melting of the composition when placed in the mouth of a user. By pressing the composition between the tongue and cheek of the user, the saliva of the user provides hydration to the composition and allows the composition to melt without any chewing. A unique feature of the present inventive compositions is that the composition becomes a liquid upon the application of pressure. The semi-solid compositions rapidly melt upon the application of pressure by the tongue of the patient, thus forming a liquid carrier for the active ingredients contained therein. The liquid helps provide the unique characteristics and features of the present inventive compositions.

The liquification of the inventive compositions can be achieved through the application of pressure by the tongue of the patient, as described above. Optionally, the liquification may be attained by the patient chewing the compositions. A slight amount of chewing will enhance the liquefication of the compositions. A further way for the composition to be liquified is by the patient sucking on the rapid-melt, semi-solid compositions of the inventive subject matter.

The rapid-melt, semi-solid technology of the present inventive subject matter has multiple applications which are ideal for the unique properties of the compositions.

One such application is the delivery of active ingredients to a mammal in need thereof.

In addition, the melting feature of the novel compositions makes the compositions ideal for uses in pediatric and geriatric care, since small children and aged individuals often have difficulty chewing items. With this intended use in mind, the compositions may be specially formulated for pediatric and geriatric patients. The unique properties will aid in drug compliance by such patients as the drugs may be administered in a way that will not require chewing by the patient.

Another application for which the inventive compositions are ideal is to enhance the saliva flow of a patient. A frequent problem for geriatric patients is dry- mouth, or the inability to salivate sufficiently. The aid of saliva flow by the use of the present inventive compositions will enhance tooth cleaning within the patient, as well as stimulate better drug delivery to the patient. Also, the increased saliva flow will facilitate better breath characteristics in the patient. The use of xylitol, as well as other polyols and sugars, in the inventive compositions will contribute to the enhancement of the saliva flow of the patient.

A further application for the inventive compositions would be the preparation of compositions for drug delivery in diabetic patients. A diabetic patient must monitor the intake of sugar and the ability to formulate the present inventive compositions with fractose and other non- cariogenic components makes them ideal for delivery of drugs to diabetic patients.

The rapid-melt, semi-solid compositions of the present inventive subject matter are preferably anhydrous, that is, they do not contain any water. The lack of water in the inventive compositions allows high doses of active materials or combinations of active materials to be incorporated into the compositions due to the stability of the active materials in the absence of the water. It is contemplated, however, that the compositions may optionally include an amount of water. The amount of water present will depend on the active ingredients to be delivered, but generally will be present in an amount less than 2.0% by weight of the composition. Preferably, the water will be present in an amount less than 1.0% by weight of the composition. The rapid-melt, semi-solid compositions of the present inventive subject matter contain at least one binder. As used herein, "binder" means at least one ingredient useful in keeping the composition in its semi-solid state, may be either solid or liquid, and may include, without limitation, a high melting point fat or waxy material such as lipid materials, polyethylene glycols (PEG), waxes and other fats. Preferably, the semi-solid compositions of the present inventive subject matter contains a mixture of binders . The solid binders useful in the compositions of the present inventive subject matter have a melting point of about 25 to 90°C, and preferably about 37 °C. When more than one binder is used in the inventive compositions, the melting point of the combination of the binders will remain within the range of 25 to 90°C, and preferably about 37°C. The inventive subject matter contemplates the use of mixtures of solid binders and liquid binders. For a non- limiting example, the present inventive subject matter contemplates mixing a small amount of a high-melting point lipid with a liquid binder to achieve a binder that attains the desired product characteristics. These characteristics include such factors as mouth feel, rapidity of melting in the mouth, appearance, flavor and compatibility with active materials and therapeutic active materials.

Among the lipid materials useful as binders in the compositions of the present inventive subject matter are those which are commercially available and commonly used in confectionery and other food products. Such lipid materials include, without limitation, cocoa butter, hydrogenated tallow, hydrogenated vegetable oils, hydrogenated cotton seed oil, palm kernel oil, soybean oil, stannol esters, and derivatives and mixtures thereof. Hydrogenated vegetable oils (such as hydrogenated palm kernel oil) , cocoa butter, and cocoa butter substitutes are among the preferred useful lipid materials.

Other materials are also suitable as binders in the present inventive subject matter. Included within the materials suitable as binders are, without limitation, polyethylene glycols and liquid binders. Examples of liquid binders are, without limitation, poly saccharides, gum solutions, water, corn syrup, hydrogenated starch hydrolates, glycerine, polypropylene glycol, and mixtures thereof.

The amount of binder present in the rapid-melt, semi-solid molded composition of the present inventive subject matter is from about 0.01% to about 70% by weight of the final composition. Preferably, the amount of binder is from about 0.01% to about 50% by weight of the composition. More preferably the binder is present from about 15% to about 30% by weight of the composition.

The binder is used to provide good melt away properties to the composition while preventing a gritty texture being imparted by the composition. The binder aids in the fast melting of the composition when placed in the mouth of a user. The rapid-melt, semi-solid molded composition of the present inventive subject matter also contains a salivating agent. As is used herein, "salivating agent" means a material that promotes greater salivation in the user of the compositions of the present inventive subject matter. The salivating agent helps create salivation in the mouth of the mammal using the inventive compositions. This is an important feature since the present compositions are intended to be taken by the patient without the aid of water to help in the transporting of the composition to the stomach of the patient. The salivating agent can be, without limitation, an emulsifier or a food acid that initiates salivation in the mouth of the patient. Examples of emulsifiers useful as salivating agents in the compositions of the present inventive subject matter include, without limitation, alkyl aryl sulfonates, alkyl sulfates, sulfonated amides and amines, sulfated and sulfonated esters and ethers, alkyl sulfonates, polyethoxlyated esters, mono- and diglycerides, diacetyl tartaric esters of monoglycerides, polyglycerol esters, sorbitan esters and ethoxylates, lactylated esters, phospholipids such as lecithin, polyoxyethylene sorbitan esters, proplyene glycol esters, sucrose esters, and mixtures thereof. The emulsifier may be either saturated or unsaturated. Examples of food acids useful as salivating agents in the inventive compositions include, without limitation, citric acid, malic acid, tartarate, food salts such as sodium chloride and salt substitutes, potassium chloride, and mixtures thereof.

The amount of salivating agent present in the rapid- melt, semi-solid molded composition of the present inventive subject matter is from about 0.05% to about 15% by weight of the final composition. Preferably, the amount of salivating agent from about 0.3% to 0.4% by weight of the composition.

Keeping the amount of salivating agent present in the inventive composition within these limits for weight percentage is important to enhance the desirable properties of the compositions. More particularly, the low amount of salivating agent present in the compositions aid in the compositions retaining the semi-solid state and the rapidity of melting in the mouth of a mammal.

The rapid-melt, semi-solid molded compositions of the present inventive subject matter further contain a diluent/bulking material. The use of a diluent/bulking material is necessary to serve as a free-flow imparting agent which aids in the moisturizing of the composition when chewed, that is, the diluent/bulking material aids in the processability of the compositions. The diluent/bulking material also serves to reduce the concentration of the active materials and add bulk to the composition. Examples of diluent/bulking materials useful in the compositons of the present inventive subject matter include, without limitation, silicon dioxide, sugars, starches, lactose, sucrose, sorbitol, fructose, talc, stearic acid, magnesium stearate, dicalcium phosphate, erythitol, xylitol, mannitol, maltitol, isomalt, dextrose, maltose, lactose, microcrystalline celluloses and mixtures thereof.

The amount of diluent/bulking material present in the semi-solid molded compositions is from about 10% to about 90% by weight of the final composition. Preferably, the amount of diluent/bulking material is from about 35% to about 55% by weight of the final composition.

The rapid-melt, semi-solid compositions of the present inventive subject matter may optionally contain a further slipping agent to aid in the palatability of the composition after it melts in the mouth of the mammal. The slipping agent may be a further lipid material, as is described above for binders, or another material which aids in the "slipping" of the composition through the mouth and down the esophagus of the mammal.

As is discussed above, the preferably anhydrous nature of the present inventive compositions allows for very high doses of active materials to be incorporated therein. The amount of active material present in the inventive compositions will vary depending on the particular active used, but generally will be present in an amount of about 0.001% to 70% by weight of the composition. Preferably, the active ingredients used in the inventive compositions are prophylactic or therapeutic active ingredients. Prophylactic or therapeutic active materials which can be used in the present invention are varied. A non-limiting list of such materials includes the following: antitussives, antihistamines, decongestants, alkaloids, mineral supplements, laxatives, vitamins, antacids, ion exchange resins, anti-cholesterolemics, antiarrhythmics, antipyretics, analgesics, appetite suppressants, expectorants, anti-anxiety agents, anti-ulcer agents, anti-inflammatory substances, coronary dilators, cerebral dilators, peripheral vasodilators, anti-infectives, psycho-tropics, antimanics, stimulants, gastrointestinal agents, sedatives, antidrrheal preparations, anti-anginal drugs, vasodialators , anti-hypertensive drugs, vasoconstrictors, migraine treatments, antibiotics, tranquilizers, anti-psychotics, antitumor drugs, anticoagulants, antithrombotic drugs, hypontics, anti-emetics, ant i-nausant s , anti-convulsant s , neuromuscular drugs, hyper- and hypoglycemic spasmodics, uterine relaxants, mineral and nutritional additives, antiobesity drugs, anabolic drugs, erythropoetic drugs, antiashmatics, cough suppressants, mucolytics, anti-uricemic drugs and mixtures thereof. Preferred prophylactic or therapeutic active materials contemplated for use in the present inventive subject matter are analgesics. Examples of analgesics useful in the present inventive subject matter, and which are the preferred therapeutic active ingredients, include, without limitation, aspirin, acetaminophen, ibuprophen and mixtures thereof .

Another preferred active material can be selected from the class of prophylactic, abortive or analgesic drugs used to treat migraines. Migraines are defined as headaches that last 4 to 72 hours wherein the patient experiences moderate to severe cranial throbbing. Migraines are also associated with nausea, vomiting, or sensitivity to light, sound or smell. For prophylactic treatment of migraines, β-blockers, calcium channel blockers, tricyclic antidepressants, or anticonvulsants can be used. Examples of drugs indicated for prophylactic treatment include amitriptyline, methysergide, popranolol, valproate, and verapamil. For abortive treatment of migraines serotonin receptor activators such as eletriptan, ergotamine, naratriptan, rizatriptan benzoate, sumatriptan succinate, and zolmitriptan can be used. Ergot alkaloid derivatives such as ergoamine tartrate and dihydroergotamine are also effective. Dopamine antagonist anti-emetics such as metoclopramide and prochlorperazine while indicated for the treatment of nausea, can also be used even if nauseau is not prominent .

For analgesic treatment acetaminophen, aspirin, non- asteroidal anti-inflammatory drugs ("NSAID") and opioids can be used in the present invention.

In general, any class of drug indicated for migraine treatment may be used in the present invention. For example, sumatriptan succinate may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver sumatriptan succinate to a patient in need thereof. In particular, sumatriptan succinate can be formulated with the present invention in doses ranging from 25, 50, to 100 mg daily. All the examples are non- limiting and it will be understood that other migraine therapeutics may be used with the present inventive subject matter.

Yet another preferred active material used in the composition of the present inventive matter is a psychotropic. Psychotropics are used to treat depression, schizophrenia, anxiety disorders, attention deficit order, obsessive compulsive disorder, senile dementia and certain sleep disorders.

The classes of drugs used in treating depression include selective serotonin reuptake inhibitors ("SSRI's"), heterocyclic antidepressants, monoamine oxidase inhibitors ("MAOI's"), serotonergic-noradrenergics, 5-HT₂ antagonists and catecholaminergics . Examples of SSRI'S include fluoxetine HCl, sertraline HCl, paroxetine HCl, and fluvoxamine . Examples of heterocyclic antidepressants include amitriptyline, nortriptyline, imipramine, desipramine, doxepin, trimipramine, clomipramine, protriptyline, amoxapine, and maprotiline. Examples of MAOI's include phenelzine and tranylcypromine . An example of a serotonergic-noradrenergics includes venlafaxine HCl. Examples of 5-HT₂ antagonists include trazadone, nefazodone, and mirtazapine. An example of a catecholaminergics includes bupropion. All examples are non-limiting and it will be understood that psychotropics of the disclosed classes may be used with the present inventive subject matter . In general, any class of psychotropic drug indicated for treating depression may be used in the present invention. For example, fluoxetine HCl may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver fluoxetine HCl to a patient in need thereof. In particular, fluoxetine HCl can be formulated with the present invention in doses ranging from about 10 to 60 mg daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs . For the treatment of anxiety, benzodiazepines may be used with the present inventive subject matter. Specific examples include alprazolam, chlordiazepoxide, clonazepam, clorazepate, diazepam, lorazepam, and oxazepam. However, any class of psychotropic drug indicated for anxiety treatment may be used in the present invention. In particular, alprazolam may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver alprazolam to a patient in need thereof. In particular, alprazolam can be formulated with the present invention in doses ranging from about 0.25 to 0.50 mg to be taken three times daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs .

For the treatment of insomnia, drugs belonging to the categories of benzodiazepines, imidazopyridines, antidepressants and non-prescription hypnotics may be used with the present inventive subject matter. Examples of benzodiazepines useful for the treatment of insomnia include midazolam, triazolam, oxazepam, temazepam, lorazepam, estazolam, nitrazepam, diazepam, quazepam, flurazepam, zopiclone and clorazepate. An example of an imidazopyridine includes zolpidem and zolpidem tartarate. Examples of antidepressants include amityiptyline and doxepin.

In particular, zolpidem may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver zolpidem to a patient in need thereof. In particular, zolpidem can be formulated with the present invention in doses ranging from about 5.0 to 30.0 mg daily, the preferred range being from about 5.0 to 10.0 mg daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non- limiting and it will be understood that other psychotrpoics may be used with the present inventive subject matter.

Still yet another preferred active material used in the composition of the present inventive matter is a gastrointestinal therapeutic. Gastrointestinal therapeutics are used to treat gastritis, nausea and vomiting, gastroesophegal reflux disease, colitis, Crohn' s disease and diarrhea. Classes of drugs include proton pump inhibitors, histamine H₂ receptor antagonists, terpene analogs, and NSAID'S.

For the treatment of gastritis, drugs such as omeprazole, lansoprazole, ranitidine HCl, famotidine, nizatidine, teprenone, cimetidine, rabeprazole sodium, and sulpiride can be used in the compositions of the present inventive subject matter.

For the treatment of nausea and vomiting, drugs such as ondansetron HCl, granisetron HCl, dolasetron mesylate, and tropisetron may be used. In particular, omeprazole may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver omeprazole to a patient in need thereof. In particular, omeprazole can be formulated with the present invention in doses ranging from about 10.0 to 60.0 mg daily, the preferred range being from about 15.0 to 25.0 mg daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non- limiting and it will be understood that other gastrointestinal therapeutics may be used with the present inventive subject matter.

Another preferred active material used in the compositions of the present invention include cardiovascular therapeutics. Cardiovascular therapeutics treat hypertension, angina, myocardial infarction, congestive heart failure, acute coronary syndrome, edema, ventricular tachycardia, hyperaldosteronism, ventricular arrhythmia, cardiac insufficiency, atrial fibrillation, arterial occlusion, cardiac decompensation, and microcirculation activation. A related class of cardiovascular therapeutics are cholesterol reducers such as 3-hydroxy-3-methylglutaryl coenzymeA ("HMG-CoA") reductase inhibitors. HMG-CoA inhibitors work by blocking an enzyme used to make cholesterol. Blocking cholesterol thereby treats hypercholesterolemia which is a significant cause of cardiovascular disease. For the treatment of hypercholesterolemia, drugs such as simvastin, atorvastatin calcium, pravastatin sodium, pravastatin, lovastatin, fluvastatin sodium, cerivastatin sodium can be used in the compositions of the present inventive subject matter.

For the treatment of hypertension, drugs such as amlodipine besylate, losartan potassium, lisinopril, felodipine, benazepril HCl, ramipril, irbesartan, verapamil HCl, bisoprolol fumarate and hydrochlorothiazide, amlodipine and benazepril HCl, clonidine, candesartan, cilexetil, diltiazem, nicardipine, imidapril, trandolapril, eprosartan mesylate, nilvadipine, verapamil HCl, temocapril, prazosin HCl, isradipine, cilazapril, celiprolol, bisoprolol, betazolol HCl, ramipril, nisoldipine, lisinopril, trandolapril, and nisoldipine can be used in the compositions of the present inventive subject matter.

For the treatment of congestive heart failure, drugs such as dioxin, carvedilol, spironolactone, trandolapril, and bisoprolol can be used in the compositions of the present inventive subject matter.

In particular, simvastin may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver simvastin to a patient in need thereof. In particular, simvastin can be formulated with the present invention in doses ranging from about 5.0 to 80 mg daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non-limiting and it will be understood that drugs from the disclosed classes may also be used with the present inventive subject matter.

Still another preferred active material used in the composition of the present invention is a therapeutic useful for treating allergic rhinitis. The classes of compounds useful for treating allergic rhinitis include alkylamines, ethanolamines, ethylenediamines, piperazines, phenothiazine, piperdines, and nonsedating compounds.

Among the non-sedating compounds that can be used in the present invention are loratadine, fexofenadine HCl, certirizine HCl, and astemizole. Other drugs which can also be used are fluticasone propionate, m metasone furoate, epinastine, beclomethasone dipropionate, triamcinolone acetonide, budesonide, and azelastine.

In particular, loratadine may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver loratadine to a patient in need thereof. In particular, loratadine can be formulated with the present invention in doses ranging from about 5.0 to 15 mg daily, with 15mg daily being the preferred dosage. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non-limiting and it will be understood that other allergic rhinitis therapeutics may be used with the present inventive subject matter.

Still yet another preferred active material used in the composition of the present invention is a therapeutic useful for treating osteoarthritis or rheumatoid arthritis. Rheumatoid arthritis is defined as non-specific, symmetrical inflammation of the peripheral joints, potentially resulting in progressive destruction of articular and periarticular structures. Osteoarthritis is characterized by loss of articular cartilage and hypertrophy of bone. Although osteoarthritis is a degenerative bone disease, symptoms associated with rheumatoid arthritis such as inflammation of the joints occur in a patient diagnosed with osteoarthritis. Accordingly, therapeutics treating rheumatoid arthritis can also be administered to an osteoarthritic patient.

Classes of drugs indicated for osteoarthritis and rheumatoid arthritis include cycloxygenase-2 inhibitors, NSAID'S, biologic response modifiers, pyrimidine synthesis inhibitors and hyaluronic acid. Specific examples of osteoarthritis and rheumatoid arthritis therapeutics include celecoxib, diclofenac sodium, rofecoxib, nabumetone, diclofenac sodium and misoprostol, oxaprozin, meloxicam, piroxicam, etodolac, naproxen, hylan G-F 20, leflunomide, tenoxicam, and naproxen sodium.

In particular, celecoxib may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver celecoxib to a patient in need thereof. In particular, celecoxib can be formulated with the present invention in doses ranging from about 150 to 250 mg daily, with 200mg daily being the preferred dosage. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non-limiting and it will be understood that other osteoarthritis and rheumatoid arthritis therapeutics from the disclosed classes may also be used with the present inventive subject matter.

Another preferred active material used in the composition of the present invention is a therapeutic useful for treating benign prostatic hypertrophy. Benign prostatic hypertrophy is defined as an adenomatous hyperplasia of the periurethral part of the prostrate gland.

Classes of drug useful for the treatment of benign prostatic hypertrophy include alpha blockers, alpha-1 selective adrenoceptor blocking agents and 5-reductase inhibitors. Specific examples of benign prostatic hypertrophy therapeutics include doxazosin mesylate, terazosin HCl, tamsulosin, finasteride, ta sulosin HCl, ethinyl estradiol and levonorgestrel . In particular, doxazosin mesylate may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver doxazosin mesylate to a patient in need thereof. In particular, doxazosin mesylate can be formulated with the present invention in doses ranging from about 1 to 16 mg daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non-limiting and it will be understood that other benign prostatic hypertrophy therapeutics from the disclosed classes may also be used with the present inventive subject matter.

Yet another preferred active material used in the composition of the present invention is a drug indicated for the treatment of fungal infections. Classes of drugs indicated for the treatment of fungal infections include synthetic triazole, ergosterol inhibitor, and polyene antifungal. Specific examples of drugs indicated for the treatment of fungal infections are itraconazole, ketoconazole, and amphotericin B.

In particular, itraconazole may be incorporated .into the rapid-melt semi-solid compositions of the present invention to effectively deliver itraconazole to a patient in need thereof. In particular, itraconazole can be formulated with the present invention in doses ranging from about 1.0 to 400 mg daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non-limiting and it will be understood that other anti- fungals from the disclosed classes may also be used with the present inventive subject matter.

Still yet another preferred active material used in the composition of the present invention is a anti- convulsant. Anti-convulsants are drugs that prevent or relieve convulsions wherein the convulsions are due to epilepsy, seizure disorders, partial seizure disorders or Huntington' s disease. Classes of drugs useful for treating these conditions include gamma-aminobutyric analogs, phenyltriazine, antiepileptic agents, benzodiazepines, polysynaptic response inhibitors, sulfamate-substituted monosaccharides, gamma-amino butyric acid uptake inhibitors and benzamides. Specific examples include carbamazepine, topiramate, and tigabine HCl.

In particular, carbamazepine may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver carbamazepine to a patient in need thereof. In particular, carbamazepine can be formulated with the present invention in doses ranging from about 100 to 1600 mg daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non-limiting and it will be understood that other anti- convulsants from the disclosed classes may also be used with the present inventive subject matter. Another preferred active material used in the composition of the present invention is an anti-herpetic. Anti-herpetics are used to treat infections from the varicella-zoster virus. Classes of drugs useful for treating herpes include synthetic purine nucleoside analogs, nucleoside analogs, and antiviral agents. Specific examples include acyclovir, valacyclovir HCL and famcyclovir .

In particular, acyclovir may be incorporated into the rapid-melt semi-solid compositions of the present invention to effectively deliver acyclovir to a patient in need thereof. In particular, acyclovir can be formulated with the present invention in doses ranging from about 200 to 800 mg daily. One of ordinary skill in the art will be able to determine the proper dosage for the remaining disclosed drugs. Moreover, all the examples are non- limiting and it will be understood that other anti- herpetics from the disclosed classes may also be used with the present inventive subject matter. Yet another active material used in the compositions of the present invention are anti-diarrheal therapeutics. Anti-diarrheal therapeutics treat the condition of diarrhea whether it is symptomatic of the disorder itself wherein diarrhea is a condition that occurs when a mammal has a low amount of stool in a bowel movement. Diarrhea results mainly from excess fecal water in the bowel of the mammal. Specific examples of anti-diarrheal therapeutics include loperamide HCl, diphenoxylate, codeine phosphate, camphorated opium tincture.

The present inventive subject matter contemplates incorporating loperamide hydrochloride into the rapid-melt semi-solid compositions as an effective means of delivering the active to a patient in need thereof. The amount of loperamide hydrochloride needed in the will depend on the intended recipient of the active ingredient. The normal dosage amount for a human adult is initially 4 milligrams, with a follow-up dosage of 2 milligrams after each unformed stool. For children, the normal dosage will depend on the age and weight of the child, pursuant to the guidelines set forth by the child's physician. The use of the present inventive subject matter to deliver loperamide hydrochloride to a child is especially effective since the rapid-melt, semi-solid compositions of the present inventive subject matter do not require any chewing by the patient. As has been previously explained, the melting feature of the novel compositions makes the compositions ideal for uses in pediatric and geriatric care, since small children and aged individuals often have difficulty chewing items. With this intended use in mind, the compositions may be specially formulated for pediatric and geriatric patients. The unique properties will aid in drug compliance by such patients as the drugs may be administered in a way that will not require chewing by the patient .

Further preferred nutritional active materials useful in the present inventive subject matter include, without limitation, calcium-containing materials such as calcium carbonate, vitamins, minerals, herbals, spices and mixtures thereof .

Examples of vitamins that are available as active ingredients include, without limitation, vitamin A (retinol) , vitamin D (cholecalciferol) , vitamin E group ( - tocopherol and other tocopherols) , vitamin K group ( phylloquinones and menaquinones) , thiamine (vitamin B_x) , riboflavin (vitamin B₂) , niacin, vitamin B₆ group, folic acid, vitamin B₁₂ (cobalamins) , biotin, vitamin C (ascorbic acid), and mixtures thereof. The amount of vitamin or vitamins present in the final encapsulated product of the present inventive subject matter is dependent on the particular vitamin and is generally the United States' Department of Agriculture Recommended Daily Allowances (USRDA) for that vitamin. For example, if vitamin C is the active ingredient and the encapsulated product is being used in a confectionery or chewing gum targeting adults, the amount of vitamin C in the encapsulated product would be 60 milligrams, which is the USRDA of vitamin C for adults.

Examples of minerals that are available as active ingredients include, without limitation, calcium, magnesium, phosphorus, iron, zinc, iodine, selenium, potassium, copper, manganese, molybdenum and mixtures thereof. As is the case with vitamins, the amount of mineral or minerals present in the final encapsulated product of the present inventive subject matter is dependent on the particular mineral and is generally the USRDA for that mineral. For example, if iodine is the active ingredient and the encapsulated product is being used in a confectionery or chewing gum targeting adults, the amount of iodine in the encapsulated product would be 150 micrograms, which is the USRDA of iodine for adults.

Examples of herbals that are available as active ingredients include, without limitation, echinacea, peppermint, licorice, goldenseal, panax pseudoginseng, grapeseed extract, bilberry, kava, ginko biloba, panax quinquefolium, Siberian ginseng, St. John's wort, bromelian, guglupids, hawthorn, garlic, ginger, angelica species, dandelion, goldenseal, and mixtures thereof. Further, examples of spices that are available as active ingredients include, without limitation, mustard, dillweed, cinnamon, garlic, black pepper, onion, sage, oregano, basil, cream of tartar, targon, cayenne pepper, red pepper, and mixtures thereof. This list of herbals and spices is for exemplary purposes and is not meant to be construed as limiting the inventive subject matter thereto. Many of the active material listed above have unpalatable tastes. Taste-masking of compositions with those unpalatable active materials is well-known in the art. The use of flavors and sweeteners to mask the unpalatability of the active materials is also well-known.

Thus, other materials which can be incorporated into the rapid-melt, semi-solid molded composition of the present inventive subject matter include flavors, colors and sweeteners. A distinct feature of the inventive rapid- melt, semi-solid compositions is that they exhibit excellent taste characteristics. Importantly, it is possible to incorporate high levels of flavors, sweeteners and other taste-masking agents, making the compositions more palatable when undesirable tastes accompany the active materials.

Flavors may be chosen from natural and synthetic flavor liquids. Flavors useful in the present inventive compositions include, without limitation, volatile oils, synthetic flavor oils, flavoring aromatics, oils, liquids, oleoresins or extracts derived from plants, leaves, flowers, fruits, stems and combinations thereof. A non-limiting list of examples include citrus oils such as lemon, orange, grape, lime and grapefruit and fruit essences including apple, pear, peach, grape, strawberry, raspberry, cherry, plum, pineapple, apricot or other fruit flavors . Other useful flavorings include aldehydes and esters such as benzaldehyde (cherry, almond), citral, i.e., alphacitral (lemon, lime), neral, i.e., betal-citral (lemon, lime) , decanal (orange, lemon) , aldehyde C-8 (citrus fruits), aldehyde C-9 (citrus fruits), aldehyde

C-12 (citrus fruits) , tolyl aldehyde (cherry, almond) , 2, 6-dimethyloctanal (green fruit), and 2-dodecenal (citrus, mandarin), and mixtures thereof.

Further examples of flavors useful in the inventive compositions include, without limitation, beef flavorings, chicken flavorings, rice flavorings, lamb flavorings, pork flavorings, seafood flavorings, and mixtures thereof.

The sweeteners may be chosen from the following non-limiting list: flucose (corn syrup), dextrose, invert sugar, fructose, and mixtures thereof; saccharin and its various salts such as the sodium salt; dipeptide sweeteners such as aspartame; dihydrochalcone compounds, glycyrrhizin; Stevia rebaudiana (Stevioside) ; chloro derivatives of sucrose such as sucralose; sugar alcohols such as sorbitol, mannitol, zylitol, and the like. Also contemplated are hydrogenated starch hydrolysates and synthetic sweetener 3, 6-dihydro-6-methyl-l-l-l,2, 3-oxathiazin-4- one-2, 2-dioxide, particularly the potassium salt (acesulfame-K) and sodium and calcium salts thereof. Other sweeteners may also be used.

The rapid-melt, semi-solid compositions of the present inventive subject matter may also be coated in order to facilitate handling of the compositions. Coatings well- known in the art are useful for keeping the compositions from melting prior to being administered to a patient in need of an active material. By coating the compositions, the composition will maintain its semi-solid state while being handled and will melt when inserted into a patient's mouth.

The present inventive subject matter also contemplates a method of preparing a rapid-melt, semi-solid molded composition. It should be recognized that the composition may be prepared by a variety of methods well-known by those of ordinary skill in the art. Such processes may be used on a batch or continuous process format and would involve melting the binders and uniformly blending them for suitable periods of time prior to adding the salivating agent. Once these two components have been blended together, the further components may be added either together or sequentially until a uniform mixture is obtained. It should be recognized that the resulting mixture should be in a semi-solid state that may be poured into a mold, cast into preformed shapes, or stamped into the final products. Clearly, other tableting techniques are contemplated to be used herein. A particularly preferred method involves the steps of: melting at least one binder having a melting point about 25 to 45°C with a salivating agent to form a mixture; mixing an active material with the lipid material to form an active mixture; mixing a diluent/bulking material with said active material to form a final mixture; and molding the final mixture into the semi-solid molded composition. The method of the present inventive subject matter also contemplates adding other materials to the final mixture prior to molding into the semi-solid molded composition. Other materials which may be added to the final mixture prior to molding include, without limitation, flavors, colors, sweeteners, and mixtures thereof.

The amount of binder melted with the salivating agent is from about 10% to about 70% by weight of the final composition. Preferably, the amount of binder is from about 10% to about 50% by weight. More preferably the binder is present from about 15% to about 30% by weight. Likewise, the amount of salivating agent melted in the first step of the method is from about 0.2% to about 0.5% by weight of the final composition. Preferably, the amount of salivating agent is from about 0.3% to 0.4% by weight of the composition.

The rapid-melt, semi-solid compositions of the present inventive subject matter produced by the above methods have increased product integrity and stability. The compositions are "storage stable", meaning that the compositions are stable in the absence of special handling procedures. The inventive compositions are stable both prior to packaging and after packaging. Importantly, the inventive compositions maintain their stability and integrity without refrigeration and without humidity controls being implemented during handling, packaging and storing of the products. Additionally, since the compositions exhibit increased integrity and stability, the compositions can be used in most of the current economical packages suitable for a global environment. Further, high temperatures are not needed when processing the inventive compositions. The only heat that needs to be used during processing is to melt the binder prior to mixing with the other elements.

The following examples are illustrative of preferred embodiments of the invention and are not to be construed as limiting the invention thereto. All percentages are given in weight percent, unless otherwise noted and equal a total of 100%.

EXAMPLES

EXAMPLE #1: PREPARATION OF 25% CALCIUM CARBONATE

SEMI-SOLID MOLDED COMPOSITION

60.00 grams of cocoa butter was melted with 0.80 grams of lecithin and 2.00 grams of sorbitan monostearate. 0.2 grams of yellow #5 was added to the above mixture after the ingredients had completely melted. To this mixture was added 50.00 grams of calcium carbonate. The mixture was then mixed for approximately three minutes. Following the mixing period, 85.80 grams of sugar and 0.80 grams of liquid peppermint flavor was added to the mixture to form 200.00 grams of the final mixture. The final mixture was mixed for approximately 5 minutes, until all of the ingredients had been thoroughly mixed.

The final mixture was molded into the final product and allowed to set-up. The resultant product contained 25% calcium carbonate.

EXAMPLE #2: PREPARATION OF 31.50% CALCIUM CARBONATE

SEMI-SOLID MOLDED COMPOSITION

30.00 grams of cocoa butter was melted with 0.6 grams of lecithin and 2.00 grams of sorbitan monstearate. 0.60 grams of red #4 was added after the ingredients had completely melted. 0.20 grams of polyoxyethylene sorbitol monostearate was then added to the mixture and the mixture was mixed for 3 minutes. To this mixture was added 31.50 grams of calcium carbonate and the mixture was further mixed for another 3 minutes. Following the mixing period, 51.30 grams of xylitol powder was added to the mixture along with 0.80 grams of cherry flavor and 0.60 grams of vanilla extract, forming 200.00 grams of final mixture. The final mixture was mixed for approximately 5 minutes, until all of the ingredients had been thoroughly mixed. The final mixture was molded into the final product and allowed to set-up. The resultant product contained 31.50% calcium carbonate.

EXAMPLE #3: PREPARATION OF 31.50% CALCIUM CARBONATE

SEMI-SOLID MOLDED COMPOSITION

38.00 grams of cocoa butter was melted with 0.68 grams of lecithin and 2.00 grams of sorbitan monstearate. 0.16 grams of red #40 was added after the ingredients had completely melted. The mixture was mixed for 8 minutes at 120°F. 0.40 grams of polyoxyethylene sorbitan ester, 0.40 grams of polyglycerol ester, and 4.00 grams of glycerine (99.7%) were added to the mixture and the mixture was further mixed for 2 minutes at 110°. To this mixture was added 63.00 grams of calcium carbonate and the mixture was further mixed for another 4 minutes. Following the mixing period, 4.00 grams of polyethylene glycol, 85.46 grams of sugar lOx, 0.18 grams of aspartame and 0.12 grams of acesulfame K were added to the mixture and the resultant mixture was mixed for 4 minutes at 90-110°F. The mixture was removed rom the heat and 0.40 grams of vanilla flavoring and 1.20 grams of strawberry flavoring was added to the mixture, resulting in 200.00 grams of mixture. The final mixture was mixed for approximately 5 minutes, until all of the ingredients had been thoroughly mixed.

The final mixture was molded into the final product and allowed to set-up. The resultant product contained 31.50% calcium carbonate.

EXAMPLE #4: PREPARATION OF 31.50% CALCIUM CARBONATE SEMI-SOLID MOLDED COMPOSITION

38.00 grams of cocoa butter, 0.80 grams of lecithin, 0.40 grams of polyoxyethylene sorbitan ester, 2.00 grams of sorbitan monostearate, 6.00 grams of polyethylene glycol, 0.16 grams of red #40, and 4.00 grams of glycerine were mixed at 130°F for 8 minutes. 63.00 grams of calcium carbonate was added and the mixture was continuously mixed until the calcium carbonate had completely dissolved at 130°F. 84.04 grams of xylitol and 1.6 grams of strawberry flavor were added, resulting in 200.00 grams of the final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed.

EXAMPLE #5: PREPARATION OF 31.50% CALCIUM CARBONATE

SEMT-SOLTD MOLDED COMPOSITION

38.00 grams of cocoa butter, 0.68 grams of lecithin,

2.00 grams of sorbitan monostearate, and 0.16 grams of red #40 were mixed at 100°F for 8 minutes. 4.00 grams of polyethylene glycol and 0.40 grams of polyoxyethylene sorbitan ester was added to the mixture. The mixture was mixed for 2 minutes at 110°F for 2 minutes. 0.40 grams of polyglycerol ester and 63.00 grams of calcium carbonate were then added and the mixture was mixed for 4 minutes at 90°F. 0.18 grams of aspartame, 0.12 grams of acesulfame K and 89.66 grams of sugar lOx were added and the mixture was mixed for 8 minutes at 90 °F. The mixture was removed from the heat and 1.00 gram of strawberry flavoring and 0.40 grams of vanilla flavorings were added, resulting in 200.00 grams of final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed.

EXAMPLE #6: PREPARATION OF 31.50% CALCIUM CARBONATE

SEMI-SOLID MOLDED COMPOSITION

30.0 grams of cocoa butter were mixed with 0.6 grams of lecithin. The mixture was heated to 90°F for 3 minutes. 2.0 grams of sorbitan monostearate, 0.2 grams of polyoxyethylenee sorbitan ester, and 4.0 grams of polyethylene glycol were added to the mixture. The mixture was mixed for 2 minutes at 110°F. 63.0 grams of calcium carbonate was added and the mixture was thoroughly mixed for 10 minutes. 49.1 grams of sugar lOx, 0.3 grams of aspartame and 49.1 grams of mannitol were added and the mixture was mixed until all ingredients were thoroughly mixed. 0.1 grams of red #40, 0.6 grams of vanilla flavoring and 1.0 grams of strawberry flavoring were added to the mixture, resulting in 200.0 grams of^' final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed. The final mixture was molded into the final product and allowed to set-up. The resultant product contained 31.50% calcium carbonate.

EXAMPLE #7: PREPARATION OF 31.50% CALCIUM CARBONATE SEMI-SOLTD MOLDED COMPOSITION

30.0 grams of cocoa butter were mixed with 0 . 6 grams of lecithin. The mixture was heated to 90°F for 3 minutes. 2.0 grams of sorbitan monostearate, 0.2 grams of polyoxyethylenee sorbitan ester, and 4.0 grams of polyethylene glycol were added to the mixture. The mixture was mixed for 2 minutes at 110°F. 63.0 grams of calcium carbonate was added and the mixture was thoroughly mixed for 10 minutes. 98.1 grams of xylitol and 0.3 grams of aspartame were added and the mixture was mixed until all ingredients were thoroughly mixed. 0.2 grams of red #40, 0.6 grams of vanilla flavoring and 1.0 grams of strawberry flavoring were added to the mixture, resulting in 200.0 grams of final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed. The final mixture was molded into the final product and allowed to set-up. The resultant product contained 31.50% calcium carbonate.

EXAMPLE #8: PREPARATION OF 13.47% ACETAMINOPHEN SEMI-SOLTD MOLDED COMPOSITION

38.00 grams of cocoa butter, 0.80 grams of lecithin and 2.00 grams of sorbitan monostearate were melted. 6.00 grams of polyethylene glycol, 4.00 grams of glycerine and 0.40 grams of polyoxyethylene sorbitan ester were added to the melt. The mixture was mixed for 6 minutes at 130°F, then for another 2 minutes at 120°F. 120.80 grams of xylitol were added to the mixture and mixed for 5 minutes at 120°F. 26.94 grams of microencapsulated acetaminophen (coated, 90% acetaminophen) were added to the mixture and the mixture was mixed for 7 minutes. 0.16 grams of red #40, 0.40 grams of vanilla flavoring and 0.80 grams of strawberry flavoring were added to the mixture, resulting in 200.30 grams of final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed.

The final mixture was molded into the final product and allowed to set-up. The resultant product contained 13.47% acetaminophen.

EXAMPLE #9: PREPARATION OF 13.57% ACETAMINOPHEN SEMI-SOLID MOLDED COMPOSITION

38.00 grams of cocoa butter, 0.68 grams of lecithin and 2.00 grams of sorbitan monostearate were melted. 4.00 grams of polyethylene glycol, 4.00 grams of glycerine and 0.40 grams of polyoxyethylene sorbitan ester were added to the melt. The mixture was mixed for 6 minutes at 130°F, then for another 2 minutes at 120°F. 122.06 grams of sugar lOx, 0.18 grams of aspartame and 0.12 grams of acesulfame K were added to the mixture and mixed for 5 minutes at 120°F. 27.14 grams of microencapsulated acetaminophen (coated, 90% acetaminophen) were added to the mixture and the mixture was mixed for 7 minutes. 0.16 grams of red #40, 0.40 grams of vanilla flavoring and 0.80 grams of strawberry flavoring were added to the mixture, resulting in 199.94 grams of final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed.

The final mixture was molded into the final product and allowed to set-up. The resultant product contained 13.57% acetaminophen. EXAMPLE #10: PREPARATION OF 13.57% ACETAMINOPHEN

SEMI-SOLID MOLDED COMPOSITION 38.00 grams of cocoa butter, 0.68 grams of lecithin and 2.00 grams of sorbitan monostearate were melted. 4.00 grams of polyethylene glycol and 0.40 grams of polyoxyethylene sorbitan ester were added to the melt. The mixture was mixed for 8 minutes at 120°F, then for another 2 minutes at 110°F. 125.94 grams of xylitol, 0.18 grams of aspartame and 0.12 grams of acesulfame K were added to the mixture and mixed for 5 minutes at 120°F. 27.14 grams of microencapsulated acetaminophen (coated, 90% acetaminophen) were added to the mixture and the mixture was mixed for 7 minutes. 0.16 grams of red #40, 0.40 grams of vanilla flavoring and 0.80 grams of strawberry flavoring were added to the mixture, resulting in 199.82 grams of final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed.

The final mixture was molded into the final product and allowed to set-up. The resultant product contained 13.57% acetaminophen.

EXAMPLE #11: PREPARATION OF 13.57% ACETAMINOPHEN

SEMI-SOLID MOLDED COMPOSITION 190.00 grams of cocoa butter, 3.40 grams of lecithin and 10.00 grams of sorbitan monostearate were melted. 20.00 grams of polyethylene glycol and 2.00 grams of polyoxyethylene sorbitan ester were added to the melt. The mixture was mixed for 8 minutes at 120°F, then for another 2 minutes at 110°F. 629.70 grams of xylitol, 0.9 grams of aspartame and 0.6 grams of acesulfame K were added to the mixture and mixed for 5 minutes at 120°F. 135.70 grams of microencapsulated acetaminophen (coated, 90% acetaminophen) were added to the mixture and the mixture was mixed for 7 minutes. 0.8 grams of red #40, 2.00 grams of vanilla flavoring and 4.00 grams of strawberry flavoring were added to the mixture, resulting in 999.10 grams of final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed.

EXAMPLE #12: PREPARATION OF 2.17% ACETAMINOPHEN

SEMI-SOLID MOLDED COMPOSITION 38.00 grams of cocoa butter, 0.68 grams of lecithin and 2.00 grams of sorbitan monostearate were melted. 4.00 grams of polyethylene glycol, 0.40 grams of polyglycerol ester, 4.00 grams of glycerine and 0.40 grams of polyoxyethylene sorbitan ester were added to the melt. The mixture was mixed for 8 minutes at 120°F, then for another 2 minutes at 110°F. 143.52 grams of sugar lOx, 0.18 grams of aspartame and 0.12 grams of acesulfame K were added to the mixture and mixed for 5 minutes at 120°F. 4.34 grams of microencapsulated acetaminophen (coated, 90% acetaminophen) were added to the mixture and the mixture was mixed for 7 minutes. 0.16 grams of red #40, 0.40 grams of vanilla flavoring and 1.20 grams of strawberry flavoring were added to the mixture, resulting in 199.40 grams of final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed.

The final mixture was molded into the final product and allowed to set-up. The resultant product contained 2.17% acetaminophen.

EXAMPLE #13: PREPARATION OF 4.34% ACETAMINOPHEN

SEMI-SOLID MOLDED COMPOSITION 38.00 grams of cocoa butter, 0.68 grams of lecithin and 2.00 grams of sorbitan monostearate were melted. 4.00 grams of polyethylene glycol and 0.40 grams of polyoxyethylene sorbitan ester were added to the melt. The mixture was mixed for 8 minutes at 120°F, then for another 2 minutes at 110°F. 144.38 grams of sugar lOx, 0.18 grams of aspartame and 0.12 grams of acesulfame K were added to the mixture and mixed for 5 minutes at 120°F. 8.69 grams of microencapsulated acetaminophen (coated, 90% acetaminophen) were added to the mixture and the mixture was mixed for 7 minutes. 0.16 grams of red #40, 0.40 grams of vanilla flavoring and 1.00 grams of strawberry flavoring were added to the mixture, resulting in 200.01 grams of final mixture. The mixture was mixed for 10 minutes, until all of the ingredients had been thoroughly mixed.

The final mixture was molded into the final product and allowed to set-up. The resultant product contained 4.34% acetaminophen.

EXAMPLE #14: PREPARATION OF 31.50% CALCIUM CARBONATE

SEMI-SOLID MOLDED COMPOSITION 19.00 grams of cocoa butter, 0.34 grams of lecithin,.

1.00 grams of sorbitan monostearate, and 0.08 grams of red #40 are mixed at 100°F for 8 minutes. 2.00 grams of polyethylene glycol, 2.00 grams of glycerine and 0.20 grams of polyoxyethylene sorbitan ester is added to the mixture. The mixture is mixed for 2 minutes at 110°F for 2 minutes. 0.20 grams of polyglycerol ester and 31.5 grams of calcium carbonate are then . added and the mixture is mixed for 4 minutes at 90°F. 0.09 grams of aspartame, 0.06 grams of acesulfame K and 42.73 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.60 gram of strawberry flavoring and 0.20 grams of vanilla flavorings are added, resulting in 100.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

The final mixture is molded into the final product and allowed to set-up. The resultant product contains 31.50% calcium carbonate.

EXAMPLE #15: PREPARATION OF 31.50% CALCIUM CARBONATE SEMI-SOLID MOLDED COMPOSITION

15.00 grams of cocoa butter, 1.00 grams of sorbitan monostearate, and 0.08 grams of red #40 are mixed at 100°F for 8 minutes. 0.80 grams of polyoxyethylene sorbitan ester is added to the mixture. The mixture is mixed for 2 minutes at 110°F for 2 minutes. 31.5 grams of calcium carbonate are then added and the mixture is mixed for 4 minutes at 90°F. 51.00 grams of xylitol are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.40 gram of strawberry flavoring and 0.22 grams of vanilla flavorings are added, resulting in 100.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

EXAMPLE #16: PREPARATION OF 31.50% CALCIUM CARBONATE

AND 13.57% ACETAMINOPHEN SEMT-SOLID MOLDED COMPOSITION

15.00 grams of cocoa butter, 0.40 grams of lecithin, and 1.00 grams of sorbitan monostearate, are mixed at 100°F for 8 minutes. 0.20 grams of polyoxyethylene sorbitan ester is added to the mixture. The mixture is mixed for 2 minutes at 110°F for 2 minutes. 0.20 grams of polyglycerol ester and 31.50 grams of calcium carbonate are then added and the mixture is mixed for 4 minutes at 90°F. 0.15 grams of aspartame, 13.57 grams of coated acetaminophen microcaps (coated, 90% acetaminophen) and 37.18 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90 °F. The mixture is removed from the heat and 0.80 grams of strawberry flavoring are added, resulting in 100.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

The final mixture is molded into the final product and allowed to set-up. The resultant product contains 31.50% calcium carbonate and 13.57% acetaminophen.

EXAMPLE #17: PREPARATION OF 13.57% ACETAMINOPHEN SEMI-SOLID MOLDED COMPOSITION 19.00 grams of cocoa butter, 0.34 grams of lecithin,

1.00 grams of sorbitan monostearate, and 0.08 grams of red #40 are mixed at 100°F for 8 minutes. 2.00 grams of polyethylene glycol are added to the mixture. The mixture is mixed for 2 minutes at 110°F for 2 minutes. 13.57 grams of coated acetaminophen microcaps (coated, 90% acetaminophen) are then added and the mixture is mixed for 4 minutes at 90°F. 0.15 grams of aspartame and 63.26 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.40 gram of strawberry flavoring and 0.20 grams of vanilla flavorings are added, resulting in 100.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

The final mixture is molded into the final product and allowed to set-up. The resultant product contains 13.57% acetaminophen.

EXAMPLE #18: PREPARATION OF 4.34% ACETAMINOPHEN

SEMI-SOLID MOLDED COMPOSITION 19.00 grams of cocoa butter, 0.34 grams of lecithin, 1.00 grams of sorbitan monostearate, and 0.08 grams of red #40 are mixed at 100°F for 8 minutes. 2.00 grams of polyethylene glycol is added to the mixture. The mixture is mixed for 2 minutes at 110°F for 2 minutes. 0.20 grams of polyglycerol ester and 4.34 grams of coated acetaminophen microcaps (coated, 90% acetaminophen) are then added and the mixture is mixed for 4 minutes at 90°F. 0.15 grams of aspartame and 72.19 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.50 grams of strawberry flavoring and 0.20 grams of vanilla flavorings are added, resulting in 100.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

The final mixture is molded into the final product and allowed to set-up. The resultant product contains 4.34% acetaminophen.

EXAMPLE #19: PREPARATION OF 10.50% IBUPROFEN

SEMI-SOLID MOLDED COMPOSITION 19.00 grams of cocoa butter, 0.34 grams of lecithin, 1.00 grams of sorbitan monostearate, and 0.08 grams of red #40 are mixed at 100°F for 8 minutes. 2.00 grams of polyethylene glycol, 2.00 grams of glycerine and 0.20 grams of polyoxyethylene sorbitan ester is added to the mixture. The mixture is mixed for 2 minutes at 110°F for 2 minutes. 0.20 grams of polyglycerol ester and 10.50 grams of coated ibuprofen microcaps (coated, 50% ibuprofen) are then added and the mixture is mixed for 4 minutes at 90°F. 0.15 grams of aspartame and 62.13 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.60 gram of strawberry flavoring, 0.20 grams of vanilla flavoring and 1.60 grams of fruit flavoring are added, resulting in 100.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed. The final mixture is molded into the final product and allowed to set-up. The resultant product contains 10.50% ibuprofen. EXAMPLE #20: PREPARATION OF 10.85mg DOSE LOPERAMIDE

HYDROCHLORIDE SEMI-SOLID MOLDED COMPOSITION

The inventive subject matter containing loperamide hydrochloride can be made by the following process. 72.00 grams of cocoa butter, 2.00 grams of lecithin, 4.40 grams of sorbitan monostearate, and 24.00 grams of kaomel are mixed at 100°F for 8 minutes. 12.00 grams of MCT oil and 0.80 grams of Polysorbate 80 are added to the mixture. The mixture is mixed for 2 minutes at 110°F. 0.20 grams of sodium laurel sulfate and 2.17 grams of loperamide hydrochloride are then added and the mixture is mixed for 4 minutes at 90°F. 1.20 grams of aspartame and 263.60 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.10 grams of light green coloring (0.01 grams of 0.0025% Blue #1 and 0.09 grams of 0.0225% Yellow #5), 1.80 grams of vanilla flavoring, 0.40 grams of flavor enhancer, 2.00 grams of natural cream powder and 13.32 grams of instant release peppermint are added, resulting in 400.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

The final mixture is molded into the final product and allowed to set-up. The final product is then cut into 200 evenly-sized pieces. Each piece of product contains 10.85 mg loperamide hydrochloride. EXAMPLE #21: PREPARATION OF lOmg DOSE OMEPRAZOLE

SEMI-SOLID MOLDED COMPOSITION

The inventive subject matter containing omeprazole can be made by the following process. 70.00 grams of cocoa butter, 2.00 grams of lecithin, 4.40 grams of sorbitan monostearate, and 24.00 grams of kaomel are mixed at 100°F for 8 minutes. 12.00 grams of MCT oil and 0.80 grams of Polysorbate 80 are added to the mixture. The mixture is mixed for 2 minutes at 110°F. 0.20 grams of sodium laurel sulfate and 2.00 grams of omeprazole are then added and the mixture is mixed for 4 minutes at 90°F. 1.20 grams of aspartame and 263.60 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.10 grams of light green coloring (0.01 grams of 0.0025% Blue #1 and 0.09 grams of 0.0225% Yellow #5), 1.80 grams of vanilla flavoring, 0.40 grams of flavor enhancer, 2.00 grams of natural cream powder and 13.32 grams of instant release peppermint are added, resulting in 400.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

The final mixture is molded into the final product and allowed to set-up. The final product is then cut into 200 evenly-sized pieces. Each piece of product contains lOmg omeprazole . EXAMPLE #22: PREPARATION OF lOmg DOSE SUMATRIPTAN

SUCCINATE SEMI-SOLID MOLDED COMPOSITION

The inventive subject matter containing sumatriptan succinate can be made by the following process. 70.00 grams of cocoa butter, 2.00 grams of lecithin, 4.40 grams of sorbitan monostearate, and 24.00 grams of kaomel are mixed at 100°F for 8 minutes. 12.00 grams of MCT oil and 0.80 grams of Polysorbate 80 are added to the mixture. The mixture is mixed for 2 minutes at 110°F. 0.20 grams of sodium laurel sulfate and 2.00 grams of sumatriptan succinate are then added and the mixture is mixed for 4 minutes at 90°F. 1.20 grams of aspartame and 263.60 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.10 grams of light green coloring (0.01 grams of 0.0025% Blue #1 and 0.09 grams of 0.0225% Yellow #5), 1.80 grams of vanilla flavoring, 0.40 grams of flavor enhancer, 2.00 grams of natural cream powder and 13.32 grams of instant release peppermint are added, resulting in 400.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

The final mixture is molded into the final product and allowed to set-up. The final product is then cut into 200 evenly-sized pieces. Each piece of product contains lOmg sumatriptan succinate. EXAMPLE #23: PREPARATION OF 60mσ DOSE FLUOXETINE

HYDROCHLORIDE SEMI-SOLID MOLDED COMPOSITION

The inventive subject matter containing fluoxetine hydrochloride can be made by the following process. 60.00 grams of cocoa butter, 2.00 grams of lecithin, 4.40 grams of sorbitan monostearate, and 24.00 grams of kaomel are mixed at 100°F for 8 minutes. 12.00 grams of MCT oil and 0.80 grams of Polysorbate 80 are added to the mixture. The mixture is mixed for 2 minutes at 110°F. 0.20 grams of sodium laurel sulfate and 12 grams of fluoxetine hydrochloride are then added and the mixture is mixed for 4 minutes at 90°F. 1.20 grams of aspartame and 263.60 grams of sugar lOx are added and the mixture is mixed for 8 minutes at 90°F. The mixture is removed from the heat and 0.10 grams of light green coloring (0.01 grams of 0.0025% Blue #1 and 0.09 grams of 0.0225% Yellow #5), 1.80 grams of vanilla flavoring, 0.40 grams of flavor enhancer, 2.00 grams of natural cream powder and 13.32 grams of instant release peppermint are added, resulting in 400.00 grams of final mixture. The mixture is mixed for 10 minutes, until all of the ingredients have been thoroughly mixed.

The final mixture is molded into the final product and allowed to set-up. The final product is then cut into 200 evenly-sized pieces. Each piece of product contains 60mg fluoxetine hydrochloride . The inventive subject matter being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the inventive subject matter, and all such modifications are intended to be included within the scope of the following claims.

Claims

WHAT IS CLAIMED IS:

1. A rapid-melt, semi-solid molded composition comprising: a) at least one binder in an amount from about 0.01% to about 70% by weight; b) a salivating agent in an amount from about 0.05% to about 15% by weight; c) a diluent/bulking material in an amount from about 10% to about 90% by weight; and d) an active material in an amount from about

2. The rapid-melt, semi-solid composition of claim 1 wherein said binder is a lipid material having a melting point about 25-90°C.

3. The rapid-melt, semi-solid composition of claim 2 wherein said binder- is a lipid material having a melting point about 37 °C.

4. The rapid-melt, semi-solid composition of claim 1 wherein said active material is a nutritional active material .

5. The rapid-melt, semi-solid composition of claim 4 wherein said nutritional active material is selected from the group consisting of calcium, vitamins, minerals, herbals, spices and mixtures thereof.

6. The rapid-melt, semi-solid composition of claim 5 wherein said nutritional active material is a vitamin.

7. The rapid-melt, semi-solid composition of claim 5 wherein said nutritional active material is a mineral.

8. The rapid-melt, semi-solid composition of claim 5 wherein said nutritional active material is calcium.

9. The rapid-melt, semi-solid composition of claim 1 wherein said active material is a prophylactic or therapeutic active material.

10. The rapid-melt, semi-solid composition of claim

9 wherein said prophylactic or therapeutic active material is selected from the group consisting of antihistamines, decongestants, alkaloids, laxatives, antacids, anti-cholesterolemics, antiarrhythmics, analgesics, appetite suppressants, expectorants, anti-anxiety agents, anti-ulcer agents, anti-inflammatory substances, stimulants, gastrointestinal agents, sedatives, migraine treatments, antibiotics, tranquilizers, antiobesity drugs, anabolic drugs, cough suppressants, aspirin, acetaminophen, ibuprofen and mixtures thereof.

11. The rapid-melt, semi-solid composition of claim 10 wherein said prophylactic or therapeutic active material is ibuprofen.

12. The rapid-melt, semi-solid composition of claim 10 wherein said prophylactic or therapeutic active material is acetaminophen.

13. The rapid-melt, semi-solid composition of claim

1 wherein said salivating agent is an emulsifier.

14. The rapid-melt, semi-solid composition of claim 1 wherein said salivating agent is a food acid or food salt .

15. A method of preparing a rapid-melt, semi-solid molded composition comprising the steps of: a) melting at least one binder in an amount from about 0.01% to about 70% by weight with a salivating agent in an amount from about 0.05% to about 15% by weight, to form a mixture b) mixing an active material with said mixture to form an active mixture; c) mixing a diluent/bulking material with said active mixture to form a final mixture; and d) molding said final mixture into said rapid- melt, semi-solid molded composition.

16. The method of claim 15 wherein said binder is a lipid material having a melting point about 25-90°C.

17. The method of claim 16 wherein said binder is a lipid material having a melting point about 37 °C.

18. The method of claim 15 wherein said active material is a nutritional active material.

19. The rapid-melt, semi-solid composition of claim 18 wherein said nutritional active material is selected from the group consisting of calcium, vitamins, minerals, herbals, spices and mixtures thereof.

20. The method of claim 19 wherein said nutritional active material is a vitamin.

21. The method of claim 19 wherein said nutritional active material is a mineral.

22. The method of claim 19 wherein said nutritional active material is calcium.

23. The method of claim 15 wherein said active material is a prophylactic or therapeutic active material.

24. The method of claim 23 wherein said prophylactic or therapeutic active material is selected from the group consisting of antihistamines, decongestants, alkaloids, laxatives, antacids, an t i - cho 1 e s t e rol emi c s , antiarrhythmics, analgesics, appetite suppressants, expectorants, anti-anxiety agents, anti-ulcer agents, anti-inflammatory substances, stimulants, gastrointestinal agents, sedatives, migraine treatments, antibiotics, tranquilizers, antiobesity drugs, anabolic drugs, cough suppressants, aspirin, acetaminophen, ibuprofen and mixtures thereof.

25. The method of claim 24 wherein said prophylactic or therapeutic active material is ibuprofen.

26. The method of claim 24 wherein said prophylactic or therapeutic active material is acetaminophen.

27. The method of claim 15 wherein said salivating agent is an emulsifier.

28. The method of claim 15 wherein said salivating agent is a food acid or food salt.

29. A method of administering an active material to a mammal comprising the step of administering the rapid- melt, semi-solid composition of claim 1 to a mammal in need thereof.

30. The method of claim 29 wherein said administering aids in drug compliance by said mammal.

31. A method of enhancing salivation in a mammal comprising administering the rapid-melt, semi-solid composition of claim 1.

32. A rapid-melt, semi-solid molded composition comprising: a) at least one binder in an amount from about 0.01% to about 70% by weight; b) a salivating agent in an amount from about 0.05% to about 15% by weight; c) a diluent/bulking material in an amount from about 10% to about 90% by weight;

Si d) water in an amount less than 2% by weight; and e) an active material in an amount from about 0.001% to about 70% by weight.

33. A rapid melt, semi-solid molded composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; and a therapeutically effective amount of a drug, wherein said drug is selected from the group consisting of psychotropics, gastrointestinal therapeutics, cardiovascular therapeutics, migraine therapeutics, inflammation therapeutics, benign prostatic hypertrophy therapeutics, fungal therapeutics, allergic rhinitis therapeutics, anticonvulsants, and viral therapeutics.

34. The composition of claim 33, wherein the said drug is a psychotropic.

35. The composition of claim 34, wherein said psychotropic is a anti-anxiety therapeutic.

36. The composition of claim 34, wherein said psychotropic is an insomnia therapeutic.

37. The composition of claim 34, wherein said psychotropic is an antidepressant.

38. The composition of claim 37, wherein said antidepressant is selected from the group consisting of Fluoxetine HCl, Paroxetine HCl, Sertraline HCl, and Venlafaxine HCl, Amitriptyline, Nortriptyline, Imipramine, Desipramine, Doxepin, Trimipramine, Clomipramine, Protriptyline, Amoxapine, Maprotiline, Phenelzine, Tranylcypromine, Fluvoxamine, Venlafaxine, Trazodone, Nefazodone, Mirtazapine, Bupropion, or mixtures thereof.

39. The composition of claim 38, wherein said drug is Fluoxetine HCl.

40. The composition of claim 33, wherein said drug is a gastrointestinal therapeutic.

41. The composition of claim 40, wherein said gastrointestinal therapeutic is a ulcer therapeutic.

42. The composition of claim 41, wherein said ulcer therapeutic is selected from the group consisting of Omeprazole, Lansoprazole, Ranitidine HCl, Famotidine, Nizatidine, Teprenone, Cimetidine, Rabeprazole sodium, Sulpiride, or mixtures thereof.

43. The composition of claim 42, wherein said ulcer therapeutic is Omeprazole.

44. The composition of claim 40, wherein said gastrointestinal therapeutic is a anti-emetic.

45. The composition of claim 44, wherein said anti- emetic is selected from the group consisting of Ondansetron

HCl, Granisetron HCl, Tropisetron, Dolasetron mesylate, Cisapride, Sulfasalazine, Balsalazide, Infliximab, or mixtures thereof.

46. The composition of claim 40, wherein said gastrointestinal therapeutic is a anti-diarrheal therapeutic.

47. The composition of claim 46, wherein said anti- diarrheal therapeutic is selected from the group consisting of Loperamide HCl, diphenoxylate, codeine phosphate, camphorated opium tincture, or mixtures thereof.

48. The composition of claim 47, wherein said anti- diarrheal therapeutic is Loperamide HCl

49. The composition of claim 33, wherein said drug is a migraine therapeutic.

50. The composition of claim 49, wherein said migraine therapeutic is selected from the group consisting of sumatriptan succinate, amitripyline, methysergide, propranolol, valproate, verapamil, dihydroergotamine, ergotamine, metoclopramide, naratriptan, prochlorperazine, rizatriptan benzoate, zolmitriptan, eletriptan, acetaminophen, aspirin, NSAID's, opioids, or mixtures thereof.

51. The composition of claim 50, wherein said migraine therapeutic is sumatriptan succinate.

52. A method of preparing a rapid-melt, semi-solid molded composition comprising the steps of: a) melting at least one binder in an amount from about 0.01% to about 70% by weight with a salivating agent in an amount from about 0.05% to about 15% by weight, to form a mixture; b) mixing a therapeutically effective amount of a drug with said mixture to form an active mixture; said drug selected from the group consisting of psychotropics, gastrointestinal therapeutics, cardiovascular therapeutics, migraine therapeutics, inflammation therapeutics, benign prostatic hypertrophy therapeutics, fungal therapeutics, allergic rhinitis therapeutics, anticonvulsants, and viral therapeutics . c) mixing a diluent/bulking material with said active mixture to form a final mixture; and d) molding said final mixture into said rapid- melt, semi-solid molded composition.

53. The method of claim 52, wherein said drug is a psychotropic.

54. The method of claim 53, wherein said psychotropic is selected from the group consisting of Fluoxetine HCl, Paroxetine HCl, Sertraline HCl, and Venlafaxine, Amitriptyline, Nortriptyline, Imipramine, Desipramine, Doxepin, Trimipramine, Clomipramine, Protriptyline, Amoxapine, Maprotiline, Phenelzine, Tranylcypromine, Fluvoxamine, Venlafaxine, Trazodone, Nefazodone, Mirtazapine, Bupropion, or mixtures thereof.

55. The method of claim 54, wherein said psychotropic is Fluoxetine HCl.

56. The method of claim 52, wherein said drug is a gastrointestinal therapeutic.

57. The method of claim 56, wherein said gastrointestinal therapeutic is a ulcer therapeutic.

58. The method of claim 57, wherein said ulcer therapeutic is selected from the group consisting of Omeprazole, Lansoprazole, Ranitidine HCL, Famotidine, Nizatidine, Teprenone, Cimetidine, Rabeprazole sodium, Sulpiride, or mixtures thereof.

59. The method of claim 58, wherein said ulcer therapeutic is Omeprazole.

60. The method of claim 56, wherein said gastrointestinal therapeutic is a anti-emetic.

61 . The method of claim 60 , wherein said anti-emetic is selected from the group consisting of Ondansetron HCl,

Granisetron HCl, Tropisetron, Dolasetron mesylate, Cisapride, Sulfasalazine, Balsalazide, Infliximab, or mixtures thereof.

62. The method of claim 56, wherein said gastrointestinal therapeutic is a anti-diarrheal therapeutic.

63. The method of claim 62, wherein said anti- diarrheal therapeutic is selected from the group consisting of Loperamide HCl, diphenoxylate, codeine phosphate, camphorated opium tincture, or mixtures thereof.

64. The method of claim 63, wherein said anti- diarrheal therapeutic is Loperamide HCl.

65. The method of claim 52, wherein said drug is a migraine therapeutic.

66. The method of claim 65, wherein said migraine therapeutic is selected from the group consisting of sumatriptan succinate, amitripyline, methysergide, propranolol, valproate, verapamil, dihydroergotamine, ergotamine, metoclopramide, naratriptan, prochlorperazine, rizatriptan benzoate, zolmitriptan, eletriptan, acetaminophen, aspirin, NSAID's, opioids, or mixtures thereof.

67. The method of claim 66, wherein said migraine therapeutic is sumatriptan succinate.

68. A method for treating depression, anxiety or insomnia comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an antidepressant, anti-anxiety therapeutic or an insomnia therapeutic and wherein said composition is prepared in the absence of free water.

69. A method for treating diarrhea and nausea comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an gastrointestinal therapeutic, a anti-emetic or a anti- diarrheal therapeutic and wherein said composition is prepared in the absence of free water.

70. A method for treating migraines comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an migraine therapeutic and wherein said composition is prepared in the absence of free water.