WO1994025068A1 - Improved pharmaceutical acceptable compositions containing an alcohol and a hydrophobic drug - Google Patents
Improved pharmaceutical acceptable compositions containing an alcohol and a hydrophobic drug Download PDFInfo
- Publication number
- WO1994025068A1 WO1994025068A1 PCT/CA1994/000222 CA9400222W WO9425068A1 WO 1994025068 A1 WO1994025068 A1 WO 1994025068A1 CA 9400222 W CA9400222 W CA 9400222W WO 9425068 A1 WO9425068 A1 WO 9425068A1
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- Prior art keywords
- composition according
- alcohol
- drug
- alcohols
- water
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/04—Peptides having up to 20 amino acids in a fully defined sequence; Derivatives thereof
- A61K38/12—Cyclic peptides, e.g. bacitracins; Polymyxins; Gramicidins S, C; Tyrocidins A, B or C
- A61K38/13—Cyclosporins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/44—Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/10—Dispersions; Emulsions
- A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
- A61K9/1075—Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4858—Organic compounds
Definitions
- This invention is directed to pharmaceutical compositions which facilitate the in vivo absorption of hydrophobic drugs, including but not limited to polypeptide and protein drugs.
- hydrophobic nature of some drugs causes them to be insoluble or poorly soluble in aqueous media. This reduces the absorption of the drug into systemic circulation after a composition containing the drug is swallowed, or the absorption into the target tissues upon topical application.
- the drug may precipitate and agglomerate into larger particles that are poorly absorbed.
- cyclosporins include cyclosporin A, also known as cyclosporine, and hereinafter referred to as "cyclosporine”, known to be therapeutically active as an immunosuppressant.
- U.S. Patent No. 4,388,307 discloses a composition comprising cyclosporine in an emulsion preconcentrate that is not water-soluble, but upon being mixed into gastrointestinal fluids forms an emulsion.
- the advantage of such compositions is that the cyclosporine in the emulsion is absorbed to a substantially greater extent than from other compositions previously known.
- the absorption is superior to that of some compositions, the absorption is still less than the maximum possible and is variable.
- cyclosporine concentration in such compositions is limited to about 10 percent by weight.
- a capsule containing 100 mg of cyclosporine weighs about 1 gram.
- Capsule strengths are thus limited to about 100 mg, as higher strength capsules would be too large to be swallowed.
- European Patent Application No. 88305138.5 discloses use of a surfactant or solubilizing agent which is alphacyclodextrin or a derivative thereof.
- compositions comprising cyclosporine together with surfactants, which also form clear solutions upon their addition to aqueous media.
- compositions have been generally impractical, as the quantities of surfactant needed to render cyclosporine entirely water-soluble have been unacceptably large. Typical therapeutic doses of such compositions would require toxic quantities of the surfactants.
- compositions in which surfactants are used in quantities less than sufficient to entirely solubilize the cyclosporine in water have provided compositions in which surfactants are used in quantities less than sufficient to entirely solubilize the cyclosporine in water.
- Japanese Patent No. 1038029 discloses preparation of powders by dissolving cyclosporine and surfactants in organic solvents and evaporating the solvents.
- the compositions described do not fully solubilize the cyclosporine, and organic solvents are costly and more difficult to use than water in the manufacturing process.
- U.K. Patent Application No. 8920597.5 discloses "microemulsion preconcentrates" which are stated to be improved over compositions disclosed in U.S. Patent No. 4,388,307.
- compositions which, in addition to the active drug, comprises a hydrophilic phase, a lipophilic phase and a surfactant will, when added to water, disperse into an emulsion of smaller droplets than prior compositions, leading to superior absorption.
- the emulsion preconcentrates disclosed in both U.S. Patent No. 4,388,307 and U.K. Patent Application No. 8920597.5 have the feature that they have a hydrophilic phase which is the primary solvent for the active drug.
- the hydrophilic solvent is ethanol
- other hydrophilic solvents are used such as Glycofurol 75, Transcutol, and Propylene Glycol.
- the use of such hydrophilic solvents in emulsion preconcentrates is a cause of some of the limitations of such compositions disclosed in the prior art.
- the hydrophilic solvent can be drawn out of the emulsified phase and into solution in the water.
- Some of the active drug will be drawn along with the hydrophilic solvent and will precipitate as the solvent dissolves in the water. This precipitation reduces the quantity of the drug available for absorption.
- hydrophilic phase also requires the use of a hydrophobic or lipophilic phase in the emulsion preconcentrate to enable the formation of an emulsion, thus increasing the total quantity of inactive ingredients required, and this in turn also requires an increased quantity of surfactant in the emulsion preconcentrates.
- ethanol and other hydrophilic solvents previously used are relatively volatile and may evaporate from the composition on storage, resulting in precipitation of the drug.
- the compositions may thus have inadequate stability on storage unless specially packaged to prevent the evaporation.
- composition as used herein and in the accompanying claims is to be understood as meaning any composition containing a drug along with inactive ingredients that are pharmaceutically acceptable by reason of not being excessively toxic in the quantity required; e.g. where oral administration is intended, acceptable for oral use, and where topical administration is intended, for topical use.
- the present invention is directed to pharmaceutical compositions which enable improved abso ⁇ tion of a hydrophobic drug while at the same time enabling the drug to be contained in the composition at relatively high concentrations.
- an emulsion preconcentrate being defined as a composition that, when added to water, readily disperses to form an emulsion.
- An object of the invention is to eliminate the need to use a hydrophilic solvent as the primary solvent, in order to obviate the problems associated in the use of hydrophilic solvents as previously described.
- solvent system means the material in which the drug is dissolved.
- the solvent system may be a single solvent or a combination or mixture of ingredients included as solvents, surfactants, diluents, or for other purposes.
- a primary feature of the invention is to use, as sole solvent or principal solvent in the solvent system, an alcohol that has a boiling point above 100°C, and that has a solubility in water of under 10 g per 100 g at 20°C.
- alcohols are less hydrophilic than ethanol or other solvents that have been previously used as the hydrophilic solvent in emulsion preconcentrates.
- Such alcohols will generally have 4 or more carbon atoms per molecule.
- the invention is applicable to drugs having adequate solubility in alcohols. Included among such drugs is cyclosporine.
- Alcohols that may be used within the scope of the present invention may include any pharmaceutically acceptable alcohol having a boiling point above 100°C and a solubility in water of under 10 g per 100 g at 20°C.
- the alcohol will have a boiling point above 150°C, and a solubility in water of under 5 g per 100 g at 20°C.
- the alcohol will have 6 to 16 carbon atoms per molecule. The use of alcohols having greater than 16 carbon atoms is generally impractical as they generally have melting points above 40 °C.
- Suitable alcohols include but are not limited to 1-hexyl, 1-octyl, 2-octyl, 1-decyl, 1-dodecyl, 1-tetradecyl, benzyl and phenethyl alcohols.
- alcohols become less hydrophilic and more hydrophobic.
- ethyl alcohol having 2 carbon atoms
- 1 -butyl alcohol having 4 carbon atoms
- 1-hexyl having 6 carbon atoms
- 1- -octyl alcohol having 8 carbon atoms
- 1-decyl alcohol having 10 carbon atoms
- the alcohols having more carbon atoms per molecule In addition to being less hydrophilic and more hydrophobic, the alcohols having more carbon atoms per molecule generally have higher boiling points and are less volatile at ambient temperature, so that use of alcohols with more carbon atoms per molecule can eliminate the problem of volatility of the hydrophilic solvents encountered with prior-art compositions.
- One alcohol may be selected as being superior as a solvent for the drug and another may be selected as superior for ease of dispersion in water.
- a combination of the two may be better than either alone to enable higher concentration of the drug and adequate ease of dispersion.
- the solvent system in which the drug is dissolved in addition to including at least one alcohol meeting the aforesaid requirements, will include at least one pharmaceutically acceptable surfactant, which serves to make the composition dispersible in water to form an emulsion.
- Suitable surfactant are:
- Polyoxyethylene-sorbitan-fatty acid esters e.g. mono- and tri- lauryl, palmityl, stearyl and oleyl esters; e.g. products of the type known as polysorbates and commercially available under the trade name Tween.
- Polyoxyethylene fatty acid esters for example, polyoxyethylene stearic acid esters of the type known and commercially available under the trade name Myrj as well as polyoxyethylene fatty acid esters known and commercially available under the trade name Cetiol HE.
- Propylene glycol mono- and di-fatty acid esters such as propylene glycol dicaprylate, propylene glycol dilaurate, propylene glycol hydroxystearate, propylene glycol isostearate, propylene glycol laurate, propylene glycol ricinoleate, propylene glycol sterate and so forth.
- Bile salts e.g. alkali metal salts, for example sodium taurocholate.
- Pentaerythritol fatty acid esters and polyalkylene glycol ethers for example pentaerythritedioleate, -distearate, -monolaurate, polyglycol ether and -monostearate as well as pentaerythrite-fatty acid esters.
- Monoglycerides e.g. glycerol monooleate, glycerol monopalmitate and glycerol monostearate; for example as known and commercially available under the trade names Myvatex, Myvaplex and Myverol, and acetylated, e.g. mono-and di-acetylated mono-glycerides; for example as known and commercially available under the trade name Myvacet.
- Suitable surfactants will not be limited to those listed above, but will be understood to include any compound which causes the composition to be more easily dispersible in water.
- the surfactant also is an effective solvent for the drug, it may be inco ⁇ orated not only as surfactant, but as an additional carrier or co-solvent, to reduce the amount of alcohol required.
- compositions in accordance with the invention may contain other ingredients in addition to the drug and one or more alcohols and one or more surfactants.
- the solvent system in which the drug is dissolved may include, in addition to one or more alcohols and one or more surfactants, one or more other ingredients that are interdissolved with the alcohol and surfactant and are included as co-solvents or diluents.
- a composition in accordance with the invention may also contain, for example, a thickening agent (i.e., viscosity increasing agent).
- a thickening agent i.e., viscosity increasing agent
- Suitable thickening agents may be of any of those known and employed in art, including, for example, pharmaceutically acceptable polymeric materials and inorganic thickening agents.
- thickening agents as aforesaid will generally not be required.
- Use of thickening agents is, on the other hand, indicated, e.g. where topical application is foreseen.
- compositions in accordance with the invention may also include one or more further ingredients; such as diluents, anti-oxidants, flavouring agents and so forth.
- compositions in accordance with the invention may be liquids at ambient temperatures or they may be solids prepared, for example, by use of alcohols or surfactants with melting points above ambient temperatures.
- the ingredients may be blended at temperatures above the melting point and then cooled to form solids.
- the solids may be ground into powder granules for further processing; for example, filling capsules or manufacture of tablets.
- the capsules or tablets may be further processed by applying coatings thereto.
- compositions in accordance with the invention may comprise end dosage forms for administration as emulsion preconcentrates.
- the emulsion preconcentrate may be directly used as liquid for oral ingestion, parenteral use, or topical application or it may be encapsulated into gelatin capsules for oral ingestion.
- the present invention also provides pharmaceutical compositions in which the emulsion preconcentrate is further processed into an emulsion.
- emulsions obtained e.g. by diluting an emulsion preconcentrate with sufficient water or other aqueous medium (for example, a sweetened or flavoured preparation for drinking), may be employed as formulations for drinking.
- compositions comprising an emulsion preconcentrate, a thickening agent, and water will provide an aqueous emulsion in gel, paste, cream or like form.
- droplet size of the emulsion formed when an emulsion preconcentrate according to the invention is dispersed in water will depend upon the identity and quantity of the ingredients used.
- droplet size will decrease as the amount of surfactant is increased.
- smaller emulsion droplet size will enable improved abso ⁇ tion, so that there is usually an advantage to using more surfactant to obtain decreased droplet size.
- increased quantity of surfactant may also imply increased toxicity from the surfactant, increased cost and increased size of the dosage form of any desired strength.
- enough surfactant has been used to achieve abso ⁇ tion close to the maximum achievable, little is to be gained by adding more surfactant.
- compositions in accordance with the present invention whether emulsion preconcentrates or emulsions may be employed for administration in any appropriate manner and form; e.g. orally, as liquids or granules or in unit dosage form, for example in hard or soft gelatin encapsulated form, parenterally or topically; e.g.
- compositions in accordance with the invention are, however, primarily intended for oral or topical application, including application to the skin or eyes.
- the relative proportion of drug and other ingredients in the compositions of the invention will, of course, vary considerably depending on the particular type of composition concerned; e.g. whether it is an emulsion preconcentrate or emulsion, the route of administration, and so forth.
- the relative proportions will also vary, depending on the identity and particular function of ingredients in the composition; for example, in the case of a surfactant component of an emulsion preconcentrate, on whether this is employed as a surfactant only or both a surfactant and a co-solvent.
- the relative proportions will also vary depending on the particular ingredients employed and the desired physical characteristics of the product composition, e.g. in the case of a composition for topical use, whether this is to be a free flowing liquid or a paste.
- compositions for topical use suitably comprise one or more carriers or diluents and/or other ingredients (e.g. thickening agents, emulsifying agents, preserving agents, moisturising agents, colourants and so forth) providing a suitable carrier.
- carriers or diluents and/or other ingredients e.g. thickening agents, emulsifying agents, preserving agents, moisturising agents, colourants and so forth.
- excipients for the preparation of such formulations will, of course, be determined by the type of formulation desired as well as the particular condition to be treated, the area to be treated, and the effect desired.
- Some conditions will more suitably be treated with hydrophobic, e.g. fat-based compositions, for example compositions in accordance with the invention comprising a petrolatum based ointment or cream as carrier medium.
- compositions for use in the treatment of some conditions will more appropriately be treated with more hydrophilic compositions, e.g. compositions in accordance with the invention in the form of an oil-in-water emulsion or gel.
- compositions in which an emulsion preconcentrate is dispersed in a suitable pharmaceutically acceptable diluent or carrier.
- Compositions as aforesaid may take the form of a water- free or substantially water- free emulsion, i.e., comprise less than 10%, preferably less than 5%, most preferably less than 1% water.
- Suitable carrier components include, for example:
- Solid hydrocarbons for example petroleum jellies, e.g. white petrolatum, ceresin and solid paraffins, as well as waxes including animal, vegetable and synthetic waxes such as, for example, spermaceti, carnauba and bees wax; Liquid hydrocarbons, e.g. liquid paraffins and fatty acid esters such as isopropylmyristate and cetyl palmitate;
- Non-volatile silicones including silicone oils and pastes, and silicone-polyalkyleneoxide co-polymers for example such as known and commercially available under the trade name Piroethicon.
- Such carrier components will suitably be present in the compositions in an amount of up to about 80%), e.g. from about 5 to about 70%, preferably from about 25 to about 60% by weight based on the total weight of the composition.
- emulsions may be obtained in liquid or semi-solid form depending on, e.g., desired requirements for topical application.
- compositions for topical use may further comprise one or more consistency promoting agents, for example microcrystalline waxes, vegetable oils such as olive oils, corn oils and kernel oils, and vegetable oil derivatives including hydrogenated vegetable oils and vegetable oil partial-glycerides, e.g. in an amount of from about 0.1 to about 10%, preferably from about 1 to about 5% weight based on the total weight of the composition.
- consistency promoting agents for example microcrystalline waxes, vegetable oils such as olive oils, corn oils and kernel oils, and vegetable oil derivatives including hydrogenated vegetable oils and vegetable oil partial-glycerides, e.g. in an amount of from about 0.1 to about 10%, preferably from about 1 to about 5% weight based on the total weight of the composition.
- compositions will also suitably contain other ingredients which may include an anti-oxidant, and anti-bacterial agent, a stabilizer, and a skin penetration enhancer.
- the present invention also provides a process for the production of a pharmaceutical composition hereinbefore defined which process comprises bringing the individual components thereof into intimate admixture and, when required compounding the obtained composition in unit dosage form, for example filling said composition into soft or hard gelatin capsules, or dispersing the composition in a carrier which may include water.
- Preferred alcohols for use as principal solvent for the drug are alcohols having a boiling point above 150°C, a melting point under 40°, and a solubility in water of under 5 g per 100 g at 20°C.
- Especially preferred alcohols are 1- octyl, 2-octyl, 1-decyl, 1-dodecyl, 1-tetradecyl, benzyl and phenethyl alcohols.
- a preferred combination is one selected from 1-octyl, 2-octyl, 1-decyl, 1-dodecyl, and 1-tetradecyl alcohols and another selected from benzyl and phenethyl.
- Preferred surfactants are reaction products of natural or hydrogenated vegetable oils and ethylene glycol; i.e., polyoxethylene glycolated natural or hydrogenated vegetable oils.
- Especially preferred surfactants are polyoxyethylene glycolated natural or hydrogenated castor oils, including those designated in the United States Pharmacopoeia and National Formulary as Polyoxyl and Polyoxyl 40 Hydrogenated Castor Oil.
- the invention will be more fully understood by the following examples which are illustrative but not limiting of compositions in accordance with the present invention.
- test tube The following were placed in a test tube:
- cyclosporine 1.04 g; 1-octyl alcohol 2.5 g; and polyoxyl 40 hydrogenated castor oil 2.0 g.
- test tube The following were placed in a test tube:
- cyclosporine 1.04 g; 1-octyl alcohol 2.5 g; and polyoxyl 35 castor oil 1.0 g.
- test tube The following were placed in a test tube:
- cyclosporine 1.04 g; 1-octyl alcohol 1.0 g; benzyl alcohol 0.25 g; and polyoxyl 35 castor oil 1.0 g.
- test tube The following were placed in a test tube:
- cyclosporine 1.04 g; 1-decyl alcohol 1.0 g; benzyl alcohol 0.25 g; and polyoxyl 35 castor oil 1.0 g.
- cyclosporine 5.20 g; 1-dodecyl alcohol 5.00 g; benzyl alcohol 1.20 g; and polyoxyl 35 castor oil 5.00 g.
- cyclosporine 1.04 g; 1-dodecyl alcohol 1.0 g; phenethyl alcohol 0.25 g; and polyoxyl 35 castor oil 1.0 g.
- the solution formed was readily dispersible in water to form an emulsion without precipitation of the cyclosporine.
- the solution of example 6 was filled into hard gelatin capsules.
- the abso ⁇ tion was compared in human volunteers to that of Sandimmure (registered trademark) capsules which is the leading brand in the world market and made in accordance with U.S. Patent No. 4,388,307. This was done by performing a comparative bioavailability study in which capsules were ingested by human volunteers, blood samples were drawn and cyclosporine levels were measured. It was found that the extent of abso ⁇ tion of the composition of example 6 was substantially greater than that of Sandimmune (registered trademark).
- they may be further processed in various ways previously described, including, for example, their inco ⁇ oration into gelatin capsules or tablets for oral ingestion, or into emulsions and various other forms for oral or topical use.
- compositions can be prepared using other drugs that are soluble in alcohols or in solvent systems containing alcohols and surfactants.
Abstract
Description
Claims
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6523695A JPH08509475A (en) | 1993-04-28 | 1994-04-22 | Pharmaceutically acceptable improved composition containing alcohol and hydrophobic drug |
AU66734/94A AU677660B2 (en) | 1993-04-28 | 1994-04-22 | Improved pharmaceutical acceptable compositions containing an alcohol and a hydrophobic drug |
US08/537,697 US5843891A (en) | 1993-04-28 | 1994-04-22 | Pharmaceutical acceptable compositions containing an alcohol and a hydrophobic drug |
EP94914284A EP0696920B1 (en) | 1993-04-28 | 1994-04-22 | Improved pharmaceutical acceptable compositions containing an alcohol and a hydrophobic drug |
PL94311294A PL311294A1 (en) | 1993-04-28 | 1994-04-22 | Improved, pharmaceutically admissible composition containing alcohol and a hydrophobous drug |
DE69414840T DE69414840T2 (en) | 1993-04-28 | 1994-04-22 | ACCEPTABLE PHARMACEUTICAL COMPOSITION CONTAINING AN ALCOHOL AND A HYDROPHALIC ACTIVE SUBSTANCE |
BR9406513A BR9406513A (en) | 1993-04-28 | 1994-04-22 | Pharmaceutical composition available in water and process for preparing composition |
FI955091A FI955091A (en) | 1993-04-28 | 1995-10-25 | Improved pharmaceutically acceptable compositions comprising an alcohol and a hydrophobic drug |
NO954329A NO954329L (en) | 1993-04-28 | 1995-10-27 | Improved pharmaceutically acceptable compositions containing an alcohol and a hydrophobic drug |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NZ247516A NZ247516A (en) | 1993-04-28 | 1993-04-28 | Water dispersible pharmaceutical compositions comprising drug dissolved in solvent system comprising at least one alcohol and at least one surfactant |
NZ247516 | 1993-04-28 |
Publications (1)
Publication Number | Publication Date |
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WO1994025068A1 true WO1994025068A1 (en) | 1994-11-10 |
Family
ID=19924336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/CA1994/000222 WO1994025068A1 (en) | 1993-04-28 | 1994-04-22 | Improved pharmaceutical acceptable compositions containing an alcohol and a hydrophobic drug |
Country Status (19)
Country | Link |
---|---|
US (1) | US5843891A (en) |
EP (1) | EP0696920B1 (en) |
JP (1) | JPH08509475A (en) |
CN (1) | CN1124457A (en) |
AT (1) | ATE173635T1 (en) |
AU (1) | AU677660B2 (en) |
BR (1) | BR9406513A (en) |
CA (1) | CA2160880A1 (en) |
CZ (1) | CZ276995A3 (en) |
DE (1) | DE69414840T2 (en) |
FI (1) | FI955091A (en) |
HU (1) | HUT73664A (en) |
IL (1) | IL109401A0 (en) |
MX (1) | MX9402922A (en) |
NO (1) | NO954329L (en) |
NZ (1) | NZ247516A (en) |
PL (1) | PL311294A1 (en) |
WO (1) | WO1994025068A1 (en) |
ZA (1) | ZA942803B (en) |
Cited By (14)
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WO1998040094A1 (en) * | 1997-03-12 | 1998-09-17 | Abbott Laboratories | Hydrophilic binary systems for the administration of cyclosporine |
US6159933A (en) * | 1997-04-29 | 2000-12-12 | Sherman; Bernard Charles | Emulsion preconcentrate comprising a cyclosporin, propylene carbonate, and glycerides |
US6258783B1 (en) | 1997-04-29 | 2001-07-10 | Bernard Charles Sherman | Emulsion preconcentrate comprising a cyclosporin and acetylated monoglyceride |
US6284268B1 (en) | 1997-12-10 | 2001-09-04 | Cyclosporine Therapeutics Limited | Pharmaceutical compositions containing an omega-3 fatty acid oil |
WO2005053727A2 (en) * | 2003-11-29 | 2005-06-16 | Sangstat Medical Corporation | Pharmaceutical compositions for bioactive peptide agents |
US8865695B2 (en) | 2009-01-08 | 2014-10-21 | Lipocine Inc. | Steroidal compositions |
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US9320801B2 (en) | 2012-04-30 | 2016-04-26 | Huons Co., Ltd | Cyclosporine-containing non-irritative nanoemulsion ophthalmic composition |
US9358241B2 (en) | 2010-11-30 | 2016-06-07 | Lipocine Inc. | High-strength testosterone undecanoate compositions |
US9498485B2 (en) | 2014-08-28 | 2016-11-22 | Lipocine Inc. | Bioavailable solid state (17-β)-hydroxy-4-androsten-3-one esters |
US10561615B2 (en) | 2010-12-10 | 2020-02-18 | Lipocine Inc. | Testosterone undecanoate compositions |
US11433083B2 (en) | 2010-11-30 | 2022-09-06 | Lipocine Inc. | High-strength testosterone undecanoate compositions |
US11559530B2 (en) | 2016-11-28 | 2023-01-24 | Lipocine Inc. | Oral testosterone undecanoate therapy |
US11707467B2 (en) | 2014-08-28 | 2023-07-25 | Lipocine Inc. | (17-ß)-3-oxoandrost-4-en-17YL tridecanoate compositions and methods of their preparation and use |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5858401A (en) | 1996-01-22 | 1999-01-12 | Sidmak Laboratories, Inc. | Pharmaceutical composition for cyclosporines |
FR2764509A1 (en) * | 1997-06-11 | 1998-12-18 | Debiopharm Sa | PHARMACEUTICAL COMPOSITIONS CONTAINING CINCHONIN DICHLORHYDRATE |
US20030216303A1 (en) * | 1998-03-06 | 2003-11-20 | Michael Ambuhl | Emulsion preconcentrates containing cyclosporin or a macrolide |
US7919109B2 (en) | 1999-02-08 | 2011-04-05 | Intarcia Therapeutics, Inc. | Stable non-aqueous single phase viscous vehicles and formulations utilizing such vehicles |
US7258869B1 (en) | 1999-02-08 | 2007-08-21 | Alza Corporation | Stable non-aqueous single phase viscous vehicles and formulations utilizing such vehicle |
AU2002240755B2 (en) * | 2001-03-13 | 2007-07-05 | Angiotech International Ag | Micellar drug delivery vehicles and uses thereof |
US20030157170A1 (en) * | 2001-03-13 | 2003-08-21 | Richard Liggins | Micellar drug delivery vehicles and precursors thereto and uses thereof |
NZ529647A (en) | 2001-04-20 | 2007-05-31 | Univ British Columbia | Micellar drug delivery systems for hydrophobic drugs |
US6592899B2 (en) | 2001-10-03 | 2003-07-15 | Macromed Incorporated | PLA/PLGA oligomers combined with block copolymers for enhancing solubility of a drug in water |
MXPA04003623A (en) * | 2001-10-19 | 2004-12-02 | Isotechnika Inc | Novel cyclosporin analog microemulsion preconcentrates. |
CA2471241A1 (en) * | 2001-12-20 | 2003-07-03 | Bernard Charles Sherman | Pharmaceutical compositions comprising a cyclosporin, a hydrophilic surfactant and a lipophilic surfactant |
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Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE684058A (en) * | 1965-07-15 | 1967-01-13 | ||
JPS5332109A (en) * | 1976-09-03 | 1978-03-27 | Takeda Chem Ind Ltd | Injection |
JPS6226220A (en) * | 1985-07-29 | 1987-02-04 | Hishiyama Seiyaku Kk | Ketoprofen injection |
GB2218334A (en) * | 1988-05-13 | 1989-11-15 | Sandoz Ltd | Cyclosporin compositions for topical application |
FR2636534A1 (en) * | 1988-09-16 | 1990-03-23 | Sandoz Sa | PHARMACEUTICAL COMPOSITIONS BASED ON CYCLOSPORINS |
WO1992009299A1 (en) * | 1990-11-27 | 1992-06-11 | BIOGAL Gyógyszergyár Rt. | Oral pharmaceutical composition containing cyclosporin and process for preparing same |
FR2678169A1 (en) * | 1991-06-27 | 1992-12-31 | Sandoz Sa | NOVEL PHARMACEUTICAL COMPOSITIONS COMPRISING CYCLOSPORINE FOR ORAL ADMINISTRATION. |
JPH0558906A (en) * | 1991-09-06 | 1993-03-09 | Sankyo Co Ltd | Cyclosporin eye-lotion |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE445174B (en) * | 1978-03-07 | 1986-06-09 | Sandoz Ag | PHARMACEUTICAL COMPOSITION CONTAINING A CYCLOSPORIN AND A HEALING SUBSTANCE |
GB8903804D0 (en) * | 1989-02-20 | 1989-04-05 | Sandoz Ltd | Improvements in or relating to organic compounds |
JP2577049B2 (en) * | 1987-06-04 | 1997-01-29 | 三共株式会社 | Cyclosporine preparation |
-
1993
- 1993-04-28 NZ NZ247516A patent/NZ247516A/en unknown
-
1994
- 1994-04-22 EP EP94914284A patent/EP0696920B1/en not_active Expired - Lifetime
- 1994-04-22 AU AU66734/94A patent/AU677660B2/en not_active Ceased
- 1994-04-22 HU HU9503075A patent/HUT73664A/en unknown
- 1994-04-22 DE DE69414840T patent/DE69414840T2/en not_active Expired - Fee Related
- 1994-04-22 JP JP6523695A patent/JPH08509475A/en active Pending
- 1994-04-22 CN CN94192265A patent/CN1124457A/en active Pending
- 1994-04-22 BR BR9406513A patent/BR9406513A/en not_active Application Discontinuation
- 1994-04-22 CA CA002160880A patent/CA2160880A1/en not_active Abandoned
- 1994-04-22 IL IL10940194A patent/IL109401A0/en unknown
- 1994-04-22 ZA ZA942803A patent/ZA942803B/en unknown
- 1994-04-22 PL PL94311294A patent/PL311294A1/en unknown
- 1994-04-22 CZ CZ952769A patent/CZ276995A3/en unknown
- 1994-04-22 MX MX9402922A patent/MX9402922A/en not_active Application Discontinuation
- 1994-04-22 WO PCT/CA1994/000222 patent/WO1994025068A1/en not_active Application Discontinuation
- 1994-04-22 US US08/537,697 patent/US5843891A/en not_active Expired - Fee Related
- 1994-04-22 AT AT94914284T patent/ATE173635T1/en not_active IP Right Cessation
-
1995
- 1995-10-25 FI FI955091A patent/FI955091A/en not_active Application Discontinuation
- 1995-10-27 NO NO954329A patent/NO954329L/en unknown
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE684058A (en) * | 1965-07-15 | 1967-01-13 | ||
JPS5332109A (en) * | 1976-09-03 | 1978-03-27 | Takeda Chem Ind Ltd | Injection |
JPS6226220A (en) * | 1985-07-29 | 1987-02-04 | Hishiyama Seiyaku Kk | Ketoprofen injection |
GB2218334A (en) * | 1988-05-13 | 1989-11-15 | Sandoz Ltd | Cyclosporin compositions for topical application |
FR2636534A1 (en) * | 1988-09-16 | 1990-03-23 | Sandoz Sa | PHARMACEUTICAL COMPOSITIONS BASED ON CYCLOSPORINS |
WO1992009299A1 (en) * | 1990-11-27 | 1992-06-11 | BIOGAL Gyógyszergyár Rt. | Oral pharmaceutical composition containing cyclosporin and process for preparing same |
FR2678169A1 (en) * | 1991-06-27 | 1992-12-31 | Sandoz Sa | NOVEL PHARMACEUTICAL COMPOSITIONS COMPRISING CYCLOSPORINE FOR ORAL ADMINISTRATION. |
JPH0558906A (en) * | 1991-09-06 | 1993-03-09 | Sankyo Co Ltd | Cyclosporin eye-lotion |
Non-Patent Citations (3)
Title |
---|
DATABASE WPI Section Ch Week 7819, Derwent World Patents Index; Class A10, AN 78-33884A * |
DATABASE WPI Section Ch Week 8711, Derwent World Patents Index; Class B04, AN 87-074911 * |
PATENT ABSTRACTS OF JAPAN vol. 17, no. 367 (C - 1082) 12 July 1993 (1993-07-12) * |
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US6008192A (en) * | 1997-03-12 | 1999-12-28 | Abbott Laboratories | Hydrophilic binary systems for the administration of lipophilic compounds |
CZ301382B6 (en) * | 1997-03-12 | 2010-02-10 | Abbott Laboratories Chad377/Ap6D-2 | Hydrophilic binary systems for administering cyclosporin |
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Also Published As
Publication number | Publication date |
---|---|
NZ247516A (en) | 1995-02-24 |
NO954329D0 (en) | 1995-10-27 |
CZ276995A3 (en) | 1996-03-13 |
EP0696920A1 (en) | 1996-02-21 |
AU6673494A (en) | 1994-11-21 |
DE69414840D1 (en) | 1999-01-07 |
FI955091A (en) | 1995-12-14 |
MX9402922A (en) | 1997-05-31 |
BR9406513A (en) | 1996-01-09 |
EP0696920B1 (en) | 1998-11-25 |
IL109401A0 (en) | 1994-11-28 |
ATE173635T1 (en) | 1998-12-15 |
ZA942803B (en) | 1996-01-22 |
NO954329L (en) | 1995-12-21 |
DE69414840T2 (en) | 1999-04-22 |
US5843891A (en) | 1998-12-01 |
HU9503075D0 (en) | 1995-12-28 |
HUT73664A (en) | 1996-09-30 |
CA2160880A1 (en) | 1994-11-10 |
PL311294A1 (en) | 1996-02-05 |
CN1124457A (en) | 1996-06-12 |
JPH08509475A (en) | 1996-10-08 |
FI955091A0 (en) | 1995-10-25 |
AU677660B2 (en) | 1997-05-01 |
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