WO2004100925A2 - Dissolvable backing layer for use with a transmucosal delivery device - Google Patents
Dissolvable backing layer for use with a transmucosal delivery device Download PDFInfo
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- WO2004100925A2 WO2004100925A2 PCT/US2004/014550 US2004014550W WO2004100925A2 WO 2004100925 A2 WO2004100925 A2 WO 2004100925A2 US 2004014550 W US2004014550 W US 2004014550W WO 2004100925 A2 WO2004100925 A2 WO 2004100925A2
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- WIPO (PCT)
- Prior art keywords
- backing layer
- hydrophilic region
- dissolvable
- hydrophilic
- layer
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Classifications
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- 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
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/006—Oral mucosa, e.g. mucoadhesive forms, sublingual droplets; Buccal patches or films; Buccal sprays
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- 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
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7007—Drug-containing films, membranes or sheets
Definitions
- the present invention is in the field of transmucosal drug delivery devices, particularly in the field of transmucosal patches for use in isolating and maintaining a drug or other active ingredient against a mucosal surface in order to promote diffusion of the drug or other active agent therethrough, and more particularly in the field of backing layers for transmucosal patches.
- Transmucosal drug delivery is an alternative method of systemic drug delivery. It offers several advantages over both injectable and enteral delivery. Drugs absorbed via the mucous membrane (e.g., oral, anal or vaginal mucosa) avoid the low pH gastric fluid and proteases, as well as first-pass metabolism in the liver. The onset of action is faster than oral administration. Unlike injections, transmucosal delivery is non-invasive and not painful. Moreover, a patient can administer the medicine without help from a medical professional.
- the mucous membrane e.g., oral, anal or vaginal mucosa
- oral and other transmucosal dosage forms can be classified in one of three categories: (1) solid forms, (2) gum, and (3) patches.
- Examples of common solid dosage forms include lozenges, lozenges having a handle (e.g., lollipops), buccal tablets, and sublingual tablets.
- This type of dosage form is referred to as an "open system" because saliva can flow freely to and from the dosage form to dissolve the formulation.
- Drug concentration is generally controlled by how fast the matrix is dissolved, which is controlled by how fast the patient sucks the unit.
- Gum like lozenges and tablets, is an open system. When this dosage form is chewed the drug is released from gum into the oral cavity where it can be absorbed by oral mucosa. Drug release from gum is controlled by the make up of the delivery device, as well as how fast the gum is chewed. In general, gum dosage forms last longer than lozenges or tablets.
- buccal patch typically refers to a flexible film that adheres to the oral mucosa and delivers a drug over a period of time.
- the buccal patch dosage form can be further divided into three types or subcategories: (1) dissolvable matrix patches, (2) patches having a non-dissolvable backing, and (3) patches with a dissolvable backing.
- Dissolvable matrix patches work similar to gum, lozenge and tablet dosage forms.
- the dissolving matrix releases the drug into the oral cavity for absorption by oral mucosa. They usually last longer than lozenges or tablets. Unlike gum, dissolvable matrix patches release the drug passively rather than actively.
- One limitation of all these systems is that the drug concentration in the mouth is not well controlled.
- buccal patches with backings were developed. Controlling drug concentration is particularly important when mucosally delivering drugs that require the help of permeation enhancers.
- Permeation enhancers are chemicals that can temporarily compromise the integrity of the oral mucosa so that drug delivery can be enhanced. The concentration of enhancers needs to be carefully controlled.
- the enhancer can cause mucosal irritation or damage. If too low, it may not provide the desired enhancement of drug delivery.
- One way to maintain control of both drug and enhancer concentration is to include a backing so that the active formulation of the buccal patch is completely isolated from the surrounding environment, especially the saliva of the oral cavity.
- Non-dissolvable backings are usually flexible. They are designed to stay in the oral cavity for long periods of time, e.g., up to 10-15 hours.
- the disadvantage is that the patch has to be removed from oral mucosa by the patient after drug administration.
- Patches with dissolvable backings are designed to stay in the oral cavity for a short period of time.
- the backing controls the local environment inside the patch so that high efficient drug delivery can be achieved in a controlled fashion. Over time, the backing dissolves or disintegrates in the oral cavity (e.g., when exposed to saliva) in order for all or part of the delivery device to go away.
- Such devices eliminate the need to remove the patch after treatment has been completed.
- One of the challenges of providing patches with a dissolvable and/or disintegratable backing has been the need to provide materials that are able to provide an adequate barrier, in order to control the drug and/or permeation enhancer concentration over the period of drug delivery, while still being able to dissolve and/or disintegrate over time.
- transmucosal delivery devices especially oral transmucosal delivery devices, that are able to dissolve and/or disintegrate over time when exposed to moisture; and that also provide sufficient barrier properties so as to prevent, or at least partially inhibit or slow, the tendency of drugs or other active agents from diffusing through the backing layer.
- the present invention overcomes shortcomings of prior art devices.
- the present invention relates to backing layers for use with transmucosal drug delivery devices that are able to dissolve or otherwise disintegrate over time when exposed to moisture (e.g., saliva found within the oral cavity) and which are able to prevent, or at least partially inhibit or slow, the diffusion of water, drugs, other active agents, or other molecules therethrough.
- moisture e.g., saliva found within the oral cavity
- dissolvable include, but are not necessarily limited to, what is meant by the terms “dissolve” and “disintegrate”, “dissolving” and “disintegrating”, or “dissolvable” and disintegratable", respectively.
- water-dissolvable includes, but is not limited to, “water-disintegratable”.
- a dissolvable layer may separate into components when exposed to moisture and optionally pass into solution or it may pass directly into solution when exposed to moisture.
- active agent broadly includes any drug, hormone, vitamin, nutrient, or molecule that is intended for transmucosal delivery.
- inventive backing layers are typically used in combination with one or more layers within a transmucosal delivery device.
- inventive backing layers are used in combination with one or more active layers in order to isolate an active agent against a mucosal surface while preventing, or at least partially inhibiting or slowing, diffusion of the active agent away from the mucosal surface and into the surrounding environment.
- the inventive backing layer prevents, inhibits or slows infusion of the active agent into the oral cavity, where it can be swallowed or expectorated.
- Backing layers according to the invention include hydrophilic and non-hydrophilic regions that allow the backing layer to provide good dissolvability in moisture over a prescribed period of time, while also inhibiting or slowing the diffusion of water from the surrounding environment into the dosage form and inhibiting or slowing the diffusion of the active agent out of the dosage form and into the surrounding environment.
- non-hydrophilic region is defined as any region other than the "hydrophilic region”.
- non-hydrophilic regions include a hydrophobic liquid phase (e.g., oil droplets or layers), a hydrophobic semisolid phase (e.g., hydrogenated vegetable oil droplets or layers), a hydrophobic solid phase (e.g., fatty acids, wax particles), voids (e.g., gaseous bubbles), and solids (e.g., non-dissolvable solid particles).
- the non-hydrophilic region may comprise one or more hydrophobic phases.
- the "hydrophilic region” comprises at least one hydrophilic polymer material that forms a matrix that holds the backing layer together prior to use, but which dissolves over time when exposed to moisture (e.g., saliva found within the oral cavity of a patient).
- moisture e.g., saliva found within the oral cavity of a patient.
- the non-hydrophilic region is included within the backing layer (e.g., within the hydrophilic region) in order to provide a barrier to the diffusion of water, drugs, or other active agents through the backing layer during the time before which the backing layer dissolves.
- the non-hydrophilic region can form a continuous barrier or, in the alternative, it can form a discontinuous barrier that, in effect, creates a more tortuous or circuitous route along which the drug or other active agent must travel before it is able to diffuse all the way through the backing layer.
- the non-hydrophilic region comprises a disperse phase within a continuous hydrophilic region (e.g., in the form of gaseous voids, oil droplets, wax particles, plastic or other solids, or insoluble inorganic particulates).
- a continuous hydrophilic region e.g., in the form of gaseous voids, oil droplets, wax particles, plastic or other solids, or insoluble inorganic particulates.
- the backing layers according to the invention may be used in any transmucosal delivery device known in the art. They are particularly well-suited for use with transmucosal delivery devices used to deliver a drug or other active agent under a closed environment.
- the backing layers according to the invention can be formulated so as to resist dissolving and provide an effective barrier layer during a prescribed period of time. In this way, the backing layers according to the invention can facilitate the manufacture of delivery devices that do not need to be peeled off and discarded in the normal manner as required with non-dissolvable buccal patches or other delivery devices known in the art.
- Figure 1 is a cross-section view illustrating an exemplary backing layer according to the invention that includes a continuous hydrophilic region or component and a disperse non-hydrophilic region or component comprising gaseous voids;
- Figure 2 is a cross-section view illustrating an alternative backing layer according to the invention comprising a continuous hydrophilic region or component and a disperse non-hydrophilic region or component comprising a liquid or solid material
- Figure 3 is a cross-section view of an inventive backing layer illustrating the concept of a tortuous or circuitous route that a drug or other active molecule must take in order to diffuse through the backing layer;
- Figure 4 is a cross-section view illustrating an alternative backing layer according to the invention that includes a continuous hydrophilic region or component surrounding a continuous non-hydrophilic region or component that is entirely encapsulated within the hydrophilic region;
- Figure 5 is a cross-section view illustrating an alternative backing layer comprising two continuous layers of a hydrophilic region separated by a non- hydrophilic region sandwiched therebetween;
- Figure 6 is a cross-section view illustrating an alternative backing layer comprising a continuous hydrophilic region or component and a plurality of elongated non-hydrophilic regions dispersed within the hydrophilic region;
- Figure 7 is a cross-sectional view illustrating a transmucosal device comprising a backing layer according to the invention and an active layer comprising a drug or other active agent adjacent to the backing layer;
- Figure 8 is a cross-section view illustrating a delivery device comprising a backing layer according to the invention adjacent to an active layer that extends along an entire length of the backing layer;
- Figure 9 is a cross-section view illustrating a delivery device comprising a backing layer according to the invention, an active layer adjacent to the backing layer, and an adhesive layer adjacent to the backing layer and circumscribing the active layer
- Figure 10 is a cross-section view illustrating a delivery device comprising a backing layer according to the invention, an adhesive layer adjacent to the backing layer, and an active layer adjacent to the adhesive layer and sized so that a portion of the adhesive layer circumscribes or extends beyond the active layer
- Figure 11 is chart depicting the results of a diffusion study that compared the diffusion rates of sumatriptan across various backing layers manufactured according to the invention, as well as a clear backing layer as a baseline comparison; and
- Figure 12 is chart depicting the results of an in vivo study that measured serum sumitriptan concentrations as a function of time using different backing layers according to the invention.
- the present invention relates to backing layers for use with transmucosal drug delivery devices that include hydrophilic and non-hydrophilic regions or components in order to provide the dual function of being able to dissolve when exposed to moisture over time while inhibiting or slowing the diffusion of water, drugs, other active agents, or other molecules through the backing layer.
- the inventive backing layers are suitable for use with any transmucosal delivery devices known in the art.
- inventive backing layers according to the invention may include a variety of components which together form hydrophilic and non-hydrophilic regions that yield a backing layer that is dissolvable when exposed to moisture and that inhibits or slows the migration of water, drugs or other molecules therethrough compared to a backing layer that does not include the non-hydrophilic region.
- a given numeric value is preceded by the term "about”
- the effect of the term "about” is to define a range that is ⁇ 10% of the given numeric value.
- the hydrophilic region or component generally comprises one or more hydrophilic polymers that have the property of being dissolvable and/or disintegratable in saliva.
- hydrophilic polymers that may be used in accordance with the invention include, but are not limited to, protein-based materials (e.g., gelatin and caseine), pectin, agarose, agar, chitosan, carrageenan, starch, cellulose and cellulose derivatives (e.g., methyl cellulose, calcium carboxymethylcellulose, sodium carboxymethylcellulose, crosslinked polymer of sodium carboxymethylcellulose (e.g., croscarmellose sodium), microcrystalline cellulose, ethylcellulose, hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropyl methylcellulose, hydroxypropylmethylcellulose phthalate, other cellulose ethers, cellulose acetate, and cellulose acetate phthalate), polyvinyl alcohol, polyvinylpyrrolidone (PVP), cross-linked povidone,
- solvents or plasticizers may be used, which make the backing layer more flexible.
- plasticizers include, but are not limted to, glycerin, propylene glycol, polyethylene glycol, polypropylene glycol, sugar alcohols, and corn syrup.
- the hydrophilic region may also include a surfactant or emulsifier so that the non-hydrophilic region is more stable in the hydrophilic region.
- the hydrophilic region may also include other components, such as flavorants, sweeteners, coloring agents, antiseptic agents, preservatives, and other ingredients so that the patch is more stable and promotes better patient compliance.
- the hydrophilic region will comprise a continuous phase that substantially or entirely surrounds or encompasses the non-hydrophilic region. Nevertheless, it is certainly within the scope of the invention to provide a non- hydrophilic region comprising two or more distinct subregions, layers or components. The time in which the hydrophilic region or component will dissolve when exposed to moisture (e.g., saliva) depends on a number of factors.
- the concentration of the hydrophilic polymer within the hydrophilic region will be in a range of about 1 % to 100% by weight of the hydrophilic region, more preferably in a range from about 5% to about 90%, and most preferably in a range from about 10% to about 80% by weight of the hydrophilic region.
- the concentration of the solvent or plasticizer within the hydrophilic region will be in a range from 0% to about 80% by weight of the hydrophilic region, more preferably in a range from about 2% to about 60%, and most preferably in a range from about 5% to about 50% by weight of the hydrophilic region.
- the hydrophilic region will preferably comprise from about 10% to about 95 % percent by volume of the overall backing layer, more preferably from about 15% to about 90%), and most preferably from about 20% to about 85% by volume of the backing layer.
- the hydrophilic region or component, as disclosed herein, may optionally contain flavorants and/or sweeteners.
- flavorants include, but are not limited to, mint (for example, peppermint or spearmintl), citrus oils (for example, lemon, lime, orange, or grapefruit), fruit essences (for example, berry or cherry), grape, coconut, chocolate, clove, wintergreen, anise, vanilla, or combinations thereof.
- sweeteners include, but are not limited to, water- soluble sweeteners such as monosaccharides, disaccharides, and polysaccharides such as xylose, ribose, glucose, mannose, galactose, fructose, dextrose, sucrose, maltose, partially hydrolyzed starch or corn syrup solids and sugar alcohols such as sorbitol, xylitol, mannitol and mixtures thereof; as well as water-soluble artificial sweeteners such as the saccharin salts, cyclamate salts, stevia, aspartame, and acesulfame potassium.
- water- soluble sweeteners such as monosaccharides, disaccharides, and polysaccharides such as xylose, ribose, glucose, mannose, galactose, fructose, dextrose, sucrose, maltose, partially hydrolyzed starch or corn syrup solids and sugar alcohols such as
- the non-hydrophilic region may comprise either a disperse phase or a continuous phase relative to the hydrophilic region.
- the main purpose of the non- hydrophilic region is to inhibit or slow migration of water, drugs or other active agents or molecules through the backing layer compared to a backing layer in the absence of the non-hydrophilic region.
- the level of inhibition or slowing of migration need not be dramatic, but appreciably measurable. Nevertheless, in more preferred embodiments according to the invention, the inhibition or slowing of migration will be substantial (e.g., so that it takes many times longer for the targeted molecule to diffuse through the backing layer compared to a backing layer in the absence of the non-hydrophilic region).
- non-hydrophilic materials that can be used as a disperse phase within the hydrophilic region include, but are not limited to, air or other gaseous bubbles or voids, droplets of one or more hydrophobic liquids, one or more types of solid hydrophobic particles, one or more types of particles that are not necessarily hydrophobic but which are not readily soluble in water, and mixtures thereof.
- hydrophobic liquids that may be dispersed in droplet form throughout the hydrophilic region so as to form a disperse non-hydrophilic region include, but are not limited to, oil, vegetable oils, mineral oil, silicones, and organic polymers.
- solid or semi-solid non-hydrophilic materials that may be dispersed throughout the hydrophilic region so as to form a disperse non-hydrophilic region include, but are not limited to, a wide variety of waxes, magnesium stearate, fats, fatty acids, salts of fatty acids, polymers, polymeric beads, and silicone particles.
- solid particles that are not necessarily chemically hydrophobic but that are not readily water soluble and that may be dispersed throughout the hydrophilic region so as to form a disperse non-hydrophilic region include water-insoluble inorganic filler particles, examples of which include, but are not limited to, talc, sand, silica, alumina, transition metal oxides (e.g., titanium dioxide), silicates, ground geologic materials, and limestone.
- water-insoluble inorganic filler particles examples of which include, but are not limited to, talc, sand, silica, alumina, transition metal oxides (e.g., titanium dioxide), silicates, ground geologic materials, and limestone.
- any material whether in a gaseous, liquid or solid phase, can comprise the non-hydrophilic region, the only limitation being that such material provides a substantially higher barrier to water, drugs, or other active agents than the hydrophilic region.
- any GRAS generally regarded as safe
- the non-hydrophilic region may comprise a continuous phase that effectively forms a continuous shield or barrier so as to prevent, inhibit or slow migration of the water, drugs, active agents, or other molecules through the backing layer.
- the continuous non-hydrophilic region may comprise a continuous phase that is entirely encapsulated within the hydrophilic region, or which bifurcates the hydrophilic region into two or more subregions or layers.
- the non-hydrophilic region may comprise a plurality of subregions that are sufficiently large so as to effectively constitute a plurality of continuous phases rather than a disperse phase, although the notion of what constitutes a disperse phase rather than a plurality of continuous phases is a sliding scale.
- the continuous non-hydrophilic region or component may comprise a thin layer of a liquid or solid non-hydrophilic material that is interposed between an active layer or region containing a drug or other target molecule and at least a portion of the hydrophilic region.
- the non-hydrophilic material may generally comprise any desired non-hydrophilic material. This is because, as the hydrophilic region disintegrates over time when exposed to moisture, the non-hydrophilic droplets or particles dispersed with the hydrophilic region will also readily disperse within the oral cavity or other place of attachment of the delivery device.
- the non-hydrophilic region comprises one or more continuous regions of substantial size, it may be preferable for the material used to form the non-hydrophilic region to comprise a material that is substantially liquid or otherwise easily broken up and dispersed, at least at body temperature.
- the material comprising the non-hydrophilic region is a liquid at room temperature, it will generally readily disperse upon disintegration of the hydrophilic region. It is also within the scope of the invention to select a material that may be a solid or semi-solid at room temperature but which softens sufficiently when raised to body temperature so as to become more easily dispersible upon disintegration of the hydrophilic region.
- the nonhydrophilic region will preferably comprise from about 5% to about 90%) by volume of the overall backing layer, more preferably from about 10% to about 85%o, and most preferably from about 15%> to about 80% by volume of the backing layer.
- the thickness of the backing layer generally correlates with the time it takes for the backing layer to become substantially disintegrated when exposed to moisture (e.g., saliva).
- the backing layer as a finished product after drying, will preferably have a thickness in a range from about 0.1 mm to about 5 rnm, more preferably in a range from about 0.2 mm to about 3.5 mm, and most preferably in a range from about 0.3 mm to about 2 mm.
- the backing layer can be formulated and sized so as to yield a backing layer that becomes dissolved within the oral cavity when exposed to saliva within a prescribed time period or range (or when exposed to moisture in some other region of the body).
- the backing layer according to the invention may have a formulation and thickness in order for the backing layer to become dissolved within the oral cavity when exposed to saliva within a time period and a range from about 1 minute to about 2 hours, more preferably in a range from about 10 minutes to about 1 hour.
- backing layers according to the invention will preferably decrease the permeability coefficient of water, drug, other active agents, or at least one other molecule by at least about 25%>, more preferably by at least about 50%, and most preferably by at least about 75% compared to a backing layer in the absence of the non-hydrophilic region.
- Figure 1 depicts a backing layer 10 that includes a hydrophilic region 12 and a plurality of gaseous voids 14 dispersed therein as a disperse non-hydrophilic region. Due to the initially solid nature of the hydrophilic region, the gaseous voids 14 will remain substantially intact during at least a portion of the predetermined time for delivery of an active agent through the mucosal layer by a delivery device incorporating the backing layer. Because molecules do not tend to diffuse through air or other gaseous voids, they are generally forced to diffuse around the voids, causing them to follow a more tortuous path through the backing layer.
- the purpose of the disperse non-hydrophilic region is to inhibit migration of a drug or other active agent contained within the active layer through the backing layer during use of the delivery device to deliver a drug or other active agent through a mucosal surface (not shown). It has been found that including a dispersed non- hydrophilic region inhibits migration of molecules by creating a tortuous or circuitous path along which the drug or other active agent must migrate to avoid the intermittent barriers foraied by the dispersed non-hydrophilic region. In this way, the dispersed non- hydrophilic region creates an effective diffusion path that is greater than the actual thickness of the backing layer. In addition, the non-hydrophilic region reduces the surface area through which drug or other active agents can diffuse through. In this way, the effective area for diffusion is smaller than the actual surface area of the backing layer.
- a backing layer having a thickness x may provide barrier properties that approximate those of a backing layer having a thickness 2x.
- FIG. 2 illustrates an alternative backing layer 20 according to the invention that includes a continuous hydrophilic region 22 and a disperse non-hydrophilic region 24 comprising a hydrophobic liquid or solid or a solid that is not readily soluble in water.
- a disperse non-hydrophilic region 24 comprising a hydrophobic liquid or solid or a solid that is not readily soluble in water.
- Figure 3 illustrates hypothetical diffusion paths 26 through an inventive backing layer, such as backing layer 20 comprising a hydrophilic region 22 and a disperse non- hydrophilic region 24 comprising a liquid or solid.
- the diffusion paths 26 deviate from a straight line and therefore necessarily lengthen the diffusion paths that would otherwise exist in the absence of the disperse non-hydrophilic region 24.
- Figure 4 depicts an alternative backing layer 30 according to the invention that includes a continuous hydrophilic region 32 that completely surrounds or encapsulates a continuous non-hydrophilic region or component 34.
- the continuous non-hydrophilic region 34 effectively forms a barrier such that any diffusion of drugs or other targeted molecules must follow diffusion path 36 that entirely bypass the continuous non- hydrophilic region 34.
- Figure 5 depicts an alternative backing layer 40 that includes a hydrophilic region 42 that is at least partially bifurcated by a non-hydrophilic region 44 sandwiched or layered between two halves of the hydrophilic region 42. It should be understood that because Figure 5 is merely a cross-section, the non-hydrophilic region 44 may terminate in unseen dimensions short of the hydrophilic region 42 such that the hydrophilic region 42 may comprise a continuous phase. Because the non-hydrophilic region 44 extends to the end of the hydrophilic region 42, it causes the diffusion paths 46 to bypass the non-hydrophilic region 42 and follow diffusion paths out the sides, rather than the top, of the backing layer 40.
- Figure 6 illustrates an alternative backing layer 50 according to the invention that includes a continuous hydrophilic region 52 and a plurality of elongated non- hydrophilic regions 54 that overlap in a manner so as to yield a nonlinear diffusion path 56 through the backing layer 50.
- the non-hydrophilic regions 54 are in one sense a disperse phase. Nevertheless, because they are elongated, they behave in some ways more like the continuous non-hydrophilic regions illustrated in Figures 4 and 5.
- the main purpose of Figure 6 is to illustrate that there are a wide range of possible non- hydrophilic regions between the highly disperse phases depicted in Figures 1 and 2 and the continuous phases depicted in Figures 4 and 5.
- Figure 7 depicts delivery device 60 comprising a backing layer 62 according to the invention that includes a hydrophilic region 64 and a disperse non-hydrophilic region 66.
- Adjacent to the backing layer 62 is an active layer 68 comprising a drug or other active agent for delivery into a patient or animal.
- the backing layer 62 will resist dissolving when exposed to saliva or other sources of moisture during a prescribed period of time in order for the delivery device 60 to isolate and maintain the active layer 68 against the delivery site for a time sufficient for a drug or other active agent therein to be delivered as desired and not diffused into the oral cavity or other location away from the targeted delivery site.
- Figure 8 depicts an alternative delivery device 70 comprising an inventive backing layer 72 having a hydrophilic region 74 and a dispersed non-hydrophilic region 76.
- An active layer 78 comprising a drug or other active agent is depicted as extending along an entire length of the backing layer 72.
- Figure 9 depicts an alternative delivery device 80 comprising an inventive backing layer 82 according to the invention, an adhesive layer 84 adjacent to a portion of the backing layer and an active layer 86 adjacent to a portion of the backing layer, with the adhesive layer 84 circumscribing at least a portion of the active layer 86.
- the adhesive layer can assist the backing layer in isolating and maintaining the drug or other active ingredient in the active layer 86 within a targeted delivery region.
- Figure 10 depicts an alternative delivery device 90 comprising an exemplary backing layer 92 according to the invention, an adhesive layer 94 adjacent to and extending along an entire length of the backing layer 92 and an active layer 96 adjacent to a portion of the adhesive layer 94.
- the adhesive layer 94 also circumscribes at least a portion of the active layer 96, at least within the cross-section depicted in Figure 10.
- the delivery device as depicted in Figures 1-10 are merely illustrative.
- the relative lengths, widths and thicknesses of the various layers can be adjusted as desired to yield a delivery device having the desired properties.
- inventive backing layers according to the invention can be used in the manufacture of transmucosal delivery devices having any desired drug or other active agent.
- the drug or other active agent will typically comprise a discrete active layer or region adjacent to the inventive backing layers according to the invention.
- inventive backing layer contains no drug or active agent initially when the transmucosal delivery devices are manufactured, it is within the scope of the invention for the active layer or region, some time after the transmucosal delivery devices are manufactured, to be at least partially dispersed within the inventive backing layer.
- the active layer or region of the transmucosal delivery devices according to the invention include a drug or other active agent and at least one enhancer.
- drugs or other active agents examples include fentanyl, codeine, sufentanil, lofentanil, carfentanil, alfentunil, mo hine, other opiates, sumatriptan, other triptans, interferons, heparin, proteins, peptides, and barbiturates, analgesics, anesthetics, anxolytics, sedatives, anti-depressants, cannobinoids, anticoagulants, anti-biotics, antihistamines, blood pressure modulators, anti-cholesterol drugs, vitamins, nutrients, etc.
- Preferred examples of drugs or other active agents that may be used in transmucosal delivery devices according to the invention include fentanyl, codeine, sufentanil, lofentanil, carfentanil, alfentunil, morphine, other opiates, triptans, in particular sumatriptan, interferons, proteins, and peptides.
- Preferred examples of drugs or other active agents that may be used in transmucosal delivery devices according to the invention include triptans, in particular sumatriptan, interferons, proteins, peptides, and any drug that requires an enhancer to promote diffusion of the drug or active agent in transmucosal delivery.
- enhancers that may be used to facilitate or accelerate delivery of a drug or other active agent through the mucosal layer, particularly high molecular weight molecules that may otherwise resist diffusion through the mucous membrane, include, but are not limited to, bile acid, their salt forms and derivatives, acyl carnitines, sodium dodecylsulfate, dimethylsulfoxide, sodium laurylsulfate, salts and other derivatives of saturated and unsaturated fatty acids, surfactants, alcohols, terpenes, cyclodextrins and their derivatives, saponins and their derivatives, chitosan, and chelators (e.g., EDTA, citric acid and salicylates).
- bile acid their salt forms and derivatives
- acyl carnitines sodium dodecylsulfate, dimethylsulfoxide, sodium laurylsulfate
- salts and other derivatives of saturated and unsaturated fatty acids surfactants, alcohols,
- bile acids examples include, but are not limited to, sodium cholate, dehydrocholate, sodium glycocholate, sodium glycodeoxycholate, sodium deoxycholate, sodium lithocholate chenocholate, chenodeoxycholate, glycochenocholate, sodium taurocholate, taurodeoxycholate, taurochenocholate, taurochenodeoxycholate, ursocholate, ursodeoxycholate, and hyodeoxycholate, and the like.
- suitable matrix materials that may optionally be included in addition to the drug and enhancer include, but are not limited to, alginic acid, its salts and derivatives, celluloses, cellulose ethers, their salts and derivatives, starches, carrageenan, polyethylene glycol, polyethylene oxide, polyvinyl alcohol, polyvinyl pyrrolidone, acacia, and polyacrylic acids.
- the backing layer according to the invention may be used together with an active layer to form a two-layer transmucosal delivery device or dosage form.
- the delivery device may include an adhesive layer adjacent to the backing layer that circumscribes the active layer in order to enhance adhesion between the backing layer and a mucosal surface or membrane to which it is attached during use (e.g., Figures 9 and 10).
- Transmucosal delivery devices may be placed against a mucosal surface or membrane of a mammal in order to deliver one or more active agents across the mucosa (e.g., within an oral cavity, vagina, or intestine).
- a typical method for delivering an active agent across mucosa comprises (1) placing the transmucosal delivery against a mucosal surface and (2) allowing the transmucosal delivery device to remain against the mucosal surface so as to provide a desired treatment.
- the transmucosal delivery is placed against a mucosal surface within an oral cavity of a mammal.
- the transmucosal delivery is typically allowed to (3) remain within the oral cavity or against other mucosa until it dissolves.
- the transmucosal delivery device may be used to deliver any active agent so as to provide any desired treatment. Such devices are particularly useful for delivering sumatriptan. They may also be used, for example, to deliver opiates or other analgesics to treat pain, including what is known as "breakthrough pain", which refers to pain that is felt by a patient who is already medicated for pain.
- Example 1 A dissolvable backing layer was manufactured by dissolving 20 parts gelatin and
- a dissolvable backing layer was manufactured from 20 parts gelatin, 10 parts glycerin, 1 part sodium alginate and 69 parts water, which together formed a hydrophilic region, and gaseous voids dispersed throughout the hydrophilic region as a disperse non- hydrophilic region.
- the forming procedure was the same as in Example 1 and yielded a gel/air mixture and subsequent cast backing layer having approximately the same concentration of air voids.
- the addition of sodium alginate within the formulation yielded a backing layer that was stronger and that lasted longer, relative to Example 1.
- a dissolvable backing layer was manufactured from 20 parts gelatin, 10 parts glycerin, and 70 parts water, which together formed a hydrophilic region, and 20% by weight of the hydrophilic region of powdered talc (magnesium silicate) dispersed throughout the hydrophilic region as a disperse non-hydrophilic region.
- the procedures for making the hydrophilic region and backing layer were the same as in the Example 1.
- Example 4
- a dissolvable backing layer was manufactured from 20 parts gelatin, 10 parts glycerin, and 70 parts water, which together formed a hydrophilic region, and 5% by weight of the hydrophilic region of Crisco® oil (a partially hydrogenated vegetable oil) dispersed throughout the hydrophilic region as a disperse non-hydrophilic region.
- Crisco® oil a partially hydrogenated vegetable oil
- Example 5 A dissolvable backing layer was manufactured from 20 parts gelatin, 10 parts glycerin, and 70 parts water, which together formed a hydrophilic region, and 10% by weight of the hydrophilic region of Lubritab® (a hydrogenated vegetable oil) dispersed throughout the hydrophilic region as a disperse non-hydrophilic region.
- the mixture was heated to 70°C in order to dissolve the gelatin within a hydrophilic region and to cause the hydrogenated vegetable oil to become a liquid as a hydrophobic phase.
- a high-speed homogenizer was used to whip the two phases together so that the mixture formed an oil-in-water emulsion. The temperature was then lowered to around 40° C while the homonegizer was running.
- the hydrogenated vegetable oil solidified while the gelatin gel remained liquid.
- the mixture thus became a solid-in- liquid suspension.
- the gelatin gel solidified and the solid hydrogenated vegetable oil particles remained permanently dispersed as a non-hydrophilic region within the continuous hydrophilic gelatin matrix.
- the thickness of the cast backing layer was 1.5 mm.
- the backing layer was dried overnight at room temperature, yielding final backing layer having a thickness of about 0.35 mm as a result of water evaporation.
- a dissolvable backing layer was manufactured from 20 parts gelatin, 10 parts glycerin, and 70 parts water, which together formed a hydrophilic region, and 5% by weight of the hydrophilic region of magnesium stearate dispersed throughout the hydrophilic region as a disperse non-hydrophilic region.
- the procedures of making the hydrophilic region and casting the backing layer were the same as in the Example 1.
- a dissolvable backing layer was manufactured from 20 parts gelatin, 10 parts glycerin, 0.5 part agarose, and 69.5 parts water, which together formed a hydrophilic region, and gaseous voids dispersed throughout the hydrophilic region as a disperse non- hydrophilic region.
- the manufacturing procedures were the same as in the Example 1.
- the addition of agarose yielded a backing layer that was stronger and that lasted longer, relative to Example 1.
- a dissolvable backing layer was manufactured from 20 parts gelatin, 10 parts glycerin, 0.53 part peppermint oil, 2.19 parts acesulfame potassium, and 67.28 parts water, which together formed a flavored hydrophilic region, and gaseous voids dispersed throughout the hydrophilic region as a disperse non-hydrophilic region.
- the manufacturing procedures were the same as in the Example 1.
- the addition of a flavorant and sweetener yielded a backing layer that tasted better. This would be expected to improve patient compliance.
- Example 9 A dissolvable backing layer was manufactured from 20 parts gelatin, 10 parts glycerin, 0.1 part sodium lauryl sulfate, and 69.9 parts water, which together fo ⁇ ned a hydrophilic region, and gaseous voids dispersed throughout the hydrophilic region as a disperse non-hydrophilic region.
- the manufacturing procedures were the same as in the Example 1.
- the surfactant sodium lauryl sulfate
- Example 1 A group of backing layers for comparative testing were manufactured using the formulations and procedures stated in Example 1 (aerated), Example 3 (talc), Example 5 (hydrogenated vegetable oil), and Example 6 (Mg stearate).
- a clear backing layer (clear) was manufactured for purposes of comparison according to Example 1 but without a non-hydrophilic region, i.e., the backing layer had the same hydrophilic region as the aerated backing layer but without any non-hydrophilic region dispersed therein. Diffusion studies were conducted to test the barrier function of the various backings discussed above using side-by-side diffusion chambers.
- Figure 11 is a chart that graphically depicts the amount of sumatriptan that crossed the membrane over time for each of the backing layers, as was determined using HPLC. As is readily shown, the diffusion of sumatriptan across the backing layer was greatest for the "clear" backing layer that did not include a non-hydrophilic region. The backing layers that included a non-hydrophilic region all demonstrated significantly reduced diffusion of sumatriptan across the backing layer, particularly during the early stages of the test. Additonal data (not shown) indicate that the addition of a non- hydrophilic region not only increased the barrier function of the backing layer, but also slowed down the hydration rate of the hydrophilic regions comprising the gelatin gel, thus further increasing the barrier function of the backing layer during its hydration period.
- Example 1 anesthetized dog
- Example 4 partially hydrogenated vegetable oil
- Example 6 Mg stearate
- the active formulation comprised 10 mg sumatriptan, 5 mg sodium taurocholic acid, and sodium alginate.
- the active layers were 0.75 inches in diameter.
- the backing layers were 0.875 inches in diameter.
- the active and backing layers were "glued" together by moistening them with water prior to the in vivo experiments. In vivo experiments were conducted on the oral mucosa of anesthetized dogs over a period of two hours.
- a transmucosal drug delivery device having a dissolvable backing layer, an adhesive layer, and an active layer.
- the dissolvable backing layer was manufactured from a gel that comprised 20% gelatin and 10%> glycerin, with the balance being water, which together formed a hydrophilic region, and gaseous voids dispersed throughout the hydrophilic region as a dispersed non-hydrophilic region.
- the hydrophilic region comprised 50% by volume of the backing layer while the voids comprised 50% by volume.
- the backing layer was cast on a plastic substrate. The thickness of the backing layer was 2 mm when first cast. The backing layer was allowed to solidify without drying.
- the adhesive layer was formed from an aqueous gel that comprised 2.5% Polyox® 750 (a polyethylene oxide), 0.5% Carbopol® 971 (a polyacrylic acid), with the balance being water.
- the gel was cast directly onto the solidified backing layer to form the adhesive layer, which had a thickness of 1 mm when first cast.
- the combined backing and adhesive layers were dried overnight at room temperature.
- the active layer was formed from an aqueous mixture that comprised 6%> sodium alginate, 4% sumatriptan as a succinate salt, 2% sodium taurocholic acid, with the balance being water.
- the mixture was cast directly onto the exposed surface of the dried adhesive layer to form the active layer having of 1 mm when first cast.
- the dosage form was then dried overnight at room temperature.
- Example 11 An oral transmucosal delivery patch containing an interferon as the active agent was made according to the current invention.
- the patch had three layers: (1) an active layer, (2) an adhesive layer, and (3) a backing layer.
- the formulations of the three layers are listed in the following tables.
- a gel composition used to form the active layer was prepared by mixing the sodium alginate, interferon oc2b, and sodium taurocholate as dry ingredients in a mixing can. Then an appropriate amount of water was added. The mixing can was rolled slowly on a roller mixer to avoid trapping excessive air inside the gel. Once the gel was adequately mixed (i.e., free of solid alginate particles), it was pipetted onto a plurality of 0.875 inch polystyrene disks at 1 ml per disk to form an active layer. The gel was dried at room temperature overnight to form the finished active layer.
- a gel composition used to form the backing layer was prepared by mixing the gelatin, glycerin and dodecyltrimethylammonium bromide in 55°C water.
- an overhead mixer was used to whip the gel at 1500 rpm until the gel turned white and the volume doubled so as to form a foamed gel composition.
- the foamed gel composition was then cast in a plastic mold having a diameter of 1 inch and a thickness of 0.125 inch. The cast gel composition was allowed to dry at room temperature overnight to form the finished backing layer.
- a gel composition used to form the adhesive layer was prepared by roll-mixing the ingredients in a mixing can. A thin layer, about 1 mm in thickness, was applied to the exposed surface of the dried backing layer. The combined backing and adhesive layers were dried together overnight at room temperature.
- An oral transmucosal delivery patch containing sumatriptan as the active agent was made according to the current invention.
- the patch had three layers: (1) an active layer, (2) an adhesive layer, and (3) a backing layer.
- the formulations of the three layers are listed in the following tables.
- a gel composition used to form the backing layer was made by dissolving the gelatin in 50°C water containing the glycerin and sodium alginate. The gel was put in an oven heated to 50°C to cause the gelatin to dissolve completely. Once the gelatin was thoroughly dissolved, the acesulfame potassium was added as sweetener. The gel composition was aerated by a high shear homogenizer to yield a foamed gel composition. The gel composition was cast on a plastic release liner to form an unsolidified sheet having a thickness of 2.2 mm using a casting block. The sheet was allowed to solidify without drying.
- a gel composition used to form the adhesive layer was made by dissolving the non- ater ingredients in the water.
- the adhesive gel composition was mixed under vacuum for about 6 hours until the gel became clear without lumps.
- the adhesive gel composition was cast on the solidified backing layer formed in the immediately preceding paragraph.
- the setting for the casting block was maintained at 2.2 mm. Since the backing layer shrank to about 1.2 mm upon solidifying, the actual thickness of the adhesive layer was about 1 mm.
- the combined backing/adhesive layers were allowed to dry at room temperature overnight.
- a gel composition used to form the active layer was made by dry mixing the non-water ingredients in a mixing container and then roll-mixing the gel on a roller for 6 hours after addition of the water.
- the active gel composition was sonicated for a few minutes to eliminate air bubbles.
- a plastic mold having a plurality of mold cavities with a diameter of 0.6875 inch and a thickness of 0.5 mm was placed over a portion of the backing/adhesive layer.
- the active gel composition was cast inside the plastic mold cavities and the excess gel composition was cut using a stainless steel blade. The plastic mold was then removed. Once the active layer was dried, tri-layer patches were cut out using a 0.8125 inch diameter die cutter.
- the finished products were tri-layer patches in which the active layers were smaller than (i.e., circumscribed by) the backing/adhesive layers.
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006532911A JP2007516222A (en) | 2003-05-09 | 2004-05-10 | Dissolvable backing layer for use with transmucosal delivery devices |
MXPA05012009A MXPA05012009A (en) | 2003-05-09 | 2004-05-10 | Dissolvable backing layer for use with a transmucosal delivery device. |
EP04751777A EP1631256A2 (en) | 2003-05-09 | 2004-05-10 | Dissolvable backing layer for use with a transmucosal delivery device |
CA002523784A CA2523784A1 (en) | 2003-05-09 | 2004-05-10 | Dissolvable backing layer for use with a transmucosal delivery device |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US46950703P | 2003-05-09 | 2003-05-09 | |
US60/469,507 | 2003-05-09 | ||
US10/841,893 | 2004-05-07 | ||
US10/841,893 US7306812B2 (en) | 2003-05-09 | 2004-05-07 | Dissolvable backing layer for use with a transmucosal delivery device |
Publications (2)
Publication Number | Publication Date |
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WO2004100925A2 true WO2004100925A2 (en) | 2004-11-25 |
WO2004100925A3 WO2004100925A3 (en) | 2005-06-02 |
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PCT/US2004/014550 WO2004100925A2 (en) | 2003-05-09 | 2004-05-10 | Dissolvable backing layer for use with a transmucosal delivery device |
Country Status (6)
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US (1) | US7306812B2 (en) |
EP (1) | EP1631256A2 (en) |
JP (1) | JP2007516222A (en) |
CA (1) | CA2523784A1 (en) |
MX (1) | MXPA05012009A (en) |
WO (1) | WO2004100925A2 (en) |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005039499A2 (en) * | 2003-10-24 | 2005-05-06 | Adhesives Research, Inc. | Rapidly disintegrating film |
US7993667B2 (en) | 2005-03-25 | 2011-08-09 | Kimberly-Clark Worldwide, Inc. | Methods of manufacturing a medicated tampon assembly |
US7744556B2 (en) | 2005-03-25 | 2010-06-29 | Kimberly-Clark Worldwide, Inc. | Delivery tube assembly for an applicator |
US7919453B2 (en) | 2005-03-25 | 2011-04-05 | Kimberly-Clark Worldwide, Inc. | Dosage cap assembly for an applicator |
US7708726B2 (en) | 2005-04-28 | 2010-05-04 | Kimberly-Clark Worldwide, Inc. | Dosage form cap for an applicator |
US8252328B2 (en) | 2006-01-06 | 2012-08-28 | Acelrx Pharmaceuticals, Inc. | Bioadhesive drug formulations for oral transmucosal delivery |
US9289583B2 (en) | 2006-01-06 | 2016-03-22 | Acelrx Pharmaceuticals, Inc. | Methods for administering small volume oral transmucosal dosage forms using a dispensing device |
US8865743B2 (en) | 2006-01-06 | 2014-10-21 | Acelrx Pharmaceuticals, Inc. | Small volume oral transmucosal dosage forms containing sufentanil for treatment of pain |
US8753308B2 (en) | 2006-01-06 | 2014-06-17 | Acelrx Pharmaceuticals, Inc. | Methods for administering small volume oral transmucosal dosage forms using a dispensing device |
US8252329B2 (en) * | 2007-01-05 | 2012-08-28 | Acelrx Pharmaceuticals, Inc. | Bioadhesive drug formulations for oral transmucosal delivery |
US8202535B2 (en) | 2006-01-06 | 2012-06-19 | Acelrx Pharmaceuticals, Inc. | Small-volume oral transmucosal dosage forms |
US8357114B2 (en) | 2006-01-06 | 2013-01-22 | Acelrx Pharmaceuticals, Inc. | Drug dispensing device with flexible push rod |
US8535714B2 (en) | 2006-01-06 | 2013-09-17 | Acelrx Pharmaceuticals, Inc. | Small volume oral transmucosal dosage forms containing sufentanil for treatment of pain |
US9066847B2 (en) | 2007-01-05 | 2015-06-30 | Aceirx Pharmaceuticals, Inc. | Storage and dispensing devices for administration of oral transmucosal dosage forms |
US8497409B2 (en) | 2008-02-29 | 2013-07-30 | Kimberly-Clark Worldwide, Inc. | Absorbent article having an olfactory wetness signal |
US8945592B2 (en) | 2008-11-21 | 2015-02-03 | Acelrx Pharmaceuticals, Inc. | Sufentanil solid dosage forms comprising oxygen scavengers and methods of using the same |
US9549842B2 (en) | 2011-02-04 | 2017-01-24 | Joseph E. Kovarik | Buccal bioadhesive strip and method of treating snoring and sleep apnea |
US8701671B2 (en) | 2011-02-04 | 2014-04-22 | Joseph E. Kovarik | Non-surgical method and system for reducing snoring |
US11951140B2 (en) | 2011-02-04 | 2024-04-09 | Seed Health, Inc. | Modulation of an individual's gut microbiome to address osteoporosis and bone disease |
US11951139B2 (en) | 2015-11-30 | 2024-04-09 | Seed Health, Inc. | Method and system for reducing the likelihood of osteoporosis |
US11844720B2 (en) | 2011-02-04 | 2023-12-19 | Seed Health, Inc. | Method and system to reduce the likelihood of dental caries and halitosis |
WO2013110340A1 (en) * | 2012-01-27 | 2013-08-01 | Beta Pharma S.A. | Edible slow dissolving film for treating oral ulcerations |
US10292806B2 (en) | 2013-01-11 | 2019-05-21 | Bvw Holding Ag | Implantable superhydrophobic surfaces |
US11839632B2 (en) | 2013-12-20 | 2023-12-12 | Seed Health, Inc. | Topical application of CRISPR-modified bacteria to treat acne vulgaris |
US11826388B2 (en) | 2013-12-20 | 2023-11-28 | Seed Health, Inc. | Topical application of Lactobacillus crispatus to ameliorate barrier damage and inflammation |
US11833177B2 (en) | 2013-12-20 | 2023-12-05 | Seed Health, Inc. | Probiotic to enhance an individual's skin microbiome |
JP6207459B2 (en) * | 2014-05-15 | 2017-10-04 | 富士フイルム株式会社 | Method for producing transdermal absorption sheet |
DE102019100483A1 (en) * | 2019-01-10 | 2020-07-16 | Lts Lohmann Therapie-Systeme Ag | Oral thin film |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4307075A (en) * | 1979-09-13 | 1981-12-22 | American Home Products Corporation | Topical treatment of aphthous stomatitis |
US5529782A (en) * | 1992-05-07 | 1996-06-25 | Staab; Robert | Dissolvable device for contraception or delivery of medication |
US5700478A (en) * | 1993-08-19 | 1997-12-23 | Cygnus, Inc. | Water-soluble pressure-sensitive mucoadhesive and devices provided therewith for emplacement in a mucosa-lined body cavity |
EP0873750A1 (en) * | 1997-04-23 | 1998-10-28 | Permatec Technologie Ag | Bioadhesive tablets |
WO1999055312A2 (en) * | 1998-04-29 | 1999-11-04 | Virotex Corporation | Pharmaceutical carrier device suitable for delivery of pharmaceutical compounds to mucosal surfaces |
US20010006677A1 (en) * | 1996-10-29 | 2001-07-05 | Mcginity James W. | Effervescence polymeric film drug delivery system |
WO2002002085A2 (en) * | 2000-07-04 | 2002-01-10 | Lts Lohmann Therapie-Systeme Ag | Rapidly-decomposing administrable form for releasing active ingredients in the oral cavity or in bodily cavities |
US6375963B1 (en) * | 1999-06-16 | 2002-04-23 | Michael A. Repka | Bioadhesive hot-melt extruded film for topical and mucosal adhesion applications and drug delivery and process for preparation thereof |
US20020068151A1 (en) * | 2000-10-17 | 2002-06-06 | Kim Won K. | Multi-layered, air-gapped sheet of chitosan |
WO2003015748A2 (en) * | 2001-08-16 | 2003-02-27 | Access Pharmaceuticals, Inc. | Mucoadhesive erodible drug delivery device for controlled administration of pharmaceuticals and other active compounds |
Family Cites Families (78)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5562012A (en) | 1978-11-06 | 1980-05-10 | Teijin Ltd | Slow-releasing preparation |
GB2042888B (en) | 1979-03-05 | 1983-09-28 | Teijin Ltd | Preparation for administration to the mucosa of the oral or nasal cavity |
JPS5758615A (en) | 1980-09-26 | 1982-04-08 | Nippon Soda Co Ltd | Film agnent and its preparation |
CA1208558A (en) | 1982-10-07 | 1986-07-29 | Kazuo Kigasawa | Soft buccal |
US4704119A (en) | 1983-02-03 | 1987-11-03 | Alza Corporation | Method comprising transdermal and buccal treatment of angina |
JPH0830004B2 (en) | 1983-11-14 | 1996-03-27 | コロンビア ラボラトリーズ インコーポレイテッド | Bioadhesive composition and method of treatment therewith |
US4573996A (en) | 1984-01-03 | 1986-03-04 | Jonergin, Inc. | Device for the administration of an active agent to the skin or mucosa |
US4740365A (en) | 1984-04-09 | 1988-04-26 | Toyo Boseki Kabushiki Kaisha | Sustained-release preparation applicable to mucous membrane in oral cavity |
US5288498A (en) | 1985-05-01 | 1994-02-22 | University Of Utah Research Foundation | Compositions of oral nondissolvable matrixes for transmucosal administration of medicaments |
US5855908A (en) | 1984-05-01 | 1999-01-05 | University Of Utah Research Foundation | Non-dissolvable drug-containing dosage-forms for use in the transmucosal delivery of a drug to a patient |
US5783207A (en) | 1985-05-01 | 1998-07-21 | University Of Utah Research Foundation | Selectively removable nicotine-containing dosage form for use in the transmucosal delivery of nicotine |
JPS61280423A (en) | 1985-06-05 | 1986-12-11 | Kiyuukiyuu Yakuhin Kogyo Kk | Mucosal application agent in oral cavity |
DE3601132A1 (en) | 1986-01-16 | 1987-07-23 | Christian Bannert | METHOD FOR TREATING THE MUCUS |
US4755386A (en) | 1986-01-22 | 1988-07-05 | Schering Corporation | Buccal formulation |
JPH0729915B2 (en) | 1986-02-01 | 1995-04-05 | 帝國製薬株式会社 | Sheet-shaped oral patch |
US4764378A (en) | 1986-02-10 | 1988-08-16 | Zetachron, Inc. | Buccal drug dosage form |
US4713243A (en) | 1986-06-16 | 1987-12-15 | Johnson & Johnson Products, Inc. | Bioadhesive extruded film for intra-oral drug delivery and process |
JPH0744940B2 (en) | 1986-12-24 | 1995-05-17 | ライオン株式会社 | Base material for oral application |
US4788209A (en) | 1987-02-17 | 1988-11-29 | Merrell Dow Pharmaceuticals Inc. | Antifungal 2-anilinothiazolines |
GB8723846D0 (en) | 1987-10-10 | 1987-11-11 | Danbiosyst Ltd | Bioadhesive microsphere drug delivery system |
US4900552A (en) | 1988-03-30 | 1990-02-13 | Watson Laboratories, Inc. | Mucoadhesive buccal dosage forms |
US4866046A (en) | 1988-05-31 | 1989-09-12 | Top Laboratories, Inc. | Low-dosage sublingual aspirin |
US5112616A (en) | 1988-11-30 | 1992-05-12 | Schering Corporation | Fast dissolving buccal tablet |
US5073374A (en) | 1988-11-30 | 1991-12-17 | Schering Corporation | Fast dissolving buccal tablet |
US5776493A (en) | 1989-07-14 | 1998-07-07 | Alza Corporation | Oral osmotic device for delivery of nystatin with hydrogel driving member |
US5021053A (en) | 1989-07-14 | 1991-06-04 | Alza Corporation | Oral osmotic device with hydrogel driving member |
US5750136A (en) | 1989-11-03 | 1998-05-12 | Riker Laboratories, Inc. | Bioadhesive composition and patch |
US5147654A (en) | 1990-07-23 | 1992-09-15 | Alza Corporation | Oral osmotic device for delivering nicotine |
US5110605A (en) | 1990-08-21 | 1992-05-05 | Oramed, Inc. | Calcium polycarbophil-alginate controlled release composition and method |
US5326685A (en) | 1991-02-13 | 1994-07-05 | Gaglio Thomas J | Viscous fluid dispensing apparatus |
US5113860A (en) | 1991-03-15 | 1992-05-19 | Minnesota Mining And Manufacturing Company | Non-invasive transmucosal drug level monitoring method |
US5248310A (en) | 1992-03-27 | 1993-09-28 | Alza Corporation | Oral osmotic device with hydrogel driving member |
US5512299A (en) | 1992-03-30 | 1996-04-30 | Alza Corporation | Method of treating oral inflammatory disease |
CA2075517C (en) | 1992-04-01 | 1997-03-11 | John Wick | Transdermal patch incorporating a polymer film incorporated with an active agent |
EP0566135A1 (en) | 1992-04-17 | 1993-10-20 | Takeda Chemical Industries, Ltd. | Transmucosal composition comprising a peptide and a cytidine derivative |
US5298256A (en) | 1992-04-28 | 1994-03-29 | Corint, Ltd. | Desmopressin buccal patch composition |
US5512293A (en) | 1992-07-23 | 1996-04-30 | Alza Corporation | Oral sustained release drug delivery device |
FI933979A0 (en) | 1992-09-10 | 1993-09-10 | Mcneil Ppc Inc | BIOERODERBAR ANORDNING FOER DOSERING AV AKTIVA INGREDIENSER |
US5573776A (en) | 1992-12-02 | 1996-11-12 | Alza Corporation | Oral osmotic device with hydrogel driving member |
US5346701A (en) | 1993-02-22 | 1994-09-13 | Theratech, Inc. | Transmucosal delivery of macromolecular drugs |
DE69422925T2 (en) | 1993-07-09 | 2000-08-17 | Cygnus Therapeutic Systems | METHOD AND DEVICE FOR THE TRANSDERMAL OR TRANSBUCCAL THERAPEUTIC ADMINISTRATION OF NICOTINE SUBSTITUTES |
US5578315A (en) | 1993-12-01 | 1996-11-26 | Rutgers, The State University Of New Jersey | Mucosal adhesive device for long-acting delivery of pharmaceutical combinations in oral cavity |
US5679714A (en) | 1995-06-07 | 1997-10-21 | Weg; Stuart L. | Administration of ketamine for detoxification and treatment of tobacco addiction |
ES2118584T3 (en) | 1994-03-02 | 1998-09-16 | Akzo Nobel Nv | SUBLINGUAL OR ORAL PHARMACEUTICAL COMPOSITION. |
US6121276A (en) | 1994-04-22 | 2000-09-19 | Pentech Pharmaceuticals, Inc. | Apomorphine-containing dosage forms for ameliorating male erectile dysfunction |
US5639469A (en) | 1994-06-15 | 1997-06-17 | Minnesota Mining And Manufacturing Company | Transmucosal delivery system |
WO1996000072A1 (en) | 1994-06-23 | 1996-01-04 | The Procter & Gamble Company | Treatment of nicotine craving and/or smoking withdrawal symptoms with a transdermal or transmucosal composition containing nicotine and caffeine or xanthine |
US5725853A (en) | 1994-10-18 | 1998-03-10 | Pioneer Hi-Bred International, Inc. | 4 strain direct-fed microbial |
US5656284A (en) | 1995-04-24 | 1997-08-12 | Balkin; Michael S. | Oral transmucosal delivery tablet and method of making it |
US5888534A (en) | 1995-06-13 | 1999-03-30 | Pentech Pharmaceuticals, Inc. | Controlled release of drugs delivered by sublingual or buccal administration |
US5624677A (en) | 1995-06-13 | 1997-04-29 | Pentech Pharmaceuticals, Inc. | Controlled release of drugs delivered by sublingual or buccal administration |
CA2184316A1 (en) | 1995-09-12 | 1997-03-13 | Wei-Chi Liao | Buccal delivery system for therapeutic agents |
US5849322A (en) | 1995-10-23 | 1998-12-15 | Theratech, Inc. | Compositions and methods for buccal delivery of pharmaceutical agents |
US5766620A (en) | 1995-10-23 | 1998-06-16 | Theratech, Inc. | Buccal delivery of glucagon-like insulinotropic peptides |
FR2742989B1 (en) | 1995-12-29 | 1998-01-23 | Adir | BIOADHESIVE PHARMACEUTICAL COMPOSITION FOR THE CONTROLLED RELEASE OF ACTIVE INGREDIENTS |
DK0906089T3 (en) | 1996-05-13 | 2003-12-08 | Novartis Consumer Health Sa | The buccal delivery system |
CA2259418A1 (en) | 1996-07-11 | 1998-01-22 | Farmarc Nederland B.V. | Pharmaceutical composition containing acid addition salt of basic drug |
US6248789B1 (en) | 1996-08-29 | 2001-06-19 | Stuart L. Weg | Administration of ketamine to manage pain and to reduce drug dependency |
US5800832A (en) | 1996-10-18 | 1998-09-01 | Virotex Corporation | Bioerodable film for delivery of pharmaceutical compounds to mucosal surfaces |
DE19646392A1 (en) | 1996-11-11 | 1998-05-14 | Lohmann Therapie Syst Lts | Preparation for use in the oral cavity with a layer containing pressure-sensitive adhesive, pharmaceuticals or cosmetics for dosed delivery |
US6197331B1 (en) | 1997-07-24 | 2001-03-06 | Perio Products Ltd. | Pharmaceutical oral patch for controlled release of pharmaceutical agents in the oral cavity |
US6146655A (en) | 1997-08-29 | 2000-11-14 | Softy-Flex Inc. | Flexible intra-oral bandage and drug delivery system |
US6228864B1 (en) | 1997-10-28 | 2001-05-08 | Vivus, Inc. | Administration of 5-HT receptor agonists and antagonists, to treat premature ejaculation |
CA2306837C (en) | 1997-10-28 | 2007-05-08 | Asivi, Llc. | Treatment of female sexual dysfunction |
US5945117A (en) | 1998-01-30 | 1999-08-31 | Pentech Pharmaceuticals, Inc. | Treatment of female sexual dysfunction |
US5981552A (en) | 1998-10-23 | 1999-11-09 | Taylor Pharmaceuticals | Sublingual and buccal compositions of droperidol and method for treating migraine |
US6200604B1 (en) | 1998-03-27 | 2001-03-13 | Cima Labs Inc. | Sublingual buccal effervescent |
US6264974B1 (en) | 1998-07-07 | 2001-07-24 | Salvagnini Italia Spa | Buccal and sublingual administration of physostigmine |
JP2000072663A (en) * | 1998-08-26 | 2000-03-07 | Sasaki Shoji Kk | Medicament-containing covering sheet |
US6180682B1 (en) | 1999-01-26 | 2001-01-30 | Virgil A. Place | Buccal drug delivery system for use in male contraception |
US6117446A (en) | 1999-01-26 | 2000-09-12 | Place; Virgil A. | Drug dosage unit for buccal administration of steroidal active agents |
US6284262B1 (en) | 1999-01-26 | 2001-09-04 | Virgil A. Place | Compact dosage unit for buccal administration of a pharmacologically active agent |
US6087362A (en) | 1999-03-16 | 2000-07-11 | Pentech Pharmaceuticals, Inc. | Apomorphine and sildenafil composition |
US6210699B1 (en) | 1999-04-01 | 2001-04-03 | Watson Pharmaceuticals, Inc. | Oral transmucosal delivery of drugs or any other ingredients via the inner buccal cavity |
US6319510B1 (en) | 1999-04-20 | 2001-11-20 | Alayne Yates | Gum pad for delivery of medication to mucosal tissues |
US6147102A (en) | 1999-10-26 | 2000-11-14 | Curatek Pharmaceuticals Holding, Inc. | Clonidine preparations |
US6264981B1 (en) | 1999-10-27 | 2001-07-24 | Anesta Corporation | Oral transmucosal drug dosage using solid solution |
US6756051B1 (en) * | 2000-11-15 | 2004-06-29 | Li-Lan H. Chen | Bioadhesive, closed-cell foam film, sustained release, delivery devices and methods of making and using same |
-
2004
- 2004-05-07 US US10/841,893 patent/US7306812B2/en not_active Expired - Fee Related
- 2004-05-10 WO PCT/US2004/014550 patent/WO2004100925A2/en active Application Filing
- 2004-05-10 JP JP2006532911A patent/JP2007516222A/en active Pending
- 2004-05-10 MX MXPA05012009A patent/MXPA05012009A/en active IP Right Grant
- 2004-05-10 EP EP04751777A patent/EP1631256A2/en not_active Withdrawn
- 2004-05-10 CA CA002523784A patent/CA2523784A1/en not_active Abandoned
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4307075A (en) * | 1979-09-13 | 1981-12-22 | American Home Products Corporation | Topical treatment of aphthous stomatitis |
US5529782A (en) * | 1992-05-07 | 1996-06-25 | Staab; Robert | Dissolvable device for contraception or delivery of medication |
US5700478A (en) * | 1993-08-19 | 1997-12-23 | Cygnus, Inc. | Water-soluble pressure-sensitive mucoadhesive and devices provided therewith for emplacement in a mucosa-lined body cavity |
US20010006677A1 (en) * | 1996-10-29 | 2001-07-05 | Mcginity James W. | Effervescence polymeric film drug delivery system |
EP0873750A1 (en) * | 1997-04-23 | 1998-10-28 | Permatec Technologie Ag | Bioadhesive tablets |
WO1999055312A2 (en) * | 1998-04-29 | 1999-11-04 | Virotex Corporation | Pharmaceutical carrier device suitable for delivery of pharmaceutical compounds to mucosal surfaces |
US6375963B1 (en) * | 1999-06-16 | 2002-04-23 | Michael A. Repka | Bioadhesive hot-melt extruded film for topical and mucosal adhesion applications and drug delivery and process for preparation thereof |
WO2002002085A2 (en) * | 2000-07-04 | 2002-01-10 | Lts Lohmann Therapie-Systeme Ag | Rapidly-decomposing administrable form for releasing active ingredients in the oral cavity or in bodily cavities |
US20020068151A1 (en) * | 2000-10-17 | 2002-06-06 | Kim Won K. | Multi-layered, air-gapped sheet of chitosan |
WO2003015748A2 (en) * | 2001-08-16 | 2003-02-27 | Access Pharmaceuticals, Inc. | Mucoadhesive erodible drug delivery device for controlled administration of pharmaceuticals and other active compounds |
Also Published As
Publication number | Publication date |
---|---|
EP1631256A2 (en) | 2006-03-08 |
US20040224008A1 (en) | 2004-11-11 |
MXPA05012009A (en) | 2006-02-03 |
US7306812B2 (en) | 2007-12-11 |
WO2004100925A3 (en) | 2005-06-02 |
JP2007516222A (en) | 2007-06-21 |
CA2523784A1 (en) | 2004-11-25 |
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