WO2013129813A1 - 도네페질-함유 경피흡수제제 및 그의 제조방법 - Google Patents
도네페질-함유 경피흡수제제 및 그의 제조방법 Download PDFInfo
- Publication number
- WO2013129813A1 WO2013129813A1 PCT/KR2013/001504 KR2013001504W WO2013129813A1 WO 2013129813 A1 WO2013129813 A1 WO 2013129813A1 KR 2013001504 W KR2013001504 W KR 2013001504W WO 2013129813 A1 WO2013129813 A1 WO 2013129813A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- drug
- layer
- donepezil
- sensitive adhesive
- containing matrix
- Prior art date
Links
Images
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
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
-
- 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
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7084—Transdermal patches having a drug layer or reservoir, and one or more separate drug-free skin-adhesive layers, e.g. between drug reservoir and skin, or surrounding the drug reservoir; Liquid-filled reservoir patches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7038—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer
- A61K9/7046—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds
- A61K9/7053—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds, e.g. polyvinyl, polyisobutylene, polystyrene
-
- 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
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7038—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer
- A61K9/7046—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds
- A61K9/7053—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds, e.g. polyvinyl, polyisobutylene, polystyrene
- A61K9/7061—Polyacrylates
-
- 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
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
- A61K9/703—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms characterised by shape or structure; Details concerning release liner or backing; Refillable patches; User-activated patches
- A61K9/7038—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer
- A61K9/7046—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds
- A61K9/7069—Transdermal patches of the drug-in-adhesive type, i.e. comprising drug in the skin-adhesive layer the adhesive comprising macromolecular compounds obtained otherwise than by reactions only involving carbon to carbon unsaturated bonds, e.g. polysiloxane, polyesters, polyurethane, polyethylene oxide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
Definitions
- the present invention relates to a donepezil-containing transdermal absorbent and a method for preparing the same, and more particularly, to a double-layer structure having a drug-containing matrix layer and an adhesive layer prepared by dissolving donepezil using a specific polymer and formulated with a pressure-sensitive adhesive.
- Percutaneous absorption preparations for example, percutaneous absorption preparations in the form of a patch
- a preparation method thereof for example, percutaneous absorption preparations in the form of a patch
- Donepezil or a salt thereof has the chemical name 2-[(1-benzyl-4-piperidinyl) methyl] -5,6-dimethoxyindan-1-one and is used as a drug for the treatment of dementia.
- Acetylcholinesterase inhibitors Acetylcholinesterase inhibitors.
- EP1437130A1 discloses a transdermal absorption agent containing donepezil, wherein the transdermal absorption agent has a structure in which an anti-dementant drug such as donepezil is dispersed in the adhesive, and adhered to the skin for 12 hours or more in plasma It is designed to keep the concentration of drug constant.
- WO2007 / 129427 discloses a three-layer transdermal absorption preparation including a pressure-sensitive adhesive layer, a drug storage layer and an interlayer to control the release rate of constant donepezil for a long time.
- patients with dementia usually require a percutaneous absorption agent designed to maintain blood drug concentration for one to several days or more, for example, one or more days, preferably about one week or more.
- a percutaneous absorption agent designed to maintain blood drug concentration for one to several days or more, for example, one or more days, preferably about one week or more.
- transdermal absorbents with high quality.
- donepezil is precipitated from the formulation, thereby causing problems such as decrease in adhesion.
- the release rate of donepezil by designing a transdermal absorption formulation in the form of a triple layer, there are disadvantages in that the process is complicated, the production is difficult, and the economic efficiency is not good.
- the percutaneous absorption can be effectively prevented by exhibiting a sudden release dumping phenomenon during use.
- a conventional solubilizer such as a surfactant
- transdermal absorbent agent e.g., a patch that is designed to have a drug-containing matrix layer and an adhesive layer formulated with an adhesive by completely dissolving donepezil using a specific polymer, i.e., polyvinylpyrrolidone. It has been found that transdermal absorbents in the form of patches may not only release donepezil at a uniform rate for a long time of more than one day, preferably more than one week, but also prevent release dumping. .
- an object of the present invention is to provide a transdermal absorption agent having the double layer structure.
- Another object of the present invention is to provide a method for preparing the transdermal absorbent preparation.
- a transdermal absorbent agent consisting of a support layer, a drug-containing matrix layer, an adhesive layer, and a release layer, wherein the drug-containing matrix layer is (i) donepezil or a pharmaceutically acceptable thereof as an active ingredient. Salts, (ii) polyvinylpyrrolidone, and (iii) acrylic pressure sensitive adhesives;
- the adhesive layer is provided with a transdermal absorbent comprising an acrylic pressure sensitive adhesive or a silicone pressure sensitive adhesive.
- the drug-containing matrix layer is 10 to 40% by weight of donepezil or a pharmaceutically acceptable salt thereof, and 0.1 to polyvinylpyrrolidone, based on the total weight of the drug-containing matrix layer. 20 wt% and 40 to 80 wt% of the acrylic pressure sensitive adhesive; Preferably, 30 to 40% by weight of donepezil or a pharmaceutically acceptable salt thereof, 1 to 20% by weight of polyvinylpyrrolidone, and 40 to 60% by weight of the acrylic pressure-sensitive adhesive based on the total weight of the drug-containing matrix layer can do.
- the weight average molecular weight of the polyvinylpyrrolidone may be in the range of 7,000 to 1,500,000.
- the pressure-sensitive adhesive layer includes a silicone-based pressure-sensitive adhesive
- the thickness of the pressure-sensitive adhesive layer may be in the range of 50 to 150 ⁇ m, preferably 90 to 110 ⁇ m.
- step (a) dissolving an acrylic pressure-sensitive adhesive in a solution containing donepezil or a pharmaceutically acceptable salt thereof and polyvinylpyrrolidone; (b) applying the solution obtained in step (a) onto a film and drying to form a drug-containing matrix layer; And (c) forming a pressure-sensitive adhesive layer comprising an acrylic pressure-sensitive adhesive or a silicone pressure-sensitive adhesive on the drug-containing matrix layer obtained in step (b).
- the solution containing Donepezil or a pharmaceutically acceptable salt thereof and polyvinylpyrrolidone is a solution of Donepezil or a pharmaceutically acceptable salt thereof and ethyl acetate, and polyvinylpyrrolidone is dissolved in ethanol. It can be obtained by mixing with the solution obtained.
- the transdermal absorption preparation of the bilayer structure according to the present invention not only can release donepezil at a uniform rate for a long time without exhibiting precipitation of donepezil in the formulation, but also release that occurs in the transdermal absorption preparation of a single layer structure. Release dumping can be prevented.
- the drug-containing matrix layer and the adhesive layer are each formulated with different pressure-sensitive adhesives, not only can they prevent excessive release, but can also control release of donepezil at a uniform rate for more than one week.
- the transdermal absorption agent of the double layer structure according to the present invention can minimize contact between air (oxygen) and donepezil, and may also contribute to securing the stability of donepezil. Therefore, the percutaneous absorption preparation according to the present invention can be usefully applied to patients with dementia, especially elderly patients without expression of side effects due to the rapid rise in blood concentration.
- Figure 3 is a result of measuring the drug concentration profile in vivo for the percutaneous absorption preparation and the comparative preparation according to the present invention for one week.
- the present invention provides a transdermal absorbent agent consisting of a support layer, a drug-containing matrix layer, an adhesive layer, and a release layer, wherein the drug-containing matrix layer is (i) donepezil or a pharmaceutically acceptable salt thereof as an active ingredient, (ii) Polyvinylpyrrolidone, and (iii) an acrylic pressure sensitive adhesive;
- the adhesive layer provides a transdermal absorbent comprising an acrylic pressure sensitive adhesive or a silicone pressure sensitive adhesive.
- the donepezil or a pharmaceutically acceptable salt thereof can be used in an amount sufficient to obtain a therapeutically effective blood concentration.
- it may be used in the range of 10 to 40% by weight, preferably 30 to 40% by weight, based on the total weight of the drug-containing matrix layer. If the content of donepezil is less than 10% by weight may not show the desired effect, if it exceeds 40% by weight may cause a decrease in adhesion and cause precipitation of crystals.
- the polyvinylpyrrolidone increases the solubility of donepezil and serves to enable complete dissolution in transdermal absorbents.
- the polyvinylpyrrolidone may have a weight average molecular weight in the range of 7,000 to 1,500,000, and is 0.1 to 20% by weight, preferably 1 to 20% by weight, more preferably 4 to 1, based on the total weight of the drug-containing matrix layer. It can be used in the range of 12% by weight. If the content of polyvinylpyrrolidone is less than 0.1% by weight, the desired solubilization effect of donepezil may not be exhibited. If it exceeds 20% by weight, the drug-containing matrix layer may be discolored or the viscosity may be too high, making it difficult to formulate.
- the acrylic pressure-sensitive adhesive is a polymer having an adhesive having a carboxyl group, a hydroxyl group, or a combination thereof as a functional group, for example, Durotak 87-202A, Durotak 387-2510, Durotak 87-4287, Durotak 387-2287, Durotak 87 -2287, Durotak 387-2516, Durotak 87-2516, Durotak 387-2525, Durotak 87-2525, Durotak 87-2979, Durotak 87-2074, Durotak 87-235A, Durotak 87-2353, Durotak 387-2353, Durotak 87 -2852, Durotak 87-2051, Durotak 387-2051, Durotak 87-2052, Durotak 387-2052, Durotak 387-2054, Durotak 87-2054, Durotak 87-2677, Durotak 87-2194, Durotak 387-2196, Durotak 387 -2825, Du
- the acrylic pressure-sensitive adhesive may be Durotak 87-2516 (Henkel), Durotak 87-235A (Henkel), Durotak 87-2353 (Henkel), Durotak 387-2353 (Henkel), Durotak 87-502A (Henkel) .
- the acrylic pressure-sensitive adhesive may be used in the range of 40 to 80% by weight, preferably 40 to 60% by weight based on the total weight of the drug-containing matrix layer.
- the drug-containing matrix layer is 10-40% by weight of donepezil or a pharmaceutically acceptable salt thereof, 0.1-20% by weight of polyvinylpyrrolidone, based on the total weight of the drug-containing matrix layer, And 40 to 80% by weight of the acrylic pressure-sensitive adhesive may be included.
- the drug-containing matrix layer is 30-40 wt% of donepezil or a pharmaceutically acceptable salt thereof, 1-20 wt% of polyvinylpyrrolidone, based on the total weight of the drug-containing matrix layer. And it may comprise 40 to 60% by weight of the acrylic pressure-sensitive adhesive.
- the drug-containing matrix layer may further include a plasticizer or stabilizer as necessary.
- the plasticizer or stabilizer may be about 40 wt% or less based on the total weight of the drug-containing matrix layer, but is not limited thereto.
- the transdermal absorbent according to the present invention includes an adhesive layer containing an acrylic pressure sensitive adhesive or a silicone pressure sensitive adhesive.
- the acrylic adhesive is as described above.
- the silicone-based pressure-sensitive adhesive is a polymer having compatibility with the drug having an amine group and at the same time, adhesiveness, for example, BIO-PSA 7-4301, BIO-PSA 7-4302, BIO-PSA 7-4303, BIO-PSA 7 -4201, BIO-PSA 7-4202, BIO-PSA 7-4302, BIO-PSA 7-4101, BIO-PSA 7-4102, BIO-PSA 7-4103 and the like.
- the silicone pressure sensitive adhesive may be BIO-PSA 7-4302 ((Dow corning), BIO-PSA 7-4202 (Dow corning), BIO-PSA 7-4102 (Dow corning).
- the pressure-sensitive adhesive layer preferably comprises a silicone pressure-sensitive adhesive
- the thickness of the pressure-sensitive adhesive layer may be 50 to 150 ⁇ m, preferably 90 to 110 ⁇ m, more preferably about 100 ⁇ m have.
- the present invention also comprises the steps of (a) dissolving an acrylic pressure-sensitive adhesive in a solution containing donepezil or a pharmaceutically acceptable salt thereof and polyvinylpyrrolidone; (b) applying the solution obtained in step (a) onto a film and drying to form a drug-containing matrix layer; And (c) forming a pressure-sensitive adhesive layer comprising an acrylic pressure-sensitive adhesive or a silicone pressure-sensitive adhesive on the drug-containing matrix layer obtained in step (b).
- the solution containing donepezil or a pharmaceutically acceptable salt thereof and polyvinylpyrrolidone may be prepared by mixing polyvinylpyrrole with a mixture solution of donepezil or a pharmaceutically acceptable salt thereof and ethyl acetate. It can be obtained by mixing with the solution obtained by dissolving the lollidon in ethanol.
- Step (b) can be carried out by applying the solution obtained in step (a) onto a film and drying to form a drug-containing matrix layer.
- the film may use a conventional PET film, for example PET film coated with silicone, the drying may be carried out by drying in an oven at about 70 °C for 15 minutes.
- a support layer may be formed by laminating a conventional backing film, for example, a polyester film on which aluminum is laminated, on a surface opposite to the film, that is, a surface on which the drug-containing matrix layer is exposed.
- the support film may be a drug-non-absorbable and flexible material commonly used in the field of transdermal absorbents, for example, polyolefin, polyether, multilayer ethylene vinyl acetate film ( Multi-layer ethylene vinyl acetate film), polyester (polyester), polyurethane (polyurethane) and the like can be used.
- Step (c) may be carried out by forming an adhesive layer containing an acrylic pressure sensitive adhesive or a silicone pressure sensitive adhesive on the drug-containing matrix layer obtained in step (b).
- a pressure-sensitive adhesive layer containing a silicone pressure-sensitive adhesive for example, by applying a silicone pressure-sensitive adhesive to a fluorine-coated PET film to a predetermined thickness, and dried for about 15 minutes in an oven at about 70 °C, step (b) It can be formed by laminating with the drug-containing matrix layer obtained in.
- the pressure-sensitive adhesive layer comprising an acrylic pressure-sensitive adhesive, for example, by applying an acrylic pressure-sensitive adhesive to a PET film coated with silicone to a predetermined thickness, drying the pressure-sensitive adhesive layer prepared for about 15 minutes in an oven at about 70 °C, step ( It can be formed by laminating with the drug-containing matrix layer obtained in b).
- a percutaneous absorption preparation in the form of a patch can be finally prepared by forming a release layer on the formulation containing the support layer, the drug-containing matrix layer, and the adhesive layer obtained as described above.
- the release layer may be a release liner or a laminate thereof commonly used in the field of transdermal absorbents, for example, polyethylene, polyester, polyvinyl chloride, polyvinylidene coated with silicone resin or fluorine resin. Films such as chloride, paper or laminates thereof can be used.
- Table 1 1-1 1-2 1-3 1-4 Raw material Donepezil Base 1 g 1 g 1 g 1 g Solvent 1 Ethyl acetate 1 g 1 g 1 g 1 g Polymer Polyvinylpyrrolidone - 0.2 g - - Eudragit E100 - - 0.2 g - Plastoid B - - - 0.2 g Solvent 2 ethanol 1 g 0.8 g 0.8 g 0.8 g Appearance of the solution opacity Transparency opacity opacity
- Polyvinylpyrrolidone having various molecular weights was used to evaluate the formulation potential into transdermal absorbents. According to the composition of Table 2, after the solution containing the donepezil base and polyvinylpyrrolidone in the same manner as in Example 1 (2-1 was added only 1g of ethanol), it was homogenized by adding an acrylic pressure-sensitive adhesive . The resulting solution was applied to a silicone coated PET film and dried in an oven at 70 ° C. for 15 minutes, then laminated with a backing film to evaluate the formulation potential.
- polyvinylpyrrolidone is PVP K17 (weight average molecular weight: 7,000 to 11,000, BASF), PVP K30 (weight average molecular weight: 44,000 to 54,000, BASF), or PVP K90 (weight average molecular weight: 1,000,000 to 1,500,000, BASF) was used, and Durotak 87-235A (Henkel) was used as the acrylic adhesive.
- the polyvinylpyrrolidone preferably has a weight average molecular weight in the range of about 7,000 to 1,500,000, the amount of use is in the range of about 1 to 20% by weight, more preferably about 4 to 12 It can be seen that the range by weight is preferred.
- each transdermal absorbent was molded into a size of 1 cm 2 and fixed on a human cadaver skin, and the sample solution diffused through the skin was automatically collected every hour.
- the internal temperature of the Franz cell was 32.5 °C, and the test solution was used a phosphate buffer solution of pH 7.4.
- the collected sample was analyzed by high performance liquid chromatography. From the results in FIG. 1, it can be seen that each transdermal absorption agent exhibits a constant flux value.
- a drug-containing matrix layer (thickness: 65 ⁇ m) coated with donepezil base, polyvinylpyrrolidone, and an acrylic pressure-sensitive adhesive on a silicone-coated PET film in the same manner as in Example 2 Formed.
- the obtained drug-containing matrix layer was laminated with a support film made of polyester laminated with aluminum to form a first layer.
- a silicone pressure sensitive adhesive (BIO-PSA-7-4302. Dow corning) was applied to the fluorine-coated PET film so that the thickness after drying was 100 ⁇ m (Example 3-1) or 50 ⁇ m (Example 3-2). Drying in an oven at 70 °C for 15 minutes to prepare a skin adhesive layer (second layer). The previously prepared silicone coated PET film of the first layer was peeled off and laminated with the second layer to prepare the transdermal absorbent preparations of Examples 3-1 and 3-2.
- the same acrylic pressure-sensitive adhesive as the acrylic pressure-sensitive adhesive used in the drug-containing matrix layer was applied to the silicone-coated PET film such that the thickness after drying was 100 ⁇ m (Example 3-3) or 50 ⁇ m (Example 3-4). Then, the mixture was dried in an oven at 70 ° C. for 15 minutes to prepare a skin adhesive layer (second layer). The previously prepared silicone coated PET film of the first layer was peeled off and laminated with the second layer to prepare the transdermal absorbent formulations of Examples 3-3 and 3-4.
- transdermal absorbents prepared in Examples 3-1 to 3-4 were evaluated using Franz cells (vertical diffusion cells).
- each transdermal absorbent was molded into a size of 1 cm 2 and fixed on a human cadaver skin, and the sample solution diffused through the skin was automatically collected every hour.
- the internal temperature of the Franz cell was 32.5 °C, and the test solution was used a phosphate buffer solution of pH 7.4.
- the collected sample was analyzed by high performance liquid chromatography. The result is shown in FIG.
- the transdermal absorbent preparations (Examples 3-3 and 3-4) having a pressure-sensitive adhesive layer composed of the same acrylic pressure-sensitive adhesives used in the drug-containing matrix layer (Examples 3-3 and 3-4) exhibited a relatively rapid release pattern of donepezil. Therefore, it is expected to be usefully used as a relatively short acting transdermal absorbent (eg, about 72 hours acting transdermal absorbent).
- transdermal absorbents (Examples 3-1 and 3-2) having a pressure-sensitive adhesive layer composed of a silicone pressure-sensitive adhesive showed a release control pattern of donepezil, in particular, a transdermal absorbent having a thickness of 100 ⁇ m of the adhesive layer (Example It can be seen that the formulation of 3-1 has an excellent effect on controlling the release of donepezil, and thus it is expected to be useful as a long-acting transdermal absorbent (for example, a functional transdermal absorbent for about 1 week). do.
- transdermal absorbent preparation prepared in Example 3-1 Long-term release control properties of the transdermal absorbent preparation prepared in Example 3-1 were evaluated using a hair less rat. For comparison, a monolayer transdermal absorbent (Comparative Example 1) was evaluated together.
- the transdermal absorption preparation of Comparative Example 1 was prepared by forming a drug-containing matrix layer (thickness: 65 ⁇ m) in the same manner as in Example 2-8, except that 0.5 g of donepezil base and 2.5 g of ethyl acetate were used. .
- the transdermal absorbent of Comparative Example 1 was 10 cm 2 and the transdermal absorbent of Example 3-1 was molded into 5 cm 2 and 10 cm 2 , respectively, and then attached to the hairless rat, followed by 2 hours for 168 hours (1 week). , 4, 6, 12, 24, 48, 72, 96, 120, 144 and 168 hours were collected and the amount of donepezil in plasma was measured.
- the blood concentration profile with time is shown in FIG. 3.
- the transdermal absorption agent of Comparative Example 1 having a monolayer structure showed low blood concentration.
- the transdermal absorbent preparation of Example 3-1 having a double layer structure was molded into 5 cm 2 and 10 cm 2 , respectively, and measured in blood concentrations of blood donepezil after adhesion to the skin. By decreasing, the drug concentration was kept constant for 1 week, showing a significant release pattern. Accordingly, it can be seen that the transdermal absorbent preparation having a bilayer structure prepared according to the present invention can release donepezil constantly and continuously for a long time.
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Dermatology (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
1-1 | 1-2 | 1-3 | 1-4 | ||
원료 | 도네페질 염기 | 1 g | 1 g | 1 g | 1 g |
용매 1 | 에틸 아세테이트 | 1 g | 1 g | 1 g | 1 g |
고분자 | 폴리비닐피롤리돈 | - | 0.2 g | - | - |
유드라짓 E100 | - | - | 0.2 g | - | |
플라스토이드 B | - | - | - | 0.2 g | |
용매 2 | 에탄올 | 1 g | 0.8 g | 0.8 g | 0.8 g |
용액의 성상 | 불투명 | 투명 | 불투명 | 불투명 |
2-1 | 2-2 | 2-3 | 2-4 | 2-5 | 2-6 | 2-7 | 2-8 | ||
원료 | 도네페질 염기(g) | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
용매1 | 에틸 아세테이트(g) | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 |
중합체 | PVP K17 (g) | - | 0.2 | 0.4 | 0.6 | - | - | - | - |
PVP K30 (g) | - | - | - | - | 0.2 | 0.4 | 0.6 | - | |
PVP K90 (g) | - | - | - | - | - | - | - | 0.2 | |
용매2 | 에탄올 | 1 | 0.8 | 0.6 | 0.4 | 0.8 | 0.6 | 0.4 | 0.8 |
점착제 | 아크릴계 점착제(g) | 3.5 | 3.5 | 3.5 | 3.5 | 3.5 | 3.5 | 3.5 | 3.5 |
총계 (g) | 7.5 | 7.5 | 7.5 | 7.5 | 7.5 | 7.5 | 7.5 | 7.5 |
실시예 | 3-1 | 3-2 | 3-3 | 3-4 | ||
약물-함유 매트릭스 층 | 활성성분 | 도네페질 염기(g) | 1 | 1 | 1 | 1 |
용매1 | 에틸 아세테이트(g) | 2 | 2 | 2 | 2 | |
중합체 | 폴리비닐피롤리돈(g) | 0.2 | 0.2 | 0.2 | 0.2 | |
용매2 | 에탄올(g) | 0.8 | 0.8 | 0.8 | 0.8 | |
점착제 | 아크릴계 점착제(g) | 3.5 | 3.5 | 3.5 | 3.5 | |
점착층 | 점착제 종류 | 실리콘계 점착제 | 실리콘계 점착제 | 아크릴계 점착제 | 아크릴계 점착제 | |
건조 후 두께 | 100 ㎛ | 50 ㎛ | 100 ㎛ | 50 ㎛ |
Claims (15)
- 지지층, 약물-함유 매트릭스층, 점착층 및 박리층으로 구성된 경피흡수제제로서, 상기 약물-함유 매트릭스층이 (i) 유효성분으로서 도네페질 또는 그의 약학적으로 허용가능한 염, (ii) 폴리비닐피롤리돈, 및 (iii) 아크릴계 점착제를 포함하고; 상기 점착층이 아크릴계 점착제 또는 실리콘계 점착제를 포함하는 경피흡수제제.
- 제1항에 있어서, 상기 약물-함유 매트릭스층이, 약물-함유 매트릭스층 총 중량에 대하여, 도네페질 또는 그의 약학적으로 허용가능한 염 10 ∼ 40 중량%, 폴리비닐피롤리돈 0.1 ∼ 20 중량%, 및 아크릴계 점착제 40 ∼ 80 중량%를 포함하는 것을 특징으로 하는 경피흡수제제.
- 제2항에 있어서, 상기 약물-함유 매트릭스층이, 약물-함유 매트릭스층 총 중량에 대하여, 도네페질 또는 그의 약학적으로 허용가능한 염 30 ∼ 40 중량%, 폴리비닐피롤리돈 1 ∼ 20 중량%, 및 아크릴계 점착제 40 ∼ 60 중량%를 포함하는 것을 특징으로 하는 경피흡수제제.
- 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 폴리비닐피롤리돈의 중량평균분자량이 7,000 내지 1,500,000의 범위인 것을 특징으로 하는 경피흡수제제.
- 제1항 내지 제3항 중 어느 한 항에 있어서, 상기 점착층이 실리콘계 점착제를 포함하는 것을 특징으로 하는 경피흡수제제.
- 제5항에 있어서, 상기 점착층의 두께가 50 ∼ 150 ㎛인 것을 특징으로 하는 경피흡수제제.
- 제5항에 있어서, 상기 점착층의 두께가 90 ∼ 110 ㎛인 것을 특징으로 하는 경피흡수제제.
- (a) 도네페질 또는 그의 약학적으로 허용가능한 염 및 폴리비닐피롤리돈을 함유하는 용액에 아크릴계 점착제를 용해시키는 단계;(b) 단계(a)에서 얻어진 용액을 필름 상에 도포하고 건조시켜, 약물-함유 매트릭스층을 형성시키는 단계; 및(c) 단계(b)에서 얻어진 약물-함유 매트릭스층 상에 아크릴계 점착제 또는 실리콘계 점착제를 포함하는 점착층을 형성시키는 단계를 포함하는, 경피흡수제제의 제조방법.
- 제8항에 있어서, 상기 도네페질 또는 그의 약학적으로 허용가능한 염 및 폴리비닐피롤리돈을 함유하는 용액이, 도네페질 또는 그의 약학적으로 허용가능한 염과 에틸 아세테이트와의 혼합액을, 폴리비닐피롤리돈을 에탄올에 용해시켜 얻어진 용액과 혼합하여 얻어진 것임을 특징으로 하는 경피흡수제제의 제조방법.
- 제8항에 있어서, 상기 약물-함유 매트릭스층이, 약물-함유 매트릭스층 총 중량에 대하여, 도네페질 또는 그의 약학적으로 허용가능한 염 10 ∼ 40 중량%, 폴리비닐피롤리돈 0.1 ∼ 20 중량%, 및 아크릴계 점착제 40 ∼ 80 중량%를 포함하는 것을 특징으로 하는 경피흡수제제의 제조방법.
- 제10항에 있어서, 상기 약물-함유 매트릭스층이, 약물-함유 매트릭스층 총 중량에 대하여, 도네페질 또는 그의 약학적으로 허용가능한 염 30 ∼ 40 중량%, 폴리비닐피롤리돈 1 ∼ 20 중량%, 및 아크릴계 점착제 40 ∼ 60 중량%를 포함하는 것을 특징으로 하는 경피흡수제제의 제조방법.
- 제8항 내지 제11항 중 어느 한 항에 있어서, 상기 폴리비닐피롤리돈의 중량평균분자량이 7,000 내지 1,500,000의 범위인 것을 특징으로 하는 경피흡수제제의 제조방법.
- 제8항 내지 제11항 중 어느 한 항에 있어서, 상기 점착층이 실리콘계 점착제를 포함하는 것을 특징으로 하는 경피흡수제제의 제조방법.
- 제13항에 있어서, 상기 점착층의 형성이 50 ∼ 150 ㎛의 점착층 두께가 얻어지도록 수행되는 것을 특징으로 하는 경피흡수제제의 제조방법.
- 제13항에 있어서, 상기 점착층의 형성이 90 ∼ 110 ㎛의 점착층 두께가 얻어지도록 수행되는 것을 특징으로 하는 경피흡수제제의 제조방법.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014559823A JP6132407B2 (ja) | 2012-02-28 | 2013-02-26 | ドネペジルを含有する経皮吸収製剤及びその製造方法 |
EP13754753.5A EP2821065B1 (en) | 2012-02-28 | 2013-02-26 | Percutaneous absorption preparation containing donepezil, and method for preparing same |
US14/381,627 US9622986B2 (en) | 2012-02-28 | 2013-02-26 | Percutaneous absorption preparation containing donepezil, and method for preparing same |
CN201380011429.4A CN104144684B (zh) | 2012-02-28 | 2013-02-26 | 含有多奈哌齐的经皮吸收制剂及其制备方法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2012-0020510 | 2012-02-28 | ||
KR1020120020510A KR101239150B1 (ko) | 2012-02-28 | 2012-02-28 | 도네페질-함유 경피흡수제제 및 그의 제조방법 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013129813A1 true WO2013129813A1 (ko) | 2013-09-06 |
Family
ID=48181058
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/KR2013/001504 WO2013129813A1 (ko) | 2012-02-28 | 2013-02-26 | 도네페질-함유 경피흡수제제 및 그의 제조방법 |
Country Status (6)
Country | Link |
---|---|
US (1) | US9622986B2 (ko) |
EP (1) | EP2821065B1 (ko) |
JP (1) | JP6132407B2 (ko) |
KR (1) | KR101239150B1 (ko) |
CN (1) | CN104144684B (ko) |
WO (1) | WO2013129813A1 (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10888533B2 (en) | 2014-12-18 | 2021-01-12 | Icure Pharmaceutical Inc. | Transdermal composition containing donepezil as active ingredient |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101770675B1 (ko) * | 2013-01-30 | 2017-08-23 | 에스케이케미칼주식회사 | 도네페질-함유 경피흡수제제 및 그의 제조방법 |
BR112015028291A2 (pt) * | 2013-05-10 | 2017-07-25 | Ctc Bio Inc | filme contendo base livre de donepezil e método para a preparação do mesmo. |
KR101485822B1 (ko) * | 2014-01-22 | 2015-01-23 | 주식회사 대웅제약 | 도네페질 또는 그의 염을 함유하는 경피흡수제제 |
IL260290B2 (en) | 2015-12-30 | 2023-11-01 | Corium Inc | Systems and methods for long-term percutaneous administration |
JP6556873B2 (ja) * | 2016-01-28 | 2019-08-07 | 久光製薬株式会社 | 経皮吸収製剤 |
CN109922796B (zh) | 2016-06-23 | 2023-04-07 | 考里安有限责任公司 | 具有亲水和疏水域的粘合剂基质和治疗剂 |
US9993466B2 (en) | 2016-07-27 | 2018-06-12 | Corium International, Inc. | Donepezil transdermal delivery system |
WO2018022814A1 (en) | 2016-07-27 | 2018-02-01 | Corium International, Inc. | Transdermal delivery systems with pharmacokinetics bioequivalent to oral delivery |
WO2018022818A1 (en) | 2016-07-27 | 2018-02-01 | Corium International, Inc. | Memantine transdermal delivery systems |
CA3086163A1 (en) | 2017-12-20 | 2019-06-27 | Corium, Inc. | Transdermal adhesive composition comprising a volatile liquid therapeutic agent having low melting point |
KR102024996B1 (ko) | 2017-12-27 | 2019-09-25 | 동아에스티 주식회사 | 도네페질을 함유하는 치매 치료용 경피흡수제제 |
US11752114B2 (en) * | 2019-04-17 | 2023-09-12 | Lts Lohmann Therapie-Systeme Ag | Transdermal therapeutic system |
KR102372630B1 (ko) * | 2019-05-15 | 2022-03-14 | 주식회사 대웅제약 | 고함량의 도네페질 또는 그의 염을 포함하는 경피흡수제제 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1437130A1 (en) | 2001-10-17 | 2004-07-14 | Hisamitsu Pharmaceutical Co. Inc. | Percutaneous absorption preparations |
WO2007129427A1 (ja) | 2006-05-08 | 2007-11-15 | Teikoku Seiyaku Co., Ltd. | 抗認知症薬物の経皮吸収製剤 |
JP2007302582A (ja) * | 2006-05-09 | 2007-11-22 | Hisamitsu Pharmaceut Co Inc | ドネペジル経皮吸収型製剤 |
US20080038328A1 (en) * | 2004-05-28 | 2008-02-14 | Naruhito Higo | Pasting Preparation |
KR20110030349A (ko) * | 2009-09-16 | 2011-03-23 | 주식회사 삼양사 | 경피 투여 제형 및 그 제조 방법 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1272445A (en) * | 1985-02-25 | 1990-08-07 | Yie W. Chien | Transdermal pharmaceutical absorption dosage unit and process of pharmaceutical administration |
JPH0818975B2 (ja) * | 1987-06-08 | 1996-02-28 | 日東電工株式会社 | 疾患治療用貼付剤 |
ZA885069B (en) * | 1987-07-24 | 1989-03-29 | Fujisawa Pharmaceutical Co | Sustained-release percutaneous preparations |
DE19728279A1 (de) * | 1996-07-03 | 1998-01-08 | Stc Corp | Ketoprofen-Pflaster mit Langzeit/Sofort-Wirkung und Verfahren zu seiner Herstellung |
US20100178307A1 (en) * | 2010-01-13 | 2010-07-15 | Jianye Wen | Transdermal anti-dementia active agent formulations and methods for using the same |
CN102188363B (zh) * | 2010-03-09 | 2013-02-27 | 上海现代药物制剂工程研究中心有限公司 | 含有多奈哌齐化合物的透皮给药系统及制剂和制备方法 |
NZ605352A (en) * | 2010-06-30 | 2013-10-25 | Nal Pharmaceuticals Ltd | Process for producing glycosaminoglycans |
-
2012
- 2012-02-28 KR KR1020120020510A patent/KR101239150B1/ko active IP Right Grant
-
2013
- 2013-02-26 EP EP13754753.5A patent/EP2821065B1/en not_active Not-in-force
- 2013-02-26 WO PCT/KR2013/001504 patent/WO2013129813A1/ko active Application Filing
- 2013-02-26 US US14/381,627 patent/US9622986B2/en not_active Expired - Fee Related
- 2013-02-26 CN CN201380011429.4A patent/CN104144684B/zh not_active Expired - Fee Related
- 2013-02-26 JP JP2014559823A patent/JP6132407B2/ja not_active Expired - Fee Related
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1437130A1 (en) | 2001-10-17 | 2004-07-14 | Hisamitsu Pharmaceutical Co. Inc. | Percutaneous absorption preparations |
US20080038328A1 (en) * | 2004-05-28 | 2008-02-14 | Naruhito Higo | Pasting Preparation |
WO2007129427A1 (ja) | 2006-05-08 | 2007-11-15 | Teikoku Seiyaku Co., Ltd. | 抗認知症薬物の経皮吸収製剤 |
KR20090009951A (ko) * | 2006-05-08 | 2009-01-23 | 데이고꾸세이약꾸가부시끼가이샤 | 항치매제를 포함하는 경피 흡수 제제 |
JP2007302582A (ja) * | 2006-05-09 | 2007-11-22 | Hisamitsu Pharmaceut Co Inc | ドネペジル経皮吸収型製剤 |
KR20110030349A (ko) * | 2009-09-16 | 2011-03-23 | 주식회사 삼양사 | 경피 투여 제형 및 그 제조 방법 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10888533B2 (en) | 2014-12-18 | 2021-01-12 | Icure Pharmaceutical Inc. | Transdermal composition containing donepezil as active ingredient |
Also Published As
Publication number | Publication date |
---|---|
CN104144684A (zh) | 2014-11-12 |
EP2821065A1 (en) | 2015-01-07 |
US20150045749A1 (en) | 2015-02-12 |
US9622986B2 (en) | 2017-04-18 |
KR101239150B1 (ko) | 2013-03-06 |
JP2015508813A (ja) | 2015-03-23 |
EP2821065B1 (en) | 2017-11-22 |
EP2821065A4 (en) | 2015-07-22 |
CN104144684B (zh) | 2016-09-07 |
JP6132407B2 (ja) | 2017-05-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
WO2013129813A1 (ko) | 도네페질-함유 경피흡수제제 및 그의 제조방법 | |
US20220151949A1 (en) | Multi-Day Patch for the Transdermal Administration of Rotigotine | |
WO2012002640A2 (ko) | 도네페질을 함유하는 경피흡수제제 | |
WO2012124966A2 (ko) | 펜타닐 경피 패치제 | |
WO2011132966A2 (ko) | 경피 흡수 제제 | |
KR20010036685A (ko) | 펜타닐을 함유하는 매트릭스형 경피투여제 | |
WO2015111862A1 (en) | Transdermal delivery system comprising donepezil or its salt | |
KR101770675B1 (ko) | 도네페질-함유 경피흡수제제 및 그의 제조방법 | |
WO2012161489A2 (ko) | 리바스티그민 함유 패취 | |
US20130101660A1 (en) | Transdermal delivery patch | |
BR112019012573A2 (pt) | sistema terapêutico transdérmico que contém asenapina e polissiloxano ou poli-isobutileno | |
CA3067938A1 (en) | Transdermal therapeutic system containing asenapine and silicone acrylic hybrid polymer | |
KR20200070305A (ko) | 실리콘 폴리머를 포함하는 구안파신의 경피 투여용 경피흡수 치료 시스템 | |
WO2012111996A2 (ko) | 갈란타민 또는 그의 염을 함유하는 경피흡수제제 | |
JP7149951B2 (ja) | ニコチン含有透明経皮吸収治療システム | |
KR101723724B1 (ko) | 수분감응성 겔이 도포된 야누스패브릭을 포함하는 구강점막용 또는 경피흡수용 패치 | |
WO2022191675A1 (ko) | 로티고틴 함유 경피 흡수 제제 | |
WO2009119992A2 (ko) | 펜타닐을 함유한 경피 흡수제 | |
KR100439659B1 (ko) | 툴로부테롤을 함유하는 경피흡수용 패취제 | |
CA3175771A1 (en) | Transdermal and/or topical delivery system comprising hydroxychloroquine and/or chloroquine | |
WO2020085809A1 (ko) | 비결정 로티고틴 함유 조성물 및 이의 제조 방법 | |
WO2015072683A1 (ko) | 셀레질린 또는 그의 약학적으로 허용가능한 염을 함유하는 경피흡수제제 | |
WO2023106506A1 (ko) | 양친매성 고분자 점착제를 포함하는 경피 패치 제조용 하이드로겔 조성물 및 이를 이용한 경피 패치 | |
CN117797125A (zh) | 含有秋水仙碱的贴剂及其制备方法和应用 | |
KR101964295B1 (ko) | 피부 자극이 감소된 메만틴 경피전달 시스템 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 13754753 Country of ref document: EP Kind code of ref document: A1 |
|
REEP | Request for entry into the european phase |
Ref document number: 2013754753 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2013754753 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 2014559823 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 14381627 Country of ref document: US |