CN101468088A - Gel patch for resisting depression and preparation method thereof - Google Patents

Gel patch for resisting depression and preparation method thereof Download PDF

Info

Publication number
CN101468088A
CN101468088A CNA2007100604783A CN200710060478A CN101468088A CN 101468088 A CN101468088 A CN 101468088A CN A2007100604783 A CNA2007100604783 A CN A2007100604783A CN 200710060478 A CN200710060478 A CN 200710060478A CN 101468088 A CN101468088 A CN 101468088A
Authority
CN
China
Prior art keywords
gel
preparation
medicine
patch
mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CNA2007100604783A
Other languages
Chinese (zh)
Inventor
高惠明
方昊
周英超
李扬
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tianjin Zhongbao Pharmaceutical Co Ltd
Original Assignee
Tianjin Zhongbao Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tianjin Zhongbao Pharmaceutical Co Ltd filed Critical Tianjin Zhongbao Pharmaceutical Co Ltd
Priority to CNA2007100604783A priority Critical patent/CN101468088A/en
Publication of CN101468088A publication Critical patent/CN101468088A/en
Pending legal-status Critical Current

Links

Landscapes

  • Medicinal Preparation (AREA)

Abstract

The present invention relates to an antidepressant traditional Chinese medicine gel plaster and its preparation method, composed of 5%-50% of extract of traditional Chinese medicine and 95%-5% of medicinal adjuvant. The antidepressant traditional Chinese medicine plaster is prepared by mixing the molecule gel, the hydrogel, active ingredients of medicine extracts with the plural gel factor. Different medicine extracts enter into the skin through different channels. The oil-soluble component in molecule gel has repulsion force to the water-soluble medicine and the water-soluble component in hydrogel has repulsion force to the oil-soluble medicine therefore the medicine absorption is promoted and the medicine efficacy is increased.

Description

A kind of gel patch for resisting depression and preparation method thereof
Technical field
The present invention relates to up-to-date molecular gel of Percutaneously administrable preparation technical field and hydrogel combines and makes the novel form of profit ampholytic gels, adopt mixing active ingredients thing that Radix Salviae Miltiorrhizae, Semen Sojae Preparatum, Fructus Gardeniae three flavor Chinese medicine compositions extract for the basis in addition the medicinal substrate preparation have antidepressant Transdermal absorption profit ampholytic gels patch and preparation method thereof, specifically be a kind of antidepressant Chinese medicine gel adhesive.
Background technology
Transdermal drug delivery system or percutaneous absorption patch refer to stick the mode medication through skin, and medicine enters the systemic blood circulation by skin absorbs and reaches a class preparation of effective blood drug concentration, realization disease treatment or prevention.The characteristics of percutaneous absorption patch are, transdermal drug delivery system can avoid the first pass effect of liver and medicine in the gastrointestinal deactivation, the absorption of medicine is not subjected to the influence of gastrointestinal factors, reduce the individual variation of medication, keep constant effective blood drug concentration or physiological effect, the blood drug level peak valley phenomenon of avoiding oral administration to cause reduces toxicity.Reduce administration number of times, improve therapeutic efficacy, prolong action time, avoid multiple dose administration, make most patient be easy to accept, simultaneously easy to use, independently medication of patient also can be cancelled medication at any time.
So-called profit ampholytic gels is not the zwitterion that we say usually, because molecular gel generally all is as solvent by oil-based solvent, organic solvent or the mixture of the two, it is gel with oleophilic properties, and used aqueous solvent accounts for greatly in the hydrogel, it is the gel of possess hydrophilic property matter, the two is used, so be called the profit ampholytic gels.
Molecular gel is that the gel factor (some micromolecule organic compound) is passed through non-covalent interaction in non-aqueous media, spontaneously assembles, assembles orderly three-dimensional fiber network structure, makes the medium gelation.Molecular gel has reversible characteristics of heat, and processing technology is simple, and gelinite contains a large amount of organic solvents, be fit to the storage storehouse as lipophilic medicament, but molecular gel exists cohesiveness low, and viscosity is little, with the skin poor compliance, is not suitable for making shortcomings such as patch.Hydrogel water content height is fit to the storage storehouse as hydrophilic medicament, and is strong to the skin compliance, but is subjected to the influence of self property, and colloid poor plasticity, elasticity are little.In sum, be advantage in conjunction with these two kinds of gels, adopt the pluralgel factor that two kinds of gelinites are disperseed mixing, with the molecular gel is framework material, the patch substrate that hydrogel is made as sticky stuff, both high resilience forms have good compliance with skin, can peel off repeatedly, paste again, improve the drug loading of hydrophilic medicament and hydrophobic drug simultaneously again.Two kinds of gels twine staggered uniform distribution in substrate, by non-covalent bond form combinations such as Van der Waals forces, by fully contacting with skin, the both sexes medicine continues to see through skin through passage separately, enters blood circulation, the performance drug effect.
Depression (depression) is that what to be caused by a variety of causes is the one group of mood disorders (mood disorders) or the affective disorder (affective disorders) of cardinal symptom with the depression, and being one group is the clinical symptom group or the state at center with the depressive mood self experience.Low based on mental state, unbecoming with situation, can be from depressed to extremely grieved, even take place numb.Psychotic disease symptoms such as hallucination, vain hope can appear in severe patient.The anxiety of some case and mobility are intense very remarkable.Depression and general " unhappy " have essential distinction, and it has obvious characteristics, has integrated three big cardinal symptoms, are exactly that depressed, retardation of thinking and motion suppress.Suicide is one of the most dangerous symptom of depression.
Modern society's life is nervous, and competitive pressure is big, and mental sickness such as depression obviously rise, and its sickness rate is also raising year by year.This mattoid of treatment is still based on medicine at present, and common drug has tricyclic antidepressant, Fourth Ring class antidepressants, monoamine oxidase, MAO, inhibitor and selectivity 5-hydroxy tryptamine, reclaims inhibitor etc.Because it is long that depressive psychosis has the course of disease, the easy characteristics of recurrence, the clinical principle that must adhere to taking medicine for a long time control again in treatment is because of the restriction of erious adverse reaction such as toxic and side effects and price endurance, make patient be difficult to adhere to treat, take for a long time also and can produce dependency.
Summary of the invention
The objective of the invention is to advantage in conjunction with up-to-date molecular gel and hydrogel, the toxic and side effects that overcomes existing antidepressants existence greatly, easily produces dependency, the oral formulations uncertain therapeutic efficacy is cut, it is frequent easily to be inactivated in gastrointestinal and to take medicine, shortcomings such as inconvenience are avoided general aqueous gel poor plasticity, oil-base gel agent again to shortcomings such as big, the easy pollution clothes of skin irritation.The invention provides a kind of to treatment depression effect remarkable and toxic and side effects is little, release slowly steadily, to little Chinese medicine composition Transdermal absorption profit ampholytic gels patch of skin irritation and preparation method thereof.The profit ampholytic gels has the strong and high resilience of cohesiveness, and is good with the skin adhesion, can peel off multiple subsides repeatedly; Water content is big, and is strong with the skin compliance, can improve the permeability of skin, helps the Transdermal absorption of medicine; Preparation is simple, is beneficial to industrialized great production.
This prescription Radix Salviae Miltiorrhizae has Radix Salviae Miltiorrhizae to have to calm the nerves, promoting blood flow to regulate menstruation, the effect of removing heat from blood eliminating carbuncle; Fructus Gardeniae has the pathogenic fire purging relieving restlessness, clearing away heat-damp and promoting diuresis, removing pathogenic heat from blood and toxic substance from the body, the effect of reducing swelling and alleviating pain; Semen Sojae Preparatum has and induces sweat the relieving restlessness effect; All medicines are harmonious, and reach the effect of treatment depression by leading pathogenic heat, removing stagnation to relieve restlessness, clearing away heart-fire for tranquillization off, are made into profit ampholytic gels patch, have evident in efficacy, release and steadily slowly continue.Used gel coherence is better, and the glue sample is flexible, and viscosity fastness is better, can peel off multiple subsides repeatedly; Water content is big, and is strong with the skin compliance, helps the Transdermal absorption of medicine; Preparation process is simple, convenient.
The technical solution used in the present invention is: a kind of antidepressant Chinese medicine compound profit ampholytic gels patch and preparation method thereof; it is made up of backing layer, adhesive-layer, protective layer, it is characterized in that the adhesive-layer in this patch mainly is made up of medicine, profit ampholytic gels and short penetrating agent.Said preparation is made up of following medicaments in part by weight extract, wherein, and Radix Salviae Miltiorrhizae 15-50, Semen Sojae Preparatum 15-30, Fructus Gardeniae 20-40; The weight part ratio of adhesive-layer Chinese medicine effective ingredient and profit ampholytic gels (molecular gel: hydrogel is 1:1-10) is 1:1-25.Transdermal enhancer 3-8 weight portions, the weight percent content of the effective ingredient of Chinese medicine mixture is 5%-50% in the profit ampholytic gels patch.Transdermal penetration agent, effective ingredient extract, molecular gel and hydrogel add with order respectively in proportion, and mix homogeneously is uniformly coated on the backing layer, the compound protective layer of going up, and after the extrusion modling, sterilization, stamping-out are made product.
Described drug molecule gel can be made as follows: 1%-30% gel factor is dissolved in the mixture of specific organic solvent or organic solvent.Medicine is dissolved in the organic solvent, adds a certain amount of gel factor then and mix, promptly get molecular gel.The gel factor that is adopted is divided into two classes, the first kind is simple tertiary amine and quaternary ammonium salt thereof as lecithin, N, N, the two octadecane amine of N-three-octadecane amine, gallbladder steroid eicosane amine, methyl, dioctadecyl dimethyl ammonium chloride and cyclodextrin derivative class as: organic molecules such as beta-schardinger dextrin-, second class are derivative of fatty acid as 12-hydroxy octadecadienoic acid and associated salts thereof, glyceryl monostearate, glyceryl tristearate, tripalmitin etc.Organic solvent comprises alkanes, arene, dimethyl sulfoxide (DMSO), acetonitrile, 1-propanol, 1-amylalcohol, 1-capryl alcohol, propylene glycol, glycerol, silicone oil, 14/isopropyl palmitate etc.
Described medicine hydrogel can be made as follows:
The first kind, 2%-15% sodium polyacrylate, 1%-30%PVP and 1%-20%CMC-NA pressed powder mix homogeneously are scattered in 15%-60% propylene glycol, the glycerol solvent, and mix homogeneously adds 40%-80% deionized water mix homogeneously promptly.The 0%-15% additive, additive comprises: Kaolin, starch, micropowder silica gel, aluminum chloride, Alumen, sodium alginate etc.
Second class, 0.1%-10% carbomer, 1%-20% sodium polyacrylate, 15%-40% glycerol, 30%-80% propylene glycol, 3%-15% ethanol, 5%-20% additive, additive comprises: Kaolin, starch, micropowder silica gel, citric acid, citric acid, ethanol, aluminum chloride, triethanolamine, ethyl hydroxybenzoate, ammonium stearate, disodium EDTA (EDTA-2Na), sodium benzoate, parabens or the like.
The above-mentioned described first kind prescription gel factor can only cooperate with first kind gel, and the second gellike factor and the second gellike agent cooperate.Because the fundamental property of two gellikes is different, intersection is combined with change or the chemical reaction that framework may take place.
Penetrating agent of the present invention comprises dimethyl sulfoxide and analog: dimethyl sulfoxide (DMSO); Azone compounds: laurocapram Azone; Alcohol compound: ethanol, propylene glycol, glycerol; Volatile oil and or their mixture etc.Described backing layer is non-woven fabrics or polyester film, and protective layer is paper or polyester film through release treatment.
Chinese crude drug extraction process of the present invention is not limited to aqueous extraction-alcohol precipitation technology, also can be that water is put forward other extraction processes such as organic solvent extractionprocess, alcohol extraction organic solvent extractionprocess and supercritical fluid extraction; Coating processes such as the also available blade coating molding of the preparation technology of patch.Gel adhesive of the present invention can be made arbitrary shape.
Process conditions:
A. extract drugs technology
(a) get a certain amount of salviamiltiorrhizabung, use 50-100% alcohol reflux 2-5 time, use 6 times of water gagings respectively, decoct 60-150min, filter merging filtrate, the distilled water that adds doubling dose is placed 1-5h, makes precipitation fully, decompression, the collecting precipitation thing, drying, so triplicate, merge precipitate, standby.
(b) get a certain amount of Chinese medicine Fructus Gardeniae, pulverize and be coarse powder, with 50-100% ethanol percolate extraction 12-48h, flow speed control is at 2-10mlmin -1, the percolate decompression recycling ethanol also is concentrated into 30-200ml.Standby.
(c) get a certain amount of Semen Sojae Preparatum, pulverize, add the ethanol of the 50%-100% of 10 times of amounts, mixing, supersound extraction 10-60 minute, decompression filtered, extract continuously three times, merging filtrate, decompression and solvent recovery also is concentrated into 30-200ml, and is standby.
B. the preparation technology of patch:
(a) preparing process of profit ampholytic gels:
The first kind: get a certain amount of sodium polyacrylate, PVP and CMC-NA pressed powder and add in the agitator, heat 20-90 ℃, be scattered in propylene glycol, the glycerol solvent, mix homogeneously, after adding molecular gel required organic solvent and drug extract mixing behind the adding deionized water mix homogeneously, after slowly mixing after the adding mixed gel factor, progressively lower the temperature, form the profit ampholytic gels until room temperature.
Second class: get in a certain amount of carbomer, sodium polyacrylate, glycerol, propylene glycol, ethanol, the additive adding agitator, heat 20-90 ℃, behind the mix homogeneously, add required organic solvent and the drug extract mixing of molecular gel, after slowly mixing after the adding mixed gel factor, progressively lower the temperature until room temperature, form the profit ampholytic gels.
(b) preparation technology of paster
The drug matrices that is mixed is evenly coated on the backing layer non-woven fabrics, will covers on the medicine glue-line through the polyester protecting film that release treatment is crossed, enter the roller bearing extrusion modling, THICKNESS CONTROL is below 5mm.Stamping-out, screening, quality inspection, packing are carried out by specification in the sterilization back.
(c) profit ampholytic gels patch application characteristic:
Respectively to hydrogel adhesive, oil-base gel agent, molecular gel agent, four kinds of gels of ampholytic gels patch from mouldability, first viscous force, peeling force, tough elastic force, seven performance indications of compliance of skin irritation, preparation stability, patient are investigated.Every definition standard is as follows.
Mouldability: four kinds of gels of equal in quality are coated on the non-woven fabrics uniformly the overall appearance of observing colloid, loosely organized degree.
First viscous force: the assay method according to the first viscous force of patch in (2005) second appendix XJ patches of Chinese Pharmacopoeia adhesive force algoscopy is measured comparison to four kinds of gels that are coated on the non-woven fabrics.
Peeling force: the assay method according to peel strength in (2005) second appendix XJ patches of Chinese Pharmacopoeia adhesive force algoscopy is measured comparison to four kinds of gels that are coated on the non-woven fabrics.
Tough elasticity: coating on the non-woven fabrics circular glass sheet of placing identical size on four kinds of gel-type vehicles, a 20g counterweight is put by sheet central authorities, after the pressure relief, observes gel shape recovery situation and compares.
Skin irritation: observe animal intact skin single and repeatedly contact gel the local excitation reaction that is produced.(300g ± 20g), male and female half and half are divided into 8 groups, 5-6 every group to choose healthy albino guinea-pig.24h is with Cavia porcellus spinal column both sides unhairing before administration, check whether skin of unhairing has wound, apply ointment or plaster in the left and right sides of every Cavia porcellus the respectively gel of same dose is observed single-dose and is removed the situation that erythema and edema appear in skin in 1h, 24h behind the gel, 48h, the 72h.Repeatedly apply ointment or plaster more than the week, observe again a week after stopping, the redness of observed and recorded skin every day and edema situation and smear the position whether pigmentation, situation such as hemorrhage are arranged.Stability: placed at ambient temperature 1 month, the character of observing each gel changes situation.
Patient's compliance: select some normal adults, stick four kinds of gels respectively, compare from situations such as the sensation of skin, degree easy to use.
Four kinds of various performance comparison results of gel
Annotate: +++for well; ++ in; + for poor
The specific embodiment
Below example by the specific embodiment, foregoing of the present invention is described in further detail, embodiment only is indicative, means that never it limits the scope of the invention by any way.But do not breaking away under the above-mentioned technological thought situation of the present invention, the various replacements of making according to ordinary skill knowledge and habitual means or the modification of change include within the scope of the invention.
Embodiment 1:
Transdermal enhancer laurocapram Azone 3.5kg
Molecular gel 2.5% lecithin,
97.5% Semen Myristicae isopropyl ester 100kg
Hydrogel 8% sodium polyacrylate, 2% polyvinylpyrrolidone
2% sodium carboxymethyl cellulose, 20% propylene glycol
20% glycerol, 48% deionized water 400kg
Effective ingredient extract 75kg
Take by weighing the 32kg sodium polyacrylate, 8kg polyvinylpyrrolidone and 8kg sodium carboxymethyl cellulose pressed powder mix homogeneously, be scattered in the 80kg propylene glycol, in the 80kg glycerol solvent, mix homogeneously in agitator, add the 192L deionized water, mix homogeneously, get 97.5kg Semen Myristicae isopropyl ester and place agitator, add 75kg effective ingredient mixture, containing the Radix Salviae Miltiorrhizae extract weight portion in the mixture is 30kg, Semen Sojae Preparatum 20kg, Fructus Gardeniae 25kg adds the 3.5Kg laurocapram, and 60 ℃ of heated and stirred are to complete mixing, add 2.5Kg lecithin, after slowly stirring with 100 rev/mins, cooling, temperature reduce to stop to stir after the room temperature leave standstill 5h the profit ampholytic gels.The drug gel substrate that is mixed is evenly sprayed cloth on the backing layer non-woven fabrics, will cover on the medicine glue-line through the polyester protecting film that release treatment is crossed, enter the roller bearing extrusion modling, THICKNESS CONTROL is below 5mm.Stamping-out is carried out by specification in the sterilization back, makes patch, and coefficient of losses 15% is pressed Chinese Pharmacopoeia patch standard through quality inspection qualification rate 85%.The certified products packing.
Embodiment 2:
Transdermal enhancer oleic acid 3.5kg
Molecular gel 5% glyceryl monostearate
95% cyclohexane extraction 150kg
Hydrogel 0.5% carbomer, 5% sodium polyacrylate
28.5% propylene glycol, 60% glycerol,
4% ethanol, 1.4% Kaolin,
0.2% citric acid, 0.4% triethanolamine 500kg
Effective ingredient extract 100kg
Take by weighing 25kg sodium polyacrylate, 2.5kg carbomer pressed powder mix homogeneously, be scattered in 142.5kg propylene glycol, the 300kg glycerol solvent, mix homogeneously in agitator, add 20Kg ethanol, 7Kg Kaolin, 1Kg citric acid, 2Kg triethanolamine, mix homogeneously is got the 142.5kg cyclohexane extraction and is placed agitator, add 100Kg effective ingredient mixture, containing the Radix Salviae Miltiorrhizae extract weight portion in the mixture is 45kg, Semen Sojae Preparatum 30kg, Fructus Gardeniae 25kg.Add 3.5Kg oleic acid, 60 ℃ of heated and stirred add the 7.5Kg glyceryl monostearate to mixings fully, after slowly stirring with 100 rev/mins, cooling, temperature reduce to stop to stir after the room temperature leave standstill 5h gel.The drug matrices that is mixed is evenly sprayed cloth on the backing layer non-woven fabrics, will cover on the medicine glue-line through the polyester protecting film that release treatment is crossed, enter the roller bearing extrusion modling, THICKNESS CONTROL is below 5mm.Stamping-out is carried out by specification in the sterilization back, makes patch, and coefficient of losses 5% is pressed Chinese Pharmacopoeia patch standard through quality inspection qualification rate 95%.The certified products packing.

Claims (7)

1. gel patch for resisting depression and preparation method thereof; it is characterized in that: it is made up of backing layer, adhesive-layer, protective layer; adhesive-layer is mixed and made into by extract and molecular gel, hydrogel, the transdermal enhancer of Radix Salviae Miltiorrhizae, Semen Sojae Preparatum, Fructus Gardeniae three herbal medicine effective ingredient; the weight portion proportioning is: effective ingredient extract 10-200 part; 3-8 parts of transdermal enhancers; 100-300 parts of molecular gels, 200-1000 parts of hydrogels.
2. according to described a kind of gel patch for resisting depression of claim 1 and preparation method thereof, it is characterized in that: described molecular gel is formed and percentage by weight is: the gel factor 1%-30%, solvent or their mixture 50%-90%.The gel factor comprises the tertiary amine of ad hoc structure and quaternary amines organic compound thereof such as lecithin, N, N, N-three-octadecane amine, gallbladder steroid eicosane amine, the two octadecane amine of methyl, dioctadecyl dimethyl ammonium chloride; Organic molecules such as cyclodextrin derivative class such as beta-schardinger dextrin-; Derivative of fatty acid such as 12-hydroxy octadecadienoic acid and associated salts thereof, glyceryl monostearate, glyceryl tristearate, tripalmitin etc.Solvent comprises alkanes, arene, dimethyl sulfoxide (DMS0), acetonitrile, 2-ethoxy ethanol, 1-propanol, 1-amylalcohol, 1-capryl alcohol, 1,2-propylene glycol, glycerol, silicone oil, 14/isopropyl palmitate etc.
3. according to described a kind of gel patch for resisting depression of claim 1 and preparation method thereof, it is characterized in that: the composition of described hydrogel and percentage by weight are water-soluble base, water-insoluble substrate or their mixture 5%-30%, solvent 50%-90%, additive 1%-10%.Water-soluble base and non-aqueous substrate comprise polypropylene acid, sodium polyacrylate, carbomer resin, polyvinylpyrrolidone, sodium carboxymethyl cellulose, methylcellulose, polyvinyl alcohol and/or their mixture of various models; Additive comprises Kaolin, starch, micropowder silica gel, aluminum chloride, Alumen, sodium alginate etc.; Solvent comprises deionized water, propylene glycol, glycerol, ethanol and/or their mixture.
4. according to described a kind of gel patch for resisting depression of claim 1 and preparation method thereof, it is characterized in that: described penetrating agent comprises dimethyl sulfoxide and analog, azone class, alcohol compound, volatile oil and/or their mixture.
5. according to described a kind of gel patch for resisting depression of claim 1 and preparation method thereof, it is characterized in that: described backing layer is non-woven fabrics or polyester film, and protective layer is paper or polyester film through release treatment.
6. according to described a kind of gel patch for resisting depression of claim 1 and preparation method thereof, it is characterized in that: described preparation process comprises:
Getting the required organic solvent of the required mixture of a certain amount of preparation hydrogel, solvent, deionized water and preparation molecular gel adds in the agitator, heat 20-90 ℃, after mixing, add the abundant mixing of effective ingredient extract, after slowly mixing after the adding mixed gel factor, progressively lower the temperature until room temperature, form gel.
7. according to described a kind of gel patch for resisting depression of claim 1 and preparation method thereof, it is characterized in that: preparation technology is spreading formation process, extrusion modling or spray mo(u)lding technology.
CNA2007100604783A 2007-12-28 2007-12-28 Gel patch for resisting depression and preparation method thereof Pending CN101468088A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNA2007100604783A CN101468088A (en) 2007-12-28 2007-12-28 Gel patch for resisting depression and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNA2007100604783A CN101468088A (en) 2007-12-28 2007-12-28 Gel patch for resisting depression and preparation method thereof

Publications (1)

Publication Number Publication Date
CN101468088A true CN101468088A (en) 2009-07-01

Family

ID=40826050

Family Applications (1)

Application Number Title Priority Date Filing Date
CNA2007100604783A Pending CN101468088A (en) 2007-12-28 2007-12-28 Gel patch for resisting depression and preparation method thereof

Country Status (1)

Country Link
CN (1) CN101468088A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113288883A (en) * 2021-05-24 2021-08-24 河南科技大学 Long-acting depression relieving microneedle patch and preparation method thereof
CN114712334A (en) * 2022-04-08 2022-07-08 季华实验室 A gel patch for treating traumatic injury, and its preparation method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113288883A (en) * 2021-05-24 2021-08-24 河南科技大学 Long-acting depression relieving microneedle patch and preparation method thereof
CN114712334A (en) * 2022-04-08 2022-07-08 季华实验室 A gel patch for treating traumatic injury, and its preparation method

Similar Documents

Publication Publication Date Title
RU2467759C2 (en) Composition for local use and its applications
JP5944325B2 (en) Methods and compositions for treating skin inflammation
TW411277B (en) Percutaneous tape preparation containing fentanyl
CN101468138A (en) Gel patch for treating insomnia and method for preparing the same
CN102552147B (en) Bullatacin ethosome gel and preparation method thereof
JP5936544B2 (en) Stable rasagiline composition
WO1993009768A1 (en) Fomentation containing ketorolac
CN101342174B (en) Phthiobuzonum/diclothane compound topical formulation
CN1322895C (en) Chinese medicinal gel formulation and its preparing process
CN101468088A (en) Gel patch for resisting depression and preparation method thereof
CN101468074A (en) Antalgic gel patch and preparation method thereof
CN101468140A (en) Gel patch for treating cardiopalmus and method for preparing the same
CN101468177A (en) Gel patch for treating scapulohumeral periarthritis and preparation method thereof
CN107961320B (en) Pharmaceutical composition for treating acute pancreatitis and preparation method thereof
CN101468082A (en) Gel patch for treating facial paralysis and preparation method thereof
CN101015538A (en) Medicinal composition of total capsicine compounds and beta-cyclodextrin or derivative of beta-cyclodextrin
CN102697664B (en) Tanshinone lipidosome and preparation method thereof
KR102105256B1 (en) Cosmetic composition containing Taeniam extracts wrapped in cubic phase lipidic nanostructure for sensitive skin care and thereof producing method
CN101468055A (en) Gel patch for preventing and treating cerebral thrombosis and preparation method thereof
CN102648922B (en) Gamuzhuer medicinal latex preparation and preparation method thereof
CN101468094A (en) Gel patch for resisting fatigue and preparation method thereof
CN101468059A (en) Gel patch for treating myopia and preparation method thereof
CN100348174C (en) Oral drop pill in use for clearing away heat and toxic material, relieving inflammation and alleviating pain, and preparation method
CN101468065A (en) Gel patch for reducing blood sugar and preparation method thereof
CN101468123A (en) Gel patch for treating migraine and method for preparing the same

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Open date: 20090701