CN102755285A - Hormone cream - Google Patents
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- CN102755285A CN102755285A CN2012102504210A CN201210250421A CN102755285A CN 102755285 A CN102755285 A CN 102755285A CN 2012102504210 A CN2012102504210 A CN 2012102504210A CN 201210250421 A CN201210250421 A CN 201210250421A CN 102755285 A CN102755285 A CN 102755285A
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Abstract
The invention relates to a hormone cream which is prepared from solid used as an oil phase matrix, a consistence regulator, a humectant, an emulsifier, a stabilizer and the balance of water, wherein active ingredients are dispersed into a suspension of the cream by a water suspension mode, and the suspension additive is also necessarily added.
Description
The application is an application number 200710060219.0, and the applying date is December in 2007 27 days, and denomination of invention is divided an application for the one Chinese patent application of " a kind of hormone emulsifiable paste ".
Technical field
The present invention relates to a kind of hormone emulsifiable paste, especially relate to a kind of methylprednisolone aceponate emulsifiable paste.
Background technology
The Methylprednisolone Aceponate emulsifiable paste is a kind of of steroids; Can suppress the reaction of inflammation and allergic skin; Also suppress simultaneously to add the related reaction of rapid regeneration and cause symptom with cell; For example erythema, oedema, thickization of skin, coarse the going down of skin surface, and alleviate problems such as itch, burning heat sensation and pain.The methylprednisolone aceponate emulsifiable paste is current superpower external corticosteroid formulations; Its curative effect all is superior to known corticosteroid; And wherein the methylprednisolone aceponate emulsifiable paste is the efficient corticosteroid of no halogen family group, and side effect is light, is a kind of corticosteroid external preparation that can be used for the child.
Methylprednisolone aceponate emulsifiable paste commodity are called Advantan, are German Schering Corp (Schering AG) exploitation listings.On Advantan description (http://www.betterhealth.vic.gov.au/bhcv2/bhcmed.nsf/pages/cscad van/$File/cscadvan.pdf), we can see that its main component is: methylprednisolone aceponate 0.1%; Adjuvant: Ceraphyl 140 (decyl oleate), the glyceryl monostearate of 40-55% content (glycerol monosteartae 40-55%), cetearyl alcohol (cetostearyl alcohol); Stearic (hard fat), caprylic/capric/myristic acid/glycerol stearate/(Softisan 378), polyoxyethylene stearate (40) ester (PEG-40-sterate); The glycerol of 85% content, Calcium Disodium Versenate, benzyl alcohol; Butoben, purified water.
2005 editions appendix I of Chinese Pharmacopoeia F mentions: ointment means medicine dissolution or is scattered in the uniform semi-solid external preparation that forms in the emulsion type substrate; The substrate of ointment should be even, fine and smooth, is applied on skin or the mucosa and answers nonirritant; Ointment should have suitable stickiness, is prone to coat on skin or the mucosa, does not melt, and stickiness should be very little with seasonal variations.
Existing methylprednisolone aceponate emulsifiable paste is had relatively high expectations for substrate; Substrate requires adjuvant more; Comparatively complicated, some adjuvant source is less, like Ceraphyl 140 (decyl oleate) and caprylic/capric/myristic acid/glycerol stearate/(Softisan 378); These adjuvants are domestic not to be had at present, import price more expensive.In addition, existing methylprednisolone aceponate emulsifiable paste stickiness is not enough, be put on the skin, since mobile excessive, the scope that bad control is applied ointment, in the time of use, the also bad control of the amount of extruding.
On Merck index, we can know as 17-hydroxy-11-dehydrocorticosterone a kind of, and methylprednisolone aceponate is to be insoluble in water and the chemical compound that is dissolved in organic solvent; In the prior art, will prepare emulsifiable paste for this corticoid chemical compound, generally be that chemical compound is dissolved in organic solvent earlier; In propylene glycol or dimethyl sulfoxine; Like authentication code is the triamcinolone acetonide acetate urea cream of H44024203, and authentication code is the compound recipe Dexamethasone Acetate Cream of H44024204, but has certain influence for the stability of the responsive active component of organic solvent; Especially methylprednisolone aceponate is this has 17; The 17-hydroxy-11-dehydrocorticosterone of 21-dibasic acid esters is being dissolved in the situation that occurs ester exchange under the situation of organic solvent easily, can have a strong impact on the stability of the emulsifiable paste that is mixed with.。
Summary of the invention
For overcoming the problems of the prior art; The invention provides a kind of brand-new methylprednisolone aceponate emulsifiable paste, compare with existing this like product Advantan emulsifiable paste of German Schering Corp, what the substrate of this emulsifiable paste related to all is conventional adjuvant; Cheaply be easy to get; Cost is lower, and the emulsifiable paste that makes is even, fine and smooth, is applied to nonirritant on skin or the mucosa; And suitable stickiness is arranged, and in the time of use, the ointment that squeezes out more easy to control can be controlled the dose that extruding is come out well, and when spreading upon on the skin, the scope of coating more easy to control.In addition, preparation technology is comparatively advanced, owing to adopted active component suspension manner of formulation, quality is more stable, and the storage time is longer.
The invention provides a kind of brand-new methylprednisolone aceponate emulsifiable paste, constitute, it is characterized in that forming by following raw materials by weight percent by solid, consistency modifiers, wetting agent, emulsifying agent, stabilizing agent and water as oil phase substrate:
As the methylprednisolone aceponate 0.05%～0.5% of active component, preferred 0.1%;
Solid as oil phase substrate; Include but are not limited to stearic acid, one or more in paraffin, Cera Flava, the higher alcohol, described higher alcohol are the monohydric alcohol of 16～22 carbon atoms; Preferred hexadecanol of solid in the said oil phase and/or octadecanol, described solid consumption is 1%～15%;
As consistency modifiers, one or more in the vaseline that includes but are not limited to, liquid paraffin, the vegetable oil, preferred vaseline and/or liquid Paraffin, the consumption of described consistency modifiers is 1%～40%, special preferable amount is 5%～20%;
With multicomponent alcoholics compound as wetting agent, include but are not limited to glycerol, propylene glycol, sorbitol, the consumption of described wetting agent is 1%～15%, preferably glycerine,
Stabilizing agent, preferred but be not limited only to Calcium Disodium Versenate, the consumption of stabilizing agent is 0.05%～3%;
And emulsifying agent; Include but are not limited to the derivant of soap class emulsifying agent, polyoxyethylene ether; Preferably as the glyceryl monostearate of soap class emulsifying agent and/or as the peregal A-20 of polyoxy ether class emulsifying agent; Total consumption of said emulsifying agent is 1～18%, and preferred soap class emulsifying agent consumption emulsifiable paste weight is 1～10%, and polyoxy ether class emulsifying agent consumption is 0.5%～8% of an emulsifiable paste weight.
Described higher alcohol also plays influence of surfactant simultaneously in substrate
And, include but are not limited in benzyl alcohol, the p-Hydroxybenzoate one or more as optional antibacterial, the consumption of described antibacterial is 0.1～5%,
The active component methylprednisolone aceponate is distributed in the emulsifiable paste with the mode of aqueous suspension; Also need add the suspendible auxiliary agent in the described active component suspension, the suspendible auxiliary agent includes but are not limited to one or more in polyvinylpyrrolidone, hydroxypropyl cellulose, hydroxypropyl emthylcellulose, hydroxyethyl-cellulose, carboxymethyl cellulose and or its salt, the carbomer; The consumption of described suspendible auxiliary agent is 0.1～5%, the preferably polyethylene ketopyrrolidine;
Surplus is a water
Above-mentioned percentage by weight is in emulsifiable paste weight.
The compound method that the invention provides a kind of brand-new methylprednisolone aceponate emulsifiable paste is following:
(1) oil phase preparation: take solid, consistency modifiers, emulsifying agent heating and melting in oil phase substrate, temperature remains on 70-80 ℃; (whether scope can strengthen)
(2) water preparation: the humectant of going bail for, stabilizing agent and water place container, heating, temperature remains on 70-80 ℃;
(3) close phase: pour the oil phase of step (1) preparation the aqueous phase of step (2) preparation into, stir, maintain the temperature at 60～90 ℃, add optional antibacterial;
(4) principal agent suspension: active component, water, suspendible auxiliary agent are placed container, and stirring or ultrasonic obtains the principal agent suspension;
(5) the control temperature is at 50-75 ℃, and the principal agent suspension that obtains in the step (4) is added in the solution that step (3) obtains, and the limit edged stirs, and is cooled to cream.
The invention provides a kind of brand-new methylprednisolone aceponate emulsifiable paste, its optimization formula is made up of following raw materials by weight percent: methylprednisolone aceponate 0.1%, white vaseline 5-10%; Octadecanol 5-8%, glyceryl monostearate 5%～10%, liquid paraffin 5%～10%; Peregal A-20 1%～5%, glycerol 5%～10%, Calcium Disodium Versenate 0.05%～1%; Benzyl alcohol 0.1～3%, polyvinylpyrrolidone 0.1%～3%, surplus is a water
The methylprednisolone aceponate of mentioning in methylprednisolone aceponate emulsifiable paste that the invention provides and the compound method, granularity is: particle size range is 0.01-50 μ m, preferred 0.1-30 μ m, most preferably 0.5-10 μ m.Directly use aqueous solution preparation suspension, and used the suspendible auxiliary agent to make the active component microgranule obtain good dispersion, not only avoid the use of the organic solvent dissolution methylprednisolone aceponate; Prevented the shortcoming that active component is degraded easily; And because the use of suspendible auxiliary agent when making active component obtain well dispersed, has also produced a kind of clathration; The active component microgranule has been produced the protection effect, thereby the feasible emulsifiable paste stability that makes by technical scheme of the present invention better.
Brand-new methylprednisolone aceponate emulsifiable paste provided by the invention and existing this like product of German Schering Corp are compared; Stickiness is suitable; With 4 batches of emulsifiable pastes of being joined by the embodiment of the invention 1～4 respectively, according to " two methods of Chinese pharmacopoeia version in 2005 are measured dynamic viscosity, adopt NDJ-1 type Rotary Viscosimeter; With No. 4 rotors, rotating speed is that per minute 6 changes.Test result such as table 1:
Two kinds of methylprednisolone aceponate emulsifiable pastes of table 1 viscosity test result
Two kinds of methylprednisolone aceponate emulsifiable pastes of table 1 viscosity test result
The result shows that the viscosity of homemade 4 lot sample article all is suitable, and this suitable stickiness is the assurance that emulsifiable paste is not stratified, principal agent is not separated out.Earlier our self-control sample is lower slightly, therefore mobile excessive relatively for clever Advantan commercial viscosimetry, is not easy to control the coating scope.
Brand-new methylprednisolone aceponate emulsifiable paste provided by the invention and existing this like product of German Schering Corp are compared, and quality stability will be got well.We are according to " the study on the stability method of the ointment formulation that Chinese pharmacopoeia version in 2005 is two ones; The homemade brand-new clever Advantan commodity of methylprednisolone aceponate emulsifiable paste and elder generation have been carried out study on the stability long-term and acceleration; Sample is from embodiment 1～4; Emulsifiable paste that each embodiment makes and lot number are that the clever Advantan emulsifiable paste of 23448C elder generation compares, and every group of sample size is 20, and specification is that 10g/ props up; Mainly liquid content and related substance are detected, detect according to following liquid phase chromatogram condition:
It is the chromatographic column of filler that a chromatographic column is selected octadecylsilane chemically bonded silica for use
B is a mobile phase with methanol: water=7:3 (volume ratio) mixed solution,
It is 243 nm that c detects wavelength
D flow velocity=1ml/min
Result of the test is following:
Two kinds of methylprednisolone aceponate emulsifiable pastes of table 2 long-time stability are investigated result's (content) (n=20,
± s)
Two kinds of methylprednisolone aceponate emulsifiable pastes of table 3 long-time stability are investigated result's (related substance)
Two kinds of methylprednisolone aceponate emulsifiable pastes of table 4 accelerated stability is investigated result's (content) (n=20,
± s)
Two kinds of methylprednisolone aceponate emulsifiable pastes of table 5 accelerated stability is investigated the result
" the ointment regulation that Chinese pharmacopoeia version in 2005 is two ones, the active component content scope is 90%-110%.Can find with earlier clever Advantan emulsifiable paste stability data contrast by table 2 and the methylprednisolone aceponate emulsifiable paste sample that 3 embodiment 1～4 makes: during pro-was investigated in 24 months; The content difference of comparing embodiment 1～4 self-control sample with the Advantan emulsifiable paste is significantly (P＞0.05) not; And its related substances difference of comparing embodiment 1～4 sample with the Advantan emulsifiable paste also not significantly (P＞0.05), and all within acceptability limit, but in 25-36 month; The content of Advantan emulsifiable paste sharply descends; Content only 80.01% in the time of 36 months, and related substance is up to 15.32%, and is defective; Content according to embodiment 1～4 self-control sample all keeps up to about 98%, compare with content, the related substance of corresponding Advantan emulsifiable paste all have significance (P＜0.01) this proved absolutely that the emulsifiable paste that makes according to the embodiment of the invention is than clever Advantan emulsifiable paste stability is good earlier.In addition, layering, metachromatism all do not take place in the emulsifiable paste that makes by the present invention program in long-time stability are investigated.
Contrasting and to find by table 4 and 5: at high temperature under condition and the high light according to embodiment 1～4 homemade methylprednisolone aceponate emulsifiable paste sample and earlier clever Advantan emulsifiable paste accelerated stability data; All samples content all slightly descends in time; Its related substances all slightly rises in time; But making the content of sample, embodiment 1～4 compares with the Advantan emulsifiable paste that though difference does not have the former content of significance (P＞0.05) and the latter generally exceeds 1% ~ 2% on year-on-year basis.Under super-humid conditions, the content of all samples and its related substances change less, explain under this condition, and be less for the emulsifiable paste stability influence.Accelerated stability data contrast table is clear, and the self-control sample is than clever Advantan emulsifiable paste accelerated stability outline is good earlier.In addition, layering, metachromatism all do not take place in our 3 lot sample article in accelerated stability is investigated.
Brand-new methylprednisolone aceponate emulsifiable paste provided by the invention and existing this like product of German Schering Corp are compared, and quality stability will be got well.This mechanism wherein is unclear as yet; Possible reason: the present invention is in preparation methylprednisolone aceponate emulsifiable paste process; Directly use the suspension of aqueous solution preparation major ingredient, an amount of suspendible auxiliary agent that in preparation suspension process, adds has produced the suitable clathration to the active component microgranule; Thereby prevented the shortcoming that major ingredient is degraded easily effectively, and used in the prior art; In addition, the adjuvant of selecting for use is suitable, and reasonable mixture ratio also is the reason of methylprednisolone aceponate emulsifiable paste good stability.
The specific embodiment
To do further description to the present invention through embodiment below, these descriptions are not that content of the present invention is done further to limit.One skilled in the art will understand that to be equal to replacement to what technical characterictic of the present invention was done, or corresponding the improvement, still belong within protection scope of the present invention.
The granularity of used methylprednisolone aceponate as active component all adopts 0.5 μ m to 10 μ m in the most preferred technical scheme in the embodiment of the invention, and the emulsifiable paste that all embodiment make is all used with the aluminum pipe subpackage equipment that 10g/ props up.
Embodiment 1
By the accurate weighing of above proportioning, moisture is two parts: 500g and 257g, gets ready, and the emulsifiable paste process for preparation is following:
(1) oil phase preparation:, get white vaseline, octadecanol, glyceryl monostearate, liquid paraffin, peregal A-20 places container, is heated to fusion, and temperature remains on 72 ± 2 ℃;
(2) water preparation: by the accurate weighing of above proportioning, get glycerol, Calcium Disodium Versenate and 500g water place container, heating, and temperature remains on 70 ± 2 ℃;
(3) close phase: pour the oil phase of step (1) preparation the aqueous phase of step (2) preparation into, stir, maintain the temperature at 75 ± 2 ℃, add benzyl alcohol;
(4) principal agent suspension: methylprednisolone aceponate, 257g water, polyvinylpyrrolidone are placed container, and stirring or ultrasonic obtains the principal agent suspension;
(5) the control temperature is at 50 ℃, and the principal agent suspension that obtains in the step (4) is added in the solution that step (3) obtains, and the limit edged stirs, and is cooled to cream.Obtain methylprednisolone aceponate emulsifiable paste 1kg.
Embodiment 2
By the accurate weighing of above proportioning, moisture is two parts: 380g and 259g, gets ready, and the emulsifiable paste process for preparation is following:
(1) oil phase preparation:, get white vaseline, octadecanol, hexadecanol, glyceryl monostearate, liquid paraffin, peregal A-20 places container, is heated to fusion, and temperature remains on 72 ± 2 ℃;
(2) water preparation: by the accurate weighing of above proportioning, get glycerol, Calcium Disodium Versenate and 380g water place container, heating, and temperature remains on 70 ± 2 ℃;
(3) close phase: pour the oil phase of step (1) preparation the aqueous phase of step (2) preparation into, stir, maintain the temperature at 75 ± 2 ℃, add benzyl alcohol;
(4) principal agent suspension: methylprednisolone aceponate, 259g water, polyvinylpyrrolidone are placed container, and stirring or ultrasonic obtains the principal agent suspension;
(5) the control temperature is at 58 ℃, and the principal agent suspension that obtains in the step (4) is added in the solution that step (3) obtains, and the limit edged stirs, and is cooled to cream.Obtain methylprednisolone aceponate emulsifiable paste 1kg.
Embodiment 3
By the accurate weighing of above proportioning, moisture is two parts: 380g and 260g, gets ready, and the emulsifiable paste process for preparation is following:
(1) oil phase preparation:, get white vaseline, octadecanol, glyceryl monostearate, liquid paraffin, peregal A-20 places container, is heated to fusion, and temperature remains on 77 ± 2 ℃;
(2) water preparation: by the accurate weighing of above proportioning, get glycerol, Calcium Disodium Versenate and 380g water place container, heating, and temperature remains on 75 ± 2 ℃;
(3) close phase: pour the oil phase of step (1) preparation the aqueous phase of step (2) preparation into, stir, maintain the temperature at 75 ± 2 ℃, add benzyl alcohol;
(4) principal agent suspension: methylprednisolone aceponate, 260g water, hydroxypropyl emthylcellulose are placed container, and stirring or ultrasonic obtains the principal agent suspension;
(5) the control temperature is at 68 ℃, and the principal agent suspension that obtains in the step (4) is added in the solution that step (3) obtains, and the limit edged stirs, and is cooled to cream.Obtain methylprednisolone aceponate emulsifiable paste 1kg.
Embodiment 4
By the accurate weighing of above proportioning, moisture is two parts: 300g and 237g, gets ready, and the emulsifiable paste process for preparation is following:
(1) oil phase preparation:, get white vaseline, octadecanol, glyceryl monostearate, liquid paraffin, peregal A-20 places container, is heated to fusion, and temperature remains on 77 ± 2 ℃;
(2) water preparation: by the accurate weighing of above proportioning, get glycerol, Calcium Disodium Versenate and 300g water place container, heating, and temperature remains on 75 ± 2 ℃;
(3) close phase: pour the oil phase of step (1) preparation the aqueous phase of step (2) preparation into, stir, maintain the temperature at 75 ± 2 ℃, add benzyl alcohol;
(4) principal agent suspension: methylprednisolone aceponate, 237g water, hydroxypropyl emthylcellulose are placed container, and stirring or ultrasonic obtains the principal agent suspension;
(5) the control temperature is at 75 ℃, and the principal agent suspension that obtains in the step (4) is added in the solution that step (3) obtains, and the limit edged stirs, and is cooled to cream.Obtain methylprednisolone aceponate emulsifiable paste 1kg.
Embodiment 5～8
The consumption of methylprednisolone aceponate is adjusted into 5g,, promptly gets active component content and be 0.5% methylprednisolone aceponate emulsifiable paste respectively according to the prescription of embodiment 1～4 and technology preparation emulsifiable paste.
Claims (10)
1. one kind is the emulsifiable paste of active component with the methylprednisolone aceponate, it is characterized in that forming by following raw materials by weight percent,
The consumption of methylprednisolone aceponate is 0.05%～0.5% by weight percentage;
The solid of oil phase substrate is selected from stearic acid, and one or more in paraffin, Cera Flava, the higher alcohol, said higher alcohol are the monohydric alcohol of 16～22 carbon atoms, and consumption is 1～15% by weight percentage;
Consistency modifiers is selected from one or more in vaseline, liquid paraffin, the vegetable oil, and consumption is 1～40% by weight percentage,
Wetting agent is a multicomponent alcoholics compound, is selected from glycerol, propylene glycol, sorbitol, and consumption is 1%～15% by weight percentage;
Stabilizing agent is selected from Calcium Disodium Versenate, and consumption is 0.05%～3% by weight percentage;
Emulsifying agent is glyceryl monostearate and/or peregal A-20, and consumption is 1～18% by weight percentage;
Also need add the suspendible auxiliary agent in the described active component suspension; Consumption is 0.1～5% by weight percentage, and described suspendible auxiliary agent is selected from one or more in polyvinylpyrrolidone, hydroxypropyl cellulose, hydroxypropyl emthylcellulose, hydroxyethyl-cellulose, carboxymethyl cellulose and/or its salt, the carbomer;
Surplus is a water.
2. one kind is the emulsifiable paste of active component with the methylprednisolone aceponate, it is characterized in that forming by following raw materials by weight percent,
The consumption of methylprednisolone aceponate is 0.05%～0.5% by weight percentage;
The solid of oil phase substrate is selected from stearic acid, and one or more in paraffin, Cera Flava, the higher alcohol, said higher alcohol are the monohydric alcohol of 16～22 carbon atoms, and consumption is 1～15% by weight percentage;
Consistency modifiers is selected from one or more in vaseline, liquid paraffin, the vegetable oil, and consumption is 1～40% by weight percentage,
Wetting agent is a multicomponent alcoholics compound, is selected from glycerol, propylene glycol, sorbitol, and consumption is 1%～15% by weight percentage;
Stabilizing agent is selected from Calcium Disodium Versenate, and consumption is 0.05%～3% by weight percentage;
Emulsifying agent is glyceryl monostearate and/or peregal A-20, and consumption is 1～18% by weight percentage;
Antibacterial is selected from benzyl alcohol, the p-Hydroxybenzoate one or more, and the consumption of described antibacterial is 0.1～5%,
Described active component is distributed in the emulsifiable paste with the mode of aqueous suspension,
Also need add the suspendible auxiliary agent in the described active component suspension; Consumption is 0.1～5% by weight percentage, and described suspendible auxiliary agent is selected from one or more in polyvinylpyrrolidone, hydroxypropyl cellulose, hydroxypropyl emthylcellulose, hydroxyethyl-cellulose, carboxymethyl cellulose and/or its salt, the carbomer;
Surplus is a water.
3. according to claim 1 or claim 2 emulsifiable paste is characterized in that described solid as oil phase substrate is selected from octadecanol and/or hexadecanol.
4. like the described emulsifiable paste of claim 1 to 2, it is characterized in that preferred vaseline of described consistency modifiers and/or liquid Paraffin, consumption is preferably 5%～20%.
5. according to claim 1 or claim 2 emulsifiable paste is characterized in that described wetting agent preferably glycerine.
6. according to claim 1 or claim 2 emulsifiable paste is characterized in that the particle size range of described methylprednisolone aceponate as active component is 0.01 μ m to 50 μ m.
7. according to claim 1 or claim 2 emulsifiable paste is characterized in that the particle size range of described methylprednisolone aceponate as active component is 0.1 μ m to 30 μ m.
8. according to claim 1 or claim 2 emulsifiable paste is characterized in that the particle size range of described methylprednisolone aceponate as active component is 0.5 μ m to 10 μ m.
9. like arbitrary described emulsifiable paste in claim 1 or 2, it is characterized in that described active component suspending agent is a polyvinylpyrrolidone.
10. emulsifiable paste as claimed in claim 2 is characterized in that filling a prescription and is made up of following raw materials by weight percent: methylprednisolone aceponate 0.1%, white vaseline 5-10%; Octadecanol 5-8%, glyceryl monostearate 5%～10%, liquid paraffin 5%～10%; Peregal A-20 1%～5%, glycerol 5%～10%, Calcium Disodium Versenate 0.05%～1%; Benzyl alcohol 0.1～3%, polyvinylpyrrolidone 0.1%～3%, surplus is a water.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 201210250421 CN102755285B (en) | 2007-12-27 | 2007-12-27 | Hormone cream |
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| Application Number | Priority Date | Filing Date | Title |
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| CN 201210250421 CN102755285B (en) | 2007-12-27 | 2007-12-27 | Hormone cream |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200710060219A Division CN101468024B (en) | 2007-12-27 | 2007-12-27 | Hormone emulsifiable paste |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103877118A (en) * | 2014-03-11 | 2014-06-25 | 天津金耀集团有限公司 | Medicine composition consisting of methylprednisolone aceponate and zinc oxide |
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2007
- 2007-12-27 CN CN 201210250421 patent/CN102755285B/en active Active
Non-Patent Citations (2)
| Title |
|---|
| 林跃: "甲基强的松龙乙酸丙酸酯", 《药学进展》 * |
| 毕殿洲: "《药剂学》", 30 April 2000 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103877118A (en) * | 2014-03-11 | 2014-06-25 | 天津金耀集团有限公司 | Medicine composition consisting of methylprednisolone aceponate and zinc oxide |
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