CN1543943A - Oral silybin sustained release agent and preparation thereof - Google Patents
Oral silybin sustained release agent and preparation thereof Download PDFInfo
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- CN1543943A CN1543943A CNA2003101051943A CN200310105194A CN1543943A CN 1543943 A CN1543943 A CN 1543943A CN A2003101051943 A CNA2003101051943 A CN A2003101051943A CN 200310105194 A CN200310105194 A CN 200310105194A CN 1543943 A CN1543943 A CN 1543943A
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- silymarin
- slow releasing
- solid dispersion
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- oral
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Abstract
The invention relates to an oral silymarin slow release preparation and process of making, wherein the preparation comprises silymarin solubilized composition 10%-80%, retarding agent 5%-80%, and balancing medicinal adjuvant. The silymarin can be prepared into solid dispersion and capsule. Compared with the existing common tablets, the preparation is characterized by the substantial curative effect for treating diseases including chronic hepatitis, persisting type hepatitis and alcohol liver.
Description
Technical field:
The present invention relates to medical technical field, exactly it be a kind of be that carrier is prepared into solid dispersion with silymarin and makes the technology of oral slow-releasing preparation-oral silymarin slow releasing preparation and preparation method thereof again with PVP K15.
Background technology:
Silymarin is insoluble in water and common organic solvents, and oral absorption is poor, and bioavailability is low, thereby influences clinical efficacy.
Chinese patent application 1391894 (application number 02125823) discloses a kind of " the silymarin injection that contains the cyclodextrin or derivatives thereof ", its technology be with silymarin under the clathration of cyclodextrin or derivatives thereof, be dissolved in the water, thus the preparation injection.
Chinese patent application 1397277 (application number 02125820) discloses a kind of " preparation method of silymarin injection ", and its technology is with behind silymarin and the alkali reaction salify, is dissolved in the water, thereby makes the silymarin injection.
Chinese patent application 1317486 (application number 01101489) discloses a kind of " process for preparing sematron by aceton method ", its technology is to adopt acetone to extract silymarin as solvent, pulverize after qualified silybum marianum seed pressed into the thick oil cake of 2mm, cross 40 mesh sieves, the extraction pot of quantitatively packing into, add quantitative acetone 60 ℃ of extractions 20 hours that circulate down, extracting solution obtains the Herba Silybi mariani ointment after concentrating, the silymarin crude product will be obtained after the ointment drying, it is dry that crude product is carried out the second time after with defat with petroleum ether, crushed after being dried is crossed 180 mesh sieves, goes out silymarin.
Chinese patent application (application number 00801319) discloses a kind of " oral micro-emulsion composition of silymarin ", it is characterized in that with organic solvent, surfactant and oil are cosurfactant, with Carduusmarianus extract, silymarin or silymarin derivant is model drug, thereby the interior bioavailability of body of silymarin is improved greatly.
Chinese patent application 1418637 (application number 02156856) discloses a kind of " silybin meglumine dispersible tablet of treatment hepatitis and preparation method thereof ", it is characterized in that forming by silybin meglumine (SilybinMeglumine) and all the other ten kinds of adjuvants, be mainly used in acute hepatitis, chronic hepatitis, first cirrhosis, fatty liver protects the liver dirty during toxic hepatitis.
Summary of the invention:
The purpose of this invention is to provide a kind of oral silymarin slow releasing preparation and preparation method thereof, it adopts solid dispersion technology, is that carrier has been made into solid dispersion with PVP K15, to increase the stripping of medicine, improves its oral administration biaavailability.
Preparation of the present invention contains following component by weight percentage:
Silymarin solid dispersion 10%-80%
Play the adjuvant 5%-80% of slow releasing function
Other adjuvant surpluses
Contain by weight percentage in the silymarin solid dispersion: silymarin 5%-80%, PVP K1520%-95%.
This preparation comprises the various preparations of film control, skeleton, gel, porous matrix type, also comprises making the various preparations that microcapsule, microsphere etc. are made preparation more earlier.
The adjuvant of above-mentioned slow releasing function is: the solubility/insoluble salt of hypromellose and/or ethyl cellulose and/or polyacrylic resin class and/or polycarboxy ethene and/or alginic acid and/or other adjuvant that plays slow releasing function, the hypromellose employing includes the extensive stock of hydroxypropyl methylcellulose (HPMC) such as U.S. many elegant (Methocel) of all size, ethyl cellulose adopts the extensive stock that includes ethyl cellulose (EC), and the polyacrylic resin class adopts and includes polyacrylic resin II, the acrylic resin of III class or analog such as all size (Eudragit).
Above-mentioned adjuvant is: porogen, binding agent, lubricant, emulsifying agent, membrane material, bleach activator, foaming agent, solvent or other adjuvant, porogen can adopt sucrose, mannitol, starch, Pulvis Talci, Polyethylene Glycol (Macrogol 200～400, polyethylene glycol 1500, Macrogol 4000, polyethylene glycol 6000), silicon dioxide etc.; Binding agent can adopt polyvinylpyrrolidone, hypromellose etc.; Wetting agent can adopt the ethanol-water solution of water, dehydrated alcohol, various concentration; Lubricant can adopt stearic acid, magnesium stearate, Pulvis Talci, starch, paraffin etc.; Solubilizing agent can be adopted medicinal surfactant Tween (as Tween-80), CremophorRH40, Poloxamer, PH regulator and sodium lauryl sulphate etc.; The PH regulator can be one or more faintly acids or alkalescence cushions such as amino acid salts, phosphate (as sodium dihydrogen phosphate, sodium hydrogen phosphate, potassium dihydrogen phosphate, dipotassium hydrogen phosphate), citrate, acetic acid and acetate, tartrate.Emulsifying agent can adopt surfactant (as Tween-80, sodium lauryl sulphate, Tween-85, Mrij 35, Migyol30, Tagat To, Migyol 812 etc.), soybean lecithin, oleic acid and oleate, oleyl alcohol, one or more in cholic acid and the cholate etc.; Membrane material can adopt cellulose acetate, polyvinyl alcohol, hydroxy methocel, hydroxyethyl-cellulose, hymetellose, methylcellulose etc.; Foaming agent can adopt basic magnesium carbonate, sodium bicarbonate etc.; Bleach activator can adopt hexadecanol, octadecanol, Cera Flava etc.; Solvent can adopt dehydrated alcohol, ethanol, water etc.
The dosage form of above-mentioned preparation has sheet type, coating type, capsule or other dosage form.
The solubilizing composition of silymarin of the present invention can adopt following method preparation:
(1), silymarin is adopted micronization pulverize
(2), adopt fusion method or solid dispersion preparations such as solvent method or solvent fusion method to prepare the silymarin solid dispersion
Advantage of the present invention is: silymarin solid dispersion slow releasing preparation, than silymarin tablet, both increased the medicine stripping, improve oral administration biaavailability, thereby minimizing dosage, improve compliance of patients, the production equipment that has conventional tablet again is simple, is convenient to the advantage of packing, storing and transport and carry.
Description of drawings:
Fig. 1 is the stripping curve figure according to the slow releasing preparation of embodiment 1 preparation
Fig. 2 is the stripping curve figure according to the slow releasing preparation of embodiment 2 preparations
The specific embodiment:
Embodiment 1:
Present embodiment 1 tablet that adopts the known method of pharmaceuticals industry to make contains following composition by weight percentage:
Silymarin solid dispersion 50%
HPMC?K4M 9％
Lactose 39%
Sodium lauryl sulphate 1%
Magnesium stearate 1%
Dehydrated alcohol is an amount of
Preparation method: preparation silymarin-PVP K15 solid dispersion: in proportion that silymarin and PVPK15 is miscible in dehydrated alcohol, adopt solvent method to make silymarin-PVP K15 solid dispersion.Add pharmaceutic adjuvants such as blocker, filler, lubricant in silymarin-PVP K15 solid dispersion, by after certain PROCESS FOR TREATMENT, evenly mixed, direct powder compression promptly gets the silymarin slow releasing tablet.HPMCK15M is a hydrophilic polymer, is framework material in said preparation, meets the expansion of water or Digestive system and forms the gel barrier, and the diffusion of control silymarin reaches the slow release purpose.
Embodiment 2:
Silymarin solid dispersion 40%
HPMC?K100 15％
Lactose 20%
Microcrystalline Cellulose 23%
Sodium lauryl sulphate 1%
Magnesium stearate 1%
Dehydrated alcohol is an amount of
Preparation method: in proportion that the blocker of silymarin, PVP K15 and recipe quantity is miscible in dehydrated alcohol, after treating all dissolvings, add mixed other adjuvants uniformly of recipe quantity again, by after certain PROCESS FOR TREATMENT, make soft material, granulate, dry below 60 ℃, granulate, get particle inspection qualified after, add an amount of magnesium stearate, mixed evenly back tabletting promptly gets the silymarin slow releasing tablet.
The silymarin slow releasing tablet technology that makes with this method is simple, low for equipment requirements, is fit to commercial production.
Embodiment 3:
Present embodiment 3 tablets that adopt the known method of pharmaceuticals industry to make contain following composition by weight percentage:
Silymarin solid dispersion 50%
Ethyl cellulose 5%
Microcrystalline Cellulose 32%
Pulvis Talci 1%
Dehydrated alcohol is an amount of
Preparation method: in proportion that the blocker of silymarin, PVP K15 and recipe quantity is miscible in dehydrated alcohol, after treating all dissolvings, add mixed other adjuvants uniformly of recipe quantity again, by after certain PROCESS FOR TREATMENT, make soft material, granulate, dry below 60 ℃, granulate, get particle inspection qualified after, add an amount of Pulvis Talci, mixed evenly back tabletting promptly gets the silymarin slow releasing tablet.
Ethyl cellulose is insoluble framework material, and medicine is dispersed in the insoluble framework material, and drug releasing rate depends on that the dissolution velocity of diffusion velocity and medicine is irrelevant.Medicine is the saturated solution state in skeleton, discharge from insoluble framework material, reaches the slow release purpose.
Embodiment 4:
Silymarin solid dispersion 30%
Carbopol 20%
Lactose 30%
Tween?80 5％
Stearic acid 1%
Dehydrated alcohol is an amount of
Preparation method: in proportion that blocker, the surfactant of silymarin, PVP K15 and recipe quantity is miscible in dehydrated alcohol, after treating all dissolvings, add mixed other adjuvants uniformly of recipe quantity again, by after certain PROCESS FOR TREATMENT, make soft material, granulate, dry below 60 ℃, granulate, get particle inspection qualified after, add an amount of stearic acid, mixed evenly back tabletting promptly gets the silymarin slow releasing tablet.
Hydrophilic polymer carbopol (carbomer) is a framework material, meets the expansion of water or Digestive system and forms the gel barrier, and the diffusion of control silymarin reaches the slow release purpose.
Embodiment 5:
Present embodiment 5 tablets that adopt the known method of pharmaceuticals industry to make contain following composition by weight percentage:
Silymarin solid dispersion 40%
Polyacrylic resin 20%
Microcrystalline Cellulose 35%
Sodium lauryl sulphate 1%
Magnesium stearate 1%
Dehydrated alcohol is an amount of
10% polyvinylpyrrolidone ethanol liquid 3%
Preparation method: in proportion that silymarin, PVP K15 is miscible in dehydrated alcohol, treat all dissolvings after, add mixed other adjuvants uniformly of recipe quantity again, by after certain PROCESS FOR TREATMENT, make soft material, granulate, dry below 60 ℃, granulate, get particle inspection qualified after, add an amount of magnesium stearate, mixed evenly back tabletting, carry out coating with mixed uniform polyacrylic resin and 10% polyvinylpyrrolidone ethanol liquid again, promptly get silymarin enteric solubility slow releasing tablet.
Polyacrylic resin is that the undissolved polymer of gastrointestinal tract is the clothing membrane material, adding a spot of polyvinylpyrrolidone ethanol liquid (PVP) in coating solution is porogen, i.e. solubilized in Digestive system, and making on the clothing film has micropore, medicine discharges from micropore, plays slow releasing function.
Embodiment 6:
Silymarin solid dispersion 30%
HPMC?K100LV 40％
Stearic acid 7%
Basic magnesium carbonate 11%
Sodium lauryl sulphate 1%
Magnesium stearate 1%
Dehydrated alcohol is an amount of
Preparation method: preparation silymarin-PVP K15 solid dispersion: in proportion that silymarin and PVPK15 is miscible in dehydrated alcohol, adopt solvent method to make silymarin-PVP K15 solid dispersion.Add pharmaceutic adjuvants such as blocker, filler, lubricant in silymarin-PVP K15 solid dispersion, by after certain PROCESS FOR TREATMENT, evenly mixed, direct powder compression promptly gets the silymarin slow releasing tablet.HPMCK100LV is a hydrophilic polymer, meets gastric juice and expands and form the gel barrier, and the density of keeping skeleton is less than gastric content density, and floats on the gastric juice; Stearic acid is a bleach activator, and can reduce the hydration rate of skeleton; Basic magnesium carbonate is a foaming agent, meets gastric acid and produces CO
2, can further alleviate the density of preparation, thereby prolong the silymarin tablet holdup time under one's belt, reach the slow release purpose.
Embodiment 7:
Present embodiment 7 tablets that adopt the known method of pharmaceuticals industry to make contain following composition by weight percentage:
Silymarin solid dispersion 50%
Icing Sugar 16%
Microcrystalline Cellulose 30%
Sodium lauryl sulphate 3%
Magnesium stearate 1%
Dehydrated alcohol is an amount of
With last component was the core.
Hypromellose 12g
Propylene glycol 3g
Titanium dioxide 3g
PEG6000 1g
Sodium lauryl sulphate 0.5g
Pulvis Talci 2g
Water 120ml
More than each medicine be the coating aqueous suspension.
Preparation method: in proportion that silymarin, PVP K15 is miscible in dehydrated alcohol, treat all dissolvings after, add mixed other adjuvants uniformly of recipe quantity again, by after certain PROCESS FOR TREATMENT, make soft material, adopt certain technology that it is prepared into micropill.Micropill is carried out coating with the coating solution that has prepared, make coated micropill, incapsulate, promptly get the silymarin slow releasing capsule.
After hydrophilic film clothing (HPMC etc.) is oral, meet Digestive system, constitute the hydrophilic polymer water absorption and swelling of film-coat, form the gel barrier, controlled drug release.
Claims (7)
1, oral silymarin slow releasing preparation, it is characterized in that: said preparation contains following composition by weight percentage:
Silymarin solid dispersion 10%-80%
Play the adjuvant 5%-80% of slow releasing function
Other adjuvant surpluses
2, oral silymarin slow releasing preparation according to claim 1, it is characterized in that: with PVP K15 is the silymarin solid dispersion of carrier, and this solid dispersion contains by weight percentage:
Silymarin 5%-80%
PVP?K15 20％-95％
3, oral silymarin slow releasing preparation according to claim 2, it is characterized in that: the carrier in the silymarin solid dispersion is PVPK15.
4, oral silymarin slow releasing preparation according to claim 1 is characterized in that: the adjuvant that plays slow releasing function is the solubility/insoluble salt of hypromellose and/or ethyl cellulose and/or polyacrylic resin class and/or polycarboxy ethene and/or alginic acid.
5, oral silymarin slow releasing preparation according to claim 1, it is characterized in that: adjuvant is pharmaceutical carrier, antiplastering aid, porogen, binding agent, lubricant, wetting agent, emulsifying agent, bleach activator, foaming agent, solubilizing agent, membrane material, solvent.
6, oral silymarin slow releasing preparation according to claim 1, it is characterized in that: the dosage form of preparation has sheet type, coating type, capsule-type.
7, a kind of preparation method of oral silymarin slow releasing preparation as claimed in claim 1 is characterized in that: a, adopt micronization to pulverize silymarin;
B, employing fusion method or solid dispersion preparations such as solvent method or solvent fusion method prepare the silymarin solid dispersion; Silymarin 5%-80% wherein, PVP K15 20%-95%;
C, in the silymarin solid dispersion, add the adjuvant that formulation ratio requires, mix homogeneously tabletting or make soft material granulation or make micropill and carry out coating and incapsulate.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2003101051943A CN100427084C (en) | 2003-11-26 | 2003-11-26 | Oral silybin sustained release agent and preparation thereof |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2003101051943A CN100427084C (en) | 2003-11-26 | 2003-11-26 | Oral silybin sustained release agent and preparation thereof |
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| CN1543943A true CN1543943A (en) | 2004-11-10 |
| CN100427084C CN100427084C (en) | 2008-10-22 |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010075664A1 (en) * | 2008-12-31 | 2010-07-08 | 江苏大学 | A highly efficient and long-acting slow-release formulation of poorly soluble drugs and preparation method thereof |
| WO2010075663A1 (en) * | 2008-12-31 | 2010-07-08 | 江苏大学 | A formulation of silymarin with high efficiency and prolonged action and the preparation method thereof |
| CN101164537B (en) * | 2006-10-16 | 2010-08-25 | 江苏大学 | High-efficient oral silibinin sustained-release preparation and preparation method thereof |
| CN101961319A (en) * | 2010-09-16 | 2011-02-02 | 中国药科大学 | Silybin meglumine enteric agent with high bioavailability and preparation method thereof |
| CN104069071A (en) * | 2014-06-25 | 2014-10-01 | 江苏大学 | Silibinin slow release micropill with double layers of coatings and preparation method of silibinin slow release micropill |
| CN106511291A (en) * | 2016-09-24 | 2017-03-22 | 济南康和医药科技有限公司 | Acotiamide hydrochloride controlled release tablet and preparation method thereof |
| CN106692980A (en) * | 2015-11-16 | 2017-05-24 | 南京卡文迪许生物工程技术有限公司 | Silibinin oral solid preparation and preparation method thereof |
-
2003
- 2003-11-26 CN CNB2003101051943A patent/CN100427084C/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101164537B (en) * | 2006-10-16 | 2010-08-25 | 江苏大学 | High-efficient oral silibinin sustained-release preparation and preparation method thereof |
| WO2010075664A1 (en) * | 2008-12-31 | 2010-07-08 | 江苏大学 | A highly efficient and long-acting slow-release formulation of poorly soluble drugs and preparation method thereof |
| WO2010075663A1 (en) * | 2008-12-31 | 2010-07-08 | 江苏大学 | A formulation of silymarin with high efficiency and prolonged action and the preparation method thereof |
| CN101444494B (en) * | 2008-12-31 | 2011-03-30 | 江苏大学 | Efficient long-acting sustained-release preparation of slightly soluble medicine and preparation method thereof |
| CN101439025B (en) * | 2008-12-31 | 2011-05-11 | 江苏大学 | Silymarin high-efficient long-acting preparation and production method thereof |
| CN101961319A (en) * | 2010-09-16 | 2011-02-02 | 中国药科大学 | Silybin meglumine enteric agent with high bioavailability and preparation method thereof |
| CN104069071A (en) * | 2014-06-25 | 2014-10-01 | 江苏大学 | Silibinin slow release micropill with double layers of coatings and preparation method of silibinin slow release micropill |
| CN106692980A (en) * | 2015-11-16 | 2017-05-24 | 南京卡文迪许生物工程技术有限公司 | Silibinin oral solid preparation and preparation method thereof |
| CN106511291A (en) * | 2016-09-24 | 2017-03-22 | 济南康和医药科技有限公司 | Acotiamide hydrochloride controlled release tablet and preparation method thereof |
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| Publication number | Publication date |
|---|---|
| CN100427084C (en) | 2008-10-22 |
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Granted publication date: 20081022 Termination date: 20111126 |