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A kind of monosialotetrahexosyl ganglioside sodium sustained-release capsule and preparation method thereof

A technology of ganglioside sodium and slow-release capsules, applied in the field of medicine, can solve the problems of loss of pharmacological effects, inability to exert curative effect, instability, etc., achieve the effects of reducing the frequency of administration, strong practicability, and improving the bonding effect

Active Publication Date: 2019-01-08
赛隆药业集团股份有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In order to solve the problem that the existing oral preparation of monosialotetrahexosylganglioside sodium is unstable in the gastrointestinal tract, it is easily decomposed in the gastrointestinal tract, and is rapidly lost under the decomposition of microorganisms and hydrolytic enzymes in the gastrointestinal tract after oral administration. Pharmacological effects, unable to exert curative effect and other problems, the invention provides a monosialotetrahexosyl ganglioside sodium sustained-release capsule and its preparation method

Method used

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  • A kind of monosialotetrahexosyl ganglioside sodium sustained-release capsule and preparation method thereof
  • A kind of monosialotetrahexosyl ganglioside sodium sustained-release capsule and preparation method thereof
  • A kind of monosialotetrahexosyl ganglioside sodium sustained-release capsule and preparation method thereof

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Embodiment 1

[0034] Embodiment 1 of the present invention provides a monosialotetrahexosylganglioside sodium slow-release capsule, the slow-release capsule is composed of a capsule filling and a capsule shell, and the capsule filling is mainly composed of the following weight grams: Composition:

[0035]

Embodiment 2

[0037]Embodiment 2 of the present invention provides a monosialotetrahexosylganglioside sodium slow-release capsule, the slow-release capsule is composed of a capsule filling and a capsule shell, and the capsule filling is mainly composed of Composition:

[0038]

[0039]

[0040] The preparation method of this slow-release capsule comprises the following steps:

[0041] S1. After dissolving monosialotetrahexosyl ganglioside sodium with ethanol aqueous solution, add lactidified polyglycerol ricinoleate and poly-L-hydroxyethyl acrylate, and stir evenly to obtain a core material;

[0042] S2. Weigh the hypromellose, slowly add distilled water under constant stirring to make a water body with a mass percentage of 1%, and put it in a spray tank for standby;

[0043] S3. Put the core material prepared in step S1 into a fluidized bed, spray into the water prepared in step S2 for microencapsulation to obtain microcapsule particles, pass the microcapsule particles through a 20-...

Embodiment 3

[0046] Embodiment 4 of the present invention provides a monosialotetrahexosylganglioside sodium sustained-release capsule, the sustained-release capsule is composed of a capsule filling and a capsule shell, and the capsule filling is mainly composed of the following grams by weight Composition:

[0047]

[0048]

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Abstract

The invention provides a monosialotetrahexosylganglioside sodium slow-release capsule and a preparation method thereof. The slow-release capsule is composed of a capsule filler and a capsule shell. The capsule filler is mainly composed of the following components in parts by weight: 10-30 parts of monosialotetrahexosylganglioside sodium, 10-20 parts of transesterified polyglycerol ricinoleate, 10-15 parts of methyl poly-L-hydroxyethylacrylate, 10-15 parts of hydroxypropyl methylcellulose, 5-8 parts of guar gum and 5-10 parts of chitosan. The capsule provided by the invention is convenient for oral administration, can effectively enhance the stability of monosialotetrahexosylganglioside sodium in the gastrointestinal tract, can ensure the regular slow constant-speed release of monosialotetrahexosylganglioside sodium, effectively prevents drugs from being quickly decomposed in the gastrointestinal tract, and keeps the drugs in the organism at a relatively constant concentration. The slow-release capsule can effectively reduce the medication frequency, reduces the pains of the patient, and enhances the drug effects.

Description

technical field [0001] The invention belongs to the technical field of medicine, in particular to a monosialotetrahexosylganglioside sodium slow-release capsule and a preparation method thereof. Background technique [0002] Gangliosides are a family of heterogeneous sialic acid-containing complex membrane glycolipids, first discovered by Klenk in 1939. Their molecules are composed of a lipophilic ceramide moiety and a hydrophilic sialooligosaccharide core group. Since Ceccarelli first proved in 1976 that exogenous gangliosides (GLs) can improve peripheral nerve regeneration and promote repair, scholars at home and abroad have conducted in-depth research on the effects of gangliosides on the central nervous system. Monosialotetrahexosyl ganglioside (GM1) is an important class of gangliosides that have multiple biological functions such as neurotrophy and central nervous system repair, and its role in the treatment of nervous system injuries is being widely recognized. Pay ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K9/62A61K31/7032A61K47/32A61K47/38A61K47/34A61K47/36A61K47/14A61P25/28
CPCA61K9/0002A61K9/4816A61K9/5036A61K9/5042A61K31/7032A61K47/14A61K47/34
Inventor 李剑峰周文
Owner 赛隆药业集团股份有限公司
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