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High-stability (S)-4-hydroxy-2-oxo-1-pyrrolidine acetamide sustained release capsule and preparation method thereof

A technology of pyrrolidine acetamide and sustained-release capsules is applied in the directions of pharmaceutical formulations, nervous system diseases, and bulk transportation, which can solve the problems of poor particle fluidity, large differences in filling amount, and many particle powder layers, etc. The preparation process is simple and feasible, the number of doses is reduced, and the granules have good fluidity.

Inactive Publication Date: 2018-02-02
CHONGQING RUNZE PHARM CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The existing (S)-4-hydroxy-2-oxo-1-pyrrolidineacetamide sustained-release capsules mainly have the problems that the release rate cannot be well controlled, and the requirements for sustained-release preparations cannot be met, the fluidity of the particles is not good, and the filling process is difficult. There is a large difference in the filling volume, which affects the dosage of the drug. There are more granular powder layers after the granulation, the yield of the finished product is low, and the capsules are easy to stick and agglomerate during storage and other technical problems.

Method used

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  • High-stability (S)-4-hydroxy-2-oxo-1-pyrrolidine acetamide sustained release capsule and preparation method thereof
  • High-stability (S)-4-hydroxy-2-oxo-1-pyrrolidine acetamide sustained release capsule and preparation method thereof
  • High-stability (S)-4-hydroxy-2-oxo-1-pyrrolidine acetamide sustained release capsule and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] A stable (S)-4-hydroxy-2-oxo-1-pyrrolidineacetamide slow-release capsule is prepared according to the following steps:

[0023]

[0024] Preparation process:

[0025] 1. Pretreatment of raw and auxiliary materials: take the prescribed amount of (S)-4-hydroxy-2-oxo-1-pyrrolidineacetamide, lactose, hydroxypropylmethylcellulose K4M, carnauba wax, calcium hydrogen phosphate, micro-powdered silica gel Put in the mixing pulverizer and mix and pulverize into fine powder (the amount that can pass through No. 5 sieve and can pass through No. 6 sieve must not be less than 95% of the total amount), and sieve;

[0026] 2. Granulation: Add povidone K30 ethanol solution, mix and granulate with 18-mesh sieve, place the prepared wet granules in a hot air oven, set the temperature at 40-60°C, and dry until the moisture content of the granules is ≤3%. Granules (through a 24-mesh sieve), set aside;

[0027] 3. Total blending: crush stearyl alcohol and magnesium stearate through a 100...

Embodiment 2

[0071] A stable (S)-4-hydroxy-2-oxo-1-pyrrolidineacetamide slow-release capsule is prepared according to the following steps:

[0072]

[0073] Preparation process: prepared according to the preparation process of Example 1. Test by the test method of Example 1, the yield test result shows that this product yield is up to more than 95%, the angle of repose result shows that this product has good fluidity, and the repose angle is less than 36 °, and the release measurement test result shows that (S)- 4-Hydroxy-2-oxo-1-pyrrolidineacetamide sustained-release capsules are slow-release, and the release time is as long as 12 hours, which can meet the requirements of sustained-release preparations. The results of the stability test show that the quality of the samples is stable after six months of acceleration. Capsule adhesion phenomenon, long-term 24 months of stable quality, no capsule adhesion phenomenon, so this product is valid for at least 24 months.

Embodiment 3

[0075] A stable (S)-4-hydroxy-2-oxo-1-pyrrolidineacetamide slow-release capsule is prepared according to the following steps:

[0076]

[0077] Preparation process: prepared according to the preparation process of Example 1. Test by the test method of embodiment 1, yield test result shows that this product yield is up to more than 94%, and angle of repose result shows that this product fluidity is good, and angle of repose is less than 38 °, and release measurement test result shows (S)- 4-Hydroxy-2-oxo-1-pyrrolidineacetamide sustained-release capsules are slow-release, and the release time is as long as 12 hours, which can meet the requirements of sustained-release preparations. The results of the stability test show that the quality of the samples is stable after six months of acceleration. Capsule adhesion phenomenon, long-term 24 months of stable quality, no capsule adhesion phenomenon, so this product is valid for at least 24 months.

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Abstract

The invention provides a high-stability (S)-4-hydroxy-2-oxo-1-pyrrolidine acetamide sustained release capsule, which is prepared from the following raw and auxiliary materials: 1 part of (S)-4-hydroxy-2-oxo-1-pyrrolidine acetamide, 0.5 to 1.1 parts of lactose, 1.8 to 2.7 parts of hydroxypropyl methyl cellulose K4M, 0.3 to 0.9 part of carnauba wax, 0.03 to 0.08 part of octadecanol, 0.12 to 0.18 part of magnesium stearate, 0.3 to 0.8 part of calcium hydrophosphate, 0.2 to 0.9 part of superfine silica gel powder and 2.8 to 3.9 parts of 7 to 10 percent polyvidone K30 ethanol solutions. The (S)-4-hydroxy-2-oxo-1-pyrrolidine acetamide sustained release capsule provided by the invention has the advantages that the particle flowability is high; the particle rest angle is smaller than 37 degrees; the powder layer is few after the particle sorting; the finished product yield is as high as 93.9 percent; the release speed is low; the release period is as long as 12 hours; meanwhile, the product stability is high; the capsule adhesion phenomenon cannot occur in the storage process; and the shelf life is as long as 24 months.

Description

technical field [0001] The invention mainly relates to the field of pharmaceutical technology, in particular to a stable (S)-4-hydroxy-2-oxo-1-pyrrolidineacetamide sustained-release capsule and a preparation method thereof. Background technique [0002] Oxiracetam (S-oxiracetam) is a synthetic cyclic derivative of hydroxyaminobutyric acid (BABOB), which is only used in the central nervous system, mainly distributed in the cerebral cortex and hippocampus, and has the function of activating, protecting or promoting nerve cells. Functional recovery can improve the memory and learning functions of patients with mental retardation, and the drug itself has no direct vasoactive or central excitatory effect, and its effect on learning and memory is a lasting promotion effect. [0003] The drug was launched in Italy in 1987, and the listed dosage forms are tablets, 800mg; capsules, 800mg; injection, 1g / 5ml. At present, only oxiracetam capsules and injections are on the market in Chi...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K9/52A61K47/38A61K31/4015A61P25/28
CPCA61K9/0002A61K9/1652A61K9/1682A61K31/4015
Inventor 叶雷
Owner CHONGQING RUNZE PHARM CO LTD
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