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脑康通泰分散片的制备及溶出度测定

王维 李洪起 邹俊忠 任晓文

天津中医药2011,Vol.28Issue(5):418-420,3.
天津中医药2011,Vol.28Issue(5):418-420,3.

脑康通泰分散片的制备及溶出度测定

Determination of preparation and dissolution with Naokangtongtai dispersible tablet

王维 1李洪起 2邹俊忠 3任晓文4

作者信息

  • 1. 天津中医药大学,天津300193
  • 2. 释药技术与药代动力学国家重点实验室,天津300193
  • 3. 天津药物研究院,天津300193
  • 4. 天津药物研究院药业有限责任公司,天津300193
  • 折叠

摘要

Abstract

[Objective] To prepare Naokangtongtai dispersible tablets and establish the dissolution method. To compare with the dissolution of other common products. [Methods] The formulation of the tablets was optimized through the indices: slope of repose, hardness, disintegration time and corpuscular liquidity. Dissolution was determined by the solvent according to the method in Chinese Pharma-copoeia(2010, Appendix Ⅱ) with 900 mL water as the solvent at a rotation speed of 100 r/min. And the detection wavelength was 270 nm. [Results] The proportion of each adjuvant in the optimal formulation consisted of 20% microcrystalline cellulose and 24% brushite as a filler, and 10% crospovidone mixed with 2% silicon dioxide as disintegrating agent, 1% magnesium stearate as lubricants. The dispersible tablets could disintegrate completely within 3 minutes and its dissolution rate could reach beyond 75% in 30 min. [Conclusion] The preparative method of Naokangtongtai dispersible tablets by wet granulation is simple. The method is accurate and suitable for the dissolution determination of Naokangtongtai dispersible tables.

关键词

脑康通泰分散片/制备工艺/溶出度

Key words

Naokangtongtai dispersible tablets preparation technology/ dissolution

分类

医药卫生

引用本文复制引用

王维,李洪起,邹俊忠,任晓文..脑康通泰分散片的制备及溶出度测定[J].天津中医药,2011,28(5):418-420,3.

基金项目

国家重点基础研究发展计划项目(2010CB735602). (2010CB735602)

天津中医药

OACSTPCD

1672-1519

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