| 对乙酰氨基酚栓的溶出度测定 |
| |
| 引用本文： | 张玲雅.对乙酰氨基酚栓的溶出度测定[J].天津药学,2003,15(2):26-27. |
| |
| 作者姓名： | 张玲雅 |
| |
| 作者单位： | 福建省泉州市药品检验所,泉州,362000 |
| |
| 摘 要： | 目的：测定对乙酰氨基酚栓的溶出度，考察不同厂家栓剂的质量。方法：用pH7．4的磷酸盐缓冲液为溶剂，浆法测定，紫外分光光度法涵定溶出度。结果：不同厂家的栓剂溶出度差异很大。结论：应建立溶出度涵定法以有效控制药品的质量。
|
| 关 键 词： | 对乙酰氨基酚栓 溶出度 测定 栓剂 质量 紫外分光光度法 解热镇痛药 |
| 文章编号： | 1006-5687(2003)02-0026-02 |
| 修稿时间： | 2003年1月13日 |
Determination of Dissolution of Paracetomal Suppositories |
| |
| Zhang Lingya.Determination of Dissolution of Paracetomal Suppositories[J].Tianjin Pharmacy,2003,15(2):26-27. |
| |
| Authors: | Zhang Lingya |
| |
| Abstract: | Objective: To study on the quality of paracetomal suppositories by dissolution testing. Methods: Phosphate buffer(pH7.4) was used as the medium, Paddles method was used at 100 r/min. UV-vis Spectrophotometer was adapted for the determination of dissolution. Results: There was a large difference of dissolution testing among varied samples. Conclusion: Dissolution testing should be established to control the paracetomal suppositories effectively. |
| |
| Keywords: | Paracetomal Suppositories Dissolution testing |
| 本文献已被 CNKI 维普 万方数据 等数据库收录！ |
