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刊物信息

期刊名称:药物分析杂志
主管单位:中国科学技术协会
主办单位:中国药学会
承办:中国食品药品检定研究院
主编:金少鸿
地址:北京天坛西里2号
邮政编码:100050
电话:010-67012819,67058427
电子邮箱:ywfx@nifdc.org.cn
国际标准刊号:ISSN 0254-1793
国内统一刊号:CN 11-2224/R
邮发代号:2-237
 

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自身对照法测定复方黄连素片溶出度

Determination of dissolution of the compound huangliansu tablets by self-control method

分类号:
出版年·卷·期(页码):2012,32 (8):0-0
DOI: 10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------

目的: 建立自身对照法测定复方黄连素片溶出度。 方法: 采用自身对照法(UV)测定复方黄连素片的溶出度。采用篮法,溶出介质为纯化水(900 mL),转速100 r·min-1,取样时间90 min。 结果: 复方黄连素片溶出度测定自身对照法在1.2~9.0 μg·mL-1 浓度范围内呈线性(r=0.9995,n=5),回收率98.9%,RSD=0.03%。 结论: 本法简便、准确、可行,可作为复方黄连素片的质量标准中控制项目之一。

-----英文摘要:---------------------------------------------------------------------------------------

Objective: To establish a self-control method for determination the dissolution of the compound huangliansu tablets. Methods: The UV spectrophotometry method was applied to determine the dissolution of the compound huangliansu tablets.Basket apparatus was used with water as the dissolution medium at a speed of 100 r·min-1 and dissolution time limit was 90 min. Results: The linear range of the compound huangliansu tablets was 1.2-9.0 μg·mL-1 and the correlation coefficient was 0.9995.The average recovery was 98.90%,and the RSD was 0.03%. Conclusion: The method is convenient,accurate and practicable.It can be applied to determine the dissolution of the tablets.

-----参考文献:---------------------------------------------------------------------------------------
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5 YANG Hui-yuan(杨慧元),LE Jian (乐健),CHEN Gui-liang(陈桂良).Determination of dissolution of cloxacillin sodium capsule by HPLC(HPLC法用于氯唑西林钠胶囊溶出度的测定).J Pharm Pract(药学实践杂志),2004,22(2):83
6 LIU Meng(刘萌),ZHOU Hui(周晖).Dissolution tests of the compound huangliansu tablets from different manufactories(不同厂家复方黄连素片的溶出度试验),Her Med(医药导报),2005,24(3):234
7 WANG Xin(王昕),TANG Su-fang(唐素芳).Development and study of method for dissolution test of furazolidone tablets(呋喃唑酮片溶出度试验方法的建立与研究).Chin J Pharm Anal(药物分析杂志),2010,30(8):1445
8 XIE Yuan-chao(谢元超),ZHANG Lei(张雷),LENG Jia-wei(冷佳蔚),et al.Determination of dissolution of Cefalexin and Trimethoprim Capsule by self-control method(自身对照法测定头孢氨苄甲氧苄啶胶囊溶出度),Qilu Pharm Aff(齐鲁药事),2009,28(3):152
9 CHEN Su-wei(陈苏伟),CHEN Qin-ming(陈琴鸣),CHEN Jian-miao(陈健苗).Research status quo and discussion of dissolution of Chinese drugs preparation(中药制剂溶出度测定测定方法研究现状与探讨).Mod J Integr Tradit Chin West Med(现代中西医结合杂志),2005,14(15):2062
10 LI Li(李丽),ZHOU Zhen-qi(周振旗).Dissolution tests of pharmaceutical preparations factors(影响药物制剂溶出度实验的因素).Northwest Pharm J(西北药学杂志),2010,6(25):479
11 JIANG Xiong-ping(姜雄平).Discussion about dissolution or drug release test of solid preparations of traditional Chinese medicin(中成药固体制剂溶出度测定的探讨).Drug Stand China(中国药品标准),2005,6(3):66
12 ZHANG Yan-ju(张艳菊),WANG Xiao-ling(王晓玲).Dissolution of baical in and berberine hydrochloride in sanhuang tablets from different pharmaceutical factories(不同厂家三黄片中黄芩苷、盐酸小檗碱的溶出度).J Anhui Tradit Chin Med Coll(安徽中医学院学报),2010,29(6):62

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