MODIFIED USP ASSAY FOR SIMULTANEOUS DETERMINATION OF ASPIRIN AND NON-ASPIRIN SALICYLATES IN ASPIRIN AND BUFFERED ASPIRIN TABLETS

被引:6
作者
LUBER, JR
VISALLI, AJ
PATEL, DM
机构
[1] Analytical and Physical Chemistry Department, Research and Development Division, William H. Rorer, Inc., Pennsylvania, 19034, Fort Washington
关键词
Analgesics—aspirin; analysis; buffered and unbuffered tablets; modified USP method; liquid chromatography; spectrophotometry; stability; Aspirin—analysis; Liquid chromatography—analysis; aspirin in buffered and unbuffered tablets;
D O I
10.1002/jps.2600680630
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Modified USP procedures are described for the simultaneous determination of nonaspirin salicylates and aspirin in aspirin and buffered aspirin tablets. The existing USP procedures are not stability indicating for intact aspirin when significant levels of nonaspirin salicylates are present, as is often the case in short‐term, high temperature stability programs. The modified procedures yield considerably shorter analysis times and stability‐indicating assays for intact aspirin without the need for sophisticated equipment other than that presently required by USP XIX. Copyright © 1979 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:780 / 782
页数:3
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