Development and Validation of a Novel UV Spectrophotometric Method for Simultaneous Analysis of Amlodipine, Indapamide and Perindopril

被引:2
|
作者
Ericaalves [1 ]
Nazareth, Celina [1 ]
Pereira, Sanelly [1 ]
机构
[1] PESs Rajaram & Tarabai Bandekar Coll Pharm, Dept Pharmaceut Chem, Farmagudi 403401, Goa, India
关键词
Absorbance correction method; amlodipine besylate; indapamide; perindopril tert-butyl amine; International Conference on Harmonisation (ICH) guidelines; BESYLATE; BULK;
D O I
10.36468/pharmaceutical-sciences.713
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A simple, accurate, precise and economical ultraviolet spectrophotometric method has been developed for the simultaneous estimation of amlodipine, perindopril and indapamide. The developed method was based on determination of the three drugs using ultraviolet absorbance correction method. The three wavelengths chosen were 365 nm for amlodipine (as absorbances due to other two drugs were nil at this wavelength), 245 nm for indapamide (corrected for absorbance due to amlodipine) and 204 nm for perindopril (corrected for absorbances due to amlodipine and indapamide) with water as diluent. The Beer Lambert's range for the three drugs was 10-60 mu g/ml, 5-20 mu g/ml and 10-100 mu g/ml for amlodipine, indapamide and perindopril respectively, with correlation coefficient (r(2)) of >= 0.999. The developed method was validated as per International Conference on Harmonisation guidelines and was found to be accurate, precise, sensitive and robust. The percentage assay results were within acceptable limits. Hence the developed method can be successfully used for the routine analysis of amlodipine, perindopril and indapamide in bulk and in combination.
引用
收藏
页码:843 / 850
页数:8
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