Development and validation of a high-performance liquid chromatographic stability-indicating method for the analysis of Synercid in quality control, stability and compatibility studies.

Abstract:

:A gradient high-performance liquid chromatographic (HPLC) method was developed for the analysis of Synercid freeze-dried powder in routine quality control, stability and compatibility studies. This method is suited for a simultaneous assay of drug substances and impurities. The method was validated for precision, reproducibility, linearity, accuracy and limits of detection. The robustness study that was performed according to an experimental design is described.

journal_name

J Pharm Biomed Anal

authors

Vasselle B,Gousset G,Bounine JP

doi

10.1016/s0731-7085(98)00242-8

subject

Has Abstract

pub_date

1999-04-01 00:00:00

pages

641-57

issue

5

eissn

0731-7085

issn

1873-264X

pii

S0731708598002428

journal_volume

19

pub_type

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