Efavirenz related compounds preparation by hydrolysis procedure: setting reference standards for chromatographic purity analysis.

Abstract:

:A simple procedure for obtaining and purifying two degradation products of efavirenz (amino alcohol and quinoline derivatives) from drug substance hydrolysis is described. These impurities are known to exhibit very different UV absorbance properties from those of the parent compound, making determination using a quantitation factor (QF) inaccurate. The obtained hydrolysis products were characterized by physicochemical methods to assure identity, purity and strength. Quinoline derivative was of high purity degree (100%) and amino alcohol was 98.74% pure. Both were set as reference standards in chromatographic related compounds test for efavirenz drug substance and tablets analyses.

journal_name

J Pharm Biomed Anal

authors

Ribeiro JA,de Campos LM,Alves RJ,Lages GP,Pianetti GA

doi

10.1016/j.jpba.2006.06.010

subject

Has Abstract

pub_date

2007-01-04 00:00:00

pages

298-303

issue

1

eissn

0731-7085

issn

1873-264X

pii

S0731-7085(06)00413-4

journal_volume

43

pub_type

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