A stability-indicating HPLC assay method for docetaxel.

Abstract:

:A novel stability-indicating high-performance liquid chromatographic assay method was developed and validated for docetaxel in the presence of degradation products generated from forced decomposition studies. A gradient HPLC method was developed to separate the drug from the degradation products, using a Hichrom RPB HPLC column. Mixture of water and acetonitrile was used as mobile phase. The flow rate was 1.0 ml/min and the detection was done at 230 nm. Using the above method one can carry out the quantitative estimation of impurity namely DCT-1 and docetaxel. The developed gradient LC method was subsequently validated.

journal_name

J Pharm Biomed Anal

authors

Rao BM,Chakraborty A,Srinivasu MK,Devi ML,Kumar PR,Chandrasekhar KB,Srinivasan AK,Prasad AS,Ramanatham J

doi

10.1016/j.jpba.2006.01.011

subject

Has Abstract

pub_date

2006-05-03 00:00:00

pages

676-81

issue

2

eissn

0731-7085

issn

1873-264X

pii

S0731-7085(06)00015-X

journal_volume

41

pub_type

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