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American Journal of PharmTech Research

Published

RP-HPLC Method development and validation for the Estimation of Etoposide in Bulk Drug and its Pharmaceutical Dosage Form.

Published in April 2015 Issue 2 (Vol. 5, Issue 2, 2015)

RP-HPLC Method development and validation for the Estimation of Etoposide in Bulk Drug and its Pharmaceutical Dosage Form. - Issue cover

Abstract

A specific and accurate HPLC method is developed for the determination of etoposidein bulk drugs and in solid capsule dosage form. Best symmetric peak shape obtained with Inertsil ODS C-18 column (250 X 4.6 mm, 5μ) column in an isocratic mode, with retention time 5 min.The mobile phase used was Water : Acetonitrile  60:40(v/v)with flow rate 1.0 ml/min and effluent was monitored at 263 nm. As per ICH guidelines method has validated. Method has found linear in the range of 5-45 µg/ml. The LOD and LOQ were found to be 0.02 and 0.06 µg/ml respectively. Method was found specific with respective of diluents, excipients and degradants.

Authors (4)

B.Lakshmi

Department of Chemistry, GITAM...

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K.Rama Krishna

Department of Chemistry, GIS, ...

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K.N.Jayaveera

Department of Chemistry, JNTU,...

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G.V.Padmakar rao

Aurobindo Research Centre, Hyd...

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Article Information

Article ID:
AJPTR52016
Paper ID:
AJPTR-01-002337
Published Date:
2015-04-01

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How to Cite

B.Lakshmi & Krishna & K.N.Jayaveera & rao (2015). RP-HPLC Method development and validation for the Estimation of Etoposide in Bulk Drug and its Pharmaceutical Dosage Form.. American Journal of PharmTech Research, 5(2), xx-xx. https://ajptr.scholarjms.com/articles/1421

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