DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING HPLC METHOD FOR ANALYSIS OF ZIDOVUDINE (ZDV) IN BULK DRUG AND IN VITRO RELEASE STUDIES OF TABLETS-Reference-Cited by-同舟云学术

DEVELOPMENT AND VALIDATION OF A STABILITY-INDICATING HPLC METHOD FOR ANALYSIS OF ZIDOVUDINE (ZDV) IN BULK DRUG AND IN VITRO RELEASE STUDIES OF TABLETS

Published:2011-04-11 Issue:8 Volume:34 Page:601-612
ISSN:1082-6076
Container-title:Journal of Liquid Chromatography & Related Technologies
language:en
Short-container-title:Journal of Liquid Chromatography & Related Technologies

Author:

Mandloi Dileep¹,Tripathi Priyanka²,Mohanraj Palanikar³,Chauhan Nagendra Singh⁴,Patel Jay Ram⁴

Affiliation:

1. a Shri Ramnath Singh Mahavidyalaya (Pharmacy), Gormi , Bhind, India

2. b Pharmaceutics Division , Central Drug Research Institute , Lucknow, India

3. c Department of Pharmaceutical Sciences , Himalayan Pharmacy Institute , E. Sikkam, India

4. d Department of Pharmaceutical Sciences , Dr. H. S. Gour University , Sagar, India

Publisher

Informa UK Limited

Subject

Clinical Biochemistry,Pharmaceutical Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/10826076.2011.557463

Reference12 articles.

1. A rapid, simple and accurate method for the bioanalysis of zidovudine

2. Validated specific HPLC method for determination of zidovudine during stability studies

3. Simultaneous determination of zidovudine and nevirapine in human plasma by RP-LC

4. Simultaneous determination of abacavir and zidovudine from rat tissues using HPLC with ultraviolet detection

5. Flow-injection spectrophotometric determination of reverse transcriptase inhibitors used for acquired immuno deficiency syndrome (AIDS) treatment

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