Development and validation of bioanalytical method for quantification of cycloserine in human plasma by liquid chromatography–tandem mass spectrometry: Application to pharmacokinetic study-Reference-Cited by-同舟云学术

Development and validation of bioanalytical method for quantification of cycloserine in human plasma by liquid chromatography–tandem mass spectrometry: Application to pharmacokinetic study

Published:2019-05-02 Issue: Volume: Page:e4548
ISSN:0269-3879
Container-title:Biomedical Chromatography
language:en
Short-container-title:Biomedical Chromatography

Author:

Dodda Sireesha¹²^ORCID,Makula Ajitha²,Kandhagatla Raj Narayana³

Affiliation:

1. Department of PharmacyAnurag group of Institutions (Formerly Lalitha College of Pharmacy) Hyderabad India

2. Department of pharmaceutical Sciences, ISTJawaharlal Nehru Technological University Hyderabad India

3. Biotechnica Pharma Hyderabad India

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/bmc.4548

Reference16 articles.

1. Synergic activity of d‐cycloserine and beta‐chloro‐d‐alanine against Mycobacterium tuberculosis;David S.;The Journal of Antimicrobial Chemotherapy,2001

2. Drug resistance in Mycobacterium tuberculosis;Johnson R.;Current Issues in Molecular Biology,2006

3. Antimicrobial resistance: The example of Staphylococcus aureus;Lowy F. D.;The Journal of Clinical Investigation,2003

4. A simplified LC–MS/MS method for rapid determination of cycloserine in small‐volume human plasma using protein precipitation coupled with dilution techniques to overcome matrix effects and its application to a pharmacokinetic study;Mao Z.;Analytical and Bioanalytical Chemistry,2017

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