Development and validation of a LC-MS/MS method for d-cycloserine determination in human plasma for bioequivalence study
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry,Analytical Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s00216-013-7521-x.pdf
Reference5 articles.
1. Johnson R, Streicher EM, Louw GE et al (2006) Drug resistance in Mycobacterium tuberculosis. Curr Issues Mol Biol 8:97–111
2. Patel DS, Sharma N, Patel MC et al (2011) Development and validation of a selective and sensitive LC–MS/MS method for determination of cycloserine in human plasma: application to bioequivalence study. J Chromatogr B 879:2265–2273
3. Pesek JJ, Matyska MT, Dang A (2012) Analysis of cycloserine and related compounds using aqueous normal phase chromatography/mass spectrometry. J Pharm Biomed Anal 64–65:72–76
4. Polagani SR, Pilli NR, Maddela R et al (2013) A rapid and sensitive liquid chromatography–tandem mass spectrometric assay for cycloserine in 50 μL of human plasma: its pharmacokinetic application. J Pharm Biomed Anal 76:21–27
5. European Medicines Agency (2011) Guideline on bioanalytical method validation. Committee for Medicinal Products for Human Use (CHMP). 21 July 2011
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