Literature DB >> 15150840

A rapid and sensitive method for simultaneous determination of lamivudine and zidovudine in human serum by on-line solid-phase extraction coupled to liquid chromatography/tandem mass spectrometry detection.

Rita de Cassia E Estrela1, Myriam C Salvadori, Guilherme Suarez-Kurtz.   

Abstract

A method based on solid-phase extraction (SPE) coupled to high-performance liquid chromatography (HPLC) with positive ion electrospray ionization tandem mass spectrometry (ESI-MS/MS) detection was developed for the simultaneous determination of lamivudine (3TC) and zidovudine (AZT) in human serum, using didanosine (ddI) as internal standard. The acquisition was performed in multiple reaction monitoring (MRM) mode, monitoring the transitions m/z 230.0 --> 111.8 for 3TC, m/z 268.1 --> 126.8 for AZT, and m/z 237.2 --> 136.8 for ddI. The limits of detection and quantitation were 3 and 10 ng/mL for 3TC, and 5 and 15 ng/mL for AZT. The method was linear in the studied ranges (10-1500 ng/mL for 3TC and 15-3000 ng/mL for AZT), with r(2) > 0.99 for each drug, and the run time was 4 min. The intra-assay precisions (%) were in the ranges 1.9-8.7 (3TC) and 2.2-8.9 (AZT), the inter-assay precisions were in the ranges 2.6-9.0 (3TC) and 4.2-8.1 (AZT), and the intra- and inter-assay accuracies were >97% for both drugs. The absolute recoveries were 95-99% for 3TC (45, 600 and 1200 ng/mL) and 104-112% for AZT (45, 1000 and 2400 ng/mL). The analytical method was applied to a bioequivalence study in which 24 healthy adult volunteers received single oral doses of the reference formulation and two test combined AZT/3TC tablets, in an open, three-period, balanced, randomized, crossover protocol. Based on the 90% confidence interval of the individual ratios (test formulation/reference formulation) for C(max) (peak serum concentration) and AUC(0-inf) (extrapolated area under the serum concentration vs. time curve from time zero to infinity), it was concluded that the two test formulations are bioequivalent to the reference formulation with respect to the rate and extent of absorption of both 3TC and AZT. Copyright 2004 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15150840     DOI: 10.1002/rcm.1446

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  6 in total

1.  Highly-parallel metabolomics approaches using LC-MS for pharmaceutical and environmental analysis.

Authors:  Sunil Bajad; Vladimir Shulaev
Journal:  Trends Analyt Chem       Date:  2007-06-01       Impact factor: 12.296

2.  Validation of a sensitive LC/MS/MS method for the determination of zidovudine and lamivudine in human plasma.

Authors:  Joseph E Rower; Brandon Klein; Lane R Bushman; Peter L Anderson
Journal:  Biomed Chromatogr       Date:  2011-04-04       Impact factor: 1.902

3.  Absence of a universal mechanism of mitochondrial toxicity by nucleoside analogs.

Authors:  Kaleb C Lund; LaRae L Peterson; Kendall B Wallace
Journal:  Antimicrob Agents Chemother       Date:  2007-04-30       Impact factor: 5.191

4.  Adenosine 3',5'-cyclic monophosphate (cAMP)-dependent phosphoregulation of mitochondrial complex I is inhibited by nucleoside reverse transcriptase inhibitors.

Authors:  Kaleb C Lund; Kendall B Wallace
Journal:  Toxicol Appl Pharmacol       Date:  2007-08-25       Impact factor: 4.219

5.  Simultaneous quantification of 9-(beta-D-1,3-dioxolan-4-yl)guanine, Amdoxovir and Zidovudine in human plasma by liquid chromatography-tandem mass spectrometric assay.

Authors:  Emilie Fromentin; Ghazia Asif; Aleksandr Obikhod; Selwyn J Hurwitz; Raymond F Schinazi
Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2009-08-27       Impact factor: 3.205

6.  Determination of genotoxic alkyl methane sulfonates and alkyl paratoluene sulfonates in lamivudine using hyphenated techniques.

Authors:  N V V S S Raman; A V S S Prasad; K Ratnakar Reddy; K Ramakrishna
Journal:  J Pharm Anal       Date:  2012-03-14
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.