Development and validation of a method for quantitative determination of valsartan in human plasma by liquid chromatography-tandem mass spectrometry-Reference-Cited by-同舟云学术

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Development and validation of a method for quantitative determination of valsartan in human plasma by liquid chromatography-tandem mass spectrometry

Published:2007-04 Issue:5 Volume:43 Page:1769-1774
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Koseki Nozomu,Kawashita Hiroto,Hara Hisanori,Niina Miyuki,Tanaka Makoto,Kawai Ryosei,Nagae Yusuke,Masuda Naoki

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference14 articles.

2. Pharmacokinetics, disposition and biotransformation of [14C]-radiolabelled valsartan in healthy male volunteers after a single oral dose

3. Absolute bioavailability and pharmacokinetics of valsartan, an angiotensin II receptor antagonist, in man

4. Automated determination of an angiotensin ii receptor antagonist, cgp 48 933, in plasma by high-performance liquid chromatography

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5. Synthesis of molecularly imprinted polymer as a nanosorbent for dispersive magnetic micro solid-phase extraction and determination of valsartan in biological samples by UV–Vis Spectrophotometry: Isotherm, kinetics, and thermodynamic studies;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2023-08

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