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Development and validation of a bioanalytical LC-UV method with solid-phase extraction for determination of valproic acid in saliva Cover

Development and validation of a bioanalytical LC-UV method with solid-phase extraction for determination of valproic acid in saliva

Open Access
|Jun 2012

Abstract

A bioanalytical HPLC method with UV detection for the determination of the antiepileptic drug valproic acid in human saliva has been developed and validated. Saliva represents an alternative matrix for therapeutic monitoring of antiepileptic drugs due to the increasing interest in free drug concentration. The proposed method involved solid-phase extraction for sample preparation and yielded very good mean recoveries of 99.4 % and 97.9 % for valproic acid and IS, respectively. The calibration function for valproic acid was linear over the concentration range of 1.0-50.0 μg mL-1 (R2 = 0.9989). Within-run and between-run precision and accuracy were studied at four concentrations and RSDs were less than 7.3 and 2.2 %, while accuracy values were higher than 96.8 and 97.5 %, respectively. The described method provides sensitivity, linearity, precision, accuracy and is suitable for analyses of valproic acid in saliva samples.

DOI: https://doi.org/10.2478/v10007-012-0015-0 | Journal eISSN: 1846-9558 | Journal ISSN: 1330-0075
Language: English
Page range: 211 - 220
Published on: Jun 28, 2012
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year
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© 2012 Jasmina Tonic-Ribarska, Arlinda Haxhiu, Zoran Sterjev, Gordana Kiteva, Ljubica Suturkova, Suzana Trajkovic-Jolevska, published by Croatian Pharmaceutical Society
This work is licensed under the Creative Commons License.

Volume 62 (2012): Issue 2 (June 2012)