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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Simple and Rapid Method by Ultra High-Performance Liquid Chromatography (UHPLC) with Ultraviolet Detection for Determination of Efavirenz in Plasma: Application in a Preclinical Pharmacokinetic Study

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Author(s):
Martins, Evelin dos Santos [1] ; Oliveira, Jonata Augusto [1] ; Franchin, Taisa Busaranho [1] ; Ulian Silva, Bruna Cristina [1] ; Candido, Caroline Damico [1] ; Peccinini, Rosangela Goncalves [1]
Total Authors: 6
Affiliation:
[1] Univ Estadual Paulista Julio de Mesquita Filho UN, Dept Nat Act Principles & Toxicol, Sch Pharmaceut Sci, Sao Paulo - Brazil
Total Affiliations: 1
Document type: Journal article
Source: Journal of Chromatographic Science; v. 57, n. 10, p. 874-880, NOV 2019.
Web of Science Citations: 0
Abstract

A simple and rapid ultra-high-performance liquid chromatography (UHPLC) method for determination of efavirenz (EFV) in plasma was developed and applied in a preclinical pharmacokinetic study. The method involves only addition of acetonitrile to precipitation of plasma proteins followed by solvent evaporation. The mobile phase consisted of methanol, acetonitrile and 0.1 M formic acid (20:50:30) at a flow rate of 0.3 mL/min with run time of 5 min. A CSH C18 column and a UHPLC-UV system operating at 245 nm were used. There was a linear response in the range of 0.078 to 10 mu g/mL, and the equation was obtained by weighting (1/x(2)) with r(2) = 0.9965. The pharmacokinetic disposition of EFV was investigated in rabbits (two groups, n = 7) following a single intravenous administration (IV group) at a dose of 2.7 mg/kg and a single oral administration (oral group) of EFV co-administered with lamivudine (3TC) and tenofovir (TNF) at a dose of 50, 25 and 25 mg, respectively. The study demonstrated the applicability of the method for determination of EFV in plasma without interference from other co-administered drugs, and the pharmacokinetic parameters were calculated. The method showed advantages over other methods in the literature, such as simplicity of sample processing and fast results. (AU)

FAPESP's process: 11/11239-9 - Preclinical pharmacokinetics of new drugs and pharmaceuticals forms
Grantee:Rosangela Gonçalves Peccinini
Support Opportunities: Regular Research Grants
FAPESP's process: 15/23843-9 - Pharmacokinetics of efavirenz administered in the form of inorganic nanoparticles in rabbits
Grantee:Evelin dos Santos Martins
Support Opportunities: Scholarships in Brazil - Master