Development and validation of a reversed-phase high-performance liquid chromatographic method with solid-phase extraction for the quantification of hydrochlorothiazide in ex vivo permeation studies

Author:

Onnainty R.1,Schenfeld E.M.1,Longhi M.R.1,Quevedo M.A.1,Granero G.E.1ORCID

Affiliation:

1. Departamento de Farmacia, UNITEFA, CONICET, Facultad de Ciencias Químicas; Universidad Nacional de Córdoba; Córdoba Argentina

Funder

Fondo para la Investigación Científica y Tecnológica

Secretaría de Ciencia y Técnica de la Universidad Nacional de Córdoba

Consejo Nacional de Investigaciones Científicas y Tecnológicas de la Nación

Publisher

Wiley

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,General Medicine,Biochemistry,Analytical Chemistry

Reference15 articles.

1. Current methodologies used for evaluation of intestinal permeability and absorption;Balimane;Journal of Pharmacological and Toxicological Methods,2000

2. Pharmacokinetics of hydrochlorothiazide in man;Beermann;European Journal of Clinical Pharmacology,1977

3. EMA 2011 Guideline on bioanalytical method validation

4. ICH 2005 Harmonized Tripartite Guideline . Validation of an Analytical Procedures: Text and Methodology Q2(R1). Guidance

5. Combined use of ivermectin and triclabendazole in sheep: In vitro and in vivo characterization of their pharmacological interaction;Lifschitz;Veterinary Journal,2009

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