Dissolution method for delapril and manidipine combination tablets based on an absorption profile of manidipine

Author:

Todeschini Vítor,Sangoi Maximiliano S.,Goelzer Gustavo K.,Machado Jaison C.,Paim Clésio S.,Araujo Bibiana V.,Volpato Nadia M.

Funder

CAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior)

CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico)

Publisher

Elsevier BV

Subject

Analytical Chemistry,Electrochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Pharmacy

Reference30 articles.

1. Food and Drug Administration, Guidance for Industry: Dissolution Testing of Immediate Release Solid Oral Dosage Forms, Rockville, 1997a.

2. Oral Drug Absorption Prediction and Assessment;Dressman,2000

3. Food and Drug Administration, Guidance for Industry: Extended Release Oral Dosage Forms: Development, Evaluation, and Application of in vitro-in vivo Correlations, Rockville, 1997b.

4. Dissolution testing as a prognostic tool for oral drug absorption: immediate release dosage forms;Dressman;Pharm. Res.,1998

5. Pharmacokinetics of a new angiotensin I converting enzyme inhibitor (delapril) in patients with deteriorated kidney function and in normal control subjects;Onoyama;Clin. Pharmacol. Ther.,1988

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