Amlodipine bioequivalence study: Quantification by liquid chromatography coupled to tandem mass spectrometry

Biopharmaceutics and Drug Disposition

Volumn 22, Issue 9, 2001, Pages 383-390

  De Nucci, G ^a   Oliveira, C ^a   Carvalho, M ^a   Sucupira, M ^b   Mendes, G ^b   Moraes, M E A ^c  

^a UNIVERSITY OF CAMPINAS   (Brazil)

^b UNIVERSITY OF SÃO PAULO   (Brazil)

^c FEDERAL UNIVERSITY OF CEARÁ   (Brazil)

Author keywords

Desipramine; HPLC; LC MS MS; Pharmacokinetics

Indexed keywords

AMLODIPINE; AMLODIPINE BESYLATE; DESIPRAMINE;

ADULT; AREA UNDER THE CURVE; ARTICLE; BIOEQUIVALENCE; BLOOD SAMPLING; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CROSSOVER PROCEDURE; DRUG ABSORPTION; DRUG BLOOD LEVEL; DRUG STRUCTURE; DYSMENORRHEA; FEMALE; FOOD AND DRUG ADMINISTRATION; HEADACHE; HUMAN; HUMAN EXPERIMENT; LIQUID CHROMATOGRAPHY; MALE; MASS SPECTROMETRY; MAXIMUM ALLOWABLE CONCENTRATION; NORMAL HUMAN; QUANTITATIVE ANALYSIS; RANDOMIZED CONTROLLED TRIAL; TABLET FORMULATION; TANDEM MASS SPECTROMETRY; VOLUNTEER;

ADOLESCENT; ADULT; AMLODIPINE; ANTIHYPERTENSIVE AGENTS; CHEMISTRY, PHARMACEUTICAL; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CONFIDENCE INTERVALS; CROSS-OVER STUDIES; FEMALE; HUMANS; LINEAR MODELS; MALE; MASS SPECTROMETRY; TABLETS; THERAPEUTIC EQUIVALENCY;

EID: 0035722796     PISSN: 01422782     EISSN: None     Source Type: Journal    
DOI: 10.1002/bdd.282     Document Type: Article

References (10)

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