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Volumn 850, Issue 1-2, 2007, Pages 59-67
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Determination of captopril in human plasma, using solid phase extraction and high-performance liquid chromatography, coupled to mass spectrometry: Application to bioequivalence study
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Author keywords
Bioequivalence; Captopril; LC MS; Pharmacokinetics; SPE; Stability validation
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Indexed keywords
EXTRACTION;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
MASS SPECTROMETRY;
PHARMACOKINETICS;
PLASMA (HUMAN);
BIOEQUIVALENCE;
CAPTOPRYL;
CONCENTRATION RANGE;
STABILITY VALIDATION;
DRUG PRODUCTS;
CAPTOPRIL;
ENALAPRIL MALEATE;
ARTICLE;
BIOEQUIVALENCE;
CLINICAL ARTICLE;
CLINICAL TRIAL;
CONTROLLED CLINICAL TRIAL;
CONTROLLED STUDY;
CROSSOVER PROCEDURE;
DRUG BLOOD LEVEL;
DRUG DETERMINATION;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
HUMAN;
MASS SPECTROMETRY;
PRIORITY JOURNAL;
RANDOMIZED CONTROLLED TRIAL;
SINGLE DRUG DOSE;
SOLID PHASE EXTRACTION;
TABLET FORMULATION;
ANGIOTENSIN-CONVERTING ENZYME INHIBITORS;
CALIBRATION;
CAPTOPRIL;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
HUMANS;
REFERENCE STANDARDS;
REPRODUCIBILITY OF RESULTS;
SENSITIVITY AND SPECIFICITY;
SPECTROMETRY, MASS, ELECTROSPRAY IONIZATION;
TANDEM MASS SPECTROMETRY;
THERAPEUTIC EQUIVALENCY;
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EID: 34247548729
PISSN: 15700232
EISSN: None
Source Type: Journal
DOI: 10.1016/j.jchromb.2006.11.007 Document Type: Article |
Times cited : (37)
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References (15)
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