Determination of nifedipine in human plasma and its use in bioequivalence study

International Journal of Pharmaceutics

Volumn 341, Issue 1-2, 2007, Pages 91-96

  Guo, Yunzhen ^a   Dai, Jinna ^a   Qian, Guiling ^b   Guo, Na ^a   Ma, Zheng ^a   Guo, XingJie ^a  

^a SHENYANG PHARMACEUTICAL UNIVERSITY   (China)

^b Disha Pharmaceutical Group Shandong Disha Pharmaceutical Co Ltd   (China)

Author keywords

Human plasma; LC MS; Nifedipine; Pharmacokinetic profile; Sustained release tablets

Indexed keywords

DIMETHOXANATE; DIMETHOXANE; ETHER; METHANOL; NIFEDIPINE; UNCLASSIFIED DRUG; WATER;

AREA UNDER THE CURVE; ARTICLE; CONFIDENCE INTERVAL; DRUG BIOAVAILABILITY; DRUG DETERMINATION; DRUG RELEASE; DRUG SOLUBILITY; EXTRACTION; FOOD AND DRUG ADMINISTRATION; HUMAN; HUMAN CELL; HUMAN EXPERIMENT; LIQUID CHROMATOGRAPHY; MALE; MASS SPECTROMETRY; MAXIMUM ALLOWABLE CONCENTRATION; NORMAL HUMAN; POSITIVE ION ELECTROSPRAY; PRIORITY JOURNAL; SINGLE DRUG DOSE;

ADMINISTRATION, ORAL; ADULT; AREA UNDER CURVE; CALCIUM CHANNEL BLOCKERS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CROSS-OVER STUDIES; DELAYED-ACTION PREPARATIONS; HUMANS; MALE; MASS SPECTROMETRY; NIFEDIPINE; REFERENCE VALUES; REPRODUCIBILITY OF RESULTS; THERAPEUTIC EQUIVALENCY;

EID: 34447645666     PISSN: 03785173     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijpharm.2007.03.053     Document Type: Article

References (13)

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