Pharmacokinetics of nifedipine.
Fabrizio Pasanisi, Peter A. Meredith, Jessica Reid
Abstract
Fabrizio Pasanisi, Peter A. Meredith, Jessica Reid
Abstract
The pharmacokinetics of a slow-release formulation of nifedipine were studied following oral administration of a single 20 mg tablet in nine young male volunteers. Blood samples were collected and nifedipine concentrations analysed by gas liquid chromatography. Compared to conventional nifedipine, there was a delay in peak concentrations and a much smaller range of peak plasma levels. The smaller interindividual variability of plasma drug levels may be useful in the treatment of hypertension.
OpenAlex reports 11 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The pharmacokinetics of a slow-release formulation of nifedipine were studied following oral administration of a single 20 mg tablet in nine young male volunteers. Blood samples were collected and nifedipine concentrations analysed by gas liquid chromatography. Compared to conventional nifedipine, there was a delay in peak concentrations and a much smaller range of peak plasma levels. The smaller interindividual variability of plasma drug levels may be useful in the treatment of hypertension.
Key concepts: Nifedipine, Pharmacokinetics, Medicine, Oral administration, Plasma concentration, Pharmacology, Bioavailability, Anesthesia