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Pharmacokinetics of nifedipine.

Fabrizio Pasanisi, Peter A. Meredith, Jessica Reid

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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.

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What this paper is about

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.

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OpenAlex reports 11 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available 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.

Key concepts: Nifedipine, Pharmacokinetics, Medicine, Oral administration, Plasma concentration, Pharmacology, Bioavailability, Anesthesia

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