Pharmacokinetics and absolute bioavailability of diltiazem in humans

Summary

Six healthy male volunteers received single doses of diltiazem hydrochloride on three occasions separated by at least 10 days. Modes of administration were: 10-minute intravenous infusion of a 20-mg dose; oral administration of 120 mg in solution form; and oral administration of 120 mg as two 60-mg sustained-release tablets. Diltiazem concentrations were measured by electroncapture gas chromatography in multiple plasma samples drawn during the 36 hours after dosage. Following intravenous administration, mean (±S.E.) pharmacokinetic variables were: elimination half-life, 11.2 (±2.1) hours; volume of distribution, 11.1 (±3.0) liters/kg; and total clearance, 11.5 (±0.7) ml/min/kg. Oral diltiazem in solution form was rapidly absorbed, with peak plasma levels attained at 38 (±6) minutes after the dose. Absolute systemic availability averaged 44% (±4%). Oral administration of sustained-release tablets yielded, as predicted, slower absorption, with peak plasma concentrations attained at an average of 165 (±22) minutes after dosage. Thus, oral diltiazem is incompletely bioavailable after oral administration, mainly because of first-pass hepatic extraction.