Abstract

We investigated the pharmacokinetics of 2 μg calcitriol in eight healthy human after a single oral administration. Plasma calcitriol was analyzed by sensitive and quantitative enzyme immunoassay following intra- and inter-day validation. In subjects, AUC 0–∞ and AUC 0–24 h were 267 and 246 pg h ml −1, respectively. Although the mean plasma concentration of calcitriol in human subjects did not return to baseline at 24 h post-dosing, the mean ratio of AUC 0–24 h to AUC 0–∞ was greater than 80%. The C max of calcitriol was measured at 3.4 h after administration as 50.0 pg ml −1. From our results, it can offer new opportunities to design and determine individually appropriate therapeutic dosage regimens based on a pharmacokinetic profile and be used for bioequivalence and revaluation study of generic drug.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call