Chen Q C, Yang C Q, Chao C H, Ma Y G, Li X N, Chen W L
Zhongshan Hospital of Shanghai.
Yao Xue Xue Bao. 1995;30(6):476-80.
The pharmacokinetics and bioavailability of glipizide were studied in 8 healthy male volunteers after a single oral dose of 5 mg in capsule or in tablet. The plasma levels of glipizide were assayed by high performance liquid chromatography. The concentration--time curves of both preparations were fitted to a one compartment model. The pharmacokinetic parameters of glipizide in capsule and in tablet were shown in tables 2 and 3. The relative bioavailability of the capsule was 109.9% compared with the tablet.
在8名健康男性志愿者单次口服5毫克胶囊或片剂形式的格列吡嗪后,对其药代动力学和生物利用度进行了研究。采用高效液相色谱法测定血浆中格列吡嗪的水平。两种制剂的浓度 - 时间曲线均符合单室模型。格列吡嗪胶囊和片剂的药代动力学参数见表2和表3。与片剂相比,胶囊的相对生物利用度为109.9%。