Peterson C M, Sims R V, Jones R L, Rieders F
Diabetes Care. 1982 Sep-Oct;5(5):497-500. doi: 10.2337/diacare.5.5.497.
The bioavailability of glipizide, plasma glucose, and insulin levels were measured in seven patients with non-insulin-dependent diabetes mellitus. Glucose and insulin response to three standard meals was measured at 11 identical time points on the day of placebo administration and on the first and 15th day of glipizide administration (mean dose of 8.7 mg glipizide orally per day). The bioavailability profile of glipizide was highly consistent between day 1 and day 15 of administration. On both days, the drug peaked within 1.2-1.8 h and displayed a plasma half-life of between 2.5 and 3.2 h. While insulin levels were significantly (P less than 0.05) increased at 4 of 11 time points of day 1, significantly elevated insulin levels were found at one time point on day 15 of glipizide administration. Insulin levels were found to be increased only in the presence of plasma drug concentrations of 200 ng/ml or greater. The hypoglycemic effect of the drug was significantly greater on day 15 than on day 1 of administration, and a significant hypoglycemic effect was noted even when drug levels were undetectable in plasma.
在7名非胰岛素依赖型糖尿病患者中测量了格列吡嗪的生物利用度、血糖水平和胰岛素水平。在给予安慰剂当天以及给予格列吡嗪的第1天和第15天(平均每日口服剂量8.7 mg格列吡嗪)的11个相同时间点,测量了对三餐标准餐的血糖和胰岛素反应。在给药第1天和第15天之间,格列吡嗪的生物利用度曲线高度一致。在这两天,药物均在1.2 - 1.8小时内达到峰值,血浆半衰期在2.5至3.2小时之间。虽然在第1天的11个时间点中的4个时间点胰岛素水平显著升高(P < 0.05),但在格列吡嗪给药第15天仅在一个时间点发现胰岛素水平显著升高。仅在血浆药物浓度达到200 ng/ml或更高时才发现胰岛素水平升高。药物的降糖作用在第15天比给药第1天显著更强,并且即使血浆中药物水平无法检测到,也观察到了显著的降糖作用。