Terakawa M, Tokuma Y, Shishido A, Yasuda K, Noguchi H
Department of Clinical Research, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.
J Clin Pharmacol. 1987 Apr;27(4):293-6. doi: 10.1002/j.1552-4604.1987.tb03016.x.
The effect of two different meals on the bioavailability of nilvadipine, a new antihypertensive and antianginal drug, was examined in 16 healthy male volunteers in two separate studies. In each study of eight subjects in a Latin-square, two-way crossover design, two groups of four subjects each were given a single 6-mg oral dose of nilvadipine after overnight fasting or 30 minutes after a 464- or 748-kcal meal. There were no significant differences in the area under the plasma concentration-time curve or the maximum plasma concentration between the fasting and fed states for either meal. Although the time to reach the maximum plasma concentration was about the same after a 464-kcal meal and after fasting, it increased slightly but significantly after a 748-kcal meal, indicating possible delay in drug absorption after meals. These studies showed that the extent of bioavailability of nilvadipine appears to be little affected in the presence of food. Although a possible delay in the onset of absorption would occur, such a delay may not have any therapeutic importance in chronic therapy.
在两项独立研究中,对16名健康男性志愿者进行了研究,以考察两种不同餐食对新型抗高血压和抗心绞痛药物尼伐地平生物利用度的影响。在每项针对8名受试者的拉丁方双向交叉设计研究中,两组各4名受试者在空腹过夜后或在摄入464千卡或748千卡餐食30分钟后,口服单剂量6毫克尼伐地平。对于两种餐食中的任何一种,空腹状态和进食状态下血浆浓度-时间曲线下面积或最大血浆浓度均无显著差异。尽管摄入464千卡餐食后和空腹后达到最大血浆浓度的时间大致相同,但摄入748千卡餐食后该时间略有延长但差异显著,表明进食后药物吸收可能延迟。这些研究表明,食物存在时尼伐地平的生物利用度似乎受影响较小。尽管吸收开始可能会有延迟,但这种延迟在长期治疗中可能没有任何治疗意义。