Francis R J, Dixon J S, Lowe J R, Harris P A
Eur J Drug Metab Pharmacokinet. 1985 Oct-Dec;10(4):309-14. doi: 10.1007/BF03189758.
A single oral dose (40 mg) of tenoxicam (Ro12-0068) was administered to six normal male volunteers pre- and post-prandially and to a further six volunteers with and without antacid to determine the effect of food and and of antacid on absorption. The rate of absorption was slower with post-prandial than with pre-prandial administration, resulting in a significantly later time for peak plasma drug levels (4.1 h compared to 1.3 h). No effect was evident on the extent of absorption or other pharmacokinetic parameters. Similarly, the rate of absorption was significantly slower after concurrent antacid than without antacid (t1/2 0.47 h compared to 0.18 h) resulting in a later peak time (4.7 h compared to 2.3 h) and significantly lower peak level (4.2 micrograms X ml-1 compared to 5.1 micrograms X ml-1) of parent drug in plasma. Again, no effect was evident on the extent of absorption or other pharmacokinetic parameters. It is concluded that food and antacids both tend to reduce the rate of absorption of tenoxicam, but that the extent of absorption is essentially unchanged. The influence on the overall kinetic profile is relatively minor, and thus unlikely to affect the therapeutic response.
给6名正常男性志愿者在餐前和餐后口服单剂量(40毫克)替诺昔康(Ro12 - 0068),并给另外6名志愿者同时服用或不服用抗酸剂,以确定食物和抗酸剂对吸收的影响。餐后给药的吸收速率比餐前给药慢,导致血浆药物峰值水平出现的时间显著延迟(分别为4.1小时和1.3小时)。对吸收程度或其他药代动力学参数没有明显影响。同样,同时服用抗酸剂后的吸收速率比不服用抗酸剂时显著减慢(半衰期分别为0.47小时和0.18小时),导致血浆中母体药物的峰值时间延迟(分别为4.7小时和2.3小时),且峰值水平显著降低(分别为4.2微克/毫升和5.1微克/毫升)。同样,对吸收程度或其他药代动力学参数没有明显影响。结论是食物和抗酸剂都倾向于降低替诺昔康的吸收速率,但吸收程度基本不变。对整体动力学曲线的影响相对较小,因此不太可能影响治疗反应。