Ryan J R, Jain A K, McMahon F G, Vargas R
Clin Pharmacol Ther. 1977 Feb;21(2):231-3. doi: 10.1002/cpt1977212231.
The effect of sulindac and tolbutamide on the control of diabetes was studied in 12 tolbutamide-treated maturity-onset diabetics with stable glycemic control. After one week of hospitalization on a metabolic ward for adjustment of diet and activity, the patients were treated with sulindac, 200 mg twice daily for one week. The time-to-peak plasma tolbutamide concentration was 3.1, 3.1, and 3.2 hr, respectively, after tolbutamide alone, after the first dose of sulindac, and after sulindac for a week. The areas under the plasma tolbutamide curve were 23.68, 22.10, and 22.78 for the same periods. The half-life for plasma tolbutamide was 7.46, 7.15, and 7.38 hr, respectively. None of the differences were statistically significant. The mean fasting plasma sugar was lower after the sulindac treatment (from 12.5 to 112.9 mg/100 ml, p less than 0.05), but the postprandial values increased slightly (from 137.7 to 142.6). It was concluded that there was no clinically significant interaction between sulindac and tolbutamide.
在12名接受甲苯磺丁脲治疗且血糖控制稳定的成年起病型糖尿病患者中,研究了舒林酸和甲苯磺丁脲对糖尿病控制的影响。在代谢病房住院一周以调整饮食和活动后,患者接受舒林酸治疗,每日两次,每次200毫克,持续一周。单独服用甲苯磺丁脲后、首次服用舒林酸后以及服用舒林酸一周后,血浆甲苯磺丁脲浓度达峰时间分别为3.1小时、3.1小时和3.2小时。同期血浆甲苯磺丁脲曲线下面积分别为23.68、22.10和22.78。血浆甲苯磺丁脲的半衰期分别为7.46小时、7.15小时和7.38小时。这些差异均无统计学意义。舒林酸治疗后空腹血糖均值降低(从12.5降至112.9毫克/100毫升,p<0.05),但餐后血糖值略有升高(从137.7升至142.6)。得出的结论是,舒林酸和甲苯磺丁脲之间不存在具有临床意义的相互作用。