Forland S C, Feng Y, Cutler R E
Clinical Pharmacology Section, Loma Linda University Medical School, CA.
J Clin Pharmacol. 1990 Jan;30(1):29-32. doi: 10.1002/j.1552-4604.1990.tb03434.x.
Colestipol and gemfibrozil may be used in combination to lower serum cholesterol and triglycerides. Since colestipol is known to bind certain anionic drugs, we studied the effect of colestipol on the pharmacokinetics of gemfibrozil in 10 patients with elevated serum cholesterol and triglycerides. Each patient received 600 mg of gemfibrozil by mouth during four different studies. Gemfibrozil was given randomly either alone, with, 2 hours before, or 2 hours after 5 grams of colestipol. The serum gemfibrozil concentration time curves were similar when gemfibrozil was given alone or two hours before or after colestipol. There was also no statistical difference in peak gemfibrozil concentration (Cmax), time to Cmax (tmax), area under the curve (AUC), or serum elimination half-life (t1/2) between any of these three treatments. However, when colestipol was given with gemfibrozil, there was a decrease in AUC (43.6 +/- 21.9 mghr/L) compared with gemfibrozil given alone (62.6 +/- 10.3 mghr/L) which was statistically different by both ANOVA and paired t-test. This finding suggests a decrease in gemfibrozil bioavailability. Cmax when colestipol was given with gemfibrozil (14.7 +/- 6.6 mg/L) was not statistically different from gemfibrozil alone (20.1 +/- 4.9 mg/L). However, the mean serum concentrations when gemfibrozil was given with colestipol were significantly lower at the 0.5, 1.0 and 1.5 hour sampling times when compared to the other regimens. Gemfibrozil serum elimination half-life was not significantly altered by combination with colestipol. The data suggest a reduction of gemfibrozil bioavailability when colestipol is administered concomitantly. Separating the administration of these two drugs by at least two hours will avoid this drug interaction.
考来替泊和吉非贝齐可联合使用以降低血清胆固醇和甘油三酯水平。由于已知考来替泊能结合某些阴离子药物,我们研究了考来替泊对10例血清胆固醇和甘油三酯升高患者体内吉非贝齐药代动力学的影响。在四项不同研究中,每位患者口服600毫克吉非贝齐。吉非贝齐随机单独给药,或与5克考来替泊同时给药、在考来替泊给药前2小时给药或在考来替泊给药后2小时给药。当吉非贝齐单独给药、在考来替泊给药前2小时或给药后2小时给药时,血清吉非贝齐浓度-时间曲线相似。这三种治疗方法在吉非贝齐的峰浓度(Cmax)、达峰时间(tmax)、曲线下面积(AUC)或血清消除半衰期(t1/2)方面也无统计学差异。然而,考来替泊与吉非贝齐同时给药时,与单独使用吉非贝齐相比,AUC降低(43.6±21.9毫克·小时/升),经方差分析和配对t检验,这一差异具有统计学意义。这一发现提示吉非贝齐的生物利用度降低。考来替泊与吉非贝齐同时给药时的Cmax(14.7±6.6毫克/升)与单独使用吉非贝齐时(20.1±4.9毫克/升)无统计学差异。然而,与其他给药方案相比,考来替泊与吉非贝齐同时给药时,在0.5、1.0和1.5小时采样时间点的平均血清浓度显著更低。考来替泊与吉非贝齐联合使用未显著改变吉非贝齐的血清消除半衰期。数据表明,考来替泊与吉非贝齐同时给药时,吉非贝齐的生物利用度会降低。将这两种药物的给药时间至少间隔两小时可避免这种药物相互作用。