Kato Ryuji, Ooi Kazuya, Ikura-Mori Megumi, Tsuchishita Yoshimasa, Hashimoto Hiroshi, Yoshimura Hironori, Uenishi Kohji, Kawai Masayuki, Tanaka Kazuhiko, Ueno Kazuyuki
Department of Pharmacy, Yokkaichi Social Insurance Hospital, Mie, Japan.
J Clin Pharmacol. 2002 Nov;42(11):1275-80. doi: 10.1177/009127002762491389.
The effect of calcium polycarbophil on the absorption of mycophenolate mofetil, an immunosuppressive agent, was evaluated in healthy subjects. In vitro studies were performed to further evaluate the mechanism of the potential interaction. In the in vitro study, the release of mycophenolate mofetil from a cellulose membrane in the presence or absence of metal cations was measured using the dissolution test procedure. In the in vivo study, a randomized crossover design with two phases was used. In one phase, 6 male healthy volunteers received 1000 mg of mycophenolate mofetil alone (treatment 1); in the other phase, they received 1000 mg of mycophenolate mofetil and 2400 mg of calcium polycarbophil fine granules concomitantly (treatment 2). They received 30 mg of lansoprazole for 5 days and, on the 6th day, received mycophenolate mofetil and 2400 mg of calcium polycarbophil fine granules concomitantly (treatment 3). The serum concentration of mycophenolic acid was measured by high-performance liquid chromatography. In the in vitro study, the release from a cellulose membrane in the presence of calcium or iron ions was slower than that in the absence of these metal ions. In the in vivo study, the AUC0-12 and C(max) in treatment 2 were less than those in treatment 1. About 50% and 25% decreases in AUC0-12 in treatment 2 and treatment 3 were observed compared with those in treatment 1, respectively. These findings suggest that when mycophenolate mofetil and calcium polycarbophil were coadministered concomitantly, a decrease in mycophenolate mofetil absorption was observed. Therefore, it appears clear that the concomitant administration of mycophenolate mofetil and calcium polycarbophil should be avoided.
在健康受试者中评估了聚卡波非钙对免疫抑制剂霉酚酸酯吸收的影响。进行了体外研究以进一步评估潜在相互作用的机制。在体外研究中,使用溶出度测试方法测量了在有或没有金属阳离子存在的情况下,霉酚酸酯从纤维素膜中的释放情况。在体内研究中,采用了两阶段随机交叉设计。在一个阶段,6名男性健康志愿者单独服用1000毫克霉酚酸酯(治疗1);在另一个阶段,他们同时服用1000毫克霉酚酸酯和2400毫克聚卡波非钙细颗粒(治疗2)。他们服用30毫克兰索拉唑,持续5天,并在第6天同时服用霉酚酸酯和2400毫克聚卡波非钙细颗粒(治疗3)。通过高效液相色谱法测量霉酚酸的血清浓度。在体外研究中,在钙或铁离子存在下从纤维素膜中的释放比在没有这些金属离子时更慢。在体内研究中,治疗2中的AUC0 - 12和C(max)低于治疗1中的值。与治疗1相比,分别观察到治疗2和治疗3中AUC0 - 12下降约50%和25%。这些发现表明,当霉酚酸酯和聚卡波非钙同时给药时,观察到霉酚酸酯吸收减少。因此,显然应避免同时给予霉酚酸酯和聚卡波非钙。