Iwasaki K, Miyazaki Y, Teramura Y, Kawamura A, Tozuka Z, Hata T, Undre N
Department of Drug Metabolism and Pharmacokinetics, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.
Res Commun Mol Pathol Pharmacol. 1996 Dec;94(3):251-7.
Protein binding of tacrolimus (FK506) in human plasma was re-evaluated by equilibration dialysis and compared with that of FK506 previously reported by two different methods (about 99 and 77% by an ultrafiltration and ultracentrifugation method, respectively). The binding determined in this study was about 99% irrespective of FK506 concentrations added (0.5-10 ng/ml) and this value was very close to that estimated by the ultrafiltration method. The effect of mycophenolic acid (MPA, an active form of the immunosuppressant mycophenolate mofetil) and its glucuronide (MPAG, a major metabolite of mycophenolate mofetil in human plasma) on the binding was studied at concentration levels of 1 and 10 ng/ml of FK506. The binding was not affected significantly by the addition of MPA (25-100 micrograms/ml) and/or MPAG (100-1500 micrograms/ml). FK506 has already been reported not to cause significant changes of plasma protein binding of MPA. The results indicate that the unbound fraction of FK506 is about 1% in human plasma and that concomitant administration of FK506 and mycophenolic mofetil does not cause the drastic change of the binding of FK506 and MPA with human plasma proteins.
采用平衡透析法对他克莫司(FK506)在人血浆中的蛋白结合率进行了重新评估,并与之前用两种不同方法报道的FK506蛋白结合率(分别采用超滤法和超速离心法,约为99%和77%)进行了比较。本研究测定的结合率约为99%,与添加的FK506浓度(0.5 - 10 ng/ml)无关,且该值与超滤法估算的值非常接近。在FK506浓度为1和10 ng/ml时,研究了霉酚酸(MPA,免疫抑制剂霉酚酸酯的活性形式)及其葡糖醛酸苷(MPAG,霉酚酸酯在人血浆中的主要代谢产物)对结合的影响。添加MPA(25 - 100微克/毫升)和/或MPAG(100 - 1500微克/毫升)对结合没有显著影响。已有报道称FK506不会引起MPA血浆蛋白结合率的显著变化。结果表明,FK506在人血浆中的未结合分数约为1%,同时给予FK506和霉酚酸酯不会导致FK506和MPA与人血浆蛋白结合的剧烈变化。