Takada K, Shibata N, Yoshimura H, Masuda Y, Yoshikawa H, Muranishi S, Oka T
J Pharmacobiodyn. 1985 Apr;8(4):320-3. doi: 10.1248/bpb1978.8.320.
The absorption of an immunosuppressive drug, cyclosporin A (CsA), with the aid of lipid-surfactant mixed micelles from the rat gastrointestinal (GI) tract and lymphatic delivery were studied. The administration of CsA in oily solution, sesame oil or linolic acid, into the rat duodenum indicated a small amount of CsA both in the plasma and lymph for about 6 h. The administration of CsA in the mixed micellar solution composing of linolic acid and HCO-60, polyoxyethylated (60 mol) hydrogenated castor oil, accelerated the absorption of CsA from the GI tract, and CsA was delivered into the lymphatics with an extremely high selectivity.
研究了免疫抑制药物环孢素A(CsA)借助脂质 - 表面活性剂混合胶束从大鼠胃肠道(GI)的吸收及淋巴转运情况。将CsA以油溶液(芝麻油或亚油酸)形式给予大鼠十二指肠后,血浆和淋巴中在约6小时内均仅有少量CsA。将CsA以由亚油酸和HCO - 60(聚氧乙烯化(60摩尔)氢化蓖麻油)组成的混合胶束溶液形式给药,加速了CsA从胃肠道的吸收,并且CsA以极高的选择性转运至淋巴管。