Bassett J B, Tacker J R, Anderson R U, Bostwick D
Division of Urology, Stanford University School of Medicine, California.
J Urol. 1988 Mar;139(3):634-6. doi: 10.1016/s0022-5347(17)42548-1.
Serially transplanted murine bladder cancer was treated with localized capacitive radiofrequency hyperthermia and liposome-delivered methotrexate (MTX). Liposomes were manufactured to retain MTX at 37C but specifically release encapsulated MTX as they passed through preheated tumors. When compared to controls, neither free MTX nor liposome-delivered MTX caused significant tumoricidal activity. Heat alone did cause a slowing of tumor growth and an increase in animal survival. Because large unilamellar liposomes are known to be cleared by the liver, sixteen animals were autopsied to determine the extent of liver toxicity which may have been a result of the various treatments. No hepatotoxic effects were observed after injection of liposomes containing MTX or other experimental combinations of drug and/or liposomes.
对连续移植的小鼠膀胱癌进行局部电容性射频热疗和脂质体递送甲氨蝶呤(MTX)治疗。脂质体经制备后可在37℃保留MTX,但当它们通过预热的肿瘤时会特异性释放包封的MTX。与对照组相比,游离MTX和脂质体递送的MTX均未引起显著的杀肿瘤活性。单独热疗确实导致肿瘤生长减缓以及动物存活率提高。由于已知大单层脂质体会被肝脏清除,因此对16只动物进行了尸检,以确定可能是各种治疗结果的肝毒性程度。注射含MTX的脂质体或药物和/或脂质体的其他实验组合后未观察到肝毒性作用。