Lopez-Berestein G, Mehta R, Hopfer R L, Mills K, Kasi L, Mehta K, Fainstein V, Luna M, Hersh E M, Juliano R
J Infect Dis. 1983 May;147(5):939-45. doi: 10.1093/infdis/147.5.939.
The toxicology of liposome-encapsulated amphotericin B in mice and its efficacy in the treatment and prophylaxis of systemic candidiasis in these animals were studied. The toxicology studies indicated that the maximal tolerated dose of free amphotericin B was 0.8 mg/kg of body weight and the 50% lethal dose (LD50) was reached at 1.2 mg/kg, while neither the maximal tolerated dose nor the LD50 for the liposomal amphotericin B was reached at a dose of 12 mg/kg. No abnormalities in blood chemistry or histology were observed in the animals injected with encapsulated amphotericin B, while the administration of free amphotericin B was associated with nephrocalcinosis and renal parenchymal edema. The encapsulated drug was as effective as the free drug when used in similar concentrations, while the animals treated with higher concentrations of liposomal amphotericin B (4 mg/kg) had a longer survival time. Thus, an improved therapeutic index resulted by encapsulating amphotericin B in liposomes.
研究了脂质体包裹的两性霉素B在小鼠体内的毒理学及其对这些动物系统性念珠菌病的治疗和预防效果。毒理学研究表明,游离两性霉素B的最大耐受剂量为0.8mg/kg体重,1.2mg/kg时达到50%致死剂量(LD50),而脂质体两性霉素B在12mg/kg剂量下既未达到最大耐受剂量也未达到LD50。注射包裹两性霉素B的动物未观察到血液化学或组织学异常,而游离两性霉素B的给药与肾钙质沉着和肾实质水肿有关。当以相似浓度使用时,包裹药物与游离药物一样有效,而用较高浓度脂质体两性霉素B(4mg/kg)治疗的动物存活时间更长。因此,将两性霉素B包裹在脂质体中可提高治疗指数。