Wiebe V J, DeGregorio M W
Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut.
Rev Infect Dis. 1988 Nov-Dec;10(6):1097-101. doi: 10.1093/clinids/10.6.1097.
Amphotericin B therapy is hampered by numerous adverse effects but remains the treatment of choice for disseminated fungal infections. A new form of amphotericin B delivery, which utilizes liposome vesicles, is currently under investigation. Preliminary evidence suggests that liposome-encapsulated amphotericin B has a wider therapeutic index than free amphotericin B and allows for the use of larger total doses. The mechanism of reduced toxicity and enhanced activity may be associated with a liposome donor effect, an erythrocyte protective effect, and a liposome-targeting ability. Liposome-encapsulated amphotericin B tends to be entrapped or taken up by organs rich in reticuloendothelial cells--a particular advantage since disseminated fungal infections localize in these areas. This liposome-encapsulated preparation appears to represent a promising new form of antifungal therapy that may reduce the dose-limiting toxicities of amphotericin B and improve treatment response.
两性霉素B疗法因诸多不良反应而受到限制,但仍然是播散性真菌感染的首选治疗方法。一种利用脂质体囊泡的新型两性霉素B给药形式目前正在研究中。初步证据表明,脂质体包裹的两性霉素B比游离两性霉素B具有更宽的治疗指数,并允许使用更大的总剂量。毒性降低和活性增强的机制可能与脂质体供体效应、红细胞保护效应和脂质体靶向能力有关。脂质体包裹的两性霉素B倾向于被富含网状内皮细胞的器官截留或摄取——这是一个特别的优势,因为播散性真菌感染就定位在这些区域。这种脂质体包裹制剂似乎代表了一种有前景的新型抗真菌疗法,可能会降低两性霉素B的剂量限制性毒性并改善治疗反应。