Janout Vaclav, Bienvenu Celine, Schell Wiley, Perfect John R, Regen Steven L
Department of Chemistry, Lehigh University , Bethlehem, Pennsylvania 18015, United States.
Bioconjug Chem. 2014 Aug 20;25(8):1408-11. doi: 10.1021/bc500277v. Epub 2014 Aug 1.
A tetrawalled and an octawalled molecular umbrella conjugate of amphotericin B (AmB) have been synthesized. Both conjugates exhibit high water solubility, a low tendency to aggregate, negligible hemolytic activity at 100 μM, and an ability to release a derivative of AmB under reducing conditions that exhibits high antifungal activity. Whereas the larger, octawalled conjugate shows slight adsorption to liposomal membranes and an ability to cross them by passive transport, the tetrawalled analogue shows significant adsorption and much lower bilayer transport activity. The potential of molecular umbrella-AmB conjugates as therapeutic agents is briefly discussed.
已合成了两性霉素B(AmB)的四面壁和八面壁分子伞缀合物。两种缀合物均表现出高水溶性、低聚集倾向、在100μM时可忽略不计的溶血活性,以及在还原条件下释放具有高抗真菌活性的AmB衍生物的能力。较大的八面壁缀合物对脂质体膜有轻微吸附,并能通过被动转运穿过脂质体膜,而四面壁类似物则表现出显著吸附且双层转运活性低得多。本文简要讨论了分子伞-AmB缀合物作为治疗剂的潜力。