Miyazaki T, Kohno S, Sasayama K, Inoue Y, Hara K, Ogasawara M, Sato T, Sunamoto J
Second Department of Internal Medicine, Nagasaki University School of Medicine.
Tohoku J Exp Med. 1992 Nov;168(3):483-90. doi: 10.1620/tjem.168.483.
Amylopectin-coated liposomal amphotericin B was investigated in a murine model of pulmonary candidiasis. The LD50 of amylopectin-coated liposomal amphotericin B in normal mice was more than 10.0 mg/kg, and that of conventional amphotericin B was 1.2 mg/kg. Amylopectin-coated liposomes showed twice the concentration in the lungs of conventional liposomes. Candida albicans was inoculated intratracheally into BALB/C mice. Twenty-four hours later, the number of Candida in the lungs of mice treated with amylopectin-coated liposomes was less than in those treated with conventional liposomes, and amylopectin-coated liposomes improved the survival rate of inoculated mice. Coating liposomes with amylopectin aids the targeting of amphotericin B to the lungs.