Otsubo T, Maesaki S, Hossain M A, Yamamoto Y, Tomono K, Tashiro T, Seki J, Tomii Y, Sonoke S, Kohno S
Second Department of Internal Medicine, Nagasaki University School of Medicine, Japan.
Antimicrob Agents Chemother. 1999 Mar;43(3):471-5. doi: 10.1128/AAC.43.3.471.
We evaluated the in vitro and in vivo potencies of a new lipid nanosphere that incorporates amphotericin B (AmB), NS-718, against Aspergillus fumigatus. The in vitro activity of NS-718 (the MIC at which 90% of strains are inhibited [MIC90], 0.25 microgram/ml) against 18 isolates of A. fumigatus was similar to that of deoxycholate AmB (D-AmB; Fungizone; MIC90, 0.25 microgram/ml), but NS-718 was more potent than liposomal AmB (L-AmB; AmBi-some; MIC90, 1.0 microgram/ml). The in vivo efficacy of NS-718 in a rat model of invasive pulmonary aspergillosis was compared with those of D-AmB and L-AmB. A low dose (1 mg/kg of body weight) of L-AmB was ineffective (survival rate, 0%), although equivalent doses of D-AmB and NS-718 were more effective (survival rate, 17%). However, a higher dose of NS-718 (3 mg/kg) was more effective (survival rate, 100%) than equivalent doses of D-AmB and L-AmB (survival rate, 0%). To explain these differences, pharmacokinetic studies showed higher concentrations of AmB in the plasma of rats treated with NS-718 than in the plasma of those treated with D-AmB. Our results suggest that NS-718, a new preparation of AmB, is a promising antifungal agent with activity against pulmonary aspergillosis.
我们评估了一种新的载有两性霉素B(AmB)的脂质纳米球NS - 718对烟曲霉的体外和体内效能。NS - 718对18株烟曲霉的体外活性(90%菌株被抑制时的最低抑菌浓度[MIC90],0.25微克/毫升)与脱氧胆酸盐两性霉素B(D - AmB;Fungizone;MIC90,0.25微克/毫升)相似,但NS - 718比脂质体两性霉素B(L - AmB;两性霉素B脂质体;MIC90,1.0微克/毫升)更有效。在大鼠侵袭性肺曲霉病模型中比较了NS - 718与D - AmB和L - AmB的体内疗效。低剂量(1毫克/千克体重)的L - AmB无效(存活率为0%),而同等剂量的D - AmB和NS - 718更有效(存活率为17%)。然而,更高剂量的NS - 718(3毫克/千克)比同等剂量的D - AmB和L - AmB更有效(存活率为100%,而D - AmB和L - AmB的存活率为0%)。为了解释这些差异,药代动力学研究表明,用NS - 718治疗的大鼠血浆中两性霉素B的浓度高于用D - AmB治疗的大鼠血浆中的浓度。我们的结果表明,NS - 718作为两性霉素B的一种新制剂,是一种有前景的抗真菌剂,对肺曲霉病具有活性。