Clinical Microbiology Laboratory, Attikon Hospital, Athens, Greece.
Antimicrob Agents Chemother. 2013 Aug;57(8):3713-8. doi: 10.1128/AAC.02484-12. Epub 2013 May 28.
Conventional MIC testing of amphotericin B results in narrow MIC ranges challenging the detection of resistant strains. In order to discern amphotericin B pharmacodynamics, the in vitro activity of amphotericin B was studied against Aspergillus isolates with the same MICs by using a new in vitro pharmacokinetic/pharmacodynamic (PK/PD) model that simulates amphotericin B human plasma levels. Clinical isolates of Aspergillus fumigatus, A. terreus, and A. flavus with the same Clinical and Laboratory Standards Institute modal MICs of 1 mg/liter were exposed to amphotericin B concentrations following the plasma concentration-time profile after single-bolus administration with C(max) values of 0.6, 1.2, 2.4, and 4.8 mg/liter. Fungal growth was monitored for up to 72 h based on galactomannan production. Complete growth inhibition was observed only against A. fumigatus with amphotericin B with a Cmax of ≥ 2.4 mg/liter. At the lower C(max) values 0.6 and 1.2 mg/liter, significant growth delays of 34 and 52 h were observed, respectively (P < 0.001). For A. flavus, there was no complete inhibition but a progressive growth delay of 1 to 50 h at an amphotericin B C(max) of 0.6 to 4.8 mg/liter (P < 0.001). For A. terreus, the growth delay was modest (up to 8 h) at all C(max)s (P < 0.05). The C(max) (95% confidence interval) associated with 50% activity for A. fumigatus was 0.60 (0.49 to 0.72) mg/liter, which was significantly lower than for A. flavus 3.06 (2.46 to 3.80) mg/liter and for A. terreus 7.90 (5.20 to 12.29) mg/liter (P < 0.001). A differential in vitro activity of amphotericin B was found among Aspergillus species despite the same MIC in the order A. fumigatus > A. flavus > A. terreus in the in vitro PK/PD model, possibly reflecting the different concentration- and time-dependent inhibitory/killing activities amphotericin B exerted against these species.
常规的两性霉素 B MIC 检测结果导致 MIC 范围狭窄,难以检测耐药菌株。为了区分两性霉素 B 的药效动力学,本研究使用新的体外药代动力学/药效动力学(PK/PD)模型,模拟两性霉素 B 人体血浆水平,研究了两性霉素 B 对具有相同临床和实验室标准协会(CLSI)模式 MIC(1 mg/L)的曲霉属分离株的体外活性。使用单次推注给药后,两性霉素 B 的 Cmax 值分别为 0.6、1.2、2.4 和 4.8 mg/L,使烟曲霉、土曲霉和黄曲霉的临床分离株暴露于两性霉素 B 浓度中,以模拟人体血浆浓度-时间曲线。根据半乳甘露聚糖的产生,监测真菌生长长达 72 小时。仅当两性霉素 B 的 Cmax 为≥2.4 mg/L 时,才能完全抑制烟曲霉的生长。在较低的 Cmax 值 0.6 和 1.2 mg/L 时,分别观察到 34 和 52 h 的显著生长延迟(P<0.001)。对于黄曲霉,在两性霉素 B 的 Cmax 值为 0.6 至 4.8 mg/L 时,没有完全抑制,但观察到 1 至 50 h 的渐进生长延迟(P<0.001)。对于土曲霉,所有 Cmax 值(0.6 至 4.8 mg/L)的生长延迟幅度较小(高达 8 h)(P<0.05)。两性霉素 B 活性为 50%的 Cmax(95%置信区间)与烟曲霉的 0.60(0.49 至 0.72)mg/L 相关,明显低于黄曲霉的 3.06(2.46 至 3.80)mg/L 和土曲霉的 7.90(5.20 至 12.29)mg/L(P<0.001)。尽管在体外 PK/PD 模型中 MIC 相同,但发现不同曲霉属之间的两性霉素 B 体外活性存在差异,烟曲霉>黄曲霉>土曲霉,这可能反映了两性霉素 B 对这些物种的浓度和时间依赖性抑制/杀伤活性不同。