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聚乙二醇包被脂质体包裹的环丙沙星:在大鼠急性或慢性铜绿假单胞菌感染模型中的疗效

Ciprofloxacin in polyethylene glycol-coated liposomes: efficacy in rat models of acute or chronic Pseudomonas aeruginosa infection.

作者信息

Bakker-Woudenberg Irma A J M, ten Kate Marian T, Guo Luke, Working Peter, Mouton Johan W

机构信息

Department of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center Rotterdam, PO Box 1738, 3000 DR Rotterdam, The Netherlands.

出版信息

Antimicrob Agents Chemother. 2002 Aug;46(8):2575-81. doi: 10.1128/AAC.46.8.2575-2581.2002.

Abstract

In a previous study in experimental Klebsiella pneumoniae pneumonia, the therapeutic potential of ciprofloxacin was significantly improved by encapsulation in polyethylene glycol-coated ("pegylated") long-circulating (STEALTH) liposomes. Pegylated liposomal ciprofloxacin in high doses was nontoxic and resulted in relatively high and sustained ciprofloxacin concentrations in blood and tissues, and hence an increase in the area under the plasma concentration-time curve (AUC). These data correspond to data from animal and clinical studies showing that for fluoroquinolones the AUC/MIC ratio is associated with favorable outcome in serious infections. Clinical failures and the development of resistance are observed for marginally susceptible organisms like Pseudomonas aeruginosa and for which sufficient AUC/MIC ratios cannot be achieved. In the present study the therapeutic efficacy of pegylated liposomal ciprofloxacin was investigated in two rat models of Pseudomonas aeruginosa pneumonia. In the acute model pneumonia developed progressively, resulting in a rapid onset of septicemia and a high mortality rate. Ciprofloxacin twice daily for 7 days was not effective at doses at or below the maximum tolerated dose (MTD). However, pegylated liposomal ciprofloxacin either at high dosage or given at low dosage in combination with free ciprofloxacin on the first day of treatment was fully effective (100% survival). Obviously, prolonged concentrations of ciprofloxacin in blood prevented death of the animals due to early-stage septicemia in this acute infection. However, bacterial eradication from the left lung was not effected. In the chronic model, pneumonia was characterized by bacterial persistence in the lung without bacteremia, and no signs of morbidity or mortality were observed. Ciprofloxacin administered for 7 days at the MTD twice daily resulted in killing of more than 99% of bacteria in the lung; this result can also be achieved with pegylated liposomal ciprofloxacin given once daily. Complete bacterial eradication is never observed.

摘要

在先前一项关于实验性肺炎克雷伯菌肺炎的研究中,环丙沙星封装于聚乙二醇包被(“聚乙二醇化”)的长循环(隐形)脂质体后,其治疗潜力得到显著提高。高剂量的聚乙二醇化脂质体环丙沙星无毒,且在血液和组织中产生相对较高且持续的环丙沙星浓度,因此血浆浓度 - 时间曲线下面积(AUC)增加。这些数据与动物和临床研究的数据一致,表明对于氟喹诺酮类药物,AUC/MIC比值与严重感染的良好预后相关。对于铜绿假单胞菌等敏感性稍差的病原体,临床治疗失败和耐药性的出现较为常见,因为无法达到足够的AUC/MIC比值。在本研究中,在两种铜绿假单胞菌肺炎大鼠模型中研究了聚乙二醇化脂质体环丙沙星的治疗效果。在急性模型中,肺炎逐渐发展,导致败血症迅速发作和高死亡率。每天两次给予环丙沙星,持续7天,在等于或低于最大耐受剂量(MTD)时无效。然而,高剂量的聚乙二醇化脂质体环丙沙星或在治疗第一天与游离环丙沙星联合低剂量给药则完全有效(100%存活)。显然,血液中环丙沙星浓度的延长预防了动物因这种急性感染早期败血症而死亡。然而,左肺中的细菌清除未受影响。在慢性模型中,肺炎的特征是肺部细菌持续存在且无菌血症,未观察到发病或死亡迹象。每天两次以MTD给予环丙沙星7天可使肺部99%以上的细菌被杀灭;每天给予一次聚乙二醇化脂质体环丙沙星也可达到此结果。从未观察到细菌被完全清除。

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本文引用的文献

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8
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9
Pharmacodynamics of fluoroquinolones.
Clin Infect Dis. 1998 Jul;27(1):33-9. doi: 10.1086/514623.
10
Administration of liposomal agents and blood clearance capacity of the mononuclear phagocyte system.
Antimicrob Agents Chemother. 1998 Jul;42(7):1677-81. doi: 10.1128/AAC.42.7.1677.

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