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抗菌药物耐药性的出现作为抗菌药物口服缓释给药系统设计中的一个关键方面所带来的影响。

Implications on emergence of antimicrobial resistance as a critical aspect in the design of oral sustained release delivery systems of antimicrobials.

作者信息

Hoffman Amnon, Horwitz Ehud, Hess Shmuel, Cohen-Poradosu Ronit, Kleinberg Lilach, Edelberg Anna, Shapiro Mervyn

机构信息

Department of Pharmaceutics, School of Pharmacy, Faculty of Medicine, Hebrew University of Jerusalem, P.O. Box 12065, Jerusalem, 91120, Israel.

出版信息

Pharm Res. 2008 Mar;25(3):667-71. doi: 10.1007/s11095-007-9373-6. Epub 2007 Oct 16.

Abstract

PURPOSE

To assess the effects of the unabsorbed fraction of an orally administered antimicrobial drug which enters the colon on the emergence of resistance among the natural microflora, a phenomenon largely overlooked so far despite its clinical importance, especially when sustained release formulations are used.

METHODS

Effects of an orally administered model beta-lactam antibiotic (amoxicillin) on emergence of resistant bacteria were assessed using a microbiological assay for qualitative and quantitative determination of resistant bacteria in fecal samples of rats following gastric administration of the drug to rats for 4 consecutive days. Time- and site-controlled administration of a beta-lactamase to the rat colon was assessed as a potential strategy for prevention the emergence of resistant bacteria following oral administration of incompletely absorbed antimicrobials.

RESULTS

Emergence of resistant bacteria was demonstrated following oral administration of amoxicillin to rats, whereas de-activation of the beta-lactam prior to entering the colon, by infusion of a beta-lactamase into the lower ileum, was shown to prevent the emergence of resistant colonic bacteria.

CONCLUSIONS

This study illustrates the need to consider the emergence of antimicrobial resistance as a goal equally important to microbiological and clinical cure, when designing oral sustained-release delivery systems of antimicrobial drugs.

摘要

目的

评估口服抗菌药物未吸收部分进入结肠后对天然微生物群中耐药性产生的影响,这一现象尽管具有临床重要性,但迄今在很大程度上被忽视,尤其是在使用缓释制剂时。

方法

使用微生物学检测方法,对连续4天给大鼠胃内给药后大鼠粪便样本中的耐药菌进行定性和定量测定,评估口服模型β-内酰胺抗生素(阿莫西林)对耐药菌出现的影响。将β-内酰胺酶定时定点注入大鼠结肠作为预防口服未完全吸收抗菌药物后耐药菌出现的潜在策略进行评估。

结果

给大鼠口服阿莫西林后出现了耐药菌,而通过向回肠下段注入β-内酰胺酶使β-内酰胺在进入结肠前失活,可防止结肠耐药菌的出现。

结论

本研究表明,在设计抗菌药物口服缓释给药系统时,需要将抗菌药物耐药性的产生视为与微生物学治愈和临床治愈同样重要的目标。

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