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利用微球技术将利福平靶向递送至结核分枝杆菌感染的巨噬细胞。

Use of microsphere technology for targeted delivery of rifampin to Mycobacterium tuberculosis-infected macrophages.

作者信息

Barrow E L, Winchester G A, Staas J K, Quenelle D C, Barrow W W

机构信息

Mycobacteriology Research Unit, Southern Research Institute, Birmingham, Alabama 35205, USA.

出版信息

Antimicrob Agents Chemother. 1998 Oct;42(10):2682-9. doi: 10.1128/AAC.42.10.2682.

Abstract

Microsphere technology was used to develop formulations of rifampin for targeted delivery to host macrophages. These formulations were prepared by using biocompatible polymeric excipients of lactide and glycolide copolymers. Release characteristics were examined in vitro and also in two monocytic cell lines, the murine J774 and the human Mono Mac 6 cell lines. Bioassay assessment of cell culture supernatants from monocyte cell lines showed release of bioactive rifampin during a 7-day experimental period. Treatment of Mycobacterium tuberculosis H37Rv-infected monocyte cell lines with rifampin-loaded microspheres resulted in a significant decrease in numbers of CFU at 7 days following initial infection, even though only 8% of the microsphere-loaded rifampin was released. The levels of rifampin released from microsphere formulations within monocytes were more effective at reducing M. tuberculosis intracellular growth than equivalent doses of rifampin given as a free drug. These results demonstrate that rifampin-loaded microspheres can be formulated for effective sustained and targeted delivery to host macrophages.

摘要

微球技术被用于开发利福平制剂,以实现向宿主巨噬细胞的靶向递送。这些制剂是通过使用丙交酯和乙交酯共聚物的生物相容性聚合物辅料制备而成。在体外以及两种单核细胞系(小鼠J774和人单核巨噬细胞6细胞系)中对释放特性进行了研究。对单核细胞系细胞培养上清液的生物测定评估显示,在为期7天的实验期内有生物活性的利福平释放。用载有利福平的微球处理结核分枝杆菌H37Rv感染的单核细胞系,在初次感染后7天,即使仅8%载于微球的利福平被释放,菌落形成单位数量也显著减少。单核细胞内从微球制剂释放的利福平水平,在减少结核分枝杆菌细胞内生长方面比等量作为游离药物给予的利福平更有效。这些结果表明,载有利福平的微球可以被制备用于向宿主巨噬细胞进行有效的持续和靶向递送。

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