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用于局部应用中控制抗生素释放的纳米杂化物。

Nanohybrids for controlled antibiotic release in topical applications.

作者信息

Tammaro L, Costantino U, Bolognese A, Sammartino G, Marenzi G, Calignano A, Tetè S, Mastrangelo F, Califano L, Vittoria V

机构信息

Department of Chemical and Food Engineering, University of Salerno, via Don Melillo, 84084 Fisciano (Sa), Italy.

出版信息

Int J Antimicrob Agents. 2007 Apr;29(4):417-23. doi: 10.1016/j.ijantimicag.2006.11.019. Epub 2007 Feb 15.

Abstract

New polymeric composite materials containing a nanohybrid to be used for the controlled release of an antibiotic molecule, chloramphenicol succinate, have been formulated, prepared and characterised. The nanohybrid consists of a layered double hydroxide of Mg-Al hydrotalcite-type, in which the nitrate anions present in the host galleries were replaced with chloramphenicol succinate anions (CFS(-)) by a simple ion-exchange reaction. Different amounts of the hybrid material were incorporated in polycaprolactone and processed as films of 0.15mm thickness. The composite materials were analysed by X-ray diffractometry and thermogravimetry and their mechanical properties were determined. They showed properties even better than those of the pristine polymer. The release process of the antibiotic molecules was found to be very interesting and promising for tuneable drug delivery. It consists of two stages: an initial stage of a very rapid burst, in which a small fraction of drug is released; and a second stage that is much slower, extending for a longer and longer time. This behaviour is profoundly different and much slower than that of a sample in which the antibiotic molecule is directly incorporated into the polymeric matrix. The parameters influencing drug release have been individuated and discussed.

摘要

已制备、表征了含有纳米杂化物的新型聚合物复合材料,该复合材料用于抗生素分子琥珀酸氯霉素的控释。该纳米杂化物由Mg-Al水滑石型层状双氢氧化物组成,通过简单的离子交换反应,主体层间存在的硝酸根阴离子被琥珀酸氯霉素阴离子(CFS(-))取代。将不同量的杂化材料掺入聚己内酯中,并加工成厚度为0.15mm的薄膜。通过X射线衍射和热重分析对复合材料进行了分析,并测定了其力学性能。它们表现出比原始聚合物更好的性能。抗生素分子的释放过程非常有趣且有望实现可调药物递送。它包括两个阶段:一个非常快速的初始爆发阶段,其中一小部分药物被释放;以及一个慢得多的第二阶段,持续时间越来越长。这种行为与抗生素分子直接掺入聚合物基质的样品有很大不同且慢得多。已确定并讨论了影响药物释放的参数。

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