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氨苄西林与膨体聚四氟乙烯的结合:导致微生物生长抑制的表面反应。

Attachment of ampicillin to expanded poly(tetrafluoroethylene): surface reactions leading to inhibition of microbial growth.

作者信息

Aumsuwan Nattharika, Danyus Ryan C, Heinhorst Sabine, Urban Marek W

机构信息

Department of Chemistry and Biochemistry, School of Polymers and High Performance Materials, Shelby F Thames Polymer Science Research Center, The University of Southern Mississippi, Hattiesburg, Mississippi 39406, USA.

出版信息

Biomacromolecules. 2008 Jul;9(7):1712-8. doi: 10.1021/bm800176t. Epub 2008 Jun 10.

DOI:10.1021/bm800176t
PMID:18540673
Abstract

The broad spectrum antibiotic, ampicillin (AM), was reacted to expanded poly (tetrafluoroethylene) (ePTFE) surfaces and resulted in the formation of antimicrobial surfaces effective against gram-positive, Staphylococcus aureus, Bacillus thuringiensis, and Enterococcus faecalis, and gram-negative, Escherichia coli, Pseudomonas putida, and Salmonella enterica bacteria. These ePTFE surface modifications were accomplished by utilization of microwave maleic anhydride (MA) plasma reactions leading to the formation of acid groups, followed by amidation reactions of heterofunctional NH 2/COOH-terminated polyethylene glycol (PEG). The final step, the attachment of AM to the PEG spacer, was achieved by amidation reactions between COOH-terminated PEG and NH 2 groups of AM. This approach protects the COOH-AM functionality and diminishes the possibility of hydrolysis of the antimicrobial active portion of AM. These studies also show that approximately 90% of AM molecules are still covalently attached to PEG-MA-ePTFE surfaces after exposure to the bacteria solutions. Even after a 24 h period, the AM volume concentration changes only from 2.25 to 2.04 microg/m3, and depending upon the bacteria type, the bacteria suspensions containing AM-PEG-MA-ePTFE specimens retain 85-99% of their initial optical density.

摘要

广谱抗生素氨苄青霉素(AM)与膨化聚四氟乙烯(ePTFE)表面发生反应,形成了对革兰氏阳性菌(金黄色葡萄球菌、苏云金芽孢杆菌和粪肠球菌)以及革兰氏阴性菌(大肠杆菌、恶臭假单胞菌和肠炎沙门氏菌)有效的抗菌表面。这些ePTFE表面改性是通过利用微波马来酸酐(MA)等离子体反应形成酸性基团,随后进行异官能团NH₂/COOH端基聚乙二醇(PEG)的酰胺化反应来实现的。最后一步,通过COOH端基PEG与AM的NH₂基团之间的酰胺化反应,将AM连接到PEG间隔基上。这种方法保护了COOH-AM官能团,并降低了AM抗菌活性部分水解的可能性。这些研究还表明,在暴露于细菌溶液后,约90%的AM分子仍共价连接在PEG-MA-ePTFE表面。即使经过24小时,AM的体积浓度仅从2.25微克/立方米变化到2.04微克/立方米,并且根据细菌类型,含有AM-PEG-MA-ePTFE标本的细菌悬液保留其初始光密度的85%-99%。

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