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合成、表征及抗菌六亚甲基二膦酸氯己定纳米粒子在生物医学材料和消费品中的应用的功效。

Synthesis, characterization, and efficacy of antimicrobial chlorhexidine hexametaphosphate nanoparticles for applications in biomedical materials and consumer products.

机构信息

Oral Nanoscience, School of Oral and Dental Sciences, University of Bristol, Bristol, UK.

出版信息

Int J Nanomedicine. 2013;8:3507-19. doi: 10.2147/IJN.S50140. Epub 2013 Sep 19.

DOI:10.2147/IJN.S50140
PMID:24092973
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3787925/
Abstract

Chlorhexidine (CHX) is an antimicrobial agent that is efficacious against gram-negative and -positive bacteria and yeasts. Its mechanism of action is based on cell membrane disruption and, as such, it does not promote the development of bacterial resistance, which is associated with the widespread use of antibiotics. In this manuscript, we report the development of novel antimicrobial nanoparticles (NPs) based on a hexametaphosphate salt of CHX. These are synthesized by instantaneous reaction between equimolar aqueous solutions of CHX digluconate and sodium hexametaphosphate, under room temperature and pressure. The reaction results in a stable colloid composed of highly negatively charged NPs (-50 mV), of size 20-160 nm. The NPs adhere rapidly to specimens of glass, titanium, and an elastomeric wound dressing, in a dose-dependent manner. The functionalized materials exhibit a gradual leaching of soluble CHX over a period of at least 50 days. The NP colloid is efficacious against methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa in both planktonic and biofilm conditions. These NPs may find application in a range of biomedical and consumer materials.

摘要

洗必泰(CHX)是一种有效的抗菌剂,可有效对抗革兰氏阴性和阳性细菌以及酵母菌。其作用机制基于细胞膜破坏,因此不会促进细菌耐药性的发展,这与抗生素的广泛使用有关。在本文中,我们报告了基于 CHX 的六偏磷酸盐盐的新型抗菌纳米颗粒(NPs)的开发。这些是通过 CHX 葡萄糖二酸的等摩尔水溶液与六偏磷酸钠在室温常压下的瞬时反应合成的。反应得到一种由带高负电荷的 NPs(-50 mV)组成的稳定胶体,尺寸为 20-160 nm。纳米颗粒以剂量依赖的方式迅速附着在玻璃、钛和弹性伤口敷料的标本上。功能化材料在至少 50 天的时间内以渐进的方式浸出可溶性 CHX。NP 胶体在浮游和生物膜条件下均对耐甲氧西林金黄色葡萄球菌(MRSA)和铜绿假单胞菌有效。这些 NPs 可能在一系列生物医学和消费品材料中得到应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/f5da65b66cac/ijn-8-3507Fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/efd935576424/ijn-8-3507Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/e345588852c2/ijn-8-3507Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/c5c54992bdcc/ijn-8-3507Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/d476a217fba6/ijn-8-3507Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/25d96d28dc52/ijn-8-3507Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/c1517358172d/ijn-8-3507Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/690f1fb97403/ijn-8-3507Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/dc237f0236a8/ijn-8-3507Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/9e6bf3ab7468/ijn-8-3507Fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/ec8734aa16c7/ijn-8-3507Fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/f5da65b66cac/ijn-8-3507Fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/efd935576424/ijn-8-3507Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/e345588852c2/ijn-8-3507Fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/c5c54992bdcc/ijn-8-3507Fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/d476a217fba6/ijn-8-3507Fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/25d96d28dc52/ijn-8-3507Fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/c1517358172d/ijn-8-3507Fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/690f1fb97403/ijn-8-3507Fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/dc237f0236a8/ijn-8-3507Fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/9e6bf3ab7468/ijn-8-3507Fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/ec8734aa16c7/ijn-8-3507Fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1cd/3787925/f5da65b66cac/ijn-8-3507Fig11.jpg

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