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一步气相沉积氟化聚阳离子涂层以制备抗耐药细菌和病毒的防污抗感染纺织品。

One-step vapor deposition of fluorinated polycationic coating to fabricate antifouling and anti-infective textile against drug-resistant bacteria and viruses.

作者信息

Song Qing, Zhao Ruixiang, Liu Tong, Gao Lingling, Su Cuicui, Ye Yumin, Chan Siew Yin, Liu Xinyue, Wang Ke, Li Peng, Huang Wei

机构信息

Ningbo Institute, Frontiers Science Center for Flexible Electronics (FSCFE), Xi'an Institute of Flexible Electronics (IFE) and Xi'an Institute of Biomedical Materials & Engineering (IBME), Northwestern Polytechnical University, 127 West Youyi Road, Xi'an 710072, China.

Key Laboratory for Organic Electronics and Information Displays, Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications, 9 Wenyuan Road, Nanjing 210023, China.

出版信息

Chem Eng J. 2021 Aug 15;418:129368. doi: 10.1016/j.cej.2021.129368. Epub 2021 Mar 16.

DOI:10.1016/j.cej.2021.129368
PMID:33746567
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7962519/
Abstract

The ongoing pandemic caused by the novel coronavirus has turned out to be one of the biggest threats to the world, and the increase of drug-resistant bacterial strains also threatens the human health. Hence, there is an urgent need to develop novel anti-infective materials with broad-spectrum anti-pathogenic activity. In the present study, a fluorinated polycationic coating was synthesized on a hydrophilic and negatively charged polyester textile via one-step initiated chemical vapor deposition of poly(dimethyl amino methyl styrene--1H,1H,2H,2H-perfluorodecyl acrylate) (P(DMAMS--PFDA), PDP). The surface characterization results of SEM, FTIR, and EDX demonstrated the successful synthesis of PDP coating. Contact angle analysis revealed that PDP coating endowed the polyester textile with the hydrophobicity against the attachment of different aqueous foulants such as blood, coffee, and milk, as well as the oleophobicity against paraffin oil. Zeta potential analysis demonstrated that the PDP coating enabled a transformation of negative charge to positive charge on the surface of polyester textile. The PDP coating exhibited excellent contact-killing activity against both gram-negative and gram-positive methicillin-resistant , with the killing efficiency of approximate 99.9%. In addition, the antiviral capacity of PDP was determined by a green fluorescence protein (GFP) expression-based method using lentivirus-EGFP as a virus model. The PDP coating inactivated the negatively charged lentivirus-EGFP effectively. Moreover, the coating showed good biocompatibility toward mouse NIH 3T3 fibroblast cells. All the above properties demonstrated that PDP would be a promising anti-pathogenic polymeric coating with wide applications in medicine, hygiene, hospital, etc., to control the bacterial and viral transmission and infection.

摘要

新型冠状病毒引发的持续大流行已成为全球面临的最大威胁之一,而耐药细菌菌株的增加也对人类健康构成威胁。因此,迫切需要开发具有广谱抗病原活性的新型抗感染材料。在本研究中,通过一步引发化学气相沉积聚(二甲基氨基甲基苯乙烯 - 1H,1H,2H,2H - 全氟癸基丙烯酸酯)(P(DMAMS - PFDA),即PDP),在亲水性带负电荷的聚酯纺织品上合成了氟化聚阳离子涂层。扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)和能量色散X射线光谱(EDX)的表面表征结果证明了PDP涂层的成功合成。接触角分析表明,PDP涂层赋予聚酯纺织品疏水性,可防止血液、咖啡和牛奶等不同水性污垢的附着,以及对石蜡油的疏油性。zeta电位分析表明,PDP涂层使聚酯纺织品表面的电荷从负电荷转变为正电荷。PDP涂层对革兰氏阴性和革兰氏阳性耐甲氧西林菌均表现出优异的接触杀灭活性,杀灭效率约为99.9%。此外,以慢病毒 - EGFP为病毒模型,通过基于绿色荧光蛋白(GFP)表达的方法测定了PDP的抗病毒能力。PDP涂层有效地灭活了带负电荷的慢病毒 - EGFP。此外,该涂层对小鼠NIH 3T3成纤维细胞表现出良好的生物相容性。上述所有特性表明,PDP将是一种有前途的抗病原聚合物涂层,在医学、卫生、医院等领域具有广泛应用,可控制细菌和病毒的传播与感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/e47e788204a7/gr9_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/34b7ba69e4c7/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/d2f4fdf8fb38/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/c0db3b3687a6/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/4550556d7f6a/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/c0136777ff6b/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/4fc4e9cde18e/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/27a3c12b6a0c/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/8ff0392ddb63/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/37d3bafc6c01/gr8_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/e47e788204a7/gr9_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/34b7ba69e4c7/ga1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/d2f4fdf8fb38/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/c0db3b3687a6/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/4550556d7f6a/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/c0136777ff6b/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/4fc4e9cde18e/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/27a3c12b6a0c/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/8ff0392ddb63/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/37d3bafc6c01/gr8_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f8c/7962519/e47e788204a7/gr9_lrg.jpg

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