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聚多巴胺介导的抗菌脂肽表面涂层用于医疗器械。

Polydopamine-Mediated Antimicrobial Lipopeptide Surface Coating for Medical Devices.

机构信息

School of Chemical Sciences and The Centre for Green Chemical Science, University of Auckland, Auckland 1142, New Zealand.

The MacDiarmid Institute for Advanced Materials and Nanotechnology, Wellington 6012, New Zealand.

出版信息

ACS Appl Bio Mater. 2024 Nov 18;7(11):7574-7584. doi: 10.1021/acsabm.4c01132. Epub 2024 Oct 30.

Abstract

Biofilm formation on medical implants such as catheters is a major issue which needs to be addressed as it leads to severe health care associated infections. This study explored the design and synthesis of a polydopamine-lipopeptide based antimicrobial coating. The coating was used to modify the surface of Ultrathane Catheters. The lipopeptide with an -terminal cysteine was covalently conjugated to the polydopamine modified catheters via a Michael addition reaction between the thiol moiety in the peptide and the aromatic ring in the polydopamine layer. The immobilization of the peptide on the polydopamine coated catheters was confirmed using water contact angle, X-ray photoelectron spectroscopy, atomic force microscopy, and scanning electron microscopy (SEM). The antimicrobial activity of the coated catheters investigated using drug resistant and clinical strains of Gram-positive (MRSA and ) and Gram-negative (, , and ) bacteria revealed that lipopeptide immobilization inhibited >90% bacterial adhesion to the catheter surface. Additionally, biofilm assays against MRSA and revealed that the lipopeptide immobilized catheters inhibited >85% bacterial growth after 1 week incubation. Finally, the cytotoxicity profile of the catheters using the human dermal fibroblast, and the human embryonic kidney cell lines demonstrated that the polydopamine-lipopeptide coating was not toxic after 72 h incubation.

摘要

在医学植入物(如导管)上形成生物膜是一个亟待解决的问题,因为它会导致严重的与医疗保健相关的感染。本研究探索了聚多巴胺-脂肽抗菌涂层的设计与合成。该涂层用于修饰 Ultrathane 导管的表面。通过肽中巯基部分和聚多巴胺层中的芳环之间的迈克尔加成反应,将带有 -末端半胱氨酸的脂肽共价偶联到经聚多巴胺修饰的导管上。使用水接触角、X 射线光电子能谱、原子力显微镜和扫描电子显微镜 (SEM) 确认了肽在聚多巴胺涂层导管上的固定。使用耐药物和临床分离株革兰氏阳性(MRSA 和 )和革兰氏阴性( 、 、 和 )细菌对涂层导管的抗菌活性进行了研究,结果表明脂肽固定化抑制了 >90%的细菌黏附到导管表面。此外,针对 MRSA 和 的生物膜测定表明,脂肽固定化导管在孵育 1 周后抑制了 >85%的细菌生长。最后,使用人真皮成纤维细胞和人胚肾细胞系评估导管的细胞毒性谱表明,聚多巴胺-脂肽涂层在孵育 72 h 后没有毒性。

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