Xiao Xixi, Zhao Wenhan, Liang Jing, Sauer Karin, Libera Matthew
Department of Chemical Engineering and Materials Science, Stevens Institute of Technology, Hoboken, NJ, USA.
Binghamton Biofilm Research Center (BBRC), Binghamton University Binghamton, NY USA.
Colloids Surf B Biointerfaces. 2020 Apr 21;192:110989. doi: 10.1016/j.colsurfb.2020.110989.
Self-defensive biomaterial surfaces are being developed in order to mitigate infection associated with tissue-contacting biomedical devices. Such infection occurs when microbes colonize the surface of a device and proliferate into a recalcitrant biofilm. A key intervention point centers on preventing the initial colonization. Incorporating antimicrobials within a surface coating can be very effective, but the traditional means of antimicrobial delivery by continuous elution can often be counterproductive. If there is no infection, continuous elution creates conditions that promote the development of resistant microbes throughout the patient. In contrast, a self-defensive coating releases antimicrobial only when and only where there is a microbial challenge to the surface. Otherwise, the antimicrobial remains sequestered within the coating and does not contribute to the development of resistance. A self-defensive surface requires a local trigger that signals the microbial challenge. Three such triggers have been identified as: (1) local pH lowering; (2) local enzyme release; and (3) direct microbial-surface contact. This short review highlights the need for self-defensive surfaces in the general context of the device-infection problem and then reviews key biomaterials developments associated with each of these three triggering mechanisms.
为了减轻与组织接触的生物医学设备相关的感染,正在开发具有自我防御功能的生物材料表面。当微生物在设备表面定植并增殖形成顽固的生物膜时,就会发生这种感染。一个关键的干预点集中在防止初始定植上。在表面涂层中加入抗菌剂可能非常有效,但通过持续洗脱进行抗菌剂递送的传统方法往往会适得其反。如果没有感染,持续洗脱会创造条件,促使患者体内产生耐药微生物。相比之下,自我防御涂层仅在表面受到微生物挑战时且仅在该位置释放抗菌剂。否则,抗菌剂会被隔离在涂层内,不会导致耐药性的产生。自我防御表面需要一个局部触发信号来表明受到了微生物挑战。已确定三种这样的触发信号为:(1)局部pH值降低;(2)局部酶释放;(3)微生物与表面的直接接触。这篇简短的综述首先强调了在设备感染问题的大背景下对自我防御表面的需求,然后回顾了与这三种触发机制中的每一种相关的关键生物材料进展。