Montdargent B, Letourneur D
Laboratoire de Recherches sur les Macromolécules, Institut Galilée, Villetaneuse, France.
Infect Control Hosp Epidemiol. 2000 Jun;21(6):404-10. doi: 10.1086/501782.
Polymers are widely used for a large range of medical devices used as biomaterials on a temporary, intermittent, and long-term basis. It is now well accepted that the initial rapid adsorption of proteins to polymeric surfaces affects the performance of these biomaterials. However, protein adsorption to a polymer surface can be modulated by an appropriate design of the interface. Extensive study has shown that these interactions can be minimized by coating with a highly hydrated layer (hydrogel), by grafting on the surface different biomolecules, or by creating domains with chemical functions (charges, hydrophilic groups). Our laboratory has investigated the latter approach over the past 2 decades, in particular the synthesis and the biological activities of polymers to improve the biocompatibility of blood-contacting devices. These soluble and insoluble polymers were obtained by chemical substitution of macromolecular chains with suitable groups able to develop specific interactions with biological components. Applied to compatibility with the blood and the immune systems, this concept has been extended to interactions of polymeric biomaterials with eukaryotic and prokaryotic cells. The design of new biomaterials with low bacterial attachment is thus under intensive study. After a brief overview of current trends in the surface modifications of biocompatible materials, we will describe how biospecific polymers can be obtained and review our recent results on the inhibition of bacterial adhesion using one type of functionalized polymer obtained by random substitution. This strategy, applied to existing or new materials, seems promising for the limitation of biomaterial-associated infections.
聚合物广泛应用于大量作为生物材料的医疗设备,这些设备可临时、间歇或长期使用。现在人们已经普遍接受,蛋白质在聚合物表面的初始快速吸附会影响这些生物材料的性能。然而,通过对界面进行适当设计,可以调节蛋白质在聚合物表面的吸附。大量研究表明,通过用高度水合层(水凝胶)包覆、在表面接枝不同生物分子或创建具有化学功能(电荷、亲水基团)的区域,可以将这些相互作用降至最低。在过去20年里,我们实验室研究了后一种方法,特别是聚合物的合成及其生物活性,以提高与血液接触设备的生物相容性。这些可溶性和不溶性聚合物是通过用能够与生物成分发生特异性相互作用的合适基团对大分子链进行化学取代而获得的。应用于与血液和免疫系统的相容性方面,这一概念已扩展到聚合物生物材料与真核细胞和原核细胞的相互作用。因此,对具有低细菌附着性的新型生物材料的设计正在深入研究。在简要概述生物相容性材料表面改性的当前趋势之后,我们将描述如何获得生物特异性聚合物,并回顾我们最近关于使用一种通过随机取代获得的功能化聚合物抑制细菌粘附的结果。这种策略应用于现有材料或新材料,对于限制生物材料相关感染似乎很有前景。