The Jacob Blaustein Institutes for Desert Research, Zuckerberg Institute for Water Research, The Albert Katz International School of Desert Studies , Ben Gurion University of the Negev , Sede Boqer Campus, Midreshet Ben-Gurion , 84990 , Israel.
Institute for Molecular Engineering , University of Chicago , Chicago , Illinois 60637 , United States.
Langmuir. 2019 Feb 5;35(5):1699-1713. doi: 10.1021/acs.langmuir.8b00181. Epub 2018 Apr 23.
There is a need for the development of antifouling materials to resist adsorption of biomacromolecules. Here we describe the preparation of a novel zwitterionic block copolymer with the potential to prevent or delay the formation of microbial biofilms. The block copolymer comprised a zwitterionic (hydrophilic) section of alternating glutamic acid (negatively charged) and lysine (positively charged) units and a hydrophobic polystyrene section. Cryo-TEM and dynamic-light-scattering (DLS) results showed that, on average, the block copolymer self-assembled into 7-nm-diameter micelles in aqueous solutions (0 to 100 mM NaCl, pH 6). Quartz crystal microbalance with dissipation monitoring (QCM-D), atomic force microscopy (AFM), and contact angle measurements demonstrated that the block copolymer self-assembled into a brush-like monolayer on polystyrene surfaces. The brush-like monolayer produced from a 100 mg/L block copolymer solution exhibited an average distance, d, of approximately 4-8 nm between each block copolymer molecule (center to center). Once the brush-like monolayer self-assembled, it reduced EPS adsorption onto the polystyrene surface by ∼70% (mass), reduced the rate of bacterial attachment by >80%, and inhibited the development of thick biofilms. QCM-D results revealed that the EPS molecules penetrate between the chains of the brush and adsorb onto the polystyrene surface. Additionally, AFM analyses showed that the brush-like monolayer prevents the adhesion of large (> d) hydrophilic colloids onto the surface via hydration repulsion; however, molecules or colloids small enough to fit between the brush polymers (< d) were able to be adsorbed onto the surface via van der Waals interactions. Overall, we found that the penetration of extracellular organelles, as well as biopolymers through the brush, is critical for the failure of the antifouling coating, and likely could be prevented through tuning of the brush density. Stability and biofilm development testing on multiple surfaces (polypropylene, glass, and stainless steel) support practical applications of this novel block copolymer.
需要开发抗生物污染材料以抵抗生物大分子的吸附。在这里,我们描述了一种新型两性离子嵌段共聚物的制备,该共聚物具有防止或延迟微生物生物膜形成的潜力。嵌段共聚物由交替的谷氨酸(带负电荷)和赖氨酸(带正电荷)单元的两性离子(亲水)部分和疏水聚苯乙烯部分组成。低温透射电子显微镜(Cryo-TEM)和动态光散射(DLS)结果表明,该嵌段共聚物在水溶液中(0 至 100 mM NaCl,pH 6)平均自组装成 7nm 直径的胶束。石英晶体微天平耗散监测(QCM-D)、原子力显微镜(AFM)和接触角测量表明,嵌段共聚物在聚苯乙烯表面自组装成刷状单层。由 100mg/L 嵌段共聚物溶液产生的刷状单层中,每个嵌段共聚物分子(中心到中心)之间的平均距离 d 约为 4-8nm。一旦刷状单层自组装,它就会减少 EPS 吸附到聚苯乙烯表面的量约 70%(质量),降低细菌附着率>80%,并抑制厚生物膜的形成。QCM-D 结果表明 EPS 分子渗透到刷的链之间并吸附到聚苯乙烯表面。此外,AFM 分析表明,刷状单层通过水化排斥防止大于 d 的亲水性胶体在表面上的粘附;然而,足够小可以通过范德华相互作用吸附到表面上的分子或胶体(<d)可以通过范德华相互作用吸附到表面上。总的来说,我们发现细胞外细胞器以及生物聚合物通过刷的渗透对于抗污染涂层的失效至关重要,并且通过刷密度的调整可能可以防止这种渗透。在多种表面(聚丙烯、玻璃和不锈钢)上进行的稳定性和生物膜发展测试支持了这种新型嵌段共聚物的实际应用。