Smith School of Chemical & Biomolecular Engineering, Cornell University, Ithaca, New York 14853, United States.
ACS Biomater Sci Eng. 2023 Jul 10;9(7):3923-3934. doi: 10.1021/acsbiomaterials.0c01691. Epub 2021 Apr 6.
Reduced biofilm formation is highly desirable in applications ranging from transportation to separations and healthcare. Biofilms often form at the three-phase interface where air, liquid, and solid coexist due to the close proximity to nutrients and oxygen. Reducing biofilm formation at the triple interface presents challenges because of the conflicting requirements for hydrophobicity at the air-solid interface (for self-cleaning properties) and for hydrophilicity at the liquid-solid interface (for reduced foulant adhesion). Meeting those needs simultaneously likely entails a dynamic surface, capable of shifting the surface energy landscape in response to wetting conditions and thus enabling hydrophobicity in air and hydrophilicity in water. Here, we designed a facile approach to render existing surfaces resistant to biofilm formation at the triple interface. By adding trace amounts (∼0.1 mM) of surfactants, biofilm formation of (known to form biofilm at the triple interface) was reduced on all surfaces tested, ranging from hydrophilic to hydrophobic, polar to nonpolar. That reduced fouling was not a result of the known antimicrobial effects. Instead, it was attributed to the surface-adsorbed surfactants that dynamically control surface energy at the triple interface. To further understand the effect of surfactant-surface interactions on biofilm reduction, we systematically varied the surfactant charge type and surface properties (surface energy and charge). Electrostatic interactions between surfactants and surfaces were identified as an influential factor when predicting the relative fouling reduction upon introduction of surfactants. Nevertheless, biofilm formation was reduced even on the charge-neutral, fluorinated surface made of poly(, , , -perfluorodecyl acrylate) by more than 2-fold simply via adding 0.2 mM dodecyl trimethylammonium chloride or 0.3 mM sodium dodecyl sulfate. Given its robustness, this strategy is broadly applicable for reducing fouling on existing surfaces, which in turn improves the cost-effectiveness of membrane separations and mitigates contaminations and nosocomial infections in healthcare.
在从运输到分离和医疗保健等各个领域,减少生物膜的形成是非常理想的。由于靠近营养物质和氧气,生物膜通常在空气、液体和固体共存的三相界面处形成。由于空气-固界面需要疏水性(用于自清洁特性)和液体-固界面需要亲水性(用于减少污染物附着),因此在三相界面处减少生物膜的形成带来了挑战。同时满足这些需求可能需要一个动态表面,能够根据润湿条件改变表面能景观,从而在空气中表现出疏水性,在水中表现出亲水性。在这里,我们设计了一种简便的方法,使现有表面能够抵抗三相界面处的生物膜形成。通过添加痕量(约 0.1mM)的表面活性剂,在所有测试的表面上,包括从亲水到疏水、从极性到非极性的表面上,都减少了(已知在三相界面处形成生物膜)的生物膜形成。减少的污染不是由于已知的抗菌作用造成的。相反,这归因于动态控制三相界面表面能的表面吸附表面活性剂。为了进一步了解表面活性剂-表面相互作用对减少生物膜的影响,我们系统地改变了表面活性剂的电荷类型和表面性质(表面能和电荷)。当引入表面活性剂时,静电相互作用被确定为预测相对污垢减少的一个影响因素。然而,即使在电荷中性的、由聚(四氟乙烯-共-六氟丙烯-共-丙烯酸羟乙酯)制成的氟化表面上,仅通过添加 0.2mM 十二烷基三甲基氯化铵或 0.3mM 十二烷基硫酸钠,生物膜的形成就减少了 2 倍以上。鉴于其稳健性,该策略广泛适用于减少现有表面的污垢,从而提高膜分离的成本效益,并减轻医疗保健中的污染和医院感染。