Xing Cheng-Mei, Meng Fan-Ning, Quan Miao, Ding Kai, Dang Yuan, Gong Yong-Kuan
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, Shaanxi, PR China.
Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an 710127, Shaanxi, PR China.
Acta Biomater. 2017 Sep 1;59:129-138. doi: 10.1016/j.actbio.2017.06.034. Epub 2017 Jun 27.
UNLABELLED: A versatile fabrication and performance optimization strategy of PEG and zwitterionic polymer coatings is developed on the sensor chip of surface plasma resonance (SPR) instrument. A random copolymer bearing phosphorylcholine zwitterion and active ester side chains (PMEN) and carboxylic PEG coatings with comparable thicknesses were deposited on SPR sensor chips via amidation coupling on the precoated polydopamine (PDA) intermediate layer. The PMEN coating showed much stronger resistance to bovine serum albumin (BSA) adsorption than PEG coating at very thin thickness (∼1nm). However, the BSA resistant efficacy of PEG coating could exceed that of PMEN due to stronger steric repelling effect when the thickness increased to 1.5∼3.3nm. Interestingly, both the PEG and PMEN thick coatings (≈3.6nm) showed ultralow fouling by BSA and bovine plasma fibrinogen (Fg). Moreover, changes in the PEG end group from -OH to -COOH, protein adsorption amount could increase by 10-fold. Importantly, the optimized PMEN and PEG-OH coatings were easily duplicated on other substrates due to universal adhesion of the PDA layer, showed excellent resistance to platelet, bacteria and proteins, and no significant difference in the antifouling performances was observed. These detailed results can explain the reported discrepancy in performances between PEG and zwitterionic polymer coatings by thickness. This facile and substrate-independent coating strategy may benefit the design and manufacture of advanced antifouling biomedical devices and long circulating nanocarriers. STATEMENT OF SIGNIFICANCE: Prevention of biofouling is one of the biggest challenges for all biomedical applications. However, it is very difficult to fabricate a highly hydrophilic antifouling coating on inert materials or large devices. In this study, PEG and zwitterion polymers, the most widely investigated polymers with best antifouling performance, are conveniently immobilized on different kinds of substrates from their aqueous solutions by precoating a polydopamine intermediate layer as the universal adhesive and readily re-modifiable surface. Importantly, the coating fabrication and antifouling performance can be monitored and optimized quantitatively by a surface plasma resonance (SPR) system. More significantly, the SPR on-line optimized coatings were successfully duplicated off-line on other substrates, and supported by their excellent antifouling properties.
未标注:在表面等离子体共振(SPR)仪器的传感器芯片上,开发了一种用于聚乙二醇(PEG)和两性离子聚合物涂层的通用制备及性能优化策略。通过在预涂覆的聚多巴胺(PDA)中间层上进行酰胺化偶联,将带有磷酰胆碱两性离子和活性酯侧链的无规共聚物(PMEN)以及具有可比厚度的羧基PEG涂层沉积在SPR传感器芯片上。在非常薄的厚度(约1nm)下,PMEN涂层对牛血清白蛋白(BSA)吸附的抗性比PEG涂层强得多。然而,当厚度增加到1.5至3.3nm时,由于更强的空间排斥效应,PEG涂层对BSA的抗吸附效果可能超过PMEN。有趣的是,PEG和PMEN厚涂层(约3.6nm)对BSA和牛血浆纤维蛋白原(Fg)均表现出超低的污垢附着。此外,PEG端基从-OH变为-COOH时,蛋白质吸附量可增加10倍。重要的是,由于PDA层的通用粘附性,优化后的PMEN和PEG-OH涂层易于在其他基材上复制,表现出对血小板、细菌和蛋白质的优异抗性,且在防污性能上未观察到显著差异。这些详细结果可以解释报道的PEG和两性离子聚合物涂层在性能上因厚度不同而产生的差异。这种简便且与基材无关的涂层策略可能有利于先进防污生物医学设备和长效循环纳米载体的设计与制造。 意义声明:防止生物污垢是所有生物医学应用面临的最大挑战之一。然而,在惰性材料或大型设备上制备高度亲水的防污涂层非常困难。在本研究中,PEG和两性离子聚合物是研究最广泛且具有最佳防污性能的聚合物,通过预涂覆聚多巴胺中间层作为通用粘合剂和易于重新改性的表面,可方便地将它们从水溶液固定在不同类型的基材上。重要的是,涂层制备和防污性能可通过表面等离子体共振(SPR)系统进行定量监测和优化。更重要的是,SPR在线优化的涂层在离线状态下成功复制到其他基材上,并具有优异的防污性能。
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