Suppr超能文献

两性离子及其他防污聚合物界面水合作用的原位分子水平研究

Molecular level studies on interfacial hydration of zwitterionic and other antifouling polymers in situ.

作者信息

Leng Chuan, Sun Shuwen, Zhang Kexin, Jiang Shaoyi, Chen Zhan

机构信息

Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States.

Department of Chemical Engineering, University of Washington, Seattle, WA 98195, United States.

出版信息

Acta Biomater. 2016 Aug;40:6-15. doi: 10.1016/j.actbio.2016.02.030. Epub 2016 Feb 23.

Abstract

UNLABELLED

Antifouling polymers have wide applications in biomedical engineering and marine industry. Recently, zwitterionic materials have been reported as promising candidates for antifouling applications, while strong hydration is believed to be the key antifouling mechanism. Zwitterionic materials can be designed with various molecular structures, which affect their hydration and antifouling performance. Although strong hydration has been proposed to occur at the material surfaces, probing the solid material/water interfaces is challenging with traditional analytical techniques. Here in this review, we will review our studies on surface hydration of zwitterionic materials and other antifouling materials by using sum frequency generation (SFG) vibrational spectroscopy, which provides molecular understanding of the water structures at various material surfaces. The materials studied include zwitterionic polymer brushes with different molecular structures, amphiphilic polymers with zwitterionic groups, uncharged hydrophilic polymer brushes, amphiphilic polypeptoids, and widely used antifouling material poly(ethylene glycol). We will compare the differences among zwitterionic materials with various molecular structures as well as the differences between antifouling materials and fouling surfaces of control samples. We will also discuss the effects of pH and biological molecules like proteins on the surface hydration of the zwitterionic materials. Using SFG spectroscopy, we have measured the hydration layers of antifouling materials and found that strong hydrogen bonds are key to the formation of strong hydration layers preventing protein fouling at the polymer interfaces.

STATEMENT OF SIGNIFICANCE

Antifouling polymers have wide applications in biomedical engineering and marine industry. Recently, zwitterionic materials have been reported as promising candidates for antifouling applications, while strong hydration is believed to be the key antifouling mechanism. However, zwitterionic materials can be designed with various molecular structures, which affect their hydration and antifouling performance. Moreover, although strong hydration has been proposed to occur at the material surfaces, probing the solid material/water interfaces is challenging with traditional analytical techniques. Here in this manuscript, we will review our studies on surface hydration of zwitterionic materials and other antifouling materials by using sum frequency generation (SFG) vibrational spectroscopy, which provides molecular understanding of the water structures at various material surfaces. The materials studied include zwitterionic polymer brushes with different molecular structures, amphiphilic polymers with zwitterionic groups, uncharged hydrophilic polymer brushes, amphiphilic polypeptoids, and widely used antifouling material poly(ethylene glycol). We will compare the differences among zwitterionic materials with various molecular structures as well as the differences between antifouling materials and fouling surfaces of control samples. We will also discuss the effects of pH and biological molecules like proteins on the surface hydration of the zwitterionic materials. All the SFG results indicate that strongly hydrogen-bonded water at the materials' surfaces (strong surface hydration) is closely correlated to the good antifouling properties of the materials. This review will be widely interested by readers of Acta Biomaterialia and will impact many different research fields in chemistry, materials, engineering, and beyond.

摘要

未标注

防污聚合物在生物医学工程和海洋工业中有着广泛应用。最近,两性离子材料被报道为防污应用的有前景的候选材料,而强水化作用被认为是关键的防污机制。两性离子材料可以设计成各种分子结构,这会影响它们的水化作用和防污性能。尽管有人提出在材料表面会发生强水化作用,但用传统分析技术探测固体材料/水界面具有挑战性。在这篇综述中,我们将回顾我们利用和频振动光谱(SFG)对两性离子材料和其他防污材料表面水化作用的研究,该技术能从分子层面理解各种材料表面的水结构。所研究的材料包括具有不同分子结构的两性离子聚合物刷、带有两性离子基团的两亲聚合物、不带电荷的亲水性聚合物刷、两亲多肽以及广泛使用的防污材料聚乙二醇。我们将比较具有不同分子结构的两性离子材料之间的差异,以及防污材料与对照样品的污染表面之间的差异。我们还将讨论pH值和蛋白质等生物分子对两性离子材料表面水化作用的影响。利用SFG光谱,我们测量了防污材料的水化层,发现强氢键是形成强水化层以防止聚合物界面蛋白质污染的关键。

重要性声明

防污聚合物在生物医学工程和海洋工业中有着广泛应用。最近,两性离子材料被报道为防污应用的有前景的候选材料,而强水化作用被认为是关键的防污机制。然而,两性离子材料可以设计成各种分子结构,这会影响它们的水化作用和防污性能。此外,尽管有人提出在材料表面会发生强水化作用,但用传统分析技术探测固体材料/水界面具有挑战性。在本手稿中,我们将回顾我们利用和频振动光谱(SFG)对两性离子材料和其他防污材料表面水化作用的研究,该技术能从分子层面理解各种材料表面的水结构。所研究的材料包括具有不同分子结构的两性离子聚合物刷、带有两性离子基团的两亲聚合物、不带电荷的亲水性聚合物刷、两亲多肽以及广泛使用的防污材料聚乙二醇。我们将比较具有不同分子结构的两性离子材料之间的差异,以及防污材料与对照样品的污染表面之间的差异。我们还将讨论pH值和蛋白质等生物分子对两性离子材料表面水化作用的影响。所有SFG结果表明,材料表面强氢键结合的水(强表面水化)与材料良好的防污性能密切相关。这篇综述将受到《生物材料学报》读者的广泛关注,并将影响化学、材料、工程及其他许多不同的研究领域。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验