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消逝波腔衰荡光谱(EW-CRDS)作为功能化界面上大分子吸附动力学的探针。

Evanescent wave cavity ring-down spectroscopy (EW-CRDS) as a probe of macromolecule adsorption kinetics at functionalized interfaces.

机构信息

Department of Chemistry, University of Warwick, Coventry, United Kingdom.

出版信息

Langmuir. 2012 May 1;28(17):6902-10. doi: 10.1021/la3006053. Epub 2012 Apr 19.

DOI:10.1021/la3006053
PMID:22489550
Abstract

Evanescent wave cavity ring-down spectroscopy (EW-CRDS) has been employed to study the interfacial adsorption kinetics of coumarin-tagged macromolecules onto a range of functionalized planar surfaces. Such studies are valuable in designing polymers for complex systems where the degree of interaction between the polymer and surface needs to be tailored. Three tagged synthetic polymers with different functionalities are examined: poly(acrylic acid) (PAA), poly(3-sulfopropyl methacrylate, potassium salt) (PSPMA), and a mannose-modified glycopolymer. Adsorption transients at the silica/water interface are found to be characteristic for each polymer, and kinetics are deduced from the initial rates. The chemistry of the adsorption interfaces has been varied by, first, manipulation of silica surface chemistry via the bulk pH, followed by surfaces modified by poly(L-glutamic acid) (PGA) and cellulose, giving five chemically different surfaces. Complementary atomic force microscopy (AFM) imaging has been used for additional surface characterization of adsorbed layers and functionalized interfaces to allow adsorption rates to be interpreted more fully. Adsorption rates for PSPMA and the glycopolymer are seen to be highly surface sensitive, with significantly higher rates on cellulose-modified surfaces, whereas PAA shows a much smaller rate dependence on the nature of the adsorption surface.

摘要

消逝波腔衰荡光谱(EW-CRDS)已被用于研究一系列功能化平面表面上香豆素标记的大分子的界面吸附动力学。这些研究对于设计用于复杂体系的聚合物非常有价值,在这些体系中,需要调整聚合物与表面之间的相互作用程度。我们研究了三种具有不同功能的标记合成聚合物:聚丙烯酸(PAA)、聚 3-磺丙基甲基丙烯酸钾(PSPMA)和甘露糖修饰的糖聚合物。在二氧化硅/水界面上的吸附瞬变对于每种聚合物都是特征性的,并且动力学是从初始速率推断出来的。首先通过改变二氧化硅表面化学性质来改变吸附界面的化学性质,然后通过聚(L-谷氨酸)(PGA)和纤维素对表面进行修饰,得到了五个化学性质不同的表面。互补原子力显微镜(AFM)成像用于吸附层和功能化界面的附加表面表征,以更全面地解释吸附速率。我们发现 PSPMA 和糖聚合物的吸附速率对表面非常敏感,在纤维素修饰的表面上的速率明显更高,而 PAA 的吸附速率对吸附表面的性质依赖性较小。

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