首页> 外文期刊>Journal of Polymer Science, Part A. Polymer Chemistry >Studies of the surface layer structure and properties of poly (styrene/alpha-t-butoxy-omega-polyglycidol) microspheres by carbon nuclear magnetic resonance, X-ray photoelectron spectroscopy, and the adsorption of human serum albumin and gamma-globuli
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Studies of the surface layer structure and properties of poly (styrene/alpha-t-butoxy-omega-polyglycidol) microspheres by carbon nuclear magnetic resonance, X-ray photoelectron spectroscopy, and the adsorption of human serum albumin and gamma-globuli

机译:通过碳核磁共振,X射线光电子能谱以及人血清白蛋白和γ-球蛋白的吸附研究聚(苯乙烯/α-叔丁氧基-ω-聚缩水甘油)微球的表面层结构和性能

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The composition and properties of the surface layers of poly(styrene/alpha-t-butoxy-omega-polyglycidol) [poly(styrene/VB-polyGL)] microspheres synthesized by the radical copolymerization of styrene and alpha-t-butoxy-omega-vinylbenzyl-polyglycidol (VB-polyGL) macromonomers [number-average molecular weight (M-n) = 950 or 2700] were investigated with X-ray photoelectron spectroscopy, C-13 NMR, and the adsorption of human serum albumin and gamma-globulins. The number-average diameter of the synthesized microspheres was 220 nm. Their surface layers were rich in polyglycidol, with polyglycidol-to-polystyrene unit ratios of 0.443 (VB-polyGL with M. = 950) and 0.427 (VB-polyGL with Mn = 2700). In suspensions of poly(styrene/VB-polyGL) particles in D2O, the polymer chains in the polyglycidol-rich surface layers were highly mobile, allowing the registration of polyglycidol C-13 NMR spectra with standard procedures for polymer solutions. In these spectra, the signals of the relatively immobile polystyrene segments were absent. The spin-lattice relaxation times (T-1) measured for polyglycidol in the microsphere surface layers and for VB-polyGL macromonomers in solution were very close, indicating similar degrees of motion in bound (in particle surface layers) and free (in solution) polyglycidol macromolecules. Studies of protein adsorption revealed that hydrophilic polyglycidol layers were protein-repellent. It was found that longer polyglycidol chains in particle surface layers were more mobile (higher T-1 values) and provided better protection against protein adsorption. (C) 2003 Wiley Periodicals, Inc. [References: 24]
机译:通过苯乙烯与α-叔丁氧基-ω-自由基的自由基共聚反应合成的聚(苯乙烯/α-叔丁氧基-ω-聚缩水甘油)[聚(苯乙烯/ VB-polyGL)]微球的表面层的组成和性质用X射线光电子能谱,C-13 NMR以及人血清白蛋白和γ-球蛋白的吸附研究了乙烯基苄基聚缩水甘油(VB-polyGL)大单体[数均分子量(Mn)= 950或2700]。合成的微球的数均直径为220nm。它们的表面层富含聚缩水甘油,聚缩水甘油与聚苯乙烯的单元比为0.443(VB-polyGL,M。= 950)和0.427(VB-polyGL,Mn = 2700)。在D2O中的聚(苯乙烯/ VB-polyGL)颗粒悬浮液中,富含聚缩水甘油的表面层中的聚合物链具有很高的流动性,从而可以用聚合物溶液的标准程序记录聚缩水甘油C-13 NMR光谱。在这些光谱中,没有相对固定的聚苯乙烯链段的信号。在微球表面层中的聚缩水甘油和溶液中VB-polyGL大分子单体的自旋晶格弛豫时间(T-1)非常接近,表明结合(在颗粒表面层)和自由(在溶液中)的运动程度相似聚缩水甘油大分子。蛋白质吸附研究表明,亲水性聚缩水甘油层具有蛋白质排斥性。发现在颗粒表面层中较长的聚缩水甘油链更具流动性(较高的T-1值),并提供了更好的蛋白质吸附保护。 (C)2003 Wiley Periodicals,Inc. [参考:24]

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