合成、天然和半天然多两性聚合物间配合物的研究进展

E. A. Bekturov, R. I. Moustafine, S. Kudaibergenov, V. Khutoryanskiy
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引用次数: 0

摘要

本文综述了合成的、天然的和半天然的聚电解质及其与其他聚电解质和非离子聚合物形成聚合物间配合物的能力。介绍了多两性电解质的定义、分类和理化性质综述。讨论了内在无序蛋白质和氨基酸衍生的半天然多两性电解质的构象和相行为。研究了合成的、天然的和半天然的多两性聚合物与水溶性聚合物形成聚合物间配合物的能力。该领域的大部分研究集中在多两性电解质与带相反电荷的多电解质之间的多电解质配合物上;然而,也有研究证明了氢键配合物的形成。络合的性质通常受溶液pH和多两性电解质等电点的影响。多两性络合物与其他聚合物之间的络合作用可能导致胶体分散体(纳米和微粒)的形成,液-液相分离(称为络合物凝聚),完全可溶的多配合物或物理交联凝胶。这一领域的大量研究集中在蛋白质形成的复合物上。讨论了多两性聚合物形成的聚合物间配合物在生物技术、医学、封装技术、分离科学、生物催化、食品科学和制药等领域的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interpolymer Complexes of Synthetic, Natural and Semi-Natural Polyampholytes: A Review
This review is focused on synthetic, natural and semi-natural polyampholytes and their ability to form interpolymer complexes with other polyelectrolytes and non-ionic polymers. It provides definition, classification and overview of physicochemical properties of polyampholytes. The conformation and phase behaviour of intrinsically disordered proteins and semi-natural polyampholytes derived from aminoacids is discussed. The ability of synthetic, natural and semi-natural polyampholytes to form interpolymer complexes with water-soluble polymers is considered. Most of the research in this area is focused on interpolyelectrolyte complexes of polyampholytes with oppositely charged polyelectrolytes; however, there are also studies demonstrating the formation of hydrogen-bonded complexes. The nature of the complexation is often affected by solution pH and also isoelectric point of polyampholytes. The complexation between polyampholytes and other polymers may lead to formation of colloidal dispersions (nano- and microparticles), liquid-liquid phase separation (called complex coacervation), fully soluble polycomplexes or physically cross-linked gels. A substantial body of studies in this area were focused on the complexes formed by proteins. Application of interpolymer complexes formed by polyampholytes in biotechnology, medicine, encapsulation technologies, separation science, biocatalysis, food science and pharmaceutics is discussed.
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