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均聚物自组装成稳定的纳米颗粒:温敏型聚(烷基丙烯酸酯)中疏水缔合和氢键协同作用。

Homopolymer self-assembly into stable nanoparticles: concerted action of hydrophobic association and hydrogen bonding in thermoresponsive poly(alkylacrylic acid)s.

机构信息

Institute of Experimental Physics, Slovak Academy of Sciences, Watsonova 47, 040 01 Košice, Slovakia.

出版信息

J Phys Chem B. 2012 Mar 1;116(8):2356-64. doi: 10.1021/jp208445p. Epub 2012 Feb 14.

Abstract

A new approach to polymer self-assembly was presented recently [M. Sedlák, Č. Koňák, J. Dybal, Macromolecules 2009, 2, 7430-7438 and 7439-7446.] (1, 2) where stable polymeric nanoparticles were formed from poly(ethylacrylic acid) homopolymers without any assembly triggering additives, simply by heating polymer solution under conditions of thermosensitivity to certain temperature. In the current Article, we present successful results on poly(propylacrylic acid), which is a more hydrophobic polymer. We also present results on a less hydrophobic polymer from this series, poly(methacrylic acid), from which nanoparticles cannot be formed. Comparison of results on all three polymers gives a solid physicochemical insight and supports the molecular mechanism of the self-assembly previously suggested: The solvent quality gradually worsens upon heating of a thermosensitive polymer solution, and polymer-polymer contacts are preferred over polymer-solvent contacts, which leads to the formation of polymer assemblies. The presence of a significant amount of charge on chains prevents macroscopic phase separation. Upon subsequent cooling to laboratory temperature, the assemblies (nanoparticles) should eventually dissolve; however, this is not the case due to the fact that polymer chains brought to a close proximity at elevated temperatures become hydrogen-bonded. In addition, hydrogen bonds strengthen upon cooling. Mainly carboxylic-carboxylate hydrogen bonds (COOH····COO(-)) are responsible for the irreversibility of the process and the stability of nanoparticles. Conclusions are supported by results from static and dynamic light scattering, FTIR spectroscopy, and cryo-TEM microscopy. Size of nanoparticles can be monitored during the growth and custom-tailored by tuning critical parameters, especially the degree of ionization, temperature, and time of heating. Nanoparticles are stable over long periods of time. They are stable in a broad range of salt concentrations, including physiological conditions, and possess a mild acceptable degree of polydispersity.

摘要

最近提出了一种新的聚合物自组装方法[M. Sedlák、Č. Koňák、J. Dybal,Macromolecules 2009,2,7430-7438 和 7439-7446](1,2),其中通过加热聚合物溶液至对特定温度敏感的条件下,无需任何组装触发添加剂,即可从聚(乙基丙烯酸)均聚物形成稳定的聚合物纳米颗粒。在当前文章中,我们展示了对疏水性更强的聚合物聚(丙基丙烯酸)的成功结果。我们还展示了该系列中疏水性较低的聚合物聚(甲基丙烯酸)的结果,无法从该聚合物形成纳米颗粒。对所有三种聚合物的结果进行比较提供了坚实的物理化学见解,并支持了先前提出的自组装的分子机制:随着热敏聚合物溶液的加热,溶剂质量逐渐恶化,聚合物-聚合物接触优先于聚合物-溶剂接触,这导致聚合物组装的形成。链上存在大量电荷可防止宏观相分离。随后冷却至实验室温度时,组装体(纳米颗粒)最终应该溶解;然而,由于在高温下靠近的聚合物链形成氢键,因此情况并非如此。此外,氢键在冷却时会增强。主要是羧酸-羧酸酯氢键(COOH····COO(-))负责该过程的不可逆性和纳米颗粒的稳定性。静态和动态光散射、傅里叶变换红外光谱和低温透射电子显微镜显微镜的结果支持了结论。可以在生长过程中监测纳米颗粒的大小,并通过调整关键参数(尤其是离子化程度、温度和加热时间)对其进行定制。纳米颗粒在很长一段时间内都很稳定。它们在广泛的盐浓度范围内稳定,包括生理条件,并且具有可接受的轻度多分散性。

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