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聚(磺酸甜菜碱甲基丙烯酸酯)-接枝二氧化硅纳米粒子的相行为及其在蛋白质溶液中的稳定性。

Phase behavior of poly(sulfobetaine methacrylate)-grafted silica nanoparticles and their stability in protein solutions.

机构信息

State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Graduate School of the Chinese Academy of Sciences, Changchun 130022, People's Republic of China.

出版信息

Langmuir. 2011 Dec 20;27(24):15282-91. doi: 10.1021/la2038558. Epub 2011 Nov 29.

Abstract

Biocompatible and zwitterionic poly(sulfobetaine methacrylate) (PSBMA) was grafted onto the surface of initiator-modified silica nanoparticles via surface-initiated atom transfer radical polymerization. The resultant samples were characterized via nuclear magnetic resonance, Fourier transform infrared spectroscopy, transmission electron microscopy, and thermogravimetric analysis. Their molecular weights and molecular weight distributions were determined via gel permeation chromatography after the removal of silica by etching. Moreover, the phase behavior of these polyzwitterionic-grafted silica nanoparticles in aqueous solutions and stability in protein/PBS solutions were systematically investigated. Dynamic light scattering and UV-visible spectroscopy results indicate that the silica-g-PSBMA nanoparticles exhibit an upper critical solution temperature (UCST) in aqueous solutions, which can be controlled by varying the PSBMA molecular weight, ionic strength, silica-g-PSBMA nanoparticle concentration, and solvent polarity. The UCSTs shift toward high temperatures with increasing PSBMA molecular weight and silica-g-PSBMA nanoparticle concentration. However, increasing the ionic strength and solvent polarity leads to a lowering of the UCSTs. The silica-g-PSBMA nanoparticles are stable for at least 72 h in both negative and positive protein/PBS solutions at 37 °C. The current study is crucial for the translation of polyzwitterionic solution behavior to surfaces to exploit their diverse properties in the development of new, smart, and responsive coatings.

摘要

通过表面引发原子转移自由基聚合,将双亲性和两性离子聚(磺基甜菜碱甲基丙烯酸酯)(PSBMA)接枝到引发剂改性的硅纳米粒子表面。通过蚀刻去除二氧化硅后,通过核磁共振、傅里叶变换红外光谱、透射电子显微镜和热重分析对所得样品进行了表征。通过凝胶渗透色谱法测定了它们的分子量和分子量分布。此外,还系统研究了这些聚两性离子接枝硅纳米粒子在水溶液中的相行为和在蛋白质/PBS 溶液中的稳定性。动态光散射和紫外-可见光谱结果表明,硅烷-g-PSBMA 纳米粒子在水溶液中表现出上临界溶解温度(UCST),通过改变 PSBMA 分子量、离子强度、硅烷-g-PSBMA 纳米粒子浓度和溶剂极性可以控制 UCST。UCST 随 PSBMA 分子量和硅烷-g-PSBMA 纳米粒子浓度的增加而向高温移动。然而,增加离子强度和溶剂极性会导致 UCST 降低。在 37°C 下,硅烷-g-PSBMA 纳米粒子在正负蛋白质/PBS 溶液中至少稳定 72 小时。本研究对于将聚两性离子溶液行为转化为表面,以利用其在新型智能响应涂层开发中的各种特性至关重要。

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