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Preparation and characterization of thermo-responsive PDMS surfaces grafted with poly(N-isopropylacrylamide) by benzophenone-initiated photopolymerization

机译:二苯甲酮引发的光聚合反应制备接枝有聚N-异丙基丙烯酰胺的热敏PDMS表面并进行表征

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摘要

In the preparation of a thereto-responsive, poly(N-isopropylacrylamide) (PNIPAAm)-grafted polydimethylsiloxane (PDMS) surface by means of benzophenone-initiated photopolymerization, we observed that thick (> 1 mm) PDMS substrates were much more difficult to be grafted with PNIPAAm than thin ones. Investigations revealed that the shortage of diffused benzophenone molecules in the surface region of the thick substrate might be the reason. By prolonging the time spent for treating the substrate with a benzophenone solution, PNIPAAm could be Successfully grafted onto thick PDMS Substrates. The PNIPAAm-grafted PDMS surface was highly thereto-responsive. The contact angle on a grafted surface increased from 38 to 91 in response to the temperature increase from 20 to 38 degrees C. An electroosmotic flow (EOF) mobility of 5 x 10(-4) cm(2)/Vs was supported by a PNIPAAm-grafted PDMS channel at 50 degrees C, whereas negligible EOF was observed at 20 degrees C. Doxorubicin (DX), an anticancer drug, was adsorbed by the grafted surface at 40 degrees C, and the majority of the adsorbed DX was quickly released from the surface to a stripping solution at 5 degrees C. Osteoblast cells adhered onto the PNIPAAm-grafted PDMS surface and proliferated therein at 37 degrees C, while the cell sheet detached from the surface by lowering the temperature to 25 degrees C without using any enzymatic agent. (c) 2008 Elsevier Inc. All rights reserved.
机译:在通过二苯甲酮引发的光聚合反应制备对之有响应的,聚(N-异丙基丙烯酰胺)(PNIPAAm)接枝的聚二甲基硅氧烷(PDMS)表面的过程中,我们发现厚(> 1 mm)的PDMS基材要困难得多PNIPAAm比薄的嫁接。研究表明,厚基底表面区域中扩散的二苯甲酮分子不足可能是其原因。通过延长用二苯甲酮溶液处理基材的时间,可以将PNIPAAm成功地接枝到厚的PDMS基材上。 PNIPAAm接枝的PDMS表面对其高度敏感。随着温度从20到38摄氏度的增加,接枝表面上的接触角从38增加到91。电渗流(EOF)迁移率为5 x 10(-4)cm(2)/ Vs PNIPAAm接枝的PDMS通道在50摄氏度时发生,而在20摄氏度时观察到的EOF可以忽略不计。抗癌药阿霉素(DX)在40摄氏度时被接枝表面吸附,大部分吸附的DX迅速释放从表面到5摄氏度的剥离溶液。成骨细胞粘附在PNIPAAm移植的PDMS表面上,并在37摄氏度下增殖,而细胞片通过不使用任何酶将温度降低至25摄氏度而从表面脱离代理商。 (c)2008 Elsevier Inc.保留所有权利。

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