4.7 Article

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

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 332, 期 1, 页码 85-90

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2008.12.046

关键词

Polydimethylsiloxane; Poly(N-isopropylacrylamide); Thermal-responsive surface; Drug release; Cell culture; Microfluidic chip

资金

  1. National Science Foundation of China [20675072, 20890020]
  2. National Basic Research Program of China [2007CB714502]

向作者/读者索取更多资源

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.

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