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|Title:||Adsorption of plasmid DNA onto, N,N′-(dimethylamino)ethyl-methacrylate graft-polymerized poly-l-lactic acid film surface for promotion of in-situ gene delivery|
|Source:||Jiang, T., Chang, J.B., Wang, C., Ding, Z., Chen, J., Zhang, J., Kang, E.-T. (2007-06). Adsorption of plasmid DNA onto, N,N′-(dimethylamino)ethyl-methacrylate graft-polymerized poly-l-lactic acid film surface for promotion of in-situ gene delivery. Biomacromolecules 8 (6) : 1951-1957. ScholarBank@NUS Repository. https://doi.org/10.1021/bm0700486|
|Abstract:||The surface of biodegradable poly-L-lactic acid (PLLA) film was modified with N,N'-(dimethylamino)ethyl-methacrylate (DMAEMA) via UV-induced graft copolymerization, and plasmid DNA molecules were adsorbed onto the surface of modified PLLA film by electrostatic interactions with cationic DMAEMA polymer. We characterized the structure of the modified PLLA film surface by Fourier transform infrared attenuated total reflection (FTIR-ATR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The weight-average molecular weight (Mw) of grafted DMAEMA polymer chains was estimated from the elution time of gel filtration chromatography. C.I. Acid Orange 7 dyeing results indicated that graft density of DMAEMA on PLLA film increased with the UV irradiation time and then reached a saturated value. DNA adsorption density was proportioned to graft density of DMAEMA. Mouse fibroblast L929 cell line was cultured on modified PLLA films, and cell viability and gene transfection efficiency were monitored after 2 days culture. It was found that the DMAEMA grafted PLLA film had obvious cytotoxicity to the cells. On the contrary, cytotoxicity of the surface was highly decreased after adsorption with plasmid DNA. This DNA adsorbed DMAEMA modified PLLA showed the ability to deliver DNA into mammalian cells cultured on the surface with high-transfection efficiency at a low DNA amount. The present results suggest that the DMAEMA grafted PLLA has potentiality to be used as a safe and effective gene delivery system in gene-activated materials. © 2007 American Chemical Society.|
|Appears in Collections:||Staff Publications|
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