Wang Ai-Jun, Xu Jing-Juan, Chen Hong-Yuan
Key Lab of Analytical Chemistry for Life Science (MOE), School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
J Chromatogr A. 2007 Apr 13;1147(1):120-6. doi: 10.1016/j.chroma.2007.02.030. Epub 2007 Feb 14.
In this paper, a simple and green modification method is developed for biomolecules analysis on poly(dimethylsiloxane) (PDMS) microchip with successful depression of nonspecific biomolecules adsorption. O-[(N-succinimdyl)succiny]-o'-methyl-poly(ethylene glycol) was explored to form hydrophilic surface via in-situ grafting onto pre-coated chitosan (Chit) from aqueous solution in the PDMS microchannel. The polysaccharide chains backbone of Chit was strongly attracted onto the surface of PDMS via hydrophobic interaction combined with hydrogen bonding in an alkaline medium. The methyl-poly(ethylene glycol) (mPEG) could produce hydrophilic domains on the mPEG/aqueous interface, which generated brush-like coating in this way and revealed perfect resistance to nonspecific adsorption of biomolecules. This strategy could greatly improve separation efficiency and reproducibility of biomolecules. Amino acids and proteins could be efficiently separated and successfully detected on the coated microchip coupled with end-channel amperometric detection at a copper electrode. In addition, it offered an effective means for preparing biocompatible and hydrophilic surface on microfluidic devices, which may have potential use in the biological analysis.
本文开发了一种简单且绿色的修饰方法,用于在聚二甲基硅氧烷(PDMS)微芯片上进行生物分子分析,成功抑制了非特异性生物分子吸附。探索了O-[(N-琥珀酰亚胺基)琥珀酰基]-O'-甲基聚乙二醇通过在PDMS微通道中从水溶液中原位接枝到预涂覆的壳聚糖(Chit)上形成亲水性表面。在碱性介质中,壳聚糖的多糖链主链通过疏水相互作用和氢键强烈吸附在PDMS表面。甲基聚乙二醇(mPEG)可以在mPEG/水界面上产生亲水性区域,从而形成刷状涂层,并对生物分子的非特异性吸附表现出完美的抗性。该策略可以大大提高生物分子的分离效率和重现性。氨基酸和蛋白质可以在涂覆的微芯片上与铜电极的通道末端安培检测相结合,实现有效分离和成功检测。此外,它为在微流控装置上制备生物相容性和亲水性表面提供了一种有效手段,这在生物分析中可能具有潜在用途。