Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering , Southwest University , Chongqing 400715 , PR China.
School of Chemistry and Chemical Engineering , Chongqing University of Technology , Chongqing 400054 , PR China.
Anal Chem. 2019 Feb 5;91(3):2273-2278. doi: 10.1021/acs.analchem.8b04863. Epub 2019 Jan 8.
Dispersion promotion of nanomaterials can significantly enhance their catalytic activities. With a new DNA-templated in situ synthesis approach, we report the preparation of highly dispersed AuNPs on nitrogen-doped graphene sheets (NGS) with significantly improved electrocatalytic ability for the monitoring of nitric oxide (NO) released from live cancer cells. The template DNA is adsorbed on NGS via π-π stacking, and the Au precursor chelates along the DNA lattice through dative bonding. Subsequent introduction of the reducing agent leads to in situ nucleation and growth of AuNPs, eventually resulting in highly dispersed AuNPs on NGS. Because of the synergistic enhancement of the catalytic activities of AuNPs and NGS, as well as the high dispersion of AuNPs, such a nanocomposite shows significant electro-oxidation capability toward NO, leading to a highly sensitive subnanomolar detection limit for NO in vitro. More importantly, the laminin glycoproteins can be readily adsorbed on the surface of the nanomaterials to render excellent biocompatibility for the adhesion and proliferation of live cells, enabling the biointerface for electrochemical detection of NO released from live cancer cells.
纳米材料的分散促进作用可以显著提高其催化活性。我们采用一种新的 DNA 模板原位合成方法,制备了高度分散在氮掺杂石墨烯片(NGS)上的 AuNPs,其对活癌细胞释放的一氧化氮(NO)的电催化监测能力得到了显著提高。模板 DNA 通过π-π 堆积吸附在 NGS 上,Au 前驱体通过配位键沿着 DNA 晶格螯合。随后引入还原剂导致 AuNPs 的原位成核和生长,最终在 NGS 上得到高度分散的 AuNPs。由于 AuNPs 和 NGS 的协同增强催化活性以及 AuNPs 的高分散性,这种纳米复合材料对 NO 表现出显著的电氧化能力,从而在体外对 NO 实现了高灵敏度的亚纳摩尔检测限。更重要的是,层粘连蛋白糖蛋白可以很容易地吸附在纳米材料表面,从而使活细胞的粘附和增殖具有优异的生物相容性,实现了电化学检测活癌细胞释放的 NO 的生物界面。