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用于心肌梗死和心肌肌钙蛋白I灵敏阻抗适体传感的纳米金刚石与氢取代石墨二炔异质纳米结构

Nanodiamonds and hydrogen-substituted graphdiyne heteronanostructure for the sensitive impedimetric aptasensing of myocardial infarction and cardiac troponin I.

作者信息

Wang Changbao, Li Jiangnan, Kang Mengmeng, Huang Xiaoyu, Liu Yang, Zhou Nan, Zhang Zhihong

机构信息

School of Materials and Chemical Engineering, Zhengzhou University of Light Industry, No. 136, Science Avenue, Zhengzhou, 450001, PR China.

Department of Orthopedics, The First Affiliated Hospital of Zhengzhou University, No. 1, Jianshe East Road, Zhengzhou, 450052, PR China.

出版信息

Anal Chim Acta. 2021 Jan 2;1141:110-119. doi: 10.1016/j.aca.2020.10.044. Epub 2020 Oct 24.

Abstract

A novel heteronanostructure of nanodiamonds (NDs) and hydrogen-substituted graphdiyne (HsGDY) (denoted as HsGDY@NDs) was prepared for the impedimetric aptasensing of biomarkers such as myoglobin (Myo) and cardiac troponin I (cTnI). Basic characterizations revealed that the HsGDY@NDs were composed of nanospheres with sizes of 200-500 nm. In these nanospheres, NDs were embedded within the HsGDY network. The HsGDY@NDs nanostructure, which integrated the good chemical stability and three-dimensional porous networks of HsGDY, and the good biocompatibility and electrochemical activity of NDs, could immobilize diverse aptamer strands and recognize target biomarkers. Compared with HsGDY- and NDs-based aptasensors, the HsGDY@NDs-based aptasensors exhibited superior sensing performances for Myo and cTnI, giving low detection limits of 6.29 and 9.04 fg mL for cTnI and Myo, respectively. In addition, the HsGDY@NDs-based aptasensors exhibited high selectivity, good stability, reproducibility, and acceptable applicability in real human serum. Thus, the construction of HsGDY@NDs-based aptasensor is expected to broaden the application of porous organic frameworks in the sensing field and provide a prospective approach for the early detection of disease biomarkers.

摘要

制备了一种新型的纳米金刚石(NDs)与氢取代石墨二炔(HsGDY)的异质纳米结构(记为HsGDY@NDs),用于对肌红蛋白(Myo)和心肌肌钙蛋白I(cTnI)等生物标志物进行阻抗适配体传感检测。基本表征显示,HsGDY@NDs由尺寸为200 - 500 nm的纳米球组成。在这些纳米球中,NDs嵌入在HsGDY网络中。HsGDY@NDs纳米结构整合了HsGDY良好的化学稳定性和三维多孔网络以及NDs良好的生物相容性和电化学活性,能够固定多种适配体链并识别目标生物标志物。与基于HsGDY和NDs的适配体传感器相比,基于HsGDY@NDs的适配体传感器对Myo和cTnI表现出优异的传感性能,cTnI和Myo的检测限分别低至6.29和9.04 fg/mL。此外,基于HsGDY@NDs的适配体传感器在实际人血清中表现出高选择性、良好的稳定性、重现性和可接受的适用性。因此,构建基于HsGDY@NDs的适配体传感器有望拓宽多孔有机框架在传感领域的应用,并为疾病生物标志物的早期检测提供一种前瞻性方法。

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