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单底物功能化氧化钼纳米酶用于黄嘌呤氧化酶活性的特异性比色监测。

Single substrate-functionalized molybdenum oxide nanozyme for specific colorimetric monitoring of xanthine oxidase activity.

机构信息

Institute of Biomedical Engineering, College of Life Sciences, School of Tourism and Geography Sciences, Qingdao University, Qingdao, 266071, China.

The Affiliated Hospital of Qingdao University, Qingdao, 266003, China.

出版信息

Mikrochim Acta. 2024 Jan 16;191(2):99. doi: 10.1007/s00604-023-06149-4.

Abstract

Xanthine-functionalized molybdenum oxide nanodots (X-MoO NDs) with peroxidase (POD)-like activity were developed for selective, sensitive, and facile colorimetric quantification of xanthine oxidase (XO). Xanthine functionalization can not only be favorable for the successful nanozyme preparation, but also for the specific recognition of XO as well as the simultaneous generation of hydrogen peroxide, which was subsequently transformed into hydroxyl radical to oxidize the chromogenic reagent based on the POD-like catalysis. Under the optimized conditions, the colorimetric biosensing platform was established for XO assay without addition of further substrates, showing good linearity relationship between absorbance difference (ΔA) and XO concentrations in the range 0.05-0.5 U/mL (R = 0.998) with a limit of detection (LOD) of 0.019 U/mL. The quantification of XO occurs in 25 min, which is superior to the previously reported and commercial XO assays. The proposed method has been successfully used in the assay of human serum samples, showing its high potential in the field of clinical monitoring.

摘要

具有过氧化物酶(POD)样活性的黄嘌呤功能化氧化钼纳米点(X-MoO NDs)被开发用于黄嘌呤氧化酶(XO)的选择性、灵敏和简便的比色定量。黄嘌呤功能化不仅有利于成功制备纳米酶,而且有利于 XO 的特异性识别以及同时产生过氧化氢,过氧化氢随后在 POD 样催化作用下转化为羟自由基,氧化基于 POD 样催化的显色试剂。在优化条件下,建立了无需添加进一步底物的 XO 比色生物传感平台,在 0.05-0.5 U/mL 范围内吸光度差(ΔA)与 XO 浓度之间呈现良好的线性关系(R=0.998),检测限(LOD)为 0.019 U/mL。XO 的定量发生在 25 分钟内,优于先前报道的和商业 XO 测定方法。该方法已成功用于人血清样品的测定,显示出其在临床监测领域的高潜力。

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