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银纳米板用于通过蚀刻/聚集/融合步骤比色测定人血浆和鱼肉中的黄嘌呤。

Silver Nanoplates for Colorimetric Determination of Xanthine in Human Plasma and in Fish Meat via Etching/Aggregation/Fusion Steps.

机构信息

Department of Chemistry, Soochow University, No. 70, LinShih Rd., Shih-Lin, Taipei 11102, Taiwan.

出版信息

Sensors (Basel). 2020 Oct 9;20(20):5739. doi: 10.3390/s20205739.

Abstract

Silver nanoplates (AgP) were prepared and used in a colorimetric method for the evaluation of Xanthine (Xan) in blood plasma and fish meat. The detection mechanism for Xan was observed to occur via etching of AgP particles/aggregation/fusion steps, resulting in a color change from blue to grey. First, the basic Xan solution is adsorbed through partial substitution of capping molecules around the AgP with Xan, and then intermolecular hydrogen bonds form between AgP and AgP. Subsequently, the titrant Xan solution further etches the AgP and finally fuses particles together. Owing to the step by step mechanism, the response range towards Xan has two linear regression ranges: 0.15-0.60 μM and 0.61-3.00 μM, respectively. The detection limit in the range of 0.15-0.60 μM is 0.011 μM (S/N = 3). AgP exhibits good selectivity for Xan over other potential interferents such as amino acids and blood proteins. AgP achieves rapid detection of Xan and can be applied to the satisfactory determination of Xan in blood plasma and fish meat. This colorimetric sensor is easy to use, cost effective, fast, selective and user friendly.

摘要

银纳米板(AgP)被制备并用于比色法评估血浆和鱼肉中的黄嘌呤(Xan)。观察到 Xan 的检测机制是通过 AgP 颗粒的蚀刻/聚集/融合步骤发生的,导致颜色从蓝色变为灰色。首先,通过 Xan 部分取代 AgP 周围的封端分子来吸附基本的 Xan 溶液,然后在 AgP 之间形成分子间氢键。随后,滴定剂 Xan 溶液进一步蚀刻 AgP,最终使颗粒融合在一起。由于这种逐步的机制,AgP 对 Xan 的响应范围具有两个线性回归范围:分别为 0.15-0.60 μM 和 0.61-3.00 μM。在 0.15-0.60 μM 范围内的检测限为 0.011 μM(S/N = 3)。AgP 对 Xan 具有良好的选择性,优于其他潜在干扰物,如氨基酸和血液蛋白。AgP 可以快速检测 Xan,并可用于满意地测定血浆和鱼肉中的 Xan。这种比色传感器易于使用、经济高效、快速、选择性好且用户友好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6166/7599804/0e120f9403dc/sensors-20-05739-sch001.jpg

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