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基于常规血糖仪的儿茶酚检测仪,用于便携式检测酪氨酸酶和苯甲酸钠。

A Catechol-Meter Based on Conventional Personal Glucose Meter for Portable Detection of Tyrosinase and Sodium Benzoate.

机构信息

Chongqing Key Laboratory of High Active Traditional Chinese Drug Delivery System, Chongqing Medical and Pharmaceutical College, Chongqing 401331, China.

School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China.

出版信息

Biosensors (Basel). 2022 Nov 27;12(12):1084. doi: 10.3390/bios12121084.

Abstract

In this study, the personal glucose meter (PGM) was first used as a fast and user-friendly meter for analyzing catechol (CA) based on the reduction of the mediator K[Fe(CN)] to K[Fe(CN)] in the glucose test strip. Then, an easy, low-cost, and convenient PGM-based method for detecting tyrosinase (TYR) activity and sodium benzoate (SBA) was developed on the basis of the TYR-catalyzed reaction. In this method, CA is oxidized to form -benzoquinone by TYR, thereby reducing the residual amount of CA and the PGM readout. On the other hand, SBA can inhibit the oxidation of CA catalyzed by TYR and increase the residual amount of CA after the enzymatic reaction. Therefore, the activity of TYR is proportional to the difference in the PGM readout of CA, and the concentration of SBA is positively correlated with the residual amount of CA. After the relevant experimental conditions were systematically optimized, the proposed PGM-based method for the detection of TYR and SBA was successfully validated. The liner ranges are 1.0-103.3 U/mL and 6.25-1000 ppm, and the quantification limits are 1.0 U/mL and 6.25 ppm for TYR and SBA, respectively. Moreover, the spiked recovery tests in normal human serum and carbonate beverages (i.e., Cola, Sprite, and Fanta) were performed, and the recoveries (91.6-106.8%) further confirm the applicability of the PGM-based method in real sample analysis.

摘要

在本研究中,我们首次使用个人血糖仪(PGM)作为一种快速且易于使用的仪器,基于葡萄糖测试条中介质 K[Fe(CN)]还原为 K[Fe(CN)]来分析儿茶酚(CA)。然后,基于 TYR 催化反应,我们开发了一种简单、低成本且方便的基于 PGM 的检测酪氨酸酶(TYR)活性和苯甲酸钠(SBA)的方法。在该方法中,CA 被 TYR 氧化为邻苯醌,从而减少 CA 的残留量和 PGM 的读数。另一方面,SBA 可以抑制 TYR 催化的 CA 氧化,从而增加酶反应后 CA 的残留量。因此,TYR 的活性与 CA 的 PGM 读数差异成正比,SBA 的浓度与 CA 的残留量呈正相关。在系统优化相关实验条件后,成功验证了所提出的基于 PGM 的 TYR 和 SBA 检测方法。该方法对 TYR 和 SBA 的线性范围分别为 1.0-103.3 U/mL 和 6.25-1000 ppm,定量限分别为 1.0 U/mL 和 6.25 ppm。此外,在正常人体血清和碳酸盐饮料(即可乐、雪碧和芬达)中进行了加标回收测试,回收率(91.6-106.8%)进一步证实了基于 PGM 的方法在实际样品分析中的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f95/9776396/0b41fdd5e39a/biosensors-12-01084-g001.jpg

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