Materials Chemistry Research Center, Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Khon Kaen University, Khon Kaen, 40002, Thailand.
Anal Sci. 2021 Dec 10;37(12):1741-1748. doi: 10.2116/analsci.21P090. Epub 2021 Jun 25.
This research work aims to propose an extraction method using chitosan as the sorbent and gold nanoparticles (AuNPs) as the colorimetric sensor for the development of a simple, cost-effective, rapid, sensitive, and selective detection method for histidine. The colorimetric assay is based on the aggregation of AuNPs in the presence of Hg ions and histidine. The state of AuNPs generally changes from dispersion to aggregation. The change in state is accompanied by a corresponding change in color (from red wine to blue). Therefore, the solid phase extraction (SPE) method using chitosan as the sorbent was used to extract the AuNPs to improve the sensitivity of detection. It was found that the extraction by means of a sensor system using chitosan could increase the detection signal for histidine by 10 times. The calibration curve, which is the plot of absorbance ratio (A/A) against the concentration of histidine, shows a linear relation in the concentration range of 100 - 800 nM. The limit of detection (LOD) and limit of quantitation (LOQ) of the method were found to be 99.88 and 107.45 nM, respectively. Good recoveries were also obtained (range: 99.75 - 104.43%) with relative standard deviations (RSDs) below 5.89% in real water samples. Moreover, this method can be used for the selective detection of histidine even in the presence of other amino acids. The proposed method has been successfully used in the determination of histidine in mineral water samples.
本研究旨在提出一种使用壳聚糖作为吸附剂和金纳米粒子(AuNPs)作为比色传感器的提取方法,用于开发一种简单、经济、快速、灵敏和选择性检测组氨酸的方法。比色测定法基于在汞离子和组氨酸存在下 AuNPs 的聚集。AuNPs 的状态通常从分散变为聚集。状态的变化伴随着相应的颜色变化(从红酒变为蓝色)。因此,使用壳聚糖作为吸附剂的固相萃取(SPE)方法用于提取 AuNPs 以提高检测灵敏度。结果发现,使用壳聚糖作为传感器系统的萃取可以将组氨酸的检测信号提高 10 倍。吸光度比(A/A)与组氨酸浓度的校准曲线显示在 100-800 nM 的浓度范围内呈线性关系。该方法的检测限(LOD)和定量限(LOQ)分别为 99.88 和 107.45 nM。在实际水样中,还获得了良好的回收率(范围:99.75-104.43%),相对标准偏差(RSD)低于 5.89%。此外,即使存在其他氨基酸,该方法也可以用于组氨酸的选择性检测。该方法已成功用于矿泉水样品中组氨酸的测定。