A disposable dual-mode electrochemical/colorimetric paper-based analytical device for simultaneous detection of hydroquinone and mercury ion

IF 6.1 1区 化学 Q1 CHEMISTRY, ANALYTICAL Talanta Pub Date : 2025-11-01 Epub Date: 2025-04-25 DOI:10.1016/j.talanta.2025.128166
Kiattisak Promsuwan , Sariktiya Chuenjitt , Ananya Kongsuwan , Jenjira Saichanapan , Asamee Soleh , Kasrin Saisahas , Kritsada Samoson , Sangay Wangchuk , Warakorn Limbut
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Abstract

In this work, we developed a paper-based analytical device (PAD) for the simultaneous detection of hydroquinone (HQ) and mercury (Hg2+) in skin whitening products. The device integrates electrochemical analysis and colorimetric detection (E/C-PAD). HQ was determined electrochemically using a bismuth oxide-graphene ink electrode screen-printed on the paper (Bi2O3-GI/PAD). Hg2+ was detected by colorimetry using a gel of Thio Michler’s Ketone and carboxymethylcellulose coated on paper (TMK-CMC gel/PAD). The morphology and structure of the E/C-PAD were characterized by scanning electron microscopy, energy dispersive X-ray analysis, and Fourier transform infra-red spectroscopy. The electrochemical properties of Bi2O3-GI/PAD were investigated, and HQ was quantified by differential pulse voltammetry. The colorimetric determination of Hg2+ was based on the value of the red channel obtained from processing digital images of reaction products. Once optimized, the Bi2O3-GI/PAD determined HQ concentrations from 1.0 to 20 μg mL−1 and 20 to 100 μg mL−1, with an LOD of 0.22 μg mL−1 and an LOQ of 0.74 μg mL−1. The TMK-CMC gel/PAD detected Hg2+ from 0.05 to 0.50 μg mL−1 and 0.50 to 40 μg mL−1, with an LOD of 0.01 μg mL−1 and an LOQ of 0.04 μg mL−1. The developed E/C-PAD demonstrated good reproducibility and stability, outstanding anti-interference capability, and high precision for the simultaneous detection of HQ and Hg2+ in real whitening products, showing results consistent with spectrophotometry. Moreover, this paper-based device is the first to combine electrochemical analysis with colorimetry for the simultaneous detection of HQ and Hg2+.

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一种同时检测对苯二酚和汞离子的一次性双模电化学/比色纸分析装置
在这项工作中,我们开发了一种同时检测皮肤美白产品中对苯二酚(HQ)和汞(Hg2+)的纸基分析装置(PAD)。该装置集成了电化学分析和比色检测(E/C-PAD)。利用丝网印刷在纸上的氧化铋-石墨烯油墨电极(Bi2O3-GI/PAD),电化学测定了HQ。采用比色法检测Hg2+,比色法采用噻吩·米歇尔酮-羧甲基纤维素纸包覆凝胶(TMK-CMC凝胶/PAD)。采用扫描电镜、x射线能谱和红外光谱对E/C-PAD的形貌和结构进行了表征。研究了Bi2O3-GI/PAD的电化学性能,并采用差分脉冲伏安法测定了HQ的含量。Hg2+的比色测定是基于处理反应产物的数字图像得到的红色通道值。优化后,Bi2O3-GI/PAD测定的HQ浓度范围为1.0 ~ 20 μ mL−1和20 ~ 100 μ mL−1,LOD为0.22 μ mL−1,LOQ为0.74 μ mL−1。TMK-CMC凝胶/PAD对Hg2+的检测范围为0.05 ~ 0.50 μ mL−1和0.50 ~ 40 μ mL−1,检出限为0.01 μ mL−1,检出限为0.04 μ mL−1。所建立的E/C-PAD重现性、稳定性好,抗干扰能力强,同时检测实际美白产品中HQ和Hg2+的精密度高,结果与分光光度法一致。此外,该纸基装置首次将电化学分析与比色法相结合,用于同时检测HQ和Hg2+。
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来源期刊
Talanta
Talanta 化学-分析化学
CiteScore
12.30
自引率
4.90%
发文量
861
审稿时长
29 days
期刊介绍: Talanta provides a forum for the publication of original research papers, short communications, and critical reviews in all branches of pure and applied analytical chemistry. Papers are evaluated based on established guidelines, including the fundamental nature of the study, scientific novelty, substantial improvement or advantage over existing technology or methods, and demonstrated analytical applicability. Original research papers on fundamental studies, and on novel sensor and instrumentation developments, are encouraged. Novel or improved applications in areas such as clinical and biological chemistry, environmental analysis, geochemistry, materials science and engineering, and analytical platforms for omics development are welcome. Analytical performance of methods should be determined, including interference and matrix effects, and methods should be validated by comparison with a standard method, or analysis of a certified reference material. Simple spiking recoveries may not be sufficient. The developed method should especially comprise information on selectivity, sensitivity, detection limits, accuracy, and reliability. However, applying official validation or robustness studies to a routine method or technique does not necessarily constitute novelty. Proper statistical treatment of the data should be provided. Relevant literature should be cited, including related publications by the authors, and authors should discuss how their proposed methodology compares with previously reported methods.
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