Novel molecularly imprinted nanogel modified microfluidic paper-based SERS substrate for simultaneous detection of bisphenol A and bisphenol S traces in plastics

双酚A 检出限 微流控 分析物 材料科学 分子印迹聚合物 基质(水族馆) 纳米技术 纳米凝胶 拉曼散射 分子印迹 化学 色谱法 拉曼光谱 选择性 环氧树脂 药物输送 光学 物理 地质学 复合材料 催化作用 海洋学 生物化学
作者
Mirkomil Sharipov,Tae Jun Ju,Shavkatjon Azizov,А. С. Тураев,Yong‐Ill Lee
出处
期刊:Journal of Hazardous Materials [Elsevier]
卷期号:461: 132561-132561 被引量:38
标识
DOI:10.1016/j.jhazmat.2023.132561
摘要

Paper-based surface-enhanced Raman scattering (SERS) optical nanoprobes provide ultrasensitive analyte detection; however, they lack selectivity, making them difficult to use in real-world sample analysis without a pretreatment process. This work describes the design of a microfluidic paper-based SERS substrate based on molecularly imprinted nanogels decorated with silver nanoparticles to simultaneously detect bisphenol A (BPA) and bisphenol S (BPS) traces in plastic toys and receipts. The synthesized nanogels have two characteristics that boost SERS performance: molecularly imprinted cavities that allow for selective adsorption and a wrinkled surface that creates uniformly distributed hot spots. Simple paper-based sensor devices were built as 'drop and read' SERS substrates with a separate reservoir to detect a single target, while advanced SERS platforms were designed as a microfluidic chip with two reservoirs connected by a channel for simultaneous detection of BPA and BPS. The SERS platform with a single reservoir showed outstanding analytical performance for the detection of BPA and BPS, with low detection limits of 0.38 pM and 0.37 pM, respectively. The microfluidic paper-based sensor allowed simultaneous and selective detection of BPA and BPS with detection limits estimated at 0.68 nM and 0.47 nM, respectively. The developed sensors are successfully applied to detect BPA and BPS in plastic products and receipts. Finally, the results obtained with our method showed greater sensitivity than those of commercially available ELISA kits, and the acquired values within the ELISA detection range were in excellent agreement.
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