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基于绿色合成分子印迹聚合物的电化学纳米传感器的研制及其用于血清和自来水中 N-亚硝基二甲胺(NDMA)的测定。

Development of a green-synthesized molecularly imprinted polymer-based electrochemical nanosensor for the determination of N-nitrosodimethylamine (NDMA) in serum and tap water.

机构信息

School of Studies in Environmental Chemistry, Jiwaji University, Gwalior, M.P., India.

Department of Analytical Chemistry, Faculty of Pharmacy, Ankara University, Ankara, Turkey.

出版信息

Mikrochim Acta. 2024 Nov 28;191(12):769. doi: 10.1007/s00604-024-06850-y.

Abstract

N-nitrosodimethylamine (NDMA) was determined using a molecularly imprinted polymer (MIP)-based electrochemical sensor. Green-synthesized silver nanoparticles were functionalized with cysteamine to enhance their integration into the electrode surface, which was used to modify a glassy carbon electrode (GCE). Furthermore, a MIP-based electrochemical sensor was constructed via electropolymerization of 3-aminophenyl boronic acid (3-APBA) as a conjugated functional monomer in the presence of lithium perchlorate (LiClO) solution as a dopant, chitosan as a carrier natural polymer, and NDMA as a template/target molecule. The polymer film was characterized by scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). The analytical performance of the silver nanomaterial-based MIP-based electrochemical (AgNPs@Chitosan/3-APBA@MIP-GCE) sensor was evaluated under optimized conditions. The linear range of NDMA was 1.0 × 10-1.0 × 10 M (0.1-1.0 pM), with a limit of detection (LOD) of 3.63 × 10 M (3.63 fM) using differential pulse voltammetry (DPV). Method validation figured out that the developed MIP-based electrochemical nanosensor exhibited excellent selectivity, accuracy, and precision, which was shown by the analysis of synthetic serum samples and tap water. The LOD and LOQ in serum samples were 17.8 fM and 59.5 fM, respectively, which were in agreement with the developed method. Good recovery results confirm the successful application of the method in serum and tap water samples. The selectivity of the developed AgNPs@Chitosan/3-APBA@MIP-GCE sensor for NDMA was demonstrated in the presence of NDEA, sartans (valsartan, losartan, irbesartan, candesartan, telmisartan), and potential interferents that are possibly present in biological fluids (dopamine, ascorbic acid, uric acid) besides ionic species (sodium, chloride, potassium, nitrate, magnesium, sulfate) and common analgesic paracetamol.

摘要

N-亚硝基二甲胺(NDMA)采用基于分子印迹聚合物(MIP)的电化学传感器进行测定。使用半胱氨酸功能化绿色合成的银纳米粒子来增强其与电极表面的整合,该电极表面用于修饰玻碳电极(GCE)。此外,通过在高氯酸锂(LiClO)溶液存在下聚合 3-氨苯基硼酸(3-APBA)作为共轭功能单体,在壳聚糖作为载体天然聚合物和 NDMA 作为模板/靶分子的情况下,构建基于 MIP 的电化学传感器。聚合物薄膜通过扫描电子显微镜(SEM)和电化学阻抗谱(EIS)进行表征。在优化条件下评估了基于银纳米材料的基于 MIP 的电化学(AgNPs@Chitosan/3-APBA@MIP-GCE)传感器的分析性能。NDMA 的线性范围为 1.0×10-1.0×10 M(0.1-1.0 pM),使用差分脉冲伏安法(DPV)的检测限(LOD)为 3.63×10 M(3.63 fM)。方法验证表明,所开发的基于 MIP 的电化学纳米传感器表现出优异的选择性、准确性和精密度,这通过对合成血清样品和自来水的分析得到证明。在血清样品中的 LOD 和 LOQ 分别为 17.8 fM 和 59.5 fM,与所开发的方法一致。良好的回收率结果证实了该方法在血清和自来水中样品中的成功应用。在可能存在于生物流体中的 NDEA、沙坦类(缬沙坦、氯沙坦、厄贝沙坦、坎地沙坦、替米沙坦)和潜在干扰物(多巴胺、抗坏血酸、尿酸)以及离子种类(钠、氯、钾、硝酸盐、镁、硫酸盐)和常见的止痛扑热息痛存在的情况下,开发的 AgNPs@Chitosan/3-APBA@MIP-GCE 传感器对 NDMA 的选择性得到了证明。

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