化学
免疫分析
光热治疗
配体(生物化学)
纳米技术
色谱法
生物化学
受体
生物
抗体
材料科学
免疫学
作者
Zongyou Chen,Jiaqi Yin,Shihai Huang,Keyang Lai,Juan Peng,Weihua Lai
标识
DOI:10.1021/acs.analchem.5c02864
摘要
The photothermal lateral flow immunoassay (LFIA) has garnered considerable attention, owing to its suitability for on-site quantitative detection. Furthermore, it has distinct advantages in further constructing sensitive detection methods for low-concentration targets. In this study, we employed a ligand engineering strategy to synthesize Fe3+-chelated quinone nanoparticles (FQNPs). Quinones with different structures, namely, naphthazarin, quinizarine, purpurin, and tetrahydroxyanthraquinone (THAQ), served as ligands to fabricate a series of FQNPs. Among them, FQNPs based on tetrahydroxyanthraquinone (FQNPs-T) exhibited exceptional light absorption ability (molar extinction coefficient = 12.71 × 1010 M-1 cm-1) and photothermal conversion efficiency (η = 60.32%). Subsequently, a photothermal LFIA based on FQNPs-T (FQNPs-LFIA) was developed for the detection of chlorantraniliprole (CHL) in apple and chili. The FQNPs-LFIA enables the highly sensitive detection of CHL within 25 min with a limit of detection (LOD) of 0.021 ng mL-1, which was 8.77-fold lower than that of conventional gold nanoparticle-based LFIA (0.193 ng mL-1). The average recovery rates of FQNPs-LFIA were 84.29-113.58%, with coefficients of variation of 4.20-14.84%. Overall, this study demonstrates the potential of FQNPs-LFIA for the sensitive and accurate detection of CHL, and it paves the way for the rapid screening of other food contaminants.
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