Song Yang, Jin Jingyi, Hu Liuling, Hu Bingqian, Wang Mengyao, Guo Lilong, Lv Xiyan
Tianjin Key Laboratory of Animal and Plant Resistance, Tianjin Normal University, Tianjin 300387, China.
Foods. 2023 Sep 15;12(18):3445. doi: 10.3390/foods12183445.
This study synthesized the NaGdF@NaGdF: Yb, Tm@NaGdF: Yb, Nd upconversion nanoparticles (UCNPs), combined with another three-layer structure NaYF@NaYF: Yb, Er@NaYF UCNPs, with a core-shell-shell structure, effectively suppressing fluorescence quenching and significantly improving upconversion luminescence efficiency. Two types of modified UCNPs were coupled with antibodies against fenpropathrin and procymidone to form signal probes, and magnetic nanoparticles were coupled with antigens of fenpropathrin and procymidone to form capture probes. A rapid and sensitive fluorescence immunoassay for the simultaneous detection of fenpropathrin and procymidone was established based on the principle of specific binding of antigen and antibody and magnetic separation technology. Under the optimal competitive reaction conditions, different concentrations of fenpropathrin and procymidone standards were added to collect the capture probe-signal probe complex. The fluorescence values at 542 nm and 802 nm were measured using 980 nm excitation luminescence. The results showed that the detection limits of fenpropathrin and procymidone were 0.114 µg/kg and 0.082 µg/kg, respectively, with sensitivities of 8.15 µg/kg and 7.98 µg/kg, and they were applied to the detection of fenpropathrin and procymidone in tomatoes, cucumbers, and cabbage. The average recovery rates were 86.5100.2% and 85.61102.43%, respectively, with coefficients of variation less than 10%. The results showed good consistency with the detection results of high-performance liquid chromatography, proving that this method has good accuracy and is suitable for the rapid detection of fenpropathrin and procymidone in food.
本研究合成了NaGdF@NaGdF:Yb,Tm@NaGdF:Yb,Nd上转换纳米颗粒(UCNPs),并将其与另一种具有核壳壳结构的三层结构NaYF@NaYF:Yb,Er@NaYF UCNPs相结合,有效抑制了荧光猝灭并显著提高了上转换发光效率。将两种修饰的UCNPs与甲氰菊酯和腐霉利抗体偶联形成信号探针,将磁性纳米颗粒与甲氰菊酯和腐霉利抗原偶联形成捕获探针。基于抗原与抗体的特异性结合原理和磁分离技术,建立了一种同时检测甲氰菊酯和腐霉利的快速灵敏荧光免疫分析方法。在最佳竞争反应条件下,加入不同浓度的甲氰菊酯和腐霉利标准品,收集捕获探针-信号探针复合物。用980nm激发发光测量542nm和802nm处的荧光值。结果表明,甲氰菊酯和腐霉利的检测限分别为0.114μg/kg和0.082μg/kg,灵敏度分别为8.15μg/kg和7.98μg/kg,并将其应用于番茄、黄瓜和白菜中甲氰菊酯和腐霉利的检测。平均回收率分别为86.5%100.2%和85.61%102.43%,变异系数小于10%。结果与高效液相色谱检测结果具有良好的一致性,证明该方法具有良好的准确性,适用于食品中甲氰菊酯和腐霉利的快速检测。