有机长余辉纳米探针介导的LFIA胃蛋白酶原检测

Ultra-long organo-phosphorescent nanoprobe for detection of pepsinogen by lateral flow immunoassay

  • 摘要: 有机长余辉材料具有激发态性能丰富、成本低、柔韧性好、易于合成、发光寿命超长等优点,在背景荧光衰减后,其余辉的收集能有效排除背景光干扰。在此基础上,该文构建了一个基于有机长余辉纳米探针的侧流免疫层析UOP-LFIAs)检测平台。首先,制备并合成长余辉晶体,然后通过在表面涂覆聚乙烯吡咯烷酮和羧甲基纤维素的步骤获得长余辉溶液。通过抗体偶联获得有机长余辉纳米探针,再设计制作出一种便携式UOP-LFIAs检测装置。最后,采用便携式UOP-LFIAs检测装置检测胃蛋白酶原(PG)Ⅰ和Ⅱ。结果表明,PG I和PG II的检测限分别为0.36 ng/mL和0.57 ng/mL,检测范围分别为0.36~1200 ng/mL和0.57~500 ng/mL。平均回收率分别为101.30%和99.30%。该研究所构造的UOP-LFIAs检测平台不仅制备过程简便、快速、高效且经济,而且能有效地降低背景光信号的干扰,提升磷光化效率。此外,该平台实现了PG I和PG II的联合检测,仅需5 min即可快速获得结果,为即时检测提供了一个高效的疾病检测平台。

     

    Abstract: Ultra-long organic phosphorescent materials have the advantages of rich excited state properties, low price and easy to synthesize, good flexibility, ultra-long luminescence lifetime. After the fluorescence decay of the background, the collection of the remaining light can effectively eliminate the background light interference. Based on this, a Lateral Flow Immunochromatographic Detection Platform Based on Ultra-Long Organo-Phosphorescent Nanoprobes (UOP-LFIAs) constructed by authors is presented in this paper. Firstly, long afterglow crystals were prepared and synthesized, and then the long afterglow solution was obtained by one-step coating polyvinylpyrrolidone and carboxymethyl cellulose on the surface. Next, it was coupled with antibodies to obtain ultra-long organic afterglow phosphorescent nanoprobes. A portable UOP-LFIAs test strip detection analyzer was then designed and manufactured. Finally, Pepsinogen (PG) I and II were detected by using a portable UOP-LFIAs detection device. The results show that the detection limits were 0.36 ng/mL and 0.57 ng/mL for PG I and PG II, with respective detection ranges of 0.36-1200 ng/mL and 0.57-500 ng/mL. The average recoveries were 101.30% and 99.30%, respectively. It is concluded that the UOP-LFIAs assay platform established in this study is not only simple, rapid, cost-effective and suitable for macro-preparation, but also can effectively reduce the interference of background light signal and enhance the phosphorescence efficiency, thereby improving the detection sensitivity. Additionally, the platform enables the combined detection of PG I and PG II, providing results in just 5 minutes. This development offers a powerful tool for bedside disease detection.

     

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