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A fluorescence immunoassay based on CdTe?:?Zn/ZnS quantum dots for the rapid detection of bacteria, taking Delftia tsuruhatensis CM’13 as an example

机译:以CdTe?:?Zn / ZnS量子点为基础的荧光免疫分析法,用于细菌的快速检测,以Derftia tsuruhatensis CM’13为例

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A fluorescence immunoassay has been widely applied in different fields due to its high sensitivity, simple operations, and high accuracy. Quantum dots (QDs) are often selected as labels in a fluorescence immunoassay due to their high fluorescence, better stability, and biocompatibility. In this study, novel doped CdTe?:?Zn/ZnS QDs with stability and a high photoluminescence quantum yield (40.78%) were prepared by the water synthesis method and used as labels to conjugate with goat anti-rabbit IgG to establish a fluorescence immunoassay (FLISA) for bacteria compared to the traditional enzyme-linked immunosorbent assay (ELISA) based on the reaction between an antibody and an antigen. A good linear relationship between the fluorescence intensity and concentrations of D. tsuruhatensis CM13 was found when the concentrations were in the range of 10 ~(3) CFU mL ~(?1) –10 ~(8) CFU mL ~(?1) . The limit of detection (LOD) of D. tsuruhatensis CM13 was 1.25 × 10 ~(3) CFU mL ~(?1) by FLISA, which was about 80 times lower than the LOD obtained from ELISA (10 ~(5) CFU mL ~(?1) ). This indicated that our FLISA method has higher sensitivity than traditional ELISA, and the CdTe?:?Zn/ZnS QDs synthesized in this paper have good applications in the rapid sensitive detection of microorganisms.
机译:荧光免疫测定法具有灵敏度高,操作简便,准确性高等优点,已广泛应用于不同领域。由于其高荧光,更好的稳定性和生物相容性,通常在荧光免疫测定中选择量子点(QD)作为标记。本研究通过水合成法制备了具有稳定性和高光致发光量子产率(40.78%)的新型掺杂的CdTe2:?Zn / ZnS量子点,并作为标记物与山羊抗兔IgG结合,建立了荧光免疫分析法。基于抗体和抗原之间的反应,将细菌(FLISA)与传统的酶联免疫吸附测定(ELISA)进行比较。当浓度在10〜(3)CFU mL〜(?1)–10〜(8)CFU mL〜(?1)范围内时,发现荧光强度与tsuruhatensis CM13浓度之间具有良好的线性关系。 。通过FLISA检测,tsuruhatensis CM13的检出限(LOD)为1.25×10〜(3)CFU mL〜(?1),比ELISA(10〜(5)CFU mL)的LOD低约80倍。 〜(?1))。这表明我们的FLISA方法比传统的ELISA方法具有更高的灵敏度,并且本文合成的CdTe2:?Zn / ZnS QD在微生物的快速灵敏检测中具有良好的应用。

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