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A sensitive sandwich structure time-resolved fluorescence method for thrombin detection

机译:灵敏的三明治结构时间分辨荧光方法检测凝血酶

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We designed a sensitive and specific time-resolved fluorescence assay for detection of human thrombin. This design was based on the amplification of nanoparticles and the specificity of aptamers. The DC@AuNPs were prepared by the conjugation of AuNPs to BSA–Eu3+–DTPA and SH-Apt29. In the presence of thrombin, the formation of a quadruplex–thrombin complex could lead to the formation of a MNPs@Apt15–thrombin–DC@AuNP sandwich structure. In the presence of enhancement solution, Eu3+ interacted with the enhancement solution to produce strong fluorescence. Under the optimized conditions, the linear range of the method was from 1 pM to 100 pM of thrombin, and the limit of detection was 0.78 pM. Furthermore, the method could specifically recognize thrombin in the presence of other analogous proteins. The method is successfully used to determine thrombin in human plasma. This method has the advantages of high sensitivity and selectivity. It showed great potential for medical diagnosis.
机译:我们设计了一种灵敏且特定时间分辨的荧光测定法,用于检测人凝血酶。该设计基于纳米颗粒的扩增和适体的特异性。 DC @ AuNPs是通过AuNPs与BSA–Eu3 + –DTPA和SH-Apt29结合而制备的。在存在凝血酶的情况下,四链体-凝血酶复合物的形成可能导致MNPs @ Apt15–凝血酶–DC @ AuNP夹心结构的形成。在增强溶液的存在下,Eu3 +与增强溶液相互作用以产生强荧光。在最佳条件下,该方法的线性范围为1 pM至100 pM凝血酶,检测限为0.78 pM。此外,该方法可以在其他类似蛋白存在下特异性识别凝血酶。该方法已成功用于测定人血浆中的凝血酶。该方法具有灵敏度高和选择性高的优点。它显示出巨大的医学诊断潜力。

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