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铕(III)螯合物键合硅胶纳米粒子在人促甲状腺激素时间分辨免疫荧光检测中的应用。

Application of europium(III) chelates-bonded silica nanoparticle in time-resolved immunofluorometric detection assay for human thyroid stimulating hormone.

机构信息

Xiamen Branch of Fujian Newborn Screening Centre and Xiamen Prenatal Diagnosis Centre, Xiamen Maternal & Children's Health Care Hospital, Xiamen, Fujian 361003, China.

出版信息

Anal Chim Acta. 2012 Apr 13;722:95-9. doi: 10.1016/j.aca.2012.01.065. Epub 2012 Feb 14.

Abstract

Eu(III) chelate-bonded silica nanoparticle was used as a fluorescent label to develop a highly sensitive time-resolved immunofluorometric assay (TrIFA) for human thyroid stimulating hormone (hTSH). The limit of detection of the assay calculated according to the 2SD method was 0.0007 mIU L(-1) and became 0.003 mIU L(-1) when serum-based matrix was used for calibrators, indicating that this TrIFA is comparable with the most sensitive assays. The linear range was from 0.005 to 100 mIU L(-1) of hTSH with coefficient of variation between 1.9% and 8.3%. The correlation study using 204 blood spot samples from newborns showed that the results from this new method were coincident with that of the commercial dissociation-enhanced lanthanide fluorescence immunoassay (DELFIA) system, with a correlation coefficient of 0.938. The fluorescent nanoparticle label allows directly reading the fluorescent signal, omitting the signal development step required for the DELFIA system, and the whole procedure of this assay is fulfilled within 2 h. Thus, we developed a novel, sensitive, quantitative and simple nanoparticle label-based TrIFA assay, suitable for routine application in hTSH screening of neonatal hypothyroidism.

摘要

Eu(III)螯合键合硅胶纳米颗粒被用作荧光标记物,开发了一种高灵敏度的时间分辨免疫荧光分析(TrIFA)用于检测人促甲状腺激素(hTSH)。根据 2SD 方法计算,该测定法的检测限为 0.0007 mIU L(-1),当使用基于血清的基质作为校准品时,检测限变为 0.003 mIU L(-1),表明该 TrIFA 可与最灵敏的测定法相媲美。线性范围为 0.005 至 100 mIU L(-1)的 hTSH,变异系数在 1.9%至 8.3%之间。使用 204 个来自新生儿的血斑样本进行的相关性研究表明,该新方法的结果与商业的解离增强镧系荧光免疫分析(DELFIA)系统的结果一致,相关系数为 0.938。荧光纳米颗粒标记物允许直接读取荧光信号,省去了 DELFIA 系统所需的信号开发步骤,该测定法的整个过程在 2 小时内完成。因此,我们开发了一种新型的、灵敏的、定量的和简单的基于纳米颗粒标记物的 TrIFA 测定法,适用于新生儿甲状腺功能减退症的 hTSH 筛查的常规应用。

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