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A Light-Up Probe for Detection of Adenosine in Urine Samples by a Combination of an AIE Molecule and an Aptamer

机译:AIE分子和适体的组合用于检测尿液样品中腺苷的发光探针。

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摘要

A light-up fluorescent probe for the detection of adenosine was constructed with an AIE (aggregation-induced emission) molecule and a DNA aptamer. The AIE molecule was used as a signal generator, and the DNA aptamer was used as a recognition element for adenosine. The emission of the AIE molecule was due to its intramolecular rotation restriction induced by the aptamer upon binding of adenosine. The optimal component ratio of the probe was AIE molecule/DNA aptamer = 100 (μM/μM). The calibration curve of adenosine detection showed a linear range of 10 pM to 0.5 μM with an R2 of 0.996, and the detection limit of the probe was 10 pM. The probe exhibited a good selectivity to adenosine against its analogs (uridine, guanosine, and cytidine). The probe was used to detect adenosine in urine samples, a recovery from 86.8% to 90.0% for the spiked concentrations of adenosine (0.01, 0.05, 0.1 μM). The relative standard deviation from 1.2% to 2.0% was obtained. The intra-day and inter-day tests also showed good precisions, with measurement RSD values of 2.3% and 2.1%, respectively.
机译:用AIE(聚集诱导发射)分子和DNA适体构建了用于检测腺苷的发光荧光探针。 AIE分子用作信号发生器,而DNA适体用作腺苷的识别元件。 AIE分子的发射是由于其在腺苷结合时由适体诱导的其分子内旋转限制。探针的最佳组分比为AIE分子/ DNA适体= 100(μM/μM)。腺苷检测的校准曲线显示,线性范围为10 pM至0.5μM,R 2 为0.996,探针的检出限为10 pM。该探针对腺苷对其类似物(尿苷,鸟苷和胞苷)表现出良好的选择性。该探针用于检测尿液样品中的腺苷,腺苷浓度(0.01、0.05、0.1μM)的回收率从86.8%降至90.0%。获得了1.2%至2.0%的相对标准偏差。日内和日间测试也显示出良好的精度,测量RSD值分别为2.3%和2.1%。

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