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谷胱甘肽保护的 CdTe/ZnS 量子点通过嵌入阳离子淀粉增强其荧光用于利福平的灵敏检测。

Fluorescence enhancement of glutathione capped CdTe/ZnS quantum dots by embedding into cationic starch for sensitive detection of rifampicin.

机构信息

Department of Chemistry, Payame Noor University, PO BOX 19395-3697, Tehran, Iran.

Department of Chemistry, Payame Noor University, PO BOX 19395-3697, Tehran, Iran.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2017 Feb 15;173:144-150. doi: 10.1016/j.saa.2016.09.006. Epub 2016 Sep 8.

Abstract

In this study, we describe the synthesis of a new quantum dots (QDs) by embedding glutathione capped CdTe/ZnS QDs into cationic starch biopolymer (CS-GSH-CdTe/ZnS QDs). The fluorescence intensity of prepared QDs was significantly enhanced. When QDs interacted with rifampicin, the fluorescence intensity of the CS-GSH-CdTe/ZnS QDs was highly quenched compared with GSH-CdTe/ZnS QDs. Based on the above, a new fluorescent nanosensor for simple, sensitive and selective detection of rifampicin was developed. The fluorescence quenching was well described by the typical Stern-Volmer equation. After optimization, the linear range of the as-prepared QDs fluorescence intensity versus the concentration of rifampicin was F/F=0.0422Q+1.109 (R=0.99). The detection limit was 0.06×10mol/L. The proposed method with satisfactory results was used to detect rifampicin in commercial capsules and tablets.

摘要

在这项研究中,我们描述了一种新的量子点(QDs)的合成方法,即将谷胱甘肽包裹的 CdTe/ZnS QDs 嵌入阳离子淀粉生物聚合物(CS-GSH-CdTe/ZnS QDs)中。制备的 QDs 的荧光强度显著增强。当 QDs 与利福平相互作用时,与 GSH-CdTe/ZnS QDs 相比,CS-GSH-CdTe/ZnS QDs 的荧光强度被高度猝灭。基于此,开发了一种用于简单、灵敏和选择性检测利福平的新型荧光纳米传感器。荧光猝灭很好地描述了典型的 Stern-Volmer 方程。经过优化,制备的 QDs 荧光强度与利福平浓度的线性范围为 F/F=0.0422Q+1.109(R=0.99)。检测限为 0.06×10mol/L。该方法检测结果令人满意,已用于检测市售胶囊和片剂中的利福平。

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