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基于荧光共振能量转移的氨基酸@gold-碳纳米粒子荧光探针用于药物分析。

FRET-based fluorescent probe for drug assay from amino acid@gold-carbon nanoparticles.

机构信息

Department of Chemistry, University of Sharjah, Sharjah, 27272, United Arab Emirates.

Department of Biology, Chemistry and Environmental Sciences, American University of Sharjah, Sharjah, 26666, United Arab Emirates.

出版信息

Anal Bioanal Chem. 2021 Feb;413(4):1117-1125. doi: 10.1007/s00216-020-03075-9. Epub 2021 Jan 6.

Abstract

Biocompatible and luminescent nanostructures synthesized by capping gold-carbon nanoparticles (HOOC-4-CH-AuNPs) with amino acids tyrosine, tryptophan, and cysteine were used for the quantitative estimation of ranitidine (RNH), a peptic ulcer and gastroesophageal reflux drug. We applied a fluorescence quenching mechanism to investigate the viability of the energy transfer based on gold-carbon nanosensors. Förster resonance energy transfer (FRET) calculations showed a donor-acceptor distance of 1.69 nm (Tyr@AuNPs), 2.27 nm (Trp@AuNPs), and 2.32 nm (Cys@AuNPs). The constant time-resolved fluorescence lifetime measurements supported the static quenching nature. This method was successfully utilized in the detection and quantification of RNH, with a limit of detection (LOD) of 0.174, 0.56, and 0.332 μM for Tyr@AuNP, Trp@AuNP, and Cys@AuNP bioconjugates, respectively. This approach was also successful in the quantification of RNH in spiked serum samples.

摘要

用氨基酸酪氨酸、色氨酸和半胱氨酸对金-碳纳米粒子(HOOC-4-CH-AuNPs)进行封端合成的生物相容性和发光纳米结构,用于定量估计雷尼替丁(RNH),一种治疗消化性溃疡和胃食管反流病的药物。我们应用荧光猝灭机制研究了基于金-碳纳米传感器的能量转移的可行性。Förster 共振能量转移(FRET)计算表明,供体-受体距离为 1.69nm(Tyr@AuNPs)、2.27nm(Trp@AuNPs)和 2.32nm(Cys@AuNPs)。恒时光谱寿命测量支持静态猝灭特性。该方法成功用于 RNH 的检测和定量,Tyr@AuNP、Trp@AuNP 和 Cys@AuNP 生物缀合物的检测限(LOD)分别为 0.174、0.56 和 0.332μM。该方法还成功地用于测定加标血清样本中的 RNH 含量。

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