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采用自放热反应合成多功能碳量子点:在长春新碱传感和细胞成像中的应用。

Adoption of self-exothermic reaction for synthesis of multifunctional carbon quantum dots: Applications to vincristine sensing and cell imaging.

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, University of Sadat City, Sadat City, 32897, Monufia, Egypt; Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt.

Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt.

出版信息

Talanta. 2025 Jan 1;282:126971. doi: 10.1016/j.talanta.2024.126971. Epub 2024 Sep 28.

DOI:10.1016/j.talanta.2024.126971
PMID:39366245
Abstract

This work introduces an extremely easy method for preparing luminescent carbon dots (CDs) at ambient temperature using 1,2-naphthoquinone sulphonate and ethylenediamine as precursors via self-exothermic reaction without energy input. The as-obtained CDs have a high quantum yield (34.1 %), a production yield of 21.2 %, and a small size diameter (3.44 nm). Various techniques (NMR, TEM, EDX-mapping, XPS, XRD, FT-IR, fluorescence, and UV-visible spectroscopy) were used to characterize the prepared CDs. The CDs exhibited an excitation-independent emission with λ of 275 nm, demonstrating their homogeneity and high purity. The anticancer drug vincristine (VCR) quantitively quenched the fluorescent signal of the synthesized CDs, allowing their application as the first fluorescent nano-sensor to determine VCR. The quenching effect was linear within the range of 0.2-5.0 μg mL, enabling the determination of VCR in vials, plasma, and for content uniformity testing with a detection limit of 0.06 μg mL. Moreover, the synthesized CDs were employed as a bio-sensing platform to detect VCR in cancer cells owing to their good selectivity, excellent biocompatibility, minimal cytotoxicity, and high stability. The fabrication of CDs with excellent properties at room temperature under mild conditions paves the way for new advancements in the room temperature synthesis of CDs and offers a highly efficient alternative to traditional synthesis approaches.

摘要

这项工作介绍了一种在环境温度下使用 1,2-萘醌磺酸盐和乙二胺作为前体,通过自放热反应在无需能量输入的情况下制备发光碳点(CDs)的极其简单方法。所得到的 CDs 具有高量子产率(34.1%)、产率为 21.2% 和小的粒径(3.44nm)。各种技术(NMR、TEM、EDX 映射、XPS、XRD、FT-IR、荧光和紫外可见光谱)用于表征制备的 CDs。CDs 表现出激发独立的发射,λ 为 275nm,证明了它们的同质性和高纯度。抗癌药物长春新碱(VCR)定量猝灭了合成 CDs 的荧光信号,使其能够作为第一个荧光纳米传感器来测定 VCR。猝灭效应在 0.2-5.0μgmL 的范围内呈线性,能够在小瓶、血浆中测定 VCR,并进行含量均匀度测试,检测限为 0.06μgmL。此外,由于合成的 CDs 具有良好的选择性、优异的生物相容性、最小的细胞毒性和高稳定性,因此被用作生物传感平台来检测癌细胞中的 VCR。在温和条件下在室温下制备具有优异性能的 CDs 为在室温下合成 CDs 的新进展铺平了道路,并为传统合成方法提供了一种高效的替代方法。

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