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可持续掺杂碳点作为治疗性药物的抗氧化剂和纳米载体

Sustainable Doped Carbon Dots as Antioxidant and Nanocarrier for Therapeutic Cargos.

作者信息

Hussain Afzal, Alajmi Mohamed Fahad, Ganguly S

机构信息

Department of Pharmacognosy, College of Pharmacy, King Saud University, PO Box 2457, Riyadh, 11451, Saudi Arabia.

Department of Chemistry, University of Waterloo, Waterloo, ON, Canada.

出版信息

J Fluoresc. 2024 Sep 25. doi: 10.1007/s10895-024-03940-1.

Abstract

Aside from their fluorescence sensing capabilities, carbon dots doped with heteroatoms show tremendous promise as nanocarriers for medicinal compounds and as antioxidants. We present a method for producing carbon dots from chitosan and lemon extract (CLCDs) using a one-step hydrothermal coupling synthesis. The as-synthesized CLCDs exhibited remarkable colloidal stability, antioxidant behavior, cytocompatibility, and nanocarrier for drug molecules. The nanoparticles was analyzed using advanced techniques such as Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), fluorescence spectroscopy, electron paramagnetic resonance (EPR) spectroscopy, and transmission electron microscopy (TEM) to determine the precise composition of their surface. In order to evaluate the drug transport properties of CLCDs, their surfaces were further modified with anticancer drug compounds. The drug release behavior was studied against physiologically simulated fluids and at different pH environments showing better delayed response in acidic condition. The plausible mechanistic pathways have been confirmed after fitting the results into Higuchi, Weibull and Korsmeyer-Peppas models. The goodness of fit was more than 95% for the Korsmeyer-Peppas model, with the release mechanism supported by anomalous transport. Moreover, the radical scavenging activity of CLCDs was also confirmed at low levels (1 mg/mL) which could be inferred > 85% efficacy against mostly employed testing agents (DPPH, ABTS, and hydroxyl radicals). Thus, the prepared CLCDs could be used as suitable nanovector in payload delivery with prominent antioxidant activity and low toxicity against living cell lines.

摘要

除了具有荧光传感能力外,掺杂杂原子的碳点作为药用化合物的纳米载体和抗氧化剂显示出巨大的潜力。我们提出了一种使用一步水热偶联合成法从壳聚糖和柠檬提取物制备碳点(CLCDs)的方法。合成的CLCDs表现出显著的胶体稳定性、抗氧化行为、细胞相容性以及作为药物分子的纳米载体。使用傅里叶变换红外光谱(FTIR)、X射线光电子能谱(XPS)、荧光光谱、电子顺磁共振(EPR)光谱和透射电子显微镜(TEM)等先进技术对纳米颗粒进行分析,以确定其表面的精确组成。为了评估CLCDs的药物传输特性,用抗癌药物化合物对其表面进行了进一步修饰。针对生理模拟流体和不同pH环境研究了药物释放行为,结果表明在酸性条件下具有更好的延迟响应。将结果拟合到Higuchi、Weibull和Korsmeyer-Peppas模型后,证实了可能的作用机制途径。Korsmeyer-Peppas模型的拟合优度超过95%,释放机制得到异常传输的支持。此外,CLCDs在低浓度(1 mg/mL)下的自由基清除活性也得到证实,对于大多数常用测试剂(DPPH、ABTS和羟基自由基),其清除效率可推断>85%。因此,制备的CLCDs可作为合适的纳米载体用于有效载荷递送,具有显著的抗氧化活性且对活细胞系毒性低。

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