揭示姜黄素负载石墨烯量子点在癌症治疗的药物输送和释放动力学方面的体内潜力

Q1 Pharmacology, Toxicology and Pharmaceutics
Nanotheranostics Pub Date : 2024-08-13 eCollection Date: 2024-01-01 DOI:10.7150/ntno.96559
Mochamad Z Fahmi, Siti F A Sugito, Aswandi Wibrianto, Siska Novania, Shinta Widyastuti, Musbahu Adam Ahmad, Satya C W Sakti, Lee H Voon
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引用次数: 0

摘要

本研究介绍了一种创新的磁性多功能抗癌药物载体,旨在提高姜黄素在癌症治疗中的疗效。该研究探讨了石墨烯量子点(GQDs)作为姜黄素给药系统抑制体内癌症生长的潜力。研究人员通过水热法和 Hummers 法合成了颗粒直径小于 10 纳米的石墨烯量子点(GQDs)。傅立叶变换红外光谱分析证实了功能化的成功,揭示了 GQDs 与姜黄素之间形成的键。使用紫外-可见分光光度计和分光荧光仪对 GQDs 的光学特性进行了评估,结果显示其荧光强度很高,量子产率为 1.32%。随后,将姜黄素添加到 GQDs(CQDs/cur)上,形成了一种高效的抗癌药物递送系统,显示出显著的体内疗效。小鼠肿瘤直径减小、体重增加就是证明。此外,在不同的 pH 值条件(4、7 和 9)下,使用 Peppas-Sahlin 方程分析了姜黄素从 GQDs 中的释放动力学,结果显示酸性条件下的释放率最高。总之,本研究强调了 GQDs 作为高效载体靶向递送姜黄素的潜力,在癌症治疗中展示了广阔的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unraveling In vivo Potential of Curcumin-loaded Graphene Quantum Dots on Drug Delivery and Release Kinetics Aspects of Cancer Treatment.

This study introduces an innovative magnetic-based multifunctional anti-cancer drug carrier aiming to enhance the efficacy of curcumin in cancer therapy. The research investigates the potential of Graphene Quantum Dots (GQDs) as a curcumin drug delivery system for inhibiting in vivo cancer growth. GQDs with a particle diameter below 10 nm were synthesized via hydrothermal and Hummers methods, exhibiting homogeneity and crystalline structure according to AFM and XRD analyses. FTIR analysis confirmed functionalization success, revealing the formation of bonds between GQDs and curcumin. The optical properties of GQDs were assessed using a UV-Vis spectrophotometer and spectrofluorometer, resulting in vigorous fluorescence with a quantum yield of 1.32%. Subsequently, loading curcumin onto GQDs (CQDs/cur) resulted in an efficient system for delivering the anti-cancer drug, demonstrating significant in vivo efficacy. It was indicated by reduced tumor diameter and increased body weight in mice. Furthermore, the release kinetics of curcumin from GQDs were analyzed using the Peppas-Sahlin equation under varying pH conditions (4, 7, and 9), revealing the highest release rate in acidic conditions. In conclusion, this study highlights the potential of GQDs as highly efficient carriers for targeted curcumin delivery, showcasing promising prospects in cancer treatment.

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来源期刊
Nanotheranostics
Nanotheranostics Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
CiteScore
10.40
自引率
0.00%
发文量
37
审稿时长
12 weeks
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