Nucleolus-Targeting Carbon Dot Nanocomplexes for Combined Photodynamic/Photothermal Therapy.

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Molecular Pharmaceutics Pub Date : 2025-02-03 Epub Date: 2024-12-30 DOI:10.1021/acs.molpharmaceut.4c01211
Shaofang Ma, Yan Zhang, Zihan Zhu, Deping Wang, Xin Zhou, Jing Wang, Wei Bian, Xinjing Tang
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Abstract

The low cure rate and high mortality associated with cancer pose significant threats to human health. Photodynamic and photothermal therapies have emerged as promising treatment strategies for various types of cancers. In this study, we successfully synthesized a novel type of carbon dot (CD) using 1,2,4-aminobenzene and ethylenediamine as precursors. Surprisingly, these CDs exhibited outstanding nucleolus-targeting capabilities coupled with a remarkable photothermal effect. Through the integration of these nucleolus-targeting CDs with indocyanine green (ICG) and folic acid (FA), we created CDs-ICG-FA nanocomplexes suitable for combined photodynamic and photothermal therapy. In vitro experiments demonstrated that CDs-ICG-FA maintained a robust photothermal ability, achieving a conversion efficiency of up to 34.3%. Furthermore, CDs-ICG-FA generated abundant reactive oxygen species, effectively inducing cancer cell death and demonstrating its potential for photodynamic therapy. In MCF-7 cancer cells, CDs-ICG-FA exhibited a pronounced synergistic photothermal/photodynamic anticancer effect. Subsequent in vivo experiments in mice revealed that CDs-ICG-FA could selectively accumulate at tumor sites, significantly inhibiting tumor growth upon exposure to an 808 nm laser. These findings suggest that the developed nucleolus-targeting CDs-ICG-FA hold promising potential for cancer targeting and the application of combined photothermal/photodynamic therapy.

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光动力/光热联合治疗核仁靶向碳点纳米配合物。
癌症的低治愈率和高死亡率对人类健康构成重大威胁。光动力和光热疗法已成为各种类型癌症的有前途的治疗策略。本研究成功地以1,2,4-氨基苯和乙二胺为前体合成了一种新型的碳点(CD)。令人惊讶的是,这些CDs表现出出色的核仁靶向能力以及显著的光热效应。通过将这些靶向核仁的CDs与吲哚菁绿(ICG)和叶酸(FA)结合,我们制备了适合于光动力和光热联合治疗的CDs-ICG-FA纳米复合物。体外实验表明,CDs-ICG-FA保持了良好的光热能力,转化效率高达34.3%。此外,CDs-ICG-FA产生丰富的活性氧,有效诱导癌细胞死亡,显示出其光动力治疗的潜力。在MCF-7癌细胞中,CDs-ICG-FA表现出明显的光热/光动力协同抗癌作用。随后的小鼠体内实验表明,在808 nm激光照射下,CDs-ICG-FA可以选择性地在肿瘤部位积累,显著抑制肿瘤生长。这些发现表明,所开发的核核靶向CDs-ICG-FA在癌症靶向和光动力联合治疗方面具有广阔的应用前景。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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