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多功能化碳点作为一种用于向胶质母细胞瘤细胞系递送药物的活性纳米载体。

Multifunctionalized Carbon Dots as an Active Nanocarrier for Drug Delivery to the Glioblastoma Cell Line.

作者信息

Algarra Manuel, Soto Juan, Pino-González Maria Soledad, Gonzalez-Munoz Elena, Dučić Tanja

机构信息

INAMAT-Institute for Advanced Materials and Mathematics, Dept. Science, Public University of Navarra, Campus Arrosadía, 31006 Pamplona, Spain.

Dept. Physical Chemistry, Faculty of Science, University of Málaga, Avda. Cervantes, 2, 29071 Málaga, Spain.

出版信息

ACS Omega. 2024 Mar 13;9(12):13818-13830. doi: 10.1021/acsomega.3c08459. eCollection 2024 Mar 26.

Abstract

Nanoparticle-based nanocarriers represent a viable alternative to conventional direct administration in cancer cells. This advanced approach employs the use of nanotechnology to transport therapeutic agents directly to cancer cells, thereby reducing the risk of damage to healthy cells and enhancing the efficacy of treatment. By approving nanoparticle-based nanocarriers, the potential for targeted, effective treatment is greatly increased. The so-called carbon-based nanoparticles, or carbon dots, have been hydrothermally prepared and initiated by a polymerization process. We synthesized and characterized nanoparticles of 2-acrylamido-2-methylpropanesulfonic acid, which showed biocompatibility with glioblastoma cells, and further, we tested them as a carrier for the drug riluzole. The obtained nanoparticles have been extensively characterized by techniques to obtain the exact composition of their surface by using Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS), and nuclear magnetic resonance (NMR) spectroscopy, as well as cryo-transmission electron microscopy. We found that the surface of the synthesized nanoparticles (NPs) is covered mainly by sulfonated, carboxylic, and substituted amide groups. These functional groups make them suitable as carriers for drug delivery in cancer cells. Specifically, we have successfully utilized the NPs as a delivery system for the drug riluzole, which has shown efficacy in treating glioblastoma cancer cells. The effect of nanoparticles as carriers for the riluzole system on glioblastoma cells was studied using live-cell synchrotron-based FTIR microspectroscopy to monitor biochemical changes. After applying nanoparticles as nanocarriers, we have observed changes in all biomacromolecules, including the nucleic acids and protein conformation. These findings provide a strong foundation for further exploration into the development of targeted treatments for glioblastoma.

摘要

基于纳米颗粒的纳米载体是癌细胞传统直接给药方式的一种可行替代方案。这种先进方法利用纳米技术将治疗剂直接输送到癌细胞,从而降低对健康细胞造成损害的风险并提高治疗效果。通过批准基于纳米颗粒的纳米载体,靶向有效治疗的潜力大大增加。所谓的碳基纳米颗粒,即碳点,是通过水热法制备并由聚合过程引发的。我们合成并表征了2-丙烯酰胺基-2-甲基丙烷磺酸纳米颗粒,其显示出与胶质母细胞瘤细胞的生物相容性,此外,我们还将它们作为药物利鲁唑的载体进行了测试。所获得的纳米颗粒已通过多种技术进行了广泛表征,以使用傅里叶变换红外光谱(FTIR)、X射线光电子能谱(XPS)和核磁共振(NMR)光谱以及低温透射电子显微镜来确定其表面的确切组成。我们发现合成的纳米颗粒(NPs)表面主要覆盖有磺化、羧基和取代酰胺基团。这些官能团使它们适合作为癌细胞中药物递送的载体。具体而言,我们已成功将NPs用作药物利鲁唑的递送系统,利鲁唑在治疗胶质母细胞瘤癌细胞方面已显示出疗效。使用基于同步加速器的活细胞FTIR显微光谱法研究了纳米颗粒作为利鲁唑系统载体对胶质母细胞瘤细胞的影响,以监测生化变化。在将纳米颗粒用作纳米载体后,我们观察到所有生物大分子都发生了变化,包括核酸和蛋白质构象。这些发现为进一步探索胶质母细胞瘤靶向治疗的发展提供了坚实的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713f/10976390/beacc2faf1c2/ao3c08459_0010.jpg

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