用于恶性肿瘤生物可视化的氧化还原敏感荧光纳米颗粒。

Sovremennye tekhnologii v meditsine Pub Date : 2025-01-01 Epub Date: 2025-02-28 DOI:10.17691/stm2025.17.1.05
O Peltek, E A Kopoleva, M V Zyuzin
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引用次数: 0

摘要

荧光氧化还原敏感纳米颗粒在当前生物医学中的应用,保证了生物可视化的高灵敏度和准确性。纳米颗粒是有效的,因为它们可以在血液中长时间循环,谷胱甘肽水平相对较低,并在肿瘤细胞中被破坏,释放负载染料或药物。本研究的目的是开发新的基于三硫氰尿酸的纳米颗粒用于恶性肿瘤的生物可视化,并研究所开发的纳米颗粒的能力。材料和方法:采用碘缩聚法制备三硫氰尿酸纳米颗粒。用扫描电镜和透射电镜对其进行表征,用分光光度法测定荧光染料的负载。采用共聚焦激光扫描显微镜研究纳米颗粒对4T1和A549细胞系活力的影响及其与细胞的相互作用。采用荧光可视化技术观察纳米颗粒在BALB/c移植瘤小鼠组织和器官中的分布。结果:经扫描显微镜观察,合成的颗粒尺寸达到100±20 nm。吸附等温线表明,每1 mg纳米颗粒可吸附0.27 mg RhB荧光染料。在谷胱甘肽和乙酰半胱氨酸的存在下,荧光染料的释放增强。颗粒对4T1和A549细胞的活力无明显影响。在肿瘤内给药后,与常规荧光染料溶液相比,他们确保肿瘤区域的荧光信号更强烈。结论:所建立的三硫氰尿酸纳米颗粒系统具有较高的恶性肿瘤生物可视化效果,具有靶向给药的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Redox-Sensitive Fluorescent Nanoparticles for Biovisualization of Malignant Tumors.

Application of fluorescent redox-sensitive nanoparticles in current biomedicine ensures high sensitivity and accuracy of biovisualization. Nanoparticles are potent as they can long circulate in the blood, where the level of glutathione is relatively low, and are destroyed in tumor cells, releasing loaded dyes or drugs. The aim of the study was to develop new nanoparticles based on trithiocyanuric acid for biovisualization of malignant tumors and study capabilities of the developed nanoparticles.

Materials and methods: Nanoparticles were obtained by polycondensation of trithiocyanuric acid using iodine. Scanning and transmission electron microscopy was used for their characterization, the loading of fluorescent dyes was assessed by means of spectrophotometry. Confocal laser scanning microscopy was applied to study the impact of nanoparticles on the viability of the 4T1 and A549 cell lines as well as their interaction with cells. The distribution of nanoparticles in tissues and organs of BALB/c model mice with grafted tumors was performed using fluorescence visualization.

Results: According to scanning microscopy, the size of the synthesized particles reached 100±20 nm. The adsorption isotherm demonstrated that adsorption of 0.27 mg of the RhB fluorescent dye per 1 mg of nanoparticles could be achieved. Enhanced release of the packed fluorescent dye was seen in the presence of glutathione and acetylcysteine. The particles did not significantly affect the viability of 4T1 and A549 cells. After intratumoral administration, they ensured a more intense fluorescent signal in the tumor area compared to a regular fluorescent dye solution.

Conclusion: The developed system of trithiocyanuric-acid-based nanoparticles demonstrated high efficiency in biovisualization of malignant tumors and has a potential for targeted delivery of treatment agents.

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