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一种新型高效的镧、氮共掺杂碳点对U251和LN229细胞的肿瘤抑制剂。

A novel and high-performance tumor inhibitor of La, N co-doped carbon dots for U251 and LN229 cells.

作者信息

Ye Xinyun, Zhong Huanglian, Liu Lin, Huang Jingtao, Xia Zhuquan, Tang Zhiji, Wei Wenjin, Huang Weilong, Ye Yuwei, Jiang Qiuhua

机构信息

Department of Neurosurgery, The Affiliated Ganzhou Hospital, Jiangxi Medical College, Nanchang University, Ganzhou 341000, China.

School of Basic Medicine Sciences, Gannan Medical University, Ganzhou 341000, China; Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases of Ministry of Education, Gannan Medical University, Ganzhou, Jiangxi Province 341000, China.

出版信息

Colloids Surf B Biointerfaces. 2025 May;249:114520. doi: 10.1016/j.colsurfb.2025.114520. Epub 2025 Jan 14.

Abstract

To address the medical challenges posed by glioblastoma, a novel and high-performance tumor inhibitor (La@FA-CDs) composed of folic acid and lanthanum nitrate hexahydrate, was successfully synthesized and demonstrated effectiveness in inhibiting the growth of U251 and LN299 cells. The microstructure of La@FA-CDs was extensively analyzed by FTIR, UV-Vis, XPS, TEM, AFM NMR, and nanoparticle size analyzer. The optical and electrical properties of La@FA-CDs were characterized using a fluorescence spectrometer and a zeta potential analyzer. Biological assays, including the CCK8 proliferation assay, scratch assay, flow cytometry, cytoskeleton staining, and live/dead staining were conducted to assess antitumor properties and cytotoxicity. The result revealed that the La@FA-CDs demonstrated significantly enhanced antitumor activity relative to the undoped sample. Furthermore, the La@FA-CDs demonstrated a dose-dependent cytotoxic effect on two glioblastoma cell lines U251 and LN299. The findings of this study suggested that treatment with La@FA-CDs effectively inhibited migration and proliferation while promoting apoptosis in glioblastoma cells. Meanwhile, the La@FA-CDs showed minimal cytotoxic effects on HEK 293 and HUVEC cells under standard conditions, with only slight toxicity observed in HUVEC cells at high (500 µM) concentrations. These results suggest that La@FA-CDs could be a promising therapeutic agent for glioblastoma treatment, demonstrating both effective inhibition and favorable safety profiles.

摘要

为应对胶质母细胞瘤带来的医学挑战,一种由叶酸和六水合硝酸镧组成的新型高性能肿瘤抑制剂(La@FA-CDs)被成功合成,并在抑制U251和LN299细胞生长方面显示出有效性。通过傅里叶变换红外光谱(FTIR)、紫外可见光谱(UV-Vis)、X射线光电子能谱(XPS)、透射电子显微镜(TEM)、原子力显微镜(AFM)、核磁共振(NMR)和纳米颗粒尺寸分析仪对La@FA-CDs的微观结构进行了广泛分析。使用荧光光谱仪和zeta电位分析仪对La@FA-CDs的光学和电学性质进行了表征。进行了包括CCK8增殖试验、划痕试验、流式细胞术、细胞骨架染色和活/死染色在内的生物学试验,以评估其抗肿瘤特性和细胞毒性。结果表明,相对于未掺杂样品,La@FA-CDs表现出显著增强的抗肿瘤活性。此外,La@FA-CDs对两种胶质母细胞瘤细胞系U251和LN299表现出剂量依赖性细胞毒性作用。本研究结果表明,用La@FA-CDs治疗可有效抑制胶质母细胞瘤细胞的迁移和增殖,同时促进其凋亡。同时,在标准条件下,La@FA-CDs对人胚肾293细胞(HEK 293)和人脐静脉内皮细胞(HUVEC)的细胞毒性作用极小,仅在高浓度(500µM)下在HUVEC细胞中观察到轻微毒性。这些结果表明,La@FA-CDs可能是一种有前途的胶质母细胞瘤治疗药物,具有有效的抑制作用和良好的安全性。

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