化学功能化单壁碳纳米管对D54MG人胶质母细胞瘤细胞形态和活力的影响

Neuroglia (Basel, Switzerland) Pub Date : 2018-12-01 Epub Date: 2018-10-16 DOI:10.3390/neuroglia1020022
Seantel Hopkins, Manoj K Gottipati, Vedrana Montana, Elena Bekyarova, Robert C Haddon, Vladimir Parpura
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引用次数: 1

摘要

单壁碳纳米管(SWCNTs)的独特性质使其成为生物医学领域的有趣候选材料。为了使这些微小的管获得各种功能,例如水溶性,可以将不同的化学基团附着在SWCNTs上。由于这些“功能化”方法的可用性,SWCNTs被视为一种潜在的抗癌治疗药物。在这种情况下,我们测试了不同的化学功能化形式的SWCNTs,以确定哪种修饰使它们更好地对抗胶质母细胞瘤(星形细胞瘤IV级),这是最致命的脑癌。我们研究了用聚乙二醇(SWCNTs - peg)或端有四氢呋喃基的聚乙二醇(SWCNTs - peg - thff)功能化的两种水溶性SWCNTs对培养的D54MG人胶质母细胞瘤细胞的形态和活力(即细胞粘附、增殖和死亡率)的影响。我们发现,当swcnts - peg - thff溶质添加到培养基中时,使D54MG细胞变得不那么圆(在形状因子上显着减少了约23%)。这种形态变化是由PEG-THFF官能团引起的,而不是由swcnts骨架本身引起的。我们还发现swcnts - peg - thff溶质降低了D54MG细胞的增殖率,同时增加了细胞死亡率。另一方面,PEG和PEG- thff官能团降低了D54MG人胶质瘤细胞的细胞死亡率。这些数据表明,SWCNTs功能化的过程可能会影响其作为胶质瘤治疗药物的生物学效应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Effects of Chemically-Functionalized Single-Walled Carbon Nanotubes on the Morphology and Vitality of D54MG Human Glioblastoma Cells.

The unique properties of single-walled carbon nanotubes (SWCNTs) have made them interesting candidates for applications in biomedicine. There are diverse chemical groups that can be attached to SWCNTs in order for these tiny tubes to gain various functionalities, for example, water solubility. Due to the availability of these "functionalization" approaches, SWCNTs are seen as agents for a potential anti-cancer therapy. In this context, we tested different chemically-functionalized forms of SWCNTs to determine which modifications make them better combatants against glioblastoma (astrocytoma grade IV), the deadliest brain cancer. We investigated the effects that two types of water soluble SWCNTs, functionalized with polyethylene glycol (SWCNT-PEG) or tetrahydrofurfuryl-terminated polyethylene glycol (SWCNT-PEG-THFF), have on the morphology and vitality, that is, cell adhesion, proliferation and death rate, of the D54MG human glioblastoma cells in culture. We found that SWCNT-PEG-THFF solute, when added to culture media, makes D54MG cells less round (measured as a significant decrease, by ~23%, in the form factor). This morphological change was induced by the PEG-THFF functional group, but not the SWCNT backbone itself. We also found that SWCNT-PEG-THFF solute reduces the proliferation rate of D54MG cells while increasing the rate of cell death. The functional groups PEG and PEG-THFF, on the other hand, reduce the cell death rate of D54MG human glioma cells. These data indicate that the process of functionalization of SWCNTs for potential use as glioma therapeutics may affect their biological effects.

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