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Synthesis method-dependent photothermal effects of colloidal solutions of platinum nanoparticles used in photothermal anticancer therapy

机译:光热抗癌治疗中铂纳米粒子胶体溶液的合成方法依赖性光热效应

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One of the most common anticancer therapies is photothermal therapy (PTT). The effectiveness of PTT depends on the photosensitizer being a molecule which is toxic for the cancer cells after electromagnetic wave irradiation. Therefore, a simulation of PTT was performed in this work on two colon cancer cells (SW480 and SW620) using platinum nanoparticles (Pt NPs). Interestingly, in the literature the dependence between the synthesis method and the photothermal properties of Pt NPs was not discussed. Consequently, in this paper, we evaluated the photothermal properties of Pt NPs synthesized by two different methods: polyol (PtI NPs) and green chemistry (PtII NPs). Scanning transmission electron microscopy revealed that the size of both Pt NPs obtained was 2 nm, the NPs were not agglomerated, and that the PtII NPs were distributed on green tea supports. The selected area electron diffraction and X-ray diffraction analysis confirmed the crystallinity of both types of Pt NPs. Fourier-transform infrared (FTIR) spectrum of the PtII NPs showed interactions between the NPs and stretching modes for C=O groups from flavonoids and polyphenols. Therefore, these chemical compounds could be responsible for reducing Pt4+ ions to Pt-0. Moreover, the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay showed that the PtII NPs exhibited 10% and 20% better cytotoxicity effect on SW480 and SW620 cells, than PtI NPs. The viability of cancer cells decreased when Pt NPs were used in PTT. The highest percentage of dead cells (82%) was observed for PtII NPs and 650-nm laser irradiation. FTIR and Raman spectroscopy showed structural changes induced by both Pt NPs and laser irradiation of cells in the range corresponding to levels of DNA, phospholipids, proteins, and lipids. Moreover, the calculated photothermal conversion efficiency showed that the value of this parameter is around 35%, regardless of the synthesis method and used wavelengths.
机译:最常见的抗癌疗法之一是光热疗(PTT)。 PTT的有效性取决于光敏剂是电磁波照射后对癌细胞有毒的分子。因此,使用铂纳米颗粒(Pt NPS)在这项结肠癌细胞(SW480和SW620)上进行PTT的模拟。有趣的是,在文献中,未讨论合成方法与Pt NP的光热性质之间的依赖性。因此,在本文中,我们评估了通过两种不同方法合成的Pt NP的光热性能:多元醇(PTI NPS)和绿色化学(PTII NPS)。扫描透射电子显微镜显示,所获得的PT NP的尺寸为2nm,NPS未凝聚,并且PTII NP分布在绿茶支撑件上。所选区域电子衍射和X射线衍射分析证实了两种类型的Pt NP的结晶度。 PTII NPS的傅立叶变换红外(FTIR)光谱在来自类黄酮和多酚的C = O基团的NPS和拉伸模式之间显示相互作用。因此,这些化合物可以负责将PT4 +离子还原为PT-0。此外,3-(4,5-二甲基噻唑-2-基)-5-(3-羧甲氧基苯基)-2-(4-磺基苯基)-2H-四唑(MTS)测定表明,PTII NPS表现出10%和20对SW480和SW620细胞的效果比PTI NP更好的细胞毒性。当PT NPS用于PTT时,癌细胞的可行性降低。对于PTII NPS和650nm激光照射,观察到最高百分比的死胞细胞(82%)。 FTIR和拉曼光谱显示出Pt NPS和激光照射的结构变化,在对应于DNA,磷脂,蛋白质和脂质水平的范围内。此外,无论合成方法和使用的波长如何,计算的光热转换效率都显示该参数的值约为35%。

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