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An NIR triphenylamine grafted BODIPY derivative with high photothermal conversion efficiency and singlet oxygen generation for imaging guided phototherapy

机译:一个近红外光谱三苯胺接枝BODIPY导数光热光谱分析转换效率高单线态氧代成像制导光疗

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摘要

Osteosarcoma, the most common malignant bone tissue tumor, with a high degree of malignancy, strong metastasis, and early lung metastasis, can result in extremely high mortality, and is a serious threat to human health. Boron dipyrromethene (BODIPY) compounds have shown great potential in photodynamic tumor therapy. In this study, an NIR triphenylamine grafted BODIPY derivative (BDPTPA) with high singlet oxygen generation efficiency (35.2%) was designed and synthesized. BDPTPA nano- particles (NPs) obtained by nanoprecipitation present high photothermal conversion efficiency (52.6%). Both MTT assay and flow cytometry experiments suggest that BDPTPA NPs are able to generate high photo-toxicity and induce apoptosis of osteosarcoma cells, while presenting negligible dark-toxicity towards osteosarcoma cells as well as normal human cells. Cell migration and transwell experiments demonstrate that BDPTPA NPs can inhibit the migration of osteosarcoma cells. Due to the enhanced permeability and retention (EPR) effects, BDPTPA NPs can accumulate in tumor tissue in 6 h. Pharmacokinetic studies in rats indicate that BDPTPA NPs eliminate much more slowly than BDPTPA in 10% DMSO. Under the irradiation of an 808 nm laser, in in vivo experiments, BDPTPA NPs can significantly inhibit tumor growth without side effects towards normal tissues. BDPTPA NPs show good biosafety and excellent therapeutic effect both in vitro and in vivo, indicating their great potential for treatment of osteosarcoma.
机译:骨肉瘤最常见的恶性骨组织肿瘤,高度恶性肿瘤,强大的转移,早期肺转移,可以导致死亡率极高,是一种严重威胁人类健康。dipyrromethene (BODIPY)化合物显示巨大的潜力在肿瘤光动力治疗。这项研究中,一个近红外光谱三苯胺接枝BODIPY导数与高单线态氧(BDPTPA)发电效率(35.2%)和设计合成。通过nanoprecipitation高光热光谱分析转换效率(52.6%)。MTT实验和流式细胞仪实验表明BDPTPA NPs能够产生高photo-toxicity和诱导细胞凋亡骨肉瘤细胞,而可以忽略不计dark-toxicity对骨肉瘤细胞正常的人类细胞。证明BDPTPA NPs transwell实验可以抑制骨肉瘤细胞的迁移。由于增强渗透性和保留(EPR)的影响,BDPTPA NPs可以积聚在肿瘤组织6 h。老鼠体内药代动力学研究表明BDPTPA NPs消除更多慢慢地比BDPTPA 10% DMSO溶液。波长808纳米的激光的辐照,在体内实验中,BDPTPA NPs可以显著抑制肿瘤的生长对正常无副作用组织。在体外和良好的治疗效果体内,来显示他们的潜力巨大治疗骨肉瘤。

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