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首页> 外文期刊>Angewandte Chemie >Stable J-Aggregation of an aza-BODIPY-Lipid in a Liposome for Optical Cancer Imaging
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Stable J-Aggregation of an aza-BODIPY-Lipid in a Liposome for Optical Cancer Imaging

机译:脂质体患者脂质体成像中AZA-BODIPY-脂质的稳定J-聚集

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摘要

Organic building blocks are the centerpieces of "one-for-all" nanoparticle development. Herein, we report the synthesis of a novel aza-BODIPY-lipid building block and its self-assembly into a liposomal nanoparticle (BODIPYsome). We observed optically stable NIR J-aggregation within the BODIPYsome that is likely attributed to J-dimerization. BODIPYsomes with cholesterol showed enhanced colloidal stability while maintaining a high extinction coefficient (128 mm(-1) cm(-1)) and high fluorescence quenching (99.70 +/- 0.09 %), which enables photoacoustic (PA) properties from its intact structure and recovered NIR fluorescence properties when it is disrupted in cancer cells. Finally, its capabilities for optical imaging (PA/fluorescence) were observed in an orthotopic prostate tumor mouse model 24 h after intravenous administration. Overall, the BODIPYsome opens the door for engineering new building blocks in the design of optically stable biophotonic imaging agents.
机译:有机构建块是“一生”纳米粒子发育的中心。 在此,我们将新型AZA-Bodipy-Lipid结构块的合成及其自组装成脂质体纳米颗粒(Bavipyome)。 我们观察到毛细血管组内的光学稳定的NIR J-聚集,其可能归因于J二聚体。 具有胆固醇的Bodipysomes显示出增强的胶体稳定性,同时保持高消光系数(128mm(-1)cm(-1))和高荧光猝灭(99.70 +/- 0.09%),这使得光声(PA)属性能够从其完整的结构中实现 当它在癌细胞中破坏时回收的NIR荧光性质。 最后,在静脉内给药后24小时的正向前列腺肿瘤小鼠模型中观察到其对光学成像(PA /荧光)的能力。 总的来说,Bodipysome在光学稳定的生物光学成像剂设计中为工程新建筑块打开门。

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