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Long-Term-Stable Near-Infrared Polymer Dots with Ultrasmall Size and Narrow-Band Emission for Imaging Tumor Vasculature in Vivo

机译:具有超小尺寸和窄带发射的长期稳定的近红外聚合物点,用于体内的肿瘤血管成像。

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摘要

Fluorescent nanoprobes have become one of the most promising classes of materials for cancer imaging. However, there remain many unresolved issues with respect to the understanding of their long-term colloidal stability and photostability in both biological systems and the environment. In this study, we report long-term-stable near-infrared (NIR) polymer dots for in vivo tumor vasculature imaging. NIR-emitting polymer dots were prepared by encapsulating an NIR dye, silicon 2,3-naphthalocyanine bis(trihexylsilyloxide) (NIR775), into a matrix of polymer dots, poly[2-methoxy-5(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV), using a nanoscale precipitation method. The prepared NIR polymer dots were sub-5 nm in diameter, exhibited narrow-band NIR emission at 778 nm with a full width at half-maximum of 20 nm, and displayed a large Stokes shift (>300 nm) between the excitation and emission maxima. In addition, no significant uptake of the prepared NIR polymer dots by either human glioblastoma U87MG cells or human non-small cell lung carcinoma H1299 cells was detected. Moreover, these NIR polymer dots showed long-term colloidal stability and photostability in water at 4 degrees C for at least 9 months, and were able to image vasculature of xenografted U87MG tumors in living mice after intravenous injection. These results thus open new opportunities for the development of whole-body imaging of mice based on NIR polymer dots as fluorescent nanoprobes.
机译:荧光纳米探针已成为用于癌症成像的最有前途的材料类别之一。然而,关于它们在生物系统和环境中的长期胶体稳定性和光稳定性的理解仍然存在许多未解决的问题。在这项研究中,我们报告了体内肿瘤血管成像的长期稳定的近红外(NIR)聚合物点。通过将NIR染料2,3,萘酞菁硅双(三己基甲硅烷基氧化物)(NIR775)封装到聚合物点的基质中制备聚NIR聚合物点,聚[2-甲氧基-5(2-乙基己基氧基)-1,4 -亚苯基亚乙烯基](MEH-PPV),采用纳米沉淀法。制备的NIR聚合物点的直径小于5 nm,在778 nm处显示窄带NIR发射,半峰全宽为20 nm,并且在激发和发射之间显示出较大的斯托克斯位移(> 300 nm)最大值。另外,未检测到人胶质母细胞瘤U87MG细胞或人非小细胞肺癌H1299细胞对制备的NIR聚合物点的显着摄取。而且,这些NIR聚合物点在4℃的水中显示出长期的胶体稳定性和光稳定性至少9个月,并且能够在活体小鼠中对异种移植的U87MG肿瘤的脉管系统进行成像。因此,这些结果为基于NIR聚合物点作为荧光纳米探针的小鼠全身成像开发提供了新的机会。

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