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聚合物胶束分子递送的荧光共振能量转移可视化

Fluorescence Resonance Energy Transfer Visualization of Molecular Delivery from Polymeric Micelles.

作者信息

Liang Yan, Huo Qingqing, Lu Wei, Jiang Lutao, Gao Wenxia, Xu Long, Han Shangcong, Cao Jie, Zhang Tingting, Sun Yong, He Bin

出版信息

J Biomed Nanotechnol. 2018 Jul 1;14(7):1308-1316. doi: 10.1166/jbn.2018.2585.

Abstract

Polymeric micelles are important carriers for anticancer drug delivery. However, rare papers focused on the dynamic of drug in the core of micelles. In this paper, we used fluorescence resonance energy transfer (FRET) technique to investigate the dynamic diffusion of drug from polymeric micelles. mPEG-PCL diblock copolymers were used as carriers. A pair of fluorescence molecules Cy3 and Cy5 was selected to evoke the FRET phenomenon. Cy5 was immobilized on the terminal group of PCL segments, Cy3 was encapsulated in the Cy5 modified polymeric micelles as the model drug. The drug loaded polymeric micelles were incubated with 4T1 breast cancer cells. The FRET was observed to explore the dynamic of Cy3 in the micelles. The results showed that the Cy3 loaded micelles were stable in aqueous solution as the energy-transfer efficiency (ETE, I660/I565) rarely decreased even when the time was as long as 120 h. The ETE increased with the content of encapsulated Cy3. The FRET spectra showed that the ETE of the Cy3 loaded polymeric micelles lowered with the release of Cy3 in PBS. The intracellular tracking of the Cy3 loaded micelles found more than 60% loaded drug was release within 12 h with the calculation of ETE in FRET spectra and it was same to confocal laser scanning and flow cytometry results.

摘要

聚合物胶束是抗癌药物递送的重要载体。然而,很少有论文关注胶束核心中药物的动态情况。在本文中,我们使用荧光共振能量转移(FRET)技术来研究药物从聚合物胶束中的动态扩散。聚乙二醇-聚己内酯(mPEG-PCL)二嵌段共聚物用作载体。选择一对荧光分子Cy3和Cy5来引发FRET现象。Cy5固定在PCL链段的末端基团上,Cy3作为模型药物被包裹在Cy5修饰的聚合物胶束中。将载药聚合物胶束与4T1乳腺癌细胞一起孵育。通过观察FRET来探究Cy3在胶束中的动态情况。结果表明,载有Cy3的胶束在水溶液中是稳定的,因为即使时间长达120小时,能量转移效率(ETE,I660/I565)也很少降低。ETE随着包裹的Cy3含量的增加而增加。FRET光谱表明,载有Cy3的聚合物胶束的ETE随着Cy3在磷酸盐缓冲液(PBS)中的释放而降低。对载有Cy3的胶束进行细胞内追踪发现,通过FRET光谱中的ETE计算,超过60%的载药在12小时内释放,这与共聚焦激光扫描和流式细胞术的结果一致。

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