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首页> 外文期刊>Biomaterials >Selective photodynamic therapy based on aggregation-induced emission enhancement of fluorescent organic nanoparticles.
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Selective photodynamic therapy based on aggregation-induced emission enhancement of fluorescent organic nanoparticles.

机译:基于聚集诱导的荧光有机纳米粒子发射增强的选择性光动力疗法。

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摘要

Three binary molecule conjugates were designed and synthesized by conjugating a chromophore (3, 6-bis-(1-methyl-4-vinylpyridinium)-carbazole diiodide, BMVC) to mono-, bis- and trishydroxyl photosensitizers, respectively. BMVC plays the role of cancer cells recognizer; AIEE (aggregation-induced emission enhancement) generator and FRET (Fluorescence Resonance Energy Transfer) donor. The self assembling properties of these binary conjugates result in different degrees of AIEE and then achieve the formations of FONs (fluorescent organic nanoparticles), which present efficient FRET and singlet oxygen generations. Biologically, FONs-photosensitizers from these compounds were much more phototoxicities to cancer cell than to normal cell without significant dark toxicity. In addition, their intracellular fluorescent colors switching upon photo-excitation are expected to be used for further cell death biomarker applications. This improved photodynamic activity might be due to the aggregation of compounds in the cell that form FONs which can promote PDT (photodynamic therapy) and are observed in cancer cell but not normal cell.
机译:通过将发色团(3,6-双-(1-甲基-4-乙烯基吡啶鎓)-咔唑二碘化物,BMVC)与单,双和三羟基光敏剂偶联,设计并合成了三种二元分子偶联物。 BMVC发挥癌细胞识别器的作用; AIEE(聚集诱导的发射增强)发生器和FRET(荧光共振能量转移)供体。这些二元共轭物的自组装特性导致不同程度的AIEE,然后实现FON(荧光有机纳米粒子)的形成,从而形成高效的FRET和单线态氧生成。从生物学上讲,这些化合物的FONs-光敏剂对癌细胞的光毒性比对正常细胞的光毒性要大得多,而对正常细胞没有明显的暗毒性。另外,预期它们在光激发后转换的细胞内荧光颜色将用于进一步的细胞死亡生物标记物应用。这种改善的光动力活性可能是由于细胞中形成FON的化合物的聚集,这些化合物可以促进PDT(光动力疗法),并且在癌细胞而非正常细胞中观察到。

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