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The mitochondria-targeted and IR780-regulated theranosomes for imaging and enhanced photodynamic/photothermal therapy

机译:用于成像和增强的光动力/光热疗法的线粒体靶向和IR780调节的托管体

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The applications of photodynamic therapy (PDT) are usually limited by the low tumor selectivity of photosensitizers. Herein, we report a near infrared (NIR) imaging multifunctional nanocarrier, so called “theranosome (TNS)”, which encapsulated both chlorin e6 (Ce6, photosensitizer) and IR780 iodide (IR780, photothermal and NIR imaging agent) to realize enhanced PDT efficacy. The phototoxicity of Ce6 was effectively restrained by IR780. Upon NIR laser irradiation at 808 nm, IR780 in the TNS could be degraded, while the phototoxicity of Ce6 could be recovered. In addition, we proved that attaching a triphenylphosphonium (TPP) group to the TNS (TPP-IR780/Ce6-TNS) could greatly facilitate its mitochondrial targeting ability so as to offer a remarkably improved PDT efficacy. This newly constructed TNS exhibited high toxicity to the tumor cells in vitro , indicating TNS was a promising nanocarrier used as a PTT combined activatable PDT.
机译:光动力治疗(PDT)的应用通常受到光敏剂的低肿瘤选择性的限制。在此,我们报告了近红外(NIR)成像多功能纳米载体,所谓的“TherAnosome(TNS)”,其封装氯e6(Ce6,光敏剂)和IR780碘化物(IR780,光热和NIR成像剂)来实现增强的PDT功效。 IR780有效抑制CE6的光毒性。在808nm处的NIR激光照射时,TNS中的IR780可能会降低,而CE6的光毒性可以回收。此外,我们证明,将三苯基膦酰基(TPP)组(TPP-IR780 / CE6-TNS)附着可以极大地促进其线粒体靶向能力,以便提供显着改善的PDT功效。这种新构建的TNS在体外对肿瘤细胞表现出高毒性,表明TNS是一种有望的纳米载体,其用作PTT合并可活性PDT。

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