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上转换介孔硅纳米颗粒中共载药物和光敏剂的光诱导解组装:一种有效的协同癌症治疗方法。

Photo-induced reactions for disassembling of coloaded photosensitizer and drug molecules from upconversion-mesoporous silica nanoparticles: An effective synergistic cancer therapy.

机构信息

Department of Chemistry, Institute of Interdisciplinary Convergence Research, Research Institute of Chem-Bio Diagnostic Technology, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul 06974, Republic of Korea.

Department of Applied Chemistry, Sardar Vallabhbhai National Institute of Technology, Surat 395 007, India.

出版信息

Mater Sci Eng C Mater Biol Appl. 2020 May;110:110545. doi: 10.1016/j.msec.2019.110545. Epub 2020 Jan 8.

Abstract

Photodynamic therapy is an emerging noninvasive cancer treatment approach, which requires a photosensitizer (PS), light, and molecular oxygen. In this study, we have successfully fabricated a dual nature (pH- and reactive-oxygen-species-responsive) upconversion nanoparticles (UCNPs) to utilize coloaded doxorubicin (DOX) and chlorin e6 (Ce6) with high antitumor efficacy. The model anticancer drug (DOX) and PS (Ce6) were conjugated in a ratio of 1:1 (w:w), and then loaded on the surface of UCNPs@mesoporous silica (mSiO) (85.63 ± 9.87 nm). Cellular uptake could be achieved by either increased permeability or ionic effect of UCNPs@mSiO, where Ce6 controlled the DOX release under a near-infrared (NIR) laser irradiation at 980 nm. A cytotoxicity analysis revealed that the dual-responsive UCNPs@mSiO could successfully deliver DOX and Ce6 at the tumor site, causing cell death with a high efficiency. This study shows that the modified UCNPs@mSiO is a promising system to realize NIR-light-triggered PS and drug delivery approach to improve synergistic therapies in vitro and in vivo, in the future.

摘要

光动力疗法是一种新兴的非侵入性癌症治疗方法,它需要一种光敏剂(PS)、光和分子氧。在本研究中,我们成功地制备了一种双功能(pH 和活性氧物种响应)上转换纳米粒子(UCNPs),以利用共负载的阿霉素(DOX)和氯乙酮(Ce6)实现高抗肿瘤功效。模型抗癌药物(DOX)和 PS(Ce6)以 1:1(w:w)的比例偶联,然后负载在介孔硅(mSiO)(85.63±9.87nm)上的 UCNPs 表面。UCNPs@mSiO 的通透性增加或离子效应可实现细胞摄取,其中 Ce6 在近红外(NIR)激光 980nm 照射下控制 DOX 的释放。细胞毒性分析表明,双响应性 UCNPs@mSiO 可成功地在肿瘤部位递送 DOX 和 Ce6,从而高效地导致细胞死亡。本研究表明,修饰后的 UCNPs@mSiO 是一种很有前途的系统,可以实现 NIR 光触发 PS 和药物递送方法,以提高体外和体内的协同治疗效果,未来可期。

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