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基于上转换诊疗一体化纳米平台的体内 808nm 图像引导光动力治疗。

In vivo 808 nm image-guided photodynamic therapy based on an upconversion theranostic nanoplatform.

机构信息

State Key Laboratory of Luminescence and Applications. Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, 130033, Changchun, Jilin, China.

出版信息

Nanoscale. 2015 Sep 28;7(36):14914-23. doi: 10.1039/c5nr03690a. Epub 2015 Aug 24.

DOI:10.1039/c5nr03690a
PMID:26300064
Abstract

A new strategy for efficient in vivo image-guided photodynamic therapy (PDT) has been demonstrated utilizing a ligand-exchange constructed upconversion-C60 nanophotosensitizer. This theranostic platform is superior to the currently reported nanophotosensitizers in (i) directly bonding photosensitizer C60 to the surface of upconversion nanoparticles (UCNPs) by a smart ligand-exchange strategy, which greatly shortened the energy transfer distance and enhanced the (1)O2 production, resulting in the improvement of the therapeutic effect; (ii) realizing in vivo NIR 808 nm image-guided PDT with both excitation (980 nm) and emission (808 nm) light falling in the biological window of tissues, which minimized auto-fluorescence, reduced light scatting and improved the imaging contrast and depth, and thus guaranteed noninvasive diagnostic accuracy. In vivo and ex vivo tests demonstrated its favorable bio-distribution, tumor-selectivity and high therapeutic efficacy. Owing to the effective ligand exchange strategy and the excellent intrinsic photophysical properties of C60, (1)O2 production yield was improved, suggesting that a low 980 nm irradiation dosage (351 J cm(-2)) and a short treatment time (15 min) were sufficient to perform NIR (980 nm) to NIR (808 nm) image-guided PDT. Our work enriches the understanding of UCNP-based PDT nanophotosensitizers and highlights their potential use in future NIR image-guided noninvasive deep cancer therapy.

摘要

一种新的高效活体影像引导光动力治疗(PDT)策略已经得到了证明,该策略利用配体交换构建的上转换-C60 纳米光敏剂。与目前报道的纳米光敏剂相比,该治疗平台具有以下优势:(i)通过智能配体交换策略,将光敏剂 C60 直接键合到上转换纳米粒子(UCNP)的表面,大大缩短了能量转移距离,增强了 (1)O2 的产生,从而提高了治疗效果;(ii)实现了体内近红外 808nm 影像引导 PDT,激发光(980nm)和发射光(808nm)均落在组织的生物窗口内,最大限度地减少了自发荧光,降低了光散射,提高了成像对比度和深度,从而保证了非侵入性诊断的准确性。体内和体外试验证明了其良好的生物分布、肿瘤选择性和高治疗效果。由于有效的配体交换策略和 C60 的优异固有光物理性质,(1)O2 的产生效率得到了提高,这表明低 980nm 辐照剂量(351 J cm(-2)) 和短的治疗时间(15 分钟)足以进行近红外(980nm)到近红外(808nm)影像引导 PDT。我们的工作丰富了基于上转换纳米粒子的 PDT 纳米光敏剂的认识,并强调了它们在未来近红外影像引导非侵入性深部癌症治疗中的潜在应用。

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