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使用含双光敏剂的上转换纳米颗粒的近红外光触发光动力疗法与细胞凋亡

Near-Infrared Light-Triggered Photodynamic Therapy and Apoptosis Using Upconversion Nanoparticles With Dual Photosensitizers.

作者信息

Lee Song Yeul, Lee Ruda, Kim Eunha, Lee Sanghee, Park Yong Il

机构信息

School of Chemical Engineering, Chonnam National University, Gwangju, South Korea.

International Research Organization for Advanced Science and Technologyn, Kumamoto University, Kumamoto, Japan.

出版信息

Front Bioeng Biotechnol. 2020 Apr 16;8:275. doi: 10.3389/fbioe.2020.00275. eCollection 2020.

Abstract

Elucidation of upconversion nanoparticles (UCNPs) that can be excited by near-infrared (NIR) light is an interesting topic in the field of photodynamic therapy (PDT). However, the PDT efficiency of conventional UCNPs is limited due to the low quantum yield and overheating effect of the 980 nm light source. In this study, a light source with a wavelength of 808 nm was used as an excitation source for Nd-doped UCNPs to solve the overheating effect. UCNPs with a core@shell structure (NaYF:Yb,Er,Nd@NaYF:Yb,Nd) were synthesized to increase the upconversion emission efficiency. Dual-color emitting Er-doped UCNPs and dual photosensitizers (Chlorin e6 and Rose Bengal) were used for enhanced PDT. Each photosensitizer could absorb red and green emissions of the UCNPs to generate reactive oxygen species (ROS), respectively. The ROS generation in a dual photosensitizer system is significantly higher than that in a single photosensitizer system. Additionally, PDT induces immunogenic apoptosis. In this study, by utilizing a highly efficient PDT agent, PDT-induced apoptosis was studied by biomarker analysis.

摘要

阐明可被近红外(NIR)光激发的上转换纳米粒子(UCNPs)是光动力疗法(PDT)领域一个有趣的课题。然而,由于980 nm光源的低量子产率和过热效应,传统UCNPs的PDT效率受到限制。在本研究中,使用波长为808 nm的光源作为掺钕UCNPs的激发源,以解决过热效应。合成了具有核壳结构(NaYF:Yb,Er,Nd@NaYF:Yb,Nd)的UCNPs,以提高上转换发射效率。双色发射的掺铒UCNPs和双光敏剂(叶绿素e6和孟加拉玫瑰红)用于增强PDT。每种光敏剂可分别吸收UCNPs的红色和绿色发射光以产生活性氧(ROS)。双光敏剂系统中的ROS生成明显高于单光敏剂系统。此外,PDT可诱导免疫原性凋亡。在本研究中,通过使用高效的PDT剂,通过生物标志物分析研究了PDT诱导的凋亡。

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