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Potentiating photodynamic therapy of ICG-loaded nanoparticles by depleting GSH with PEITC

机译:其余ICG-loaded光动力治疗纳米粒子通过消耗与PEITC谷胱甘肽

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摘要

Photodynamic therapy (PDT) is a clinically approved cancer treatment which utilizes reactive oxygen species (ROS) to eradicate cancer cells. But the high concentration of GSH inside tumor cells can neutralize the generated ROS during PDT, resulting in an insufficient therapeutic effect. To address this issue, we combined ICG-loaded nanoparticles with PEITC for potent PDT. ICG encapsulated in novel hydroxyethyl starch-oleic acid conjugate (HES-OA) nanoparticles (approximate to 50 nm) exhibited excellent stability and efficient singlet oxygen generation under laser irradiation, promoted cellular uptake, and enhanced tumor accumulation, whilst PEITC depleted intracellular GSH significantly. As a result, PDT based on ICG-loaded NPs combined with PEITC synergistically suppressed cancer cells both in vitro and in vivo. Potentiating ICG-loaded NPs with PEITC represents a novel and efficient strategy to enhance PDT efficacy.
机译:光动力疗法(PDT)是一种临床通过利用反应性的癌症治疗氧物种(ROS)根除癌细胞。但高浓度的肿瘤内谷胱甘肽细胞可以中和期间生成的活性氧PDT,导致一个治疗不足的效果。ICG-loaded纳米粒子与PEITC有力PDT。starch-oleic共轭酸(HES-OA)纳米颗粒(近似50 nm)展出优秀的稳定和高效的单线态氧代在激光辐照下,晋升肿瘤细胞吸收,和增强的积累,同时PEITC耗尽细胞内谷胱甘肽显著。ICG-loaded NPs与PEITC相结合抑制癌细胞的增效剂体外和体内。PEITC代表小说和高效策略增强PDT功效。

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