L. Bretin, D. Léger, A. Pinon, Soukaina Bouramtane, Frédérique Brégier, Vincent Sol, V. Chaleix, B. Liagre
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引用次数: 2
Abstract
Photodynamic therapy (PDT) using porphyrins has been approved in treatment of several solid tumors thanks to generation of cytotoxic reactive oxygen species (ROS). However, low physiological solubility and lack of selectivity towards tumors sites are the main limitations of their clinical use. Nanoparticles are able to spontaneously accumulate in solid tumors through the enhanced permeability and retention (EPR) effect due to leaky vasculature, poor lymphatic drainage and increased vessel permeability. Herein, we demonstrated added value of nanoparticles vectorization strategy on anticancer efficacy of the 5-(4-hydroxyphenyl)-10,15,20-triphenylporphyrin (TPPOH). Using the 80 nm silica nanoparticles (SNPs) coated with xylan-TPPOH conjugate (TPPOH-X), we highlighted on HT-29 tumor-bearing nude mice, a high anticancer efficacy of TPPOH-X SNPs compared to TPPOH free.
由于产生细胞毒性活性氧(ROS),使用卟啉的光动力疗法(PDT)已被批准用于治疗几种实体肿瘤。然而,低生理溶解度和对肿瘤部位缺乏选择性是其临床应用的主要限制。由于血管渗漏、淋巴引流不良和血管通透性增加,纳米颗粒能够通过增强的渗透性和滞留(EPR)效应在实体肿瘤中自发积聚。在此,我们证明了纳米粒子矢量化策略对5-(4-羟基苯基)-10,15,20-三苯基卟啉(TPPOH)抗癌功效的附加价值。利用80 nm包被木聚糖-TPPOH偶联物(TPPOH- x)的二氧化硅纳米颗粒(SNPs),我们在HT-29荷瘤裸鼠身上发现,与不含TPPOH的SNPs相比,TPPOH- x SNPs具有更高的抗癌功效。