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Biocompatible astaxanthin as a novel marine-oriented agent for dual chemo-photothermal therapy

机译:生物相容性虾青素作为一种新型海洋定向药物用于双化学光热疗法

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摘要

The photothermal effect of a marine-oriented xanthophyll carotenoid, astaxanthin (AXT), was characterized based on its potential absorption of visible laser light and conversion of optical light energy into heat for thermal treatment. As an antioxidant and anticancer agent, AXT extracted from marine material can be utilized for photothermal therapy due to its strong light absorption. The current study investigated the feasibility of the marine-based material AXT to increase the therapeutic efficacy of chemo-photothermal therapy (PTT) by assessing photothermal sessions in both cells and tumor tissues. A quasi-cw Q-switched 80 W 532 nm laser system was utilized to induce thermal necrosis in in vitro and in vivo models. An in vitro cytotoxicity study of AXT was implemented using squamous cell carcinoma (VX2) and macrophage (246.7) cell lines. In vivo PTT experiments were performed on 17 rabbits bearing VX2 tumors on their eyes that were treated with or without intratumoral injection of AXT at a dose of 100 μl (300 μg/ml) followed by laser irradiation at a low irradiance of 0.11 W/cm2. Fluorescence microscopy images revealed cellular death via apoptosis and necrosis owing to the dual chemo-photothermal effects induced by AXT. In vivo experimental results demonstrated that the AXT-assisted irradiation entailed a temperature increase by 30.4°C after tumor treatment for 4 min. The relative variations in tumor volume confirmed that the tumors treated with both AXT and laser irradiation completely disappeared 14 days after treatment, but the tumors treated under other conditions gradually grew. Due to selective light absorption, AXT-assisted laser treatment could be an effective thermal therapy for various drug-resistant cancers.
机译:基于面向海洋的叶黄素类胡萝卜素虾青素(AXT)的光热效应是基于其对可见激光的潜在吸收并将光能转化为热进行热处理而表征的。从海洋材料中提取的AXT作为抗氧化剂和抗癌剂,由于其强大的光吸收能力,可用于光热疗法。当前的研究通过评估细胞和肿瘤组织中的光热疗程,研究了海洋材料AXT在提高化学光热疗法(PTT)的治疗功效方面的可行性。在体外和体内模型中,使用准连续Q调Q 80 W 532 nm激光系统诱导热坏死。使用鳞状细胞癌(VX2)和巨噬细胞(246.7)细胞系进行了AXT的体外细胞毒性研究。体内PTT实验是对17只眼睛上有VX2肿瘤的兔子进行的,这些兔子接受或不接受肿瘤内注射AXT的剂量为100μl(300μg/ ml),然后以低辐照度0.11 W / cm进行激光照射 2 。荧光显微镜图像显示由于AXT诱导的双重化学光热效应,细胞通过凋亡和坏死而死亡。体内实验结果表明,在肿瘤治疗4分钟后,AXT辅助照射会使温度升高30.4°C。肿瘤体积的相对变化证实了用AXT和激光照射治疗的肿瘤在治疗后14天完全消失,但是在其他条件下治疗的肿瘤逐渐生长。由于选择性的光吸收,AXT辅助激光治疗可能成为各种耐药性癌症的有效热疗法。

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