首页> 外文期刊>Photodiagnosis and Photodynamic Therapy >Photodynamic therapeutic effect of indocyanine green entrapped in polymeric nanoparticles and their anti-EGFR- conjugate in skin cancer in CD1 mice
【24h】

Photodynamic therapeutic effect of indocyanine green entrapped in polymeric nanoparticles and their anti-EGFR- conjugate in skin cancer in CD1 mice

机译:高分子纳米颗粒中吲哚菁绿及其抗EGFR结合物对CD1小鼠皮肤癌的光动力治疗作用

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Background: Indocyanine green (ICG) is a promising photosensitive agent for photodynamic therapy (PDT) of tumors. Encapsulating ICG dye in polymeric nanoparticles based on PEBBLE technology forming (ICG-PEBBLE) could improve the aqueous stability of the entrapped ICG molecules. The study objective is to investigate the PDT effect of free ICG-PEBBLE and its Anti-EGFR conjugate. Methods: Skin squamous cell carcinoma was induced in CD1 mice by dimethylbenzanthracene (DMBA) and 12-O-tetradecanoyl-phorbol-13-acetate (TPA) followed by a PDT protocol for four weeks. Results: PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR decreased skin tumor sizes. Our findings revealed that the inflammatory mediators tumor necrosis factor (TNF-α ), nitric oxide (NO), cycloxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX), the angiogenic mediator vascular endothelial growth factor (VEGF), and proliferating cell nuclear antigen (PCNA) were decreased, while apoptosis, caspase-3 and histone acetylation were induced in tumor bearing groups after PDT using both of ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR. Conclusion: The present study indicated the effectiveness of PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR as an inhibitor modality for tumor size, apoptosis, angiogenesis and tumor inflammation. The conjugating of ICG-PEBBLE to anti-EGFR was found to be more effective in inhibiting VEGF and in increasing caspase-3 compared to free ICG-PEBBLE, but there were no other preferential PDT efficacy.
机译:背景:吲哚菁绿(ICG)是一种有前景的光敏剂,用于肿瘤的光动力疗法(PDT)。基于PEBBLE技术形成(ICG-PEBBLE)将ICG染料包埋在聚合物纳米颗粒中可以提高所捕获ICG分子的水稳定性。研究目的是研究游离ICG-PEBBLE及其抗EGFR共轭物的PDT效应。方法:用二甲基苯并蒽(DMBA)和12-O-十四烷酰基-phorbol-13-乙酸盐(TPA)诱导CD1小鼠皮肤鳞状细胞癌,然后进行PDT方案持续4周。结果:使用ICG-PEBBLE或ICG-PEBBLE-Anti-EGFR的PDT减少了皮肤肿瘤的大小。我们的发现表明,炎性介质肿瘤坏死因子(TNF-α),一氧化氮(NO),环氧化酶2(COX-2)和5-脂氧合酶(5-LOX)是血管生成介质血管内皮生长因子(VEGF)。 PDT后,使用ICG-PEBBLE或ICG-PEBBLE-Anti-EGFR均可降低荷瘤组的凋亡,增殖细胞核抗原(PCNA),并诱导凋亡,caspase-3和组蛋白乙酰化。结论:本研究表明使用ICG-PEBBLE或ICG-PEBBLE-抗-EGFR作为肿瘤形态,凋亡,血管生成和肿瘤炎症的抑制剂,PDT的有效性。发现ICG-PEBBLE与抗EGFR的结合与游离ICG-PEBBLE相比,在抑制VEGF和增加caspase-3方面更有效,但没有其他优先的PDT功效。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号