光热治疗
光毒性
光敏剂
化学
壳聚糖
药物输送
人血清白蛋白
生物物理学
癌症研究
光动力疗法
毒品携带者
药理学
医学
纳米技术
材料科学
体外
生物化学
光化学
生物
有机化学
作者
Haiyan Hu,Qi Qi,Ziyi Dong,Xianglong Yu,Yu-Jia Mo,Juyuan Luo,Yan Wang,Shouying Du,Yang Lu
标识
DOI:10.1016/j.carbpol.2020.116335
摘要
Current metastatic breast cancer therapies are not only affected by limited drug delivery options, but also restricted to the monotherapies. Here, we synthesized trimethyl chitosan (TMC), loaded it with photosensitizer IR780 or bufalin by ionic gelation, and coated it with human serum albumin (HSA) by electrostatic absorption (designated TIH or TBH, respectively). The near-spherical nanoparticles had a size of approximately 30 nm, exerted strong photothermal effects, and enhanced cellular mitochondrion colocation and phototoxicity. Tumor microenvironments were disrupted by TIH-mediated photothermal effects, which enhanced the accumulation of a second TBH dose in the tumor that promoted deep penetration in the whole tumor mass. After laser irradiation our nanoplatform enhanced cancer tissue accessibility and substantially suppressed tumor growth, and causing a 98.46 % inhibition of lung metastasis. Thus HSA-masked TMC represents a promising tumor-targeted drug delivery strategy with synergistic modality that may improve the therapeutic outcome of metastatic breast cancer.
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