Delivery of coumarin-containing all-trans retinoic acid derivatives via targeted nanoparticles encapsulating indocyanine green for chemo/photothermal/photodynamic therapy of breast cancer

被引:11
|
作者
Jiao, Jia [1 ]
Wu, Hongshuai [1 ]
Chen, Fanghui [1 ]
Chen, Renjie [2 ]
Sun, Baiwang [1 ]
Wang, Mingliang [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Nanjing 210089, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 2, Nanjing 210011, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
PRODRUG NANOPARTICLES; SYNERGISTIC THERAPY; DRUG-DELIVERY; IN-VIVO; MICELLES; RELEASE; CELLS; CHEMOTHERAPY; DOXORUBICIN; PH;
D O I
10.1039/c8nj00578h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Development of chemo/photothermal/photodynamic therapy with nanoplatforms offers a promising strategy for effective cancer treatment. Recently, all-trans retinoic acid (ATRA), as a potential antitumor drug, has attracted great attention due to its antitumor activity. In this study, a novel coumarin-containing ATRA (AC) and indocyanine green (ICG) dye-loaded nanoparticles with the targeted ligand cyclic (Arg-Gly-Asp-d-Phe-Lys) (cRGD) peptide were fabricated by self-assembly and used as a new theranostic nanoplatform for chemo/photothermal/photodynamic therapy. The as-formed nanoparticles (AC/ICG-TNPs) had a diameter of around 133 nm with uniform monodispersity. Additionally, AC/ICG-TNPs showed marked stability under normal physiological conditions. However, it could rapidly release drugs in a mild acidic microenvironment. Moreover, confocal microscopic observations confirmed that the uptake of AC/ICG-TNPs increased in the breast cancer cells, particularly in MDA-MB-231 cells, probably mediated by cRGD via specific recognition of the overexpressed integrin (v3). Moreover, free AC exhibited stronger cytotoxic effects than free ATRA in the MTT assay, and AC/ICG-TNPs were demonstrated to possess excellent antitumor efficacy when exposed to NIR irradiation through the combination therapy. Hence, the therapeutic method designed in this study is a good candidate for improved bioactivity of ATRA and site-specific combinational therapy against breast cancer.
引用
收藏
页码:8805 / 8814
页数:10
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