Heparinmodified photosensitizer-loaded liposomes for tumor treatment and alleviating metastasis in phototherapy

被引:23
作者
Cao, Dinglingge [1 ,2 ]
Li, Huangjuan [1 ,3 ]
Luo, Yuan [3 ]
Feng, Nianping [1 ]
Ci, Tianyuan [1 ,2 ,3 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Dept Pharmaceut Sci, Shanghai 201203, Peoples R China
[2] Fudan Univ, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[3] China Pharmaceut Univ, Dept Pharmaceut, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Phototherapy; Tumor metastasis; Low molecular weight heparin; Indocyanine green; Liposomes; PHOTODYNAMIC THERAPY; CANCER; HEPARIN; NANOPARTICLES; ACTIVATION; STABILITY;
D O I
10.1016/j.ijbiomac.2020.12.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Phototherapy holds promise in cancer treatment for its prominent antitumor efficacy and low systematic toxicity compared with traditional chemotherapy. However, the higher risk of tumor metastasis caused by the severe hypoxic state during phototherapy is a threat in practical use. Here, in order to tackle this challenge, we developed a delivery system via loading the photosensitizer indocyanine green (ICG) into the low molecular weight heparin (LMWH) modified liposomes (LMWH-ICG-Lip) to realize the synergistic effects between photosensitizer and drug vehicle, achieving better phototherapeutic efficacy and meanwhile alleviating the potential risk of tumor metastasis caused by phototherapy. In this system, besides elongating the photosensitizers' circulation time and enhancing their accumulating efficacy to tumor tissues, LMWH itself also exhibited anti-metastasis efficacy via inhibiting adhesion of platelets to tumor cells and decreasing migration and invasion capability of tumor cells. In vivo efficacy evaluation was conducted on orthotopic 4T1 breast cancer model, and the system of LMWH-ICG-Lip could alleviate metastasis potential of residual tumor cells after irradiation, and elicit optimistic antitumor and anti-metastasis efficacy for phototherapy. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:526 / 536
页数:11
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