Porphyrin-based Nanosonosensitizers Combined with Targeting Peptides for Sonodynamic Therapy of Glioma

被引:5
作者
Jiang, Mei-Yu [1 ,2 ,3 ]
Wu, Jia-Sheng [1 ,2 ]
Liu, Wei-Min [1 ,2 ,3 ]
Ren, Hao-Hui [1 ,2 ]
Wang, Xin [1 ,2 ,3 ]
Wang, Peng-Fei [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Photochem Convers & Optoelect Mat, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Tech Inst Phys & Chem, CityU CAS Joint Lab Funct Mat & Devices, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Sch Future Technol, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Sonodynamic therapy; Glioma; Cyclic peptide; Target enrichment; Deep penetration; CANCER; ULTRASOUND;
D O I
10.1007/s10118-022-2795-0
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Traditional cancer treatments have disadvantages of large trauma area and toxic side effects while killing cancer cells. Peptide-targeted sonodynamic therapy (SDT) can effectively improve specificity of cancer treatment and overcome the problem of low tissue penetration depth caused by a photo-driven therapy. Herein, we developed a porphyrin-based sonosensitizer with a water-soluble polymer as a biological carrier and a cRGD peptide for tumor targeting, which constituted a nano sonosensitizer (T-cRGD NPs) for fluorescence imaging-guided sonodynamic therapy. A comparable sonosensitizer (T-PEG NPs) without the targeting unit was also prepared for illustration of therapeutic performance. Attribute to the role of peptide targeting, T-cRGD NPs can accumulate and enter tumor cells for fluorescence imaging and show a superior SDT effect than T-PEG NPsin vitro. The imaging in vivo reveals that T-cRGD NPs can enrich in tumor tissues within 14 h with a good biocompatibility.
引用
收藏
页码:1120 / 1128
页数:9
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