Self-adjuvanting photosensitizer nanoparticles for combination photodynamic immunotherapy

被引:13
作者
Zhang, Guiqiang [1 ]
Wang, Ning [1 ]
Sun, Haifeng [1 ]
Fu, Xiao [1 ]
Zhai, Shumei [1 ]
Cui, Jiwei [1 ,2 ,3 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Key Lab Colloid & Interface Chem, Minist Educ, Jinan 250100, Shandong, Peoples R China
[2] Shandong Univ, State Key Lab Microbial Technol, Qingdao 266237, Shandong, Peoples R China
[3] Shandong Univ, Adv Med Res Inst, Jinan 250012, Shandong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
IMMUNOGENIC CELL-DEATH; CANCER-IMMUNOTHERAPY; INCREASES; DELIVERY; BLOCKADE; THERAPY;
D O I
10.1039/d1bm01139a
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Combination cancer immunotherapy that synergizes the advantages of multiple therapeutic agents has shown great potential in tumor treatment. Herein, we report the one-step assembly of therapeutic nanoparticles (NPs) to co-deliver photosensitizers and adjuvants for combination photodynamic therapy (PDT) and immunotherapy. The NPs are obtained via self-assembly of chlorin e6 (Ce6) and imidazoquinoline-based TLR7 agonists (IMDQ), which results in a high loading efficacy of 72.2% and 27.8% for Ce6 and IMDQ, respectively. Upon laser irradiation, the resulting NPs could not only effectively induce photodynamic immunogenic cancer cell death, but also elicit robust antitumor immunity, leading to significant inhibition of both primary and distant tumors in a bilateral tumor model. This study demonstrates the potential of self-assembled NPs in co-delivering multiple therapeutics for potential immunotherapy to enhance the antitumor efficacy.
引用
收藏
页码:6940 / 6949
页数:10
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