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自佐剂光敏剂纳米颗粒用于联合光动力免疫治疗。

Self-adjuvanting photosensitizer nanoparticles for combination photodynamic immunotherapy.

机构信息

Key Laboratory of Colloid and Interface Chemistry of the Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, Shandong 250100, China.

State Key Laboratory of Microbial Technology, Shandong University, Qingdao, Shandong 266237, China.

出版信息

Biomater Sci. 2021 Oct 12;9(20):6940-6949. doi: 10.1039/d1bm01139a.

Abstract

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 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.

摘要

联合癌症免疫疗法通过协同多种治疗药物的优势,在肿瘤治疗中显示出巨大的潜力。在此,我们报告了一种一步法组装治疗性纳米粒子(NPs)的方法,用于共递送光敏剂和佐剂以进行联合光动力疗法(PDT)和免疫疗法。 NPs 是通过氯乙酮(Ce6)和咪唑并喹啉基 TLR7 激动剂(IMDQ)的自组装获得的,分别实现了 Ce6 和 IMDQ 的高载药效率 72.2%和 27.8%。激光照射后,所得 NPs 不仅能有效诱导光动力免疫原性癌细胞死亡,还能引发强烈的抗肿瘤免疫,显著抑制双侧肿瘤模型中的原发性和远处肿瘤。本研究证明了自组装 NPs 在共递递送多种治疗药物以增强抗肿瘤疗效方面的潜力。

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