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通过一步融合方法工程化的血小板-药物偶联物用于转移性和术后癌症治疗。

Platelet-Drug Conjugates Engineered via One-step Fusion Approach for Metastatic and Postoperative Cancer Treatment.

机构信息

State Key Laboratory of Advanced Drug Delivery and Release Systems, Zhejiang Provincial Key Laboratory for Advanced Drug Delivery Systems, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou, 310058, China.

Department of Hepatobiliary and Pancreatic Surgery, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, 310009, China.

出版信息

Angew Chem Int Ed Engl. 2024 Sep 9;63(37):e202403541. doi: 10.1002/anie.202403541. Epub 2024 Jun 26.

Abstract

The exploration of cell-based drug delivery systems for cancer therapy has gained growing attention. Approaches to engineering therapeutic cells with multidrug loading in an effective, safe, and precise manner while preserving their inherent biological properties remain of great interest. Here, we report a strategy to simultaneously load multiple drugs in platelets in a one-step fusion process. We demonstrate doxorubicin (DOX)-encapsulated liposomes conjugated with interleukin-15 (IL-15) could fuse with platelets to achieve both cytoplasmic drug loading and surface cytokine modification with a loading efficiency of over 70 % within minutes. Due to their inherent targeting ability to metastatic cancers and postoperative bleeding sites, the engineered platelets demonstrated a synergistic therapeutic effect to suppress lung metastasis and postoperative recurrence in mouse B16F10 melanoma tumor models.

摘要

细胞为基础的药物输送系统在癌症治疗中的探索得到了越来越多的关注。以有效、安全和精确的方式对治疗细胞进行多药物加载的方法,同时保持其固有生物特性,仍然是非常有意义的。在这里,我们报告了一种在一步融合过程中同时将多种药物装载到血小板中的策略。我们证明了阿霉素(DOX)包封的脂质体与白细胞介素 15(IL-15)偶联后可以与血小板融合,在几分钟内实现细胞质药物加载和表面细胞因子修饰,载药效率超过 70%。由于它们对转移性癌症和术后出血部位的固有靶向能力,工程化血小板在小鼠 B16F10 黑色素瘤肿瘤模型中表现出协同治疗效果,抑制肺转移和术后复发。

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