Biohybrid Microrobot Enteric‐Coated Microcapsule for Oral Treatment of Colorectal Cancer

材料科学 肿瘤微环境 纳米技术 癌症研究 免疫系统 免疫原性细胞死亡 免疫疗法 免疫学 医学
作者
Yong Kang,Yaoguang She,Yang Zang,Mengyu Yuan,Gaoli Niu,Xinghua Tian,Lei Zhang,Jingjing Lin,Mengxiang Yang,Zhengcun Pei,Ximo Wang,Xiaoyuan Ji
出处
期刊:Advanced Materials [Wiley]
卷期号:37 (40): e20586-e20586 被引量:11
标识
DOI:10.1002/adma.202420586
摘要

Abstract The oral treatment of colorectal cancer is highly desirable due to its noninvasiveness and potential for localized drug action, yet it remains challenged by gastrointestinal barriers and limited intratumoral penetration. This study presents the first oral biohybrid microrobot system that integrates ultrasound‐activated piezoelectric catalysis with bacterial therapy, achieving synergistic tumor targeting, reactive oxygen species generation, and immune activation. By leveraging Enterobacter aerogenes (EA) and BaTiO 3 nanoparticles, this strategy induces immunogenic tumor cell death and metabolic remodeling. It utilizes BaTiO 3 incorporated into EA (EA@BTO) microrobots, which are encapsulated in enteric microcapsules. These microcapsules, encapsulated in enteric microcapsules via photocurable 3D printing, protect during digestion, target tumors, penetrate mucus, and release gases. They thrive in anaerobic, acidic environments, enabling precise, responsive delivery within the intestinal tract. Once the microrobots reach the tumor, the BaTiO 3 nanoparticles catalyze reduction and oxidation reactions upon ultrasound irradiation, leading to the induction of immunogenic tumor cell death. Notably, the consumption of lactic acid by BaTiO 3 and EA alleviates the immunosuppressive microenvironment within the tumor. This promotes the maturation of dendritic cells and the polarization of macrophages toward the M1 phenotype, thereby reducing the proportion of regulatory T cells and enhancing the population of effector T cells.
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