炎症
中枢神经系统
地塞米松
血脑屏障
金黄色葡萄球菌
抗生素
脑膜炎
医学
免疫学
趋化性
药理学
微生物学
细菌
生物
内科学
外科
受体
遗传学
作者
Anwei Zhou,Delian Kong,Xinyuan Zhou,Yao Liu,Yiping Zhang,Junrong Li,Yurui Xu,Xinghai Ning
标识
DOI:10.1002/adma.202311661
摘要
Abstract Brain infections, frequently accompanied by significant inflammation, necessitate comprehensive therapeutic approaches targeting both infections and associated inflammation. A major impediment to such combined treatment is the blood–brain barrier (BBB), which significantly restricts therapeutic agents from achieving effective concentrations within the central nervous system. Here, a neutrophil‐centric dual‐responsive delivery system, coined “CellUs,” is pioneered. This system is characterized by live neutrophils enveloping liposomes of dexamethasone, ceftriaxone, and oxygen‐saturated perfluorocarbon (Lipo@D/C/P). CellUs is meticulously engineered to co‐deliver antibiotics, anti‐inflammatory agents, and oxygen, embodying a comprehensive strategy against brain infections. CellUs leverages the intrinsic abilities of neutrophils to navigate through BBB, accurately target infection sites, and synchronize the release of Lipo@D/C/P with local inflammatory signals. Notably, the incorporation of ultrasound‐responsive perfluorocarbon within Lipo@D/C/P ensures the on‐demand release of therapeutic agents at the afflicted regions. CellUs shows considerable promise in treating Staphylococcus aureus infections in mice with meningitis, particularly when combined with ultrasound treatments. It effectively penetrates BBB, significantly eliminates bacteria, reduces inflammation, and delivers oxygen to the affected brain tissue, resulting in a substantial improvement in survival rates. Consequently, CellUs harnesses the natural chemotactic properties of neutrophils and offers an innovative pathway to improve treatment effectiveness while minimizing adverse effects.
科研通智能强力驱动
Strongly Powered by AbleSci AI