炎症
药物输送
药品
癌症
中性粒细胞胞外陷阱
肿瘤微环境
医学
靶向给药
药理学
癌症研究
肿瘤细胞
免疫学
纳米技术
内科学
材料科学
作者
Yunfei Guo,Yiming Li,Jianmin Li,Haoran Cai,Kangkang Liu,Dengyi Duan,Wenyi Zhang,Gang Han,Yang Zhao
标识
DOI:10.1002/advs.202411307
摘要
Abstract Tumor heterogeneity remains a formidable obstacle in targeted cancer therapy, often leading to suboptimal treatment outcomes. This study presents an innovative approach that harnesses controlled inflammation to guide neutrophil‐mediated drug delivery, effectively overcoming the limitations imposed by tumor heterogeneity. By inducing localized inflammation within tumors using lipopolysaccharide, it significantly amplify the recruitment of drug‐laden neutrophils to tumor sites, irrespective of specific tumor markers. This strategy not only enhances targeted drug delivery but also triggers the release of neutrophil extracellular traps, further potentiating the anti‐tumor effect. Crucially, this study demonstrates that potential systemic inflammatory responses can be effectively mitigated through neutrophil transfusion, ensuring the safety and clinical viability of this approach. In a murine breast cancer model, the method significantly impedes tumor growth compared to conventional treatments. This work offers a versatile strategy for precise drug delivery across diverse tumor types. The findings pave the way for more effective and broadly applicable cancer treatments, potentially addressing the long‐standing challenge of tumor heterogeneity.
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