Zhou Mi, Tang Yuanlin, Lu Yifei, Zhang Tianxu, Zhang Shunhao, Cai Xiaoxiao, Lin Yunfeng
State Key Laboratory of Oral Diseases, National Center for Stomatology, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, Sichuan 610041, China.
Sichuan Provincial Engineering Research Center of Oral Biomaterials, Chengdu, Sichuan 610041, China.
ACS Nano. 2025 Jan 28;19(3):3455-3469. doi: 10.1021/acsnano.4c12917. Epub 2025 Jan 16.
Targeted drug delivery is a promising strategy for treating inflammatory diseases, with recent research focusing on the combination of neutrophils and nanomaterials. In this study, a targeted nanodrug delivery platform (Ac-PGP-tFNA, APT) was developed using tetrahedral framework nucleic acid (tFNA) along with a neutrophil hitchhiking mechanism to achieve precise delivery and anti-inflammatory effects. The tFNA structure, known for its excellent drug-loading capacity and cellular uptake efficiency, was used to carry a therapeutic agent─baicalin. The results demonstrate that the development of this drug delivery platform not only considerably enhances the bioavailability and effective concentration of the drug (baicalin) but also promotes the polarization of pro-inflammatory M1 macrophages to anti-inflammatory M2 macrophages by modulating the interactions between the neutrophils and macrophages. This targeted therapeutic method effectively treats inflammatory conditions such as sepsis and introduces a strategy for managing inflammatory diseases characterized by neutrophil infiltration.
靶向药物递送是一种治疗炎症性疾病的有前景的策略,近期研究聚焦于中性粒细胞与纳米材料的结合。在本研究中,利用四面体框架核酸(tFNA)开发了一种靶向纳米药物递送平台(Ac-PGP-tFNA,APT),并结合中性粒细胞搭载机制以实现精准递送和抗炎效果。tFNA结构以其出色的载药能力和细胞摄取效率而闻名,被用于携带治疗剂——黄芩苷。结果表明,该药物递送平台的开发不仅显著提高了药物(黄芩苷)的生物利用度和有效浓度,还通过调节中性粒细胞与巨噬细胞之间的相互作用,促进促炎M1巨噬细胞向抗炎M2巨噬细胞极化。这种靶向治疗方法有效治疗了脓毒症等炎症性病症,并引入了一种针对以中性粒细胞浸润为特征的炎症性疾病的管理策略。