DNA
小RNA
抗生素
伤口愈合
四面体
材料科学
药物输送
纳米技术
化学
医学
基因
生物化学
结晶学
免疫学
作者
Xiaoying Lyu,Haoyan Wu,Ye Chen,Yue Sun,Xiaoxiao Cai,Songhang Li,Yunfeng Lin
出处
期刊:Small
[Wiley]
日期:2024-09-16
标识
DOI:10.1002/smll.202406629
摘要
Abstract Infected wounds are a complex disease involving bacterial infections and dysregulated inflammation. However, current research has mostly focused on bacterial inhibition rather than on inflammation. Thus, combined therapeutic strategies with anti‐bacterial and anti‐inflammation efficacies are urgently needed. Antibiotics are the main treatment strategy for infections. However, the excessive use of antibiotics throughout the body can cause serious side effects. In addition, miRNA‐based therapeutics are superior for the treatment of wounds, but their rapid degradation and poor cellular uptake limit their clinical application. Tetrahedral framework DNA (tFNA) is an ideal drug delivery system owing to its excellent stability and remarkable transport ability. Herein, a novel multi‐functional miRNA and antibiotic co‐delivery system based on tFNA is presented for the first time, called B/L. B/L has heightened resistance to serum and excellent codelivery ability. After transdermal administration, B/L can specifically target TNF receptor‐associated factor 6(TRAF6) and IL‐1receptor‐associated kinase 1(IRAK1), thereby regulating nuclear factor kappa‐B (NF‐𝜿B) and thus effectively reducing inflammation and promoting the healing of infected wounds. This novel multi‐functional co‐delivery system provides a versatile, simple, biocompatible, and powerful platform for the personalized and combined treatment of multiple diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI