体内
光热治疗
一氧化碳
化学
生物医学工程
生物物理学
纳米技术
医学
材料科学
生物
生物化学
生物技术
催化作用
作者
Xiaoting Gao,Lei Yan,Wei Zhang,Yuanliang Lv,Peiyan Ou,Ruiqiang Hang,Ang Gao,Liping Tong,Paul K. Chu,Huaiyu Wang
出处
期刊:Nano Today
[Elsevier]
日期:2023-11-02
卷期号:53: 102047-102047
被引量:5
标识
DOI:10.1016/j.nantod.2023.102047
摘要
Carbon monoxide (CO) has great potential in the therapy of osteoarthritis (OA), but its controllable delivery in vivo is still an intractable problem. To optimize CO gas therapy for OA, a stable CO release platform with multi-stimulus responsiveness must be designed. Herein, we describe a local delivery system (Fe3(CO)12 @Croc-PEG5K) for near-infrared fluorescence (NIRF) imaging-guided photothermal treatment and CO gas synergistic therapy. As a nano gas tank, Fe3(CO)12 @Croc-PEG5K releases CO on-demand under near infrared (NIR) laser irradiation, scavenges free radicals and regulates the pH in the OA microenvironment, and relieves the inflammatory response of macrophages to maintain the vitality of chondrocytes. Furthermore, the pH-dependent NIRF imaging properties of Fe3(CO)12 @Croc-PEG5K can be exploited to determine the administration interval and auto-monitor the curative effects during the therapeutic process. Owing to these merits, the photothermal and CO gas synergistic therapy mediated by Fe3(CO)12 @Croc-PEG5K can be optimized to deliver outstanding therapeutic performance in vivo, as demonstrated by the OA rat model. Our study is the first to validate the therapeutic effect of CO against OA in vivo, reveals a promising strategy for precision medicine pertaining to the treatment of OA and broadens the scope of CO gas therapy.
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