光热治疗
体内
荧光
材料科学
荧光寿命成像显微镜
热疗
生物物理学
生物医学工程
纳米技术
医学
生物
光学
物理
内科学
生物技术
作者
Zhuqing Sun,Tuanwei Li,Feng Wu,Tingfeng Yao,Hongchao Yang,Xiaohu Yang,Hongqiang Yin,Yajuan Gao,Yejun Zhang,Chunyan Li,Qiangbin Wang
标识
DOI:10.1002/adfm.202311622
摘要
Abstract Photothermal therapy (PTT) is considered a promising treatment strategy for solid tumors. However, local hyperthermia (over 45°C) during PTT can cause severe side effects in neighboring healthy tissues. PTT with accurate temperature feedback is a compelling strategy to ablate tumors and reduce side effects, but it still faces challenges. Here, a new kind of phototheranostic nanoparticle, namely 17‐RF@Ag 2 Se is developed, enabling in vivo NIR‐II fluorescence tracking, PTT and fluorescence nanothermometry as well as synergistic heat‐shock protein (HSP) inhibition. Precise PTT with high spatiotemporal resolution is achieved with the help of the designed NIR‐II fluorescence imaging‐photothermal therapy linkage apparatus. Upon intravenous injection, 17‐RF@Ag 2 Se is specifically accumulated in tumors targeted by the overexpressed integrin α v β 3 , which is monitored by NIR‐II fluorescence imaging of Ag 2 Se QDs. Further, the release of HSP inhibitor, tanespimycin (17‐AAG), enhances the thermosensitivity of tumor cells. Subsequently, the internal temperature of the tumor is precisely monitored and adjusted during PTT via the temperature‐dependent NIR‐II fluorescence feedback of Ag 2 Se QDs and the linkage apparatus calibration, thereby achieving efficient and safe tumor PTT. Also, the results present a new method for accurate temperature monitoring and control in vivo, which can be applied to other biomedical studies.
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