中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Mitochondria-Targeting Small-Molecule NIR-II Fluorescent Probes for Imaging and Treatment of Tumor

文献类型:期刊论文

作者Li, Mingxun1,2; Wu, Yibin1,2; He, Chunfeng2,3; Li, Xinxin2,5; Tao, Ji2; Qu, Chunrong2; Chen, Wen-Hua1; Cheng, Zhen2,3,4
刊名ADVANCED THERAPEUTICS
出版日期2023-07-24
页码10
关键词mitochondrial membrane potential NIR-II imaging photothermal therapy small molecule probes tumors
DOI10.1002/adtp.202300151
通讯作者Qu, Chunrong(crqu@simm.ac.cn) ; Chen, Wen-Hua(whchen@wyu.edu.cn) ; Cheng, Zhen(zcheng@simm.ac.cn)
英文摘要Mitochondrial membrane potential (& UDelta;& psi;m)-targeting molecular probes play an essential role in diagnosing and treating diseases. Recently, the second near-infrared window (NIR-II, 1000-1700 nm) fluorescent imaging has been actively studied as an attractive imaging modality. However, small molecule & UDelta;& psi;m-targeting NIR-II probes are rarely reported, especially for highly efficient imaging and treatment of tumors. Herein, a small molecule probe named TQPTPP is designed and synthesized by conjugation of a novel D-A type dye TQT1009 with & UDelta;& psi;m-targeting molecule alkyl triphenylphosphine (TPP) through a polyethylene glycol-8 (PEG(8)) linker. The conventional ICG dye is also coupled with TPP through PEG(8) to produce ICGTPP as a comparison. TQPTPP showed a fluorescence quantum yield of 0.041% and excellent photothermal conversion efficiency (61.4%). It can be self-assembled into nanoparticles and still preserve & UDelta;& psi;m-targeting capability. Tumor imaging is further performed, and results showed a long tumor retention time of TQPTPP (maximum tumor signal on day five and signal-to-noise ratio up to nine). As a comparison, ICGTPP remained a single molecule with & UDelta;& psi;m-targeting capability. But it has shorter tumor retention and lower photostability. These results suggested the novel D-A small molecule & UDelta;& psi;m-targeting NIR-II probe TQPTPP provided a new tool for diagnosing and treating tumors.
WOS关键词FLUOROPHORES ; DELIVERY ; THERAPY ; DYE
资助项目National Natural Science Foundation of China[U2267221] ; National Natural Science Foundation of China[81901799] ; Chinese Academy of Sciences
WOS研究方向Pharmacology & Pharmacy
语种英语
出版者WILEY
WOS记录号WOS:001032188600001
源URL[http://119.78.100.183/handle/2S10ELR8/306770]  
专题新药研究国家重点实验室
通讯作者Qu, Chunrong; Chen, Wen-Hua; Cheng, Zhen
作者单位1.Wuyi Univ, Sch Biotechnol & Hlth Sci, Jiangmen 529020, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Mat Med, Mol Imaging Ctr, State Key Lab Drug Res, Shanghai 201203, Peoples R China
3.Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
4.Bohai Rim Adv Res Inst Drug Discovery, Shandong Lab Yantai Drug Discovery, Yantai 264117, Shandong, Peoples R China
5.First Hosp Jilin Univ, Dept Radiol, Changchun 130021, Peoples R China
推荐引用方式
GB/T 7714
Li, Mingxun,Wu, Yibin,He, Chunfeng,et al. Mitochondria-Targeting Small-Molecule NIR-II Fluorescent Probes for Imaging and Treatment of Tumor[J]. ADVANCED THERAPEUTICS,2023:10.
APA Li, Mingxun.,Wu, Yibin.,He, Chunfeng.,Li, Xinxin.,Tao, Ji.,...&Cheng, Zhen.(2023).Mitochondria-Targeting Small-Molecule NIR-II Fluorescent Probes for Imaging and Treatment of Tumor.ADVANCED THERAPEUTICS,10.
MLA Li, Mingxun,et al."Mitochondria-Targeting Small-Molecule NIR-II Fluorescent Probes for Imaging and Treatment of Tumor".ADVANCED THERAPEUTICS (2023):10.

入库方式: OAI收割

来源:上海药物研究所

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