Recent advances in stimuli-responsive theranostic systems with aggregation-induced emission characteristics

被引:113
作者
Hu, Jing-Jing [1 ]
Jiang, Wenlian [1 ]
Yuan, Lizhen [1 ]
Duan, Chong [1 ]
Yuan, Qiming [1 ]
Long, Zi [1 ]
Lou, Xiaoding [1 ]
Xia, Fan [1 ]
机构
[1] China Univ Geosci, Fac Mat Sci & Chem, Engn Res Ctr Nanogeomat, Minist Educ, Wuhan 430074, Peoples R China
来源
AGGREGATE | 2021年 / 2卷 / 01期
基金
中国国家自然科学基金;
关键词
aggregation induced emission; imaging; stimuli-responsive; theranostics; tumor therapy; FLUORESCENT ORGANIC NANOPARTICLES; MESOPOROUS SILICA NANOPARTICLES; TARGETED PHOTODYNAMIC THERAPY; DEMAND DRUG-RELEASE; INTRACELLULAR DRUG; CANCER-THERAPY; AIE CHARACTERISTICS; MATRIX METALLOPROTEINASES; PLATINUM(IV) PRODRUG; NANO-GRAPHENE;
D O I
10.1002/agt2.10
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Theranostic systems by integrating the tumor imaging and tumor therapeutic capabilities into one platform have attracted numerous attentions from worldwide researchers. Despite the great developments, their clinical application is still in the nascent stage, owing to the unsatisfied imaging quality and limited therapeutic efficacy. Fortunately, the emerging of aggregation-induced emission (AIE) molecules with unique fluorescence property offers an opportunity to solve the imaging problem. Besides, further utilizing the tumor microenvironments and external triggers to design the stimuli-responsive imaging-guided therapy could enhance the therapeutic efficacy and reduce the side effects. In this review, the advancements in stimuli-responsive theranostic systems with AIE characteristics are summarized. Theranostic systems are first classified according to their treatment modes, and then subdivided based on various stimuli, including pH, redox, enzyme, and light. In each section, the design strategies and application examples are introduced. At last, the current state of the art, limitations, as well as prospects are also discussed.
引用
收藏
页码:48 / 65
页数:18
相关论文
共 137 条
[41]   MMP-responsive theranostic nanoplatform based on mesoporous silica nanoparticles for tumor imaging and targeted drug delivery [J].
Hu, Jing-Jing ;
Liu, Li-Han ;
Li, Ze-Yong ;
Zhuo, Ren-Xi ;
Zhang, Xian-Zheng .
JOURNAL OF MATERIALS CHEMISTRY B, 2016, 4 (11) :1932-1940
[42]   Redox-Responsive Biomimetic Polymeric Micelle for Simultaneous Anticancer Drug Delivery and Aggregation-Induced Emission Active Imaging [J].
Hu, Jun ;
Zhuang, Weihua ;
Ma, Boxuan ;
Su, Xin ;
Yu, Tao ;
Li, Gaocan ;
Hu, Yanfei ;
Wang, Yunbing .
BIOCONJUGATE CHEMISTRY, 2018, 29 (06) :1897-1910
[43]   Near-infrared AIEgen-functionalized and diselenide-linked oligo-ethylenimine with self-sufficing ROS to exert spatiotemporal responsibility for promoted gene delivery [J].
Huang, Yongkang ;
Chen, Qixian ;
Lu, Hongguang ;
An, Jinxia ;
Zhu, Huajie ;
Yan, Xiangjie ;
Li, Wei ;
Gao, Hui .
JOURNAL OF MATERIALS CHEMISTRY B, 2018, 6 (41) :6660-6666
[44]   Enzyme-instructed self-assembly leads to the activation of optical properties for selective fluorescence detection and photodynamic ablation of cancer cells [J].
Ji, Shenglu ;
Gao, Heqi ;
Mu, Wancen ;
Ni, Xiang ;
Yi, Xiaoyong ;
Shen, Jing ;
Liu, Qian ;
Bao, Pingping ;
Ding, Dan .
JOURNAL OF MATERIALS CHEMISTRY B, 2018, 6 (17) :2566-2573
[45]   Dual Intratumoral Redox/Enzyme-Responsive NO-Releasing Nanomedicine for the Specific, High-Efficacy, and Low-Toxic Cancer Therapy [J].
Jia, Xiaobo ;
Zhang, Yihua ;
Zou, Yu ;
Wang, Yao ;
Niu, Dechao ;
He, Qianjun ;
Huang, Zhangjian ;
Zhu, Weihong ;
Tian, He ;
Shi, Jianlin ;
Li, Yongsheng .
ADVANCED MATERIALS, 2018, 30 (30)
[46]   Lipid Droplet-Targetable Fluorescence Guided Photodynamic Therapy of Cancer Cells with an Activatable AIE-Active Fluorescent Probe for Hydrogen Peroxide [J].
Jiang, Guoyu ;
Li, Chunbin ;
Liu, Xiang ;
Chen, Qingqing ;
Li, Xiaokang ;
Gu, Xinggui ;
Zhang, Pengfei ;
Lai, Qingfang ;
Wang, Jianguo .
ADVANCED OPTICAL MATERIALS, 2020, 8 (20)
[47]   Multifunctional organic nanoparticles with aggregation-induced emission (AIE) characteristics for targeted photodynamic therapy and RNA interference therapy [J].
Jin, Guorui ;
Feng, Guangxue ;
Qin, Wei ;
Tang, Ben Zhong ;
Liu, Bin ;
Li, Kai .
CHEMICAL COMMUNICATIONS, 2016, 52 (13) :2752-2755
[48]   Understanding endocytic pathways and intracellular trafficking: a prerequisite for effective design of advanced drug delivery systems [J].
Jones, AT ;
Gumbleton, M ;
Duncan, R .
ADVANCED DRUG DELIVERY REVIEWS, 2003, 55 (11) :1353-1357
[49]   Notch1 increases Snail expression under high reactive oxygen species conditions in hepatocellular carcinoma cells [J].
Kim, H. S. ;
Jung, G. .
FREE RADICAL RESEARCH, 2014, 48 (07) :806-813
[50]   Disulfide-cross-linked PEG-poly(amino acid)s copolymer micelles for glutathione-mediated intracellular drug delivery [J].
Koo, Ahn Na ;
Lee, Hong Jae ;
Kim, Sung Eun ;
Chang, Jeong Ho ;
Park, Chiyoung ;
Kim, Chulhee ;
Park, Jae Hyung ;
Lee, Sang Cheon .
CHEMICAL COMMUNICATIONS, 2008, (48) :6570-6572