Light-triggered theranostics based on photosensitizer-conjugated carbon dots for simultaneous enhanced-fluorescence imaging and photodynamic therapy.
Light-triggered theranostics based on photosensitizer-conjugated carbon dots for simultaneous enhanced-fluorescence imaging and photodynamic therapy.
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DOI:
10.1002/adma.201200650
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发表时间:
2012-09-25
影响因子:
29.4
通讯作者:
Chen, Xiaoyuan
中科院分区:
文献类型:
--
作者:
Huang, Peng;Lin, Jing;Wang, Xiansong;Wang, Zhe;Zhang, Chunlei;He, Meng;Wang, Kan;Chen, Feng;Li, Zhiming;Shen, Guangxia;Cui, Daxiang;Chen, Xiaoyuan
Theranostics, combining both medical diagnostics and therapeutics to achieve an optimizing efficacy and safety of comprehensive regime, is an emerging interdiscipline that is paving the avenue towards the goal of personalized medicine.[1] Activatable theranostic agents can enhance the selectivity and specificity for disease destruction with high localized cytotoxicity and little collateral damage.[2] So far, controllable activation by an external stimulus such as temperature, pH, applied magnetic or electrical field, ultrasound, light, or enzymatic action have been proposed as triggered delivery systems.[3] Over the past decade, light-triggered theranostics, such as photodynamic-, photothermal-and photo-triggered chemotherapy have received increased attention due to the advantage of highly specific spatial and temporal control of compound release.[4] The theranostic constructs could advance a novel category of clinical solution which possesses early recognition of the disease by enhancing contrast in various imaging modalities followed by the tailored guidance of therapy.Photodynamic therapy (PDT) is an extraordinary theranostic modality for a number of malignant and nonmalignant diseases.[5] The general procedure of PDT involves the systemic, local, or topical administration of a non-toxic drug or dye known as a photosensitizer (PS) followed by selective illumination with appropriate wavelength and power of light.[2e, 6] In the presence of oxygen, PS can transfer the absorbed photon energy to surrounding oxygen molecules, generating reactive oxygen species (ROS) including singlet oxygen (SO) or free radicals and consequently causing cell death and tissue destruction. Meanwhile, upon light activation, PS can emit fluorescence due to the relaxation of the excited-singlet-state PS back to the ground state.[1e] The emitted fluorescence can be employed for locating diseases, photodiagnosis and molecular imaging, which is known as photosensitizer fluorescence detection (PFD).[4a, 7] Therefore, organic fusion of PFD and PDT enables online imaging of drug for the detection of disease, imageguided drug delivery and treatments, guidance of surgical resection, and monitoring of treatment response.[8]
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影响因子:
12.4
作者:
Huang P;Xu C;Lin J;Wang C;Wang X;Zhang C;Zhou X;Guo S;Cui D
通讯作者:
Cui D
影响因子:
14
作者:
Huang, Peng;Bao, Le;Cui, Daxiang
通讯作者:
Cui, Daxiang
影响因子:
14
作者:
Huang, Peng;Li, Zhiming;Cui, Daxiang
通讯作者:
Cui, Daxiang
影响因子:
6.7
作者:
Anilkumar, Parambath;Wang, Xin;Sun, Ya-Ping
通讯作者:
Sun, Ya-Ping
影响因子:
2.5
作者:
Huang, Zheng;Li, Libo;Hetzel, Fred W.
通讯作者:
Hetzel, Fred W.