TY - JOUR
T1 - All-in-One Phototheranostics
T2 - Single Laser Triggers NIR-II Fluorescence/Photoacoustic Imaging Guided Photothermal/Photodynamic/Chemo Combination Therapy
AU - Wang, Qi
AU - Dai, Yeneng
AU - Xu, Jingzeng
AU - Cai, Jie
AU - Niu, Xinrui
AU - Zhang, Lei
AU - Chen, Runfeng
AU - Shen, Qingming
AU - Huang, Wei
AU - Fan, Quli
N1 - Publisher Copyright:
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Development of single near-infrared (NIR) laser triggered phototheranostics for multimodal imaging guided combination therapy is highly desirable but is still a big challenge. Herein, a novel small-molecule dye DPP-BT is designed and synthesized, which shows strong absorption in the first NIR window (NIR-I) and fluorescence emission in the second NIR region (NIR-II). Such a dye not only acts as a dual-modal contrast agent for NIR-II fluorescence and photoacoustic (PA) imaging, but also serves as a combined therapeutic agent for photothermal therapy (PTT) and photodynamic therapy (PDT). The single NIR laser triggered all-in-one phototheranostic nanoparticles are constructed by encapsulating the dye DPP-BT, chemotherapy drug DOX, and natural phase-change materials with a folic acid functionalized amphiphile. Notably, under NIR laser irradiation, DOX can effectively release from such nanoparticles via NIR-induced hyperthermia of DPP-BT. By intravenous injection of such nanoparticles into Hela tumor-bearing mice, the tumor size and location can be accurately observed via NIR-II fluorescence/PA dual-modal imaging. From in vitro and in vivo therapy results, such nanoparticles simultaneously present remarkable antitumor efficacy by PTT/PDT/chemo combination therapy, which is triggered by a single NIR laser. Overall, this work provides an innovative strategy to design and construct all-in-one nanoplatforms for clinical phototheranostics.
AB - Development of single near-infrared (NIR) laser triggered phototheranostics for multimodal imaging guided combination therapy is highly desirable but is still a big challenge. Herein, a novel small-molecule dye DPP-BT is designed and synthesized, which shows strong absorption in the first NIR window (NIR-I) and fluorescence emission in the second NIR region (NIR-II). Such a dye not only acts as a dual-modal contrast agent for NIR-II fluorescence and photoacoustic (PA) imaging, but also serves as a combined therapeutic agent for photothermal therapy (PTT) and photodynamic therapy (PDT). The single NIR laser triggered all-in-one phototheranostic nanoparticles are constructed by encapsulating the dye DPP-BT, chemotherapy drug DOX, and natural phase-change materials with a folic acid functionalized amphiphile. Notably, under NIR laser irradiation, DOX can effectively release from such nanoparticles via NIR-induced hyperthermia of DPP-BT. By intravenous injection of such nanoparticles into Hela tumor-bearing mice, the tumor size and location can be accurately observed via NIR-II fluorescence/PA dual-modal imaging. From in vitro and in vivo therapy results, such nanoparticles simultaneously present remarkable antitumor efficacy by PTT/PDT/chemo combination therapy, which is triggered by a single NIR laser. Overall, this work provides an innovative strategy to design and construct all-in-one nanoplatforms for clinical phototheranostics.
KW - combination therapy
KW - photoacoustic imaging
KW - phototheranostics
KW - second near-infrared fluorescence imaging
KW - single near-infrared laser
UR - https://www.scopus.com/pages/publications/85066915528
U2 - 10.1002/adfm.201901480
DO - 10.1002/adfm.201901480
M3 - 文章
AN - SCOPUS:85066915528
SN - 1616-301X
VL - 29
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 31
M1 - 1901480
ER -