期刊
MOLECULAR PHARMACEUTICS
卷 14, 期 11, 页码 3978-3986出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.7b00649
关键词
programmed cell death-I (PD-I); near-infrared fluorescence (NIRF) imaging PET imaging; doxorubicin (DOX); breast cancer; therapy
资金
- National Natural Science Foundation of China [81227901, 81470083, 81527805, 81571810, 61231004, 81771846]
- Research and Development Program of China (973) [2014CB748600, 2015CB755500]
- Strategic Priority Research Program from Chinese Academy of Sciences [XDB02060010]
- Beijing Natural Science Foundation [Z16110200010000]
- Peking University Third Hospital [BYSY2015023]
The overexpression of programmed cell death-1 (PD 1) in tumors as breast cancer makes it a possible target for cancer imaging and therapy. Advances in molecular imaging, including radionuclide imaging and near-infrared fluorescence (NIRF) imaging, enable the detection of tumors with high sensitivity. In this study, we aim to develop a novel PD-1 antibody targeted positron emission tomography (PET) and NIRF labeled liposome loaded with doxorubicin (DOX) and evaluate its application for in vivo cancer imaging and therapy. IRDye800CW and Cu-60 were conjugated to liposomes with PD-1 antibody labeling, and DOX was inside the liposomes to form theranostic nanopartides. The 4T1 tumors were successfully visualized with PD-1-LiposomeDOX-Cu-64/IRDye800CW using NIRF/PET imaging. The bioluminescent imaging (BLI) results showed that tumor growth was significantly inhibited in the PD-1-Liposome-DOX-treated group than the IgG control. Our results highlight the potential of using dual-labeled theranostic PD-1 mAb-targeted Liposome-DOX-Cu-64/IRDye800CW for the management of breast tumor.
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