| Literature DB >> 29635107 |
Fangfang Xia1, Wenxiu Hou1, Yanlei Liu1, Wentao Wang2, Yu Han1, Meng Yang1, Xiao Zhi1, Chenlu Li1, Daizong Qi1, Tianliang Li1, Jesus Martinez de la Fuente3, Chunlei Zhang1, Jie Song4, Daxiang Cui5.
Abstract
The cytotoxicity and unique tumor-tropic properties of cytokine-induced killer (CIK) cells render them promising in the field of cancer immunotherapy and delivery systems. Here, we report a novel and facile approach to assemble gold nanoclusters (GNCs) into stable and monodispersed nanoparticles (NPs) using Chlorin e6 (Ce6) molecules. Notably, the fluorescence intensity of the GNCs-Ce6 NPs was about 4.5 folds stronger than the GNCs counterparts. The as-prepared GNCs-Ce6 NPs were conjugated with CD3 antibody (Ab) and further employed to label CIK cells to create a CIK cell-based drug delivery system (Ce6-GNCs-Ab-CIK). The Ce6-GNCs-Ab-CIK exhibited high tumor-targeting efficiency and excellent therapeutic efficacy toward MGC-803 tumor-bearing mice. Benefiting from the synergistic therapeutic effect between GNCs-Ce6-Ab NPs and CIK cells, the GNCs-Ce6-Ab-CIK strategy may present an ideal cancer theranostic platform for tumor targeted imaging and combination therapy.Entities:
Keywords: CIK cells; Chlorin e6; Gold nanoclusters; Immunotherapy; Near-infrared fluorescence imaging; Photodynamic therapy
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Year: 2018 PMID: 29635107 DOI: 10.1016/j.biomaterials.2018.03.048
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479