Please use this identifier to cite or link to this item: https://doi.org/10.1002/adfm.201908865
Title: Biodegradable Nanoscale Coordination Polymers for Targeted Tumor Combination Therapy with Oxidative Stress Amplification
Authors: Liu, Jingjing 
Wu, Min 
Pan, Yutong 
Duan, Yukun 
Dong, Ziliang
Chao, Yu
Liu, Zhuang
Liu, Bin 
Keywords: Science & Technology
Physical Sciences
Technology
Chemistry, Multidisciplinary
Chemistry, Physical
Nanoscience & Nanotechnology
Materials Science, Multidisciplinary
Physics, Applied
Physics, Condensed Matter
Chemistry
Science & Technology - Other Topics
Materials Science
Physics
Cancer targeting
Cisplatin
Combination therapy
Nanoscale coordination polymer
Reactive oxygen species
METAL-ORGANIC FRAMEWORKS
DRUG-RELEASE
CANCER-CELLS
NANOPARTICLES
TOXICITY
NEPHROTOXICITY
OXIDE
MOFS
Issue Date: 12-Feb-2020
Publisher: WILEY-VCH VERLAG
Citation: Liu, Jingjing, Wu, Min, Pan, Yutong, Duan, Yukun, Dong, Ziliang, Chao, Yu, Liu, Zhuang, Liu, Bin (2020-02-12). Biodegradable Nanoscale Coordination Polymers for Targeted Tumor Combination Therapy with Oxidative Stress Amplification. ADVANCED FUNCTIONAL MATERIALS 30 (13). ScholarBank@NUS Repository. https://doi.org/10.1002/adfm.201908865
Abstract: © 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim Nowadays various inorganic nanoparticles that generate highly reactive hydroxyl radical (·OH) on the basis of Fenton-like catalytic activity of metal ions have been designed for chemodynamic therapy. However, the high level of adaptive antioxidants [glutathione (GSH)] in cancer cells could effectively consume ·OH to compromise the treatment efficiency and biosafety of these inorganic nanoparticles, and this is a general concern in chemodynamic therapy. Herein, a new biodegradable nanoscale coordination polymer (NCP) is developed by integration of cisplatin prodrug (DSCP) and iron (III) ions through a reverse microemulsion method. The DSCP in the NCPs could react with GSH to release free cisplatin, while the iron (III) ions could be reduced by GSH into iron (II) to enable Fenton reaction, subsequently leading to amplified intracellular oxidative stress. After surface modification of polyethylene glycol (PEG) and cyclo[Arg-Gly-Asp-D-Phe-Lys(mpa)] peptide (cRGD), Fe-DSCP-PEG-cRGD shows an excellent targeting effect against αvβ3-integrin overexpressed tumor cells. Furthermore, Fe-DSCP-PEG-cRGD enables significant chemo and chemodynamic therapy with dramatically enhanced therapeutic efficiency in comparison to relative monotherapies. Importantly, Fe-DSCP-PEG-cRGD could be efficiently cleared out from mice through feces and urine postinjection 7 days. The NCP presented in this work is simple and economical, which shows great biodegradability and biosafety for potential clinical translation.
Source Title: ADVANCED FUNCTIONAL MATERIALS
URI: https://scholarbank.nus.edu.sg/handle/10635/169491
ISSN: 1616301X
16163028
DOI: 10.1002/adfm.201908865
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