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ICG and Sunitinib-loaded NH2-MOFs for Folate-mediated Hepatocellular Carcinoma Dual-modal Therapy

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Chemical Research in Chinese Universities Aims and scope

Abstract

This research investigated a novel folic acid(FA)-modified zirconium core metal-organic framework(MOF) Uio-66 as a nanocarrier to deliver indocyanine green(ICG) and Sunitinib to cancer cells for combination therapy. Platinum-loaded Uio-66 nanoparticles(Pu) were synthesized via a one-pot method, followed by the modification with FA on their surfaces. This afforded FPu that enabled subsequent loading of ICG and Sunitinib to achieve dual-modal cancer therapy. Drug loading/release test and singlet oxygen detection were also conducted in vitro, and the nanoparticles showed considerable drug loading efficiency for both ICG and Sunitinib, coupled with a high singlet oxygen generation rate. Specifically, drug loading and encapsulation efficiency of Sunitinib were 2.30% and 72.67%, while those for ICG were 2.87% and 90.28%, respectively. Additionally, cytotoxicity test on HepG2 human hepatocellular carcinoma cancer cell line revealed that the fully functional nanoparticles possess excellent biocompatibility and as such could be further investigated as a potential drug delivery system for effectual carcinoma cancer treatment.

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Acknowledgements

This work was supported by the Ningbo Natural Science Foundation, China(No.202003N4253) and the Southeast University-China Pharmaceutical University Cooperative Research Project, China(No.2242019K3DZ06).

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Correspondence to Aiguo Wu or Yewei Zhang.

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Zhang, Z., Liu, C., Akakuru, O. et al. ICG and Sunitinib-loaded NH2-MOFs for Folate-mediated Hepatocellular Carcinoma Dual-modal Therapy. Chem. Res. Chin. Univ. 37, 967–974 (2021). https://doi.org/10.1007/s40242-021-1206-3

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  • DOI: https://doi.org/10.1007/s40242-021-1206-3

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