| Literature DB >> 32447953 |
Jimin Zhou, Xiangfeng Zhu, Qianya Cheng, Yuxuan Wang1, Ruiqi Wang, Xingwen Cheng2, Jiajia Xu2, Kuntang Liu, Lin Li2, Xueming Li, Mingfang He, Jian Wang3, Heng Xu, Su Jing, Ling Huang2.
Abstract
By taking advantage of the efficient Förster resonance energy transfer (FRET) between near-infrared (NIR)-responsive lanthanide-doped upconversion nanoparticles (UCNPs) and Fenton reagent ferrocenyl compounds (Fc), a series of Fc-UCNPs was designed by functionalizing NaYF4:Yb,Tm nanoparticles with Fc1-Fc5 via surface-coordination chemistry. Fc-UCNP-Lipo nanosystems were then constructed by encapsulating Fc-UCNP inside liposomes for efficient delivery. Fc-UCNP can effectively release ·OH via a NIR-promoted Fenton-like reaction. In vitro and in vivo studies of Fc1-UCNP-Lipo confirmed the preferential accumulation in a tumor site followed by an enhanced uptake of cancer cells. After cellular internalization, the released Fc1-UCNP can effectively promote ·OH generation for tumor growth suppression. Such a Fc1-UCNP-Lipo nanosystem exhibits advantages such as easy fabrication, low drug dosage, and no ferrous ion release.Entities:
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Year: 2020 PMID: 32447953 DOI: 10.1021/acs.inorgchem.0c01073
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165