| Literature DB >> 26855313 |
Bo Thingholm1, Philipp Schattling1, Yan Zhang1, Brigitte Städler1.
Abstract
Cell mimicry is an approach which aims at substituting missing or lost activity. In this context, the goal of artificial organelles is to provide intracellularly active nanoreactors to affect the cellular performance. So far, only a handful of reports discuss concepts addressing this challenge based on single-component reactors. Here, the assembly of nanoreactors equipped with glucose oxidase (GOx)-loaded liposomal subunits coated with a poly(dopamine) polymer layer and RGD targeting units is reported. When comparing different surface modifications, the uptake of the nanoreactors by endothelial cells and macrophages with applied shear stress is confirmed without inherent cytotoxicity. Furthermore, the encapsulation and preserved activity of GOx within the nanoreactors is shown. The intracellular activity is demonstrated by exposing macrophages with internalized nanoreactors to glucose and assessment of the cell viability after 6 and 24 h. The macrophage viability is found to be reduced due to the intracellularly produced hydrogen peroxide by GOx. This report on the first intracellular active subcompartmentalized nanoreactors is a considerable step in therapeutic cell mimicry.Entities:
Keywords: artificial organelles; encapsulated catalysis; intracellular activity; macrophages; shear stress
Mesh:
Year: 2016 PMID: 26855313 DOI: 10.1002/smll.201502109
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281