Biological characterization of a novel hybrid copolymer carrier system based on glycogen
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
15-25781a
the Grant Agency of the Ministry of Health - International
13-08336S
the Czech Science Foundation - International
P108/12/1168
the Czech Science Foundation - International
282216
the Charles University in Prague (Faculty of Science), project GA UK - International
PubMed
29134553
DOI
10.1007/s13346-017-0436-x
PII: 10.1007/s13346-017-0436-x
Knihovny.cz E-resources
- Keywords
- Cancer, Contrast agents, Drug delivery, Glycogen, Polymers,
- MeSH
- Hep G2 Cells MeSH
- Endocytosis MeSH
- Fluorescein-5-isothiocyanate administration & dosage pharmacokinetics MeSH
- Fluorescent Dyes administration & dosage pharmacokinetics MeSH
- Glycogen administration & dosage pharmacokinetics MeSH
- Heterocyclic Compounds administration & dosage pharmacokinetics MeSH
- Humans MeSH
- Mice, Inbred C57BL MeSH
- Drug Carriers administration & dosage pharmacokinetics MeSH
- Organometallic Compounds administration & dosage pharmacokinetics MeSH
- Polyamines administration & dosage pharmacokinetics MeSH
- Tissue Distribution MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Fluorescein-5-isothiocyanate MeSH
- Fluorescent Dyes MeSH
- gadolinium 1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetate MeSH Browser
- Glycogen MeSH
- Heterocyclic Compounds MeSH
- Drug Carriers MeSH
- Organometallic Compounds MeSH
- poly(2-methyl-2-oxazoline) MeSH Browser
- Polyamines MeSH
The effective drug delivery systems for cancer treatment are currently on high demand. In this paper, biological behavior of the novel hybrid copolymers based on polysaccharide glycogen were characterized. The copolymers were modified by fluorescent dyes for flow cytometry, confocal microscopy, and in vivo fluorescence imaging. Moreover, the effect of oxazoline grafts on degradation rate was examined. Intracellular localization, cytotoxicity, and internalization route of the modified copolymers were examined on HepG2 cell line. Biodistribution of copolymers was addressed by in vivo fluorescence imaging in C57BL/6 mice. Our results indicate biocompatibility, biodegradability, and non-toxicity of the glycogen-based hybrid copolymers. Copolymers were endocyted into the cytoplasm, most probably via caveolae-mediated endocytosis. Higher content of oxazoline in polymers slowed down cellular uptake. No strong colocalization of the glycogen-based probe with lysosomes was observed; thus, it seems that the modified externally administered glycogen is degraded in the same way as an endogenous glycogen. In vivo experiment showed relatively fast biodistribution and biodegradation. In conclusion, this novel nanoprobe offers unique chemical and biological attributes for its use as a novel drug delivery system that might serve as an efficient carrier for cancer therapeutics with multimodal imaging properties.
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