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Influence of serum albumin on intracellular delivery of drug-loaded hyaluronan polymeric micelles
K. Nešporová, J. Šógorková, D. Šmejkalová, J. Kulhánek, G. Huerta-Angeles, L. Kubala, V. Velebný,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články
- MeSH
- buňky HT-29 MeSH
- HCT116 buňky MeSH
- intracelulární tekutina účinky léků metabolismus MeSH
- kyselina hyaluronová aplikace a dávkování metabolismus MeSH
- lidé MeSH
- micely * MeSH
- nosiče léků aplikace a dávkování metabolismus MeSH
- polymery aplikace a dávkování metabolismus MeSH
- sérový albumin aplikace a dávkování metabolismus MeSH
- systémy cílené aplikace léků metody MeSH
- vazba proteinů fyziologie MeSH
- viabilita buněk účinky léků fyziologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Polymeric micelles are attractive drug delivery systems for intravenously administered nonpolar drugs. Although physical parameters like size, shape and loading capacity are considered as the most important for their efficiency, here we demonstrate that the effects of serum protein interaction and characteristics of loaded compound cannot be neglected during the micelle development and design of experimental set up. Polymeric micelles prepared from amphiphilic hyaluronic acid grafted with short (hexanoic) and long fatty acids (oleic) were tested after loading with two different hydrophobic models, Nile red and curcumin. The composition of micelles affected mainly the loading capacity. Both encapsulated compounds behaved differently in the in vitro cell uptake, which was also influenced by serum concentration, where serum albumin was found to be the primary destabilizing component. This destabilization was found to be influenced by polymeric micelle concentration. Thus, the chemical structure of micelle, the properties of non-covalently loaded substance and serum albumin/polymeric micelle ratio modulate the in vitro intracellular uptake of drugs loaded in nanocarriers.
Citace poskytuje Crossref.org
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- $a Polymeric micelles are attractive drug delivery systems for intravenously administered nonpolar drugs. Although physical parameters like size, shape and loading capacity are considered as the most important for their efficiency, here we demonstrate that the effects of serum protein interaction and characteristics of loaded compound cannot be neglected during the micelle development and design of experimental set up. Polymeric micelles prepared from amphiphilic hyaluronic acid grafted with short (hexanoic) and long fatty acids (oleic) were tested after loading with two different hydrophobic models, Nile red and curcumin. The composition of micelles affected mainly the loading capacity. Both encapsulated compounds behaved differently in the in vitro cell uptake, which was also influenced by serum concentration, where serum albumin was found to be the primary destabilizing component. This destabilization was found to be influenced by polymeric micelle concentration. Thus, the chemical structure of micelle, the properties of non-covalently loaded substance and serum albumin/polymeric micelle ratio modulate the in vitro intracellular uptake of drugs loaded in nanocarriers.
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