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Inne
Near-infrared Ag2S quantum dots loaded in phospholipid nanostructures : physical properties, stability and cytotoxicity.
Autorzy
Rok wydania
2019
Czasopismo
Colloids and Surfaces A: Physicochemical and Engineering Aspects
Numer woluminu
579
Strony
123631/1-123631/9
DOI
10.1016/j.colsurfa.2019.123631
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
In this paper, we report the encapsulation of near-infrared emitting Ag2S quantum dots (QDs) in the phospholipid nanostructures with different functional head-groups of phospholipids. Ag2S QDs were prepared using single-source precursor approach by thermal decomposition of silver diethyldithiocarbamate (Ag(DDTC)). Water dispersion of the QDs were accomplished by their encapsulation within cationic, anionic, neutral or PEGylated phospholipid nanostructures. The influence of different head-groups of phospholipids on physicochemical properties, encapsulation efficiency, luminescence efficiency, type of aggregates and stability of phospholipid nanostructures containing Ag2S QDs was determined and discussed. The basic biocompability of Ag2S QDs preparates was tested in vitro using NIH3T3 and HCT116 cell lines. In this regard the viability was assessed using MTS assay along with induction of apoptosis in cultures treated with selected phospholipid formulations of Ag2S. The anionic and PEGylated phospholipids showed greater encapsulation efficacy, stability and lower cytotoxicity than neutral and cationic phospholipids used for QDs encapsulation. Such low-toxic phospholipid structures can be used as carriers for different types of QDs. Our study revealed that the DSPE-PEG2000-based formulations of Ag2S QDs are well suited for applications in living biological systems Combination of outstanding optical properties of QDs and phospholipids biocompatibility makes such particles potentially useful in fluorescent microscopy as fluorescent contrast agents.
Słowa kluczowe
Quantum dots, Ag2S, Phospholipids, Encapsulation
Adres publiczny
http://dx.doi.org/10.1016/j.colsurfa.2019.123631
Strona internetowa wydawcy
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