Encapsulation of α-lipoic acid intochitosan and alginate/gelatin hydrogel microparticles and its in vitro antioxidant activity

Alpha-lipoic acidis an organosulphur compound well-known for its therapeutic potential and antioxidant properties. However, the effective use of ?-lipoic acid depends on biological plasma half-life and its preserving stability, which could be improved by encapsulation. In this study, ?-lipoic acid w...

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Published inHemijska industrija Vol. 70; no. 1; pp. 49 - 58
Main Authors Vidovic, Bojana, Milasinovic, Nikola, Kotur-Stevuljevic, Jelena, Dilber, Sanda, Kalagasidis-Krusic, Melina, Djordjevic, Brizita, Knezevic-Jugovic, Zorica
Format Journal Article
LanguageEnglish
Serbian
Published Belgrade Hemijska Industrija 2016
Association of Chemical Engineers of Serbia
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Summary:Alpha-lipoic acidis an organosulphur compound well-known for its therapeutic potential and antioxidant properties. However, the effective use of ?-lipoic acid depends on biological plasma half-life and its preserving stability, which could be improved by encapsulation. In this study, ?-lipoic acid was incorporated into chitosan microparticles obtained by reverse emulsion crosslinking technique, as well as into microparticles of alginate/gelatin crosslinked with zinc ions. Encapsulation of ?-lipoic acid in both cases was carried out by swelling of synthesized dried microparticles by their dipping in a solution of the active substance under strictly controlled conditions. Encapsulation efficiency of ?-lipoic acid obtained in this study was up to 53.9 %. The structural interaction of ?-lipoic acid with the carriers was revealed by Fourier transform infrared spectroscopy. In vitro released studies showed that controlled release of ?-lipoic acid was achieved through its encapsulation into chitosan microparticles. The results of in vitro antioxidative activity assays of released ?-lipoic acid indicated that antioxidant activity was preserved at a satisfactory level. These obtained results suggested that chitosan microparticles could be suitable for modeling the controlled release of ?-lipoic acid.
ISSN:0367-598X
2217-7426
DOI:10.2298/HEMIND141119010V