2015
DOI: 10.1016/j.carbpol.2015.04.038
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Complexes of dextran sulfate and anthocyanins from Vaccinium myrtillus: Formation and stability

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Cited by 44 publications
(20 citation statements)
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“…Similar protection was observed in samples exposed to white light for 10 days (−20% vs. −80%). Sulfonylated polysaccharides, such as dextran sulfate and carrageenans, can also be used to encapsulate bilberry anthocyanins from acidic solutions (pH ≈ 3) with high efficiency and improved stability [ 64 , 65 ]. The binding of isotherms and HPLC analysis showed that the binding is selective of anthocyanins (the other phenols remaining in solution) and is stronger when the sulfonylation degree is higher.…”
Section: The Importance Of Anthocyanin Chemistry In Food and Nutrimentioning
confidence: 99%
“…Similar protection was observed in samples exposed to white light for 10 days (−20% vs. −80%). Sulfonylated polysaccharides, such as dextran sulfate and carrageenans, can also be used to encapsulate bilberry anthocyanins from acidic solutions (pH ≈ 3) with high efficiency and improved stability [ 64 , 65 ]. The binding of isotherms and HPLC analysis showed that the binding is selective of anthocyanins (the other phenols remaining in solution) and is stronger when the sulfonylation degree is higher.…”
Section: The Importance Of Anthocyanin Chemistry In Food and Nutrimentioning
confidence: 99%
“…However, the relatively low stability and bioavailability of anthocyanins are the primary barrier to limit the wide and effective applications [9][10][11], raising up the importance of reducing the degradation of anthocyanins and controlling release. So far, encapsulation [12][13][14][15], composite [16][17][18][19] and group substitution [20][21][22][23][24] are the three main means used for anthocyanin stabilization. Some studies have been carried out on the adsorption of pigments by Fe 3 O 4 [25] and the stabilization of Fe 3+ [26,27].…”
Section: Introductionmentioning
confidence: 99%
“…In our previous work (Klimaviciute et al, 2015) we maintained that only the charge-charge interaction was responsible for the formation of complexes between strongly negative sulfate groups of dextran sulfate and the flavylium cation. These results were in contrast with the formation of complexes between chondroitin sulfate and ATCs (Jeong et al, 2012) where authors suggested that, besides the electrostatic, also the hydrophobic interaction and intermolecular stacking play a significant role in complex formation.…”
Section: Equilibrium Adsorption Of Atcs On Cross-linked Cargmentioning
confidence: 90%
“…A new approach to stabilizing ATCs is their introduction into a nanocarrier system. ATCs containing stable nanoparticles were obtained during complex formation between ATCs and chondroitin (Jeong & Na, 2012) or dextran (Klimaviciute, Navikaite, Jakstas, & Ivanauskas, 2015) sulfate. First of all, the charge-charge interactions between strongly negative groups of sulfated polysaccharide and the flavylium cation were responsible for the complex formation.…”
Section: Introductionmentioning
confidence: 99%