2013
DOI: 10.1016/j.ijbiomac.2013.04.059
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Selenylation modification can enhance antioxidant activity of Potentilla anserina L. polysaccharide

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Cited by 82 publications
(31 citation statements)
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“…Selenium could prevent free radicals from damaging cells and tissues in vivo . Zhao and others () studied the selenylation‐modified polysaccharides from P. anserine L., and found that their antioxidant activities were significantly enhanced. Selenylation of polysaccharides from L. barbarum significantly enhanced glutathione peroxidase (GSH‐Px) and superoxide dismutase (SOD) activities, and decreased malondialdehyde (MDA) content, showing significantly stronger antioxidant activities and bioactivities than the original polysaccharide (Qiu and others ).…”
Section: Influence Of Molecular Modification On Bioactivities Of Polymentioning
confidence: 99%
“…Selenium could prevent free radicals from damaging cells and tissues in vivo . Zhao and others () studied the selenylation‐modified polysaccharides from P. anserine L., and found that their antioxidant activities were significantly enhanced. Selenylation of polysaccharides from L. barbarum significantly enhanced glutathione peroxidase (GSH‐Px) and superoxide dismutase (SOD) activities, and decreased malondialdehyde (MDA) content, showing significantly stronger antioxidant activities and bioactivities than the original polysaccharide (Qiu and others ).…”
Section: Influence Of Molecular Modification On Bioactivities Of Polymentioning
confidence: 99%
“…However, their limited water-solubility and relatively low biological activities hinder their application. Chemical modification of polysaccharide chains, such as phosphorylation (Song, Ni, Hu, & Li, 2015), sulphation (Jin, Wang, Huang, Lu, & Wang, 2014), selenylation (Zhao et al, 2013), or the introduction of hydroxamates (Aiedeh & Taha, 2001), leads to changes in the physicochemical and biological properties of polysaccharides.…”
Section: Introductionmentioning
confidence: 99%
“…Absorption bands for the polysaccharides in the range of 950–1200 cm −1 were found in cases in which C–O–C and C–O–H link band positions were found. Absent in the spectrogram of CEPS, a weak characteristic absorption band in that of Se-CEPS was found at 882.9 cm −1 , indicating an asymmetrical Se = O stretching vibration of selenium ester [19], and another characteristic absorption band was found at 610.6 cm −1 , indicating an asymmetrical Se − O − C stretching vibration [20], which demonstrated that Se-CEPS was successfully modified by selenylation.
Fig. 2IR spectra of the CEPS ( a ) and Se-CEPS ( b ) in the range of 400–4000 nm
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Section: Resultsmentioning
confidence: 99%