2018
DOI: 10.1016/j.ijbiomac.2017.10.163
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A novel iron supplements preparation from Grifola frondosa polysaccharide and assessment of antioxidant, lymphocyte proliferation and complement fixing activities

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Cited by 41 publications
(34 citation statements)
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“…These results demonstrate that the AAPS-iron(III) complex maintained high thermal stability in the temperature ranging from 50°C to 256°C, indicating that the AAPS-iron(III) complex is sufficiently stable if used as a type of nutritional fortifiers which are generally required to be stable below 250°C in the food industry. Similar thermal stability was also reported in Grifola frondosa [13], where the AAPS-iron(III) complex showed increased high stability in the temperature ranging from room temperature to 275°C in comparison to AAPS.…”
Section: Resultssupporting
confidence: 84%
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“…These results demonstrate that the AAPS-iron(III) complex maintained high thermal stability in the temperature ranging from 50°C to 256°C, indicating that the AAPS-iron(III) complex is sufficiently stable if used as a type of nutritional fortifiers which are generally required to be stable below 250°C in the food industry. Similar thermal stability was also reported in Grifola frondosa [13], where the AAPS-iron(III) complex showed increased high stability in the temperature ranging from room temperature to 275°C in comparison to AAPS.…”
Section: Resultssupporting
confidence: 84%
“…The optimum preparation conditions of the AAPS-iron(III) complex included a ratio of AAPS to FeCl 3 ∙ 6H 2 O of 2:3 (w/w), pH 8.0, reaction temperature of 50°C, and reaction time of 3 h. The AAPS-iron(III) complex had a relatively high iron content (28.40%) compared to those previously reported and showed increased water solubility. For example, Xu et al [13] have obtained iron content of 24.15% in the AAPS-iron(III) complex in a fungal species of Grifola frondosa under the optimum preparation conditions based on the single factor and orthogonal optimization experiments, including a ratio of AAPS to the catalyst (sodium citrate) of 1:1 (g/g), reaction temperature of 80°C, reaction time of 1.5 h, and pH 8.0.…”
Section: Resultsmentioning
confidence: 99%
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“…AOS had an absorption peak at 1725 cm −1 (–COOH) (Dolamic et al ., ) that was absent in the AOS–iron (III) spectrum, which indicates that –COOH might be chelated with iron (III). In addition, bands at 1636 and 1412 cm −1 in the AOS spectrum indicated the presence of a free carboxylic carbonyl group (Siqueira et al ., ; Pouyet et al ., ) and carboxylic acids group (Xu et al ., ), respectively. In the AOS–iron (III) spectrum, the two peaks showed some migration (1605 and 1386 cm −1 ), which means that iron (III) and AOS might be combined by the –OH groups (Tang et al ., ).…”
Section: Resultsmentioning
confidence: 95%
“…Iron content was highest (11.89 ± 0.24%) at the mass ratio of 2:1 g:g. Sodium citrate and AOS are ligands for iron (III) (Gautier‐Luneau et al ., ; Wang et al ., ). Sodium citrate acts as a bridge to link AOS and iron (III), and then it separates from AOS–iron (III) (Xu et al ., b). Therefore, sodium citrate was available for further reaction to get more AOS–iron (III).…”
Section: Resultsmentioning
confidence: 99%