2020
DOI: 10.1016/j.arabjc.2018.11.013
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Environmentally-friendly strategy for separation of α-lactalbumin from whey by aqueous two phase flotation

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Cited by 30 publications
(22 citation statements)
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“…Rather than using alcohol-based LBS, a recent study had showed the extraction of α-Lactalbumin from whey used a different phase forming component (i.e., PEG 1000 and citrate salts) along with bubble-assisted technologies showed a separation efficiency and purification fold of 87.54% and 5.33 [64]. The advantages of this study had showed the feasibility of bubble-assisted technology compared to conventional liquid-liquid extraction providing a low processing cost, rapid, and good separation yield.…”
Section: Bubble-assisted Lbsmentioning
confidence: 99%
“…Rather than using alcohol-based LBS, a recent study had showed the extraction of α-Lactalbumin from whey used a different phase forming component (i.e., PEG 1000 and citrate salts) along with bubble-assisted technologies showed a separation efficiency and purification fold of 87.54% and 5.33 [64]. The advantages of this study had showed the feasibility of bubble-assisted technology compared to conventional liquid-liquid extraction providing a low processing cost, rapid, and good separation yield.…”
Section: Bubble-assisted Lbsmentioning
confidence: 99%
“…It can enhance the viability of probiotic cells during processing, storage, subsequent consumption, and gastrointestinal digestion [ 6 , 7 ]. It has been reported that different methods such as emulsification, phase separation, and spray drying have been used to microencapsulate bioactive substances [ 7 , 8 , 9 , 10 ]. However, many of these methods involve high temperatures or a large amount of organic reagents, which may adversely affect the survival rate of probiotics or cause potential hazards to the human body.…”
Section: Introductionmentioning
confidence: 99%
“…The Pv was analyzed by SDS-PAGE (Bio-Rad Co., Ltd., Guangzhou, China) as described by Jiang [36,37]. The resolving gel concentration was 12%, and the concentration of the stacking gel was 5%, and the molecular weight of the pre-stained protein Marker ranged from 14.4~116.0 kDa.…”
Section: Methodsmentioning
confidence: 99%