2014
DOI: 10.1007/s13228-014-0035-y
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Bioefficacy of Tea Catechins Associated with Milk Caseins Tested Using Different In Vitro Digestion Models

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Cited by 25 publications
(29 citation statements)
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“…The anti-proliferation activity of curcumin encapsulated in SSPS before and after treatment in simulated gastric and intestinal digestive fluids was compared to free curcumin dissolved in dimethyl sulfoxide (DMSO). The simulated gastric and intestinal digestion conditions followed literature methods, with slight modification (Guri, Haratifar, & Corredig, 2014; Luo, Pan, & Zhong, 2015). Pepsin and pancreatin were dispersed separately at 8.0 mg/ml and 80.0 mg/ml in 10 mM phosphate-buffered saline adjusted to pH 2.0 and pH 7.0, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…The anti-proliferation activity of curcumin encapsulated in SSPS before and after treatment in simulated gastric and intestinal digestive fluids was compared to free curcumin dissolved in dimethyl sulfoxide (DMSO). The simulated gastric and intestinal digestion conditions followed literature methods, with slight modification (Guri, Haratifar, & Corredig, 2014; Luo, Pan, & Zhong, 2015). Pepsin and pancreatin were dispersed separately at 8.0 mg/ml and 80.0 mg/ml in 10 mM phosphate-buffered saline adjusted to pH 2.0 and pH 7.0, respectively.…”
Section: Methodsmentioning
confidence: 99%
“…In our study, catechins were selectively incorporated into rice bran, which provides a promising way to enrich catechins on food matrix directly from caffeine‐containing crude tea extract. Yet, the selectivity of food matrix for carrying catechins has not been fully discussed, since most studies investigated the incorporation with neat catechins or individual catechin (Dube and others ; Shpigelman and others ; Guri and others ; Wu and others ,b). Defatting pretreatment enhanced the adsorption of tea catechins on rice bran, which is possibly attributed to a relative increased content of key components responsible for catechins adsorption, as lipids were removed.…”
Section: Resultsmentioning
confidence: 99%
“…These cells are able to create a tight monolayer with well-developed tight junctions once they reach full confluency, as a close representation of the epithelial layer in the human gut 22 . We have been successfully using this cell model either in isolate or in combination with HT-29-MTX cells as a valid approach to access the uptake of bioactives in the small intestine 4, 5,23 . DMEM supplied with 10 FBS, 1 antibiotic solution 10,000 units/mL of penicillin and 10,000 μg/mL of streptomycin , 1 NAA and 0.25 HEPES, was used for propagation of the cells.…”
Section: Cell Culturementioning
confidence: 99%