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논문 기본 정보

자료유형
학술저널
저자정보
Chang, Oun Ki (Animal Products and Development Division, National Institute of Animal Science, Rural Development Administration) Ha, Go Eun (Animal Products and Development Division, National Institute of Animal Science, Rural Development Administration) Jeong, Seok-Geun (Animal Products and Development Division, National Institute of Animal Science, Rural Development Administration) Seol, Kuk-Hwan (Animal Products and Development Division, National Institute of Animal Science, Rural Development Administration) Oh, Mi-Hwa (Animal Products and Development Division, National Institute of Animal Science, Rural Development Administration) Kim, Dong Wook (Department of Animal Products and Food Science, Kangwon National University) Jang, Aera (Department of Animal Products and Food Science, Kangwon National University) Kim, Sae Hun (Department of Food Bioscience and Technology, Korea University) Park, Beom-Young (Animal Products and Development Division, National Institute of Animal Science, Rural Development Administration) Ham, Jun-Sang (Animal Products and Development Division, National Institute of Animal Science, Rural Dev)
저널정보
한국축산식품학회 한국축산식품학회지 한국축산식품학회지 제33권 제4호
발행연도
2013.1
수록면
493 - 500 (8page)

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초록· 키워드

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Gelatin is a collagen-containing thermohydrolytic substance commonly incorporated in cosmetic and pharmaceutical products. This study investigated the antioxidant activity of gelatin by using different reagents, such as 2,2-azinobis-(3-ethylbenzothiazoline- 6-sulfonic acid) (ABTS), 2,2-di (4-tert-octylphenyl)-1-picrylhydrazyl (DPPH), and oxygen radical absorbance capacity-fluorescein (ORAC-FL) in a porcine gelatin hydrolysate obtained using gastrointestinal enzymes. Electrophoretic analysis of the gelatin hydrolysis products showed extensive degradation by pepsin and pancreatin, resulting in an increase in the peptide concentration (12.1 mg/mL). Antioxidant activity, as measured by ABTS, exhibited the highest values after 48-h incubation with pancreatin treatment after pepsin digestion. Similar effects were observed at 48 h incubation, that is, 61.5% for the DPPH assay and 69.3% for the ABTS assay. However, the gallic acid equivalent (GE) at 48 h was $87.8{\mu}M$, whereas $14.5{\mu}M$ GE was obtained using the ABTS and DPPH assays, indicating about sixfold increase. In the ORACFL assay, antioxidant activity corresponding to $45.7{\mu}M$ of trolox equivalent was found in the gelatin hydrolysate after 24 h hydrolysis with pancreatin treatment after pepsin digestion, whereas this activity decreased at 48 h. These antioxidant assay results showed that digestion of gelatin by gastrointestinal enzymes prevents oxidative damage.

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