Degradation kinetics of anthocyanins from purple sweet potato (Ipomoea batatas L.) as affected by ascorbic acid
被引:22
作者:
Li, Jing
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Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R ChinaSouthwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
Li, Jing
[1
]
Song, Huige
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Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
Neijiangshizhongqun Food & Drug Adm, Neijing 641000, Peoples R ChinaSouthwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
Song, Huige
[1
,2
]
Dong, Nan
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Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R ChinaSouthwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
Dong, Nan
[1
]
Zhao, Guohua
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Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
Food Engn & Technol Res Ctr Chongqing, Chongqing 400715, Peoples R China
Chongqing Sweet Potato Engn & Technol Ctr, Chongqing 400715, Peoples R ChinaSouthwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
Zhao, Guohua
[1
,3
,4
]
机构:
[1] Southwest Univ, Coll Food Sci, Chongqing 400715, Peoples R China
[2] Neijiangshizhongqun Food & Drug Adm, Neijing 641000, Peoples R China
[3] Food Engn & Technol Res Ctr Chongqing, Chongqing 400715, Peoples R China
[4] Chongqing Sweet Potato Engn & Technol Ctr, Chongqing 400715, Peoples R China
Storage (4A degrees C and 25A degrees C, 28 days) and thermal (70A degrees C-90A degrees C, 6 h) stabilities of purple sweet potato anthocyanins (PSPAs) with varying concentrations of ascorbic acid (AA) were investigated in a model soft drink medium. For storage stability, the model drink was sterilized at 85A degrees C for 15 min prior to storage. Zero-order kinetics and first-order kinetics were fitted for storage degradation at 4A degrees C and 25A degrees C, respectively. However, all data for thermal degradation fitted first-order kinetics. The temperature dependence on degradation was modeled after the Arrhenius equation. Storage degradation of PSPAs was increased by the presence of AA (40-360 mg/L). Retarded thermal degradation was be achieved by adding 120 mg/L of AA, while accelerated thermal degradation resulted from 360 mg/L of AA. Heat treatment did not markedly change the DPPH radical-scavenging activity of PSPAs.