食品安全质量检测学报
食品安全質量檢測學報
식품안전질량검측학보
FOOD SAFETY AND QUALITY DETECTION TECHNOLOGY
2015年
5期
1907-1912
,共6页
虞哲高%林冰东%邢月寒%王晓燕
虞哲高%林冰東%邢月寒%王曉燕
우철고%림빙동%형월한%왕효연
维生素C%总黄酮%固相萃取%D101大孔树脂%硝酸铝比色法?
維生素C%總黃酮%固相萃取%D101大孔樹脂%硝痠鋁比色法?
유생소C%총황동%고상췌취%D101대공수지%초산려비색법?
vitamin?C%total?flavonoids%solid?phase?extraction%D101?macro-porous?resin%aluminum?nitrate?colorimetric?
目的:建立富含维生素 C 食品中总黄酮的定量分析方法,解决维生素 C 干扰络合法测定总黄酮的问题。方法使用Waters Sep-Pak C18固相萃取小柱对提取物进行脱脂和去除色素, D101大孔固相萃取(SPE)小柱去除维生素C,得到总黄酮洗脱液,用硝酸铝比色法进行测定,检测波长510 nm。结果总黄酮在0~48μg/mL具有良好的线性关系,相关系数为0.9998,相对标准偏差(RSD)小于5%,三个水平的添加回收率为95.31%~98.38%。考察三种不同总黄酮和维生素C比例含量的食品(Vc:总黄酮=1:1,2:1,10:1),发现随着维生素C含量增加,对总黄酮测定结果的影响越大。因此,对样品进行前处理,可以测得较为准确的总黄酮含量。结论本方法样品前处理简单、环保、快速、准确,适用于富含维生素C食品中总黄酮的含量测定。
目的:建立富含維生素 C 食品中總黃酮的定量分析方法,解決維生素 C 榦擾絡閤法測定總黃酮的問題。方法使用Waters Sep-Pak C18固相萃取小柱對提取物進行脫脂和去除色素, D101大孔固相萃取(SPE)小柱去除維生素C,得到總黃酮洗脫液,用硝痠鋁比色法進行測定,檢測波長510 nm。結果總黃酮在0~48μg/mL具有良好的線性關繫,相關繫數為0.9998,相對標準偏差(RSD)小于5%,三箇水平的添加迴收率為95.31%~98.38%。攷察三種不同總黃酮和維生素C比例含量的食品(Vc:總黃酮=1:1,2:1,10:1),髮現隨著維生素C含量增加,對總黃酮測定結果的影響越大。因此,對樣品進行前處理,可以測得較為準確的總黃酮含量。結論本方法樣品前處理簡單、環保、快速、準確,適用于富含維生素C食品中總黃酮的含量測定。
목적:건립부함유생소 C 식품중총황동적정량분석방법,해결유생소 C 간우락합법측정총황동적문제。방법사용Waters Sep-Pak C18고상췌취소주대제취물진행탈지화거제색소, D101대공고상췌취(SPE)소주거제유생소C,득도총황동세탈액,용초산려비색법진행측정,검측파장510 nm。결과총황동재0~48μg/mL구유량호적선성관계,상관계수위0.9998,상대표준편차(RSD)소우5%,삼개수평적첨가회수솔위95.31%~98.38%。고찰삼충불동총황동화유생소C비례함량적식품(Vc:총황동=1:1,2:1,10:1),발현수착유생소C함량증가,대총황동측정결과적영향월대。인차,대양품진행전처리,가이측득교위준학적총황동함량。결론본방법양품전처리간단、배보、쾌속、준학,괄용우부함유생소C식품중총황동적함량측정。
Objective To establish a quantitative analysis of total flavonoids with high content of ascorbic acid(vitamin C) in food and solve the interference of ascorbic acid on the measurement of total flavonoids by complexation reaction. Methods A solid phase extraction procedure was developed to degrease and remove pigments by Sep-Pak C18, vitamin C was removed with D101 macro-porous resin, total flavonoids were determined by aluminum nitrate colorimetric using detection wavelength at 510 nm. Results The developed method was successfully used to determine total flavonoids in vitamin C rich fruits/plant extracts. It showed a good linearity in the range of 0~48 μg/mL with r=0.9998. The recoveries were 95.31%~98.38% at 3 spiked levels, and the relative standard deviations (RSDs) were less than 5%. Three kinds of food (ascorbic acid:flavonoids=1:1, 2:1, 10:1) were analyzed, which showed that higher ascorbic acid content could affect the testing result. So, it is necessary to remove the ascorbic acid before coloration in rich ascorbic acid products. Conclusion The method is suitable for simple, environmental, and effective determination of total flavonoids in rich ascorbic acid foods.