新疆大学学报(自然科学版)
新疆大學學報(自然科學版)
신강대학학보(자연과학판)
XINJIANG UNIVERSITY JOURNAL(NATURAL SCIENCE EDITION)
2014年
3期
258-260
,共3页
林江丽%朱亚娟%王金霞%封顺%王吉德
林江麗%硃亞娟%王金霞%封順%王吉德
림강려%주아연%왕금하%봉순%왕길덕
HPLC%葡萄%贮藏%糖分
HPLC%葡萄%貯藏%糖分
HPLC%포도%저장%당분
HPLC%grape%storage%saccharide
利用高效液相色谱法测定鲜食葡萄采后贮藏过程中糖分的变化.色谱柱为Inertsil NH2柱,流动相为75%的乙腈水溶液,用示差折光检测器检测不同贮藏期鲜食葡萄果实中的糖分.本方法的相对标准偏差为0.52%~1.22%,相关系数分别为0.9973和0.9993,加标回收率为99.81%~100.4%.该方法简便、灵敏、结果可靠,两种糖都得到了较好的分离,适用于鲜食葡萄果实中糖分的分析.
利用高效液相色譜法測定鮮食葡萄採後貯藏過程中糖分的變化.色譜柱為Inertsil NH2柱,流動相為75%的乙腈水溶液,用示差摺光檢測器檢測不同貯藏期鮮食葡萄果實中的糖分.本方法的相對標準偏差為0.52%~1.22%,相關繫數分彆為0.9973和0.9993,加標迴收率為99.81%~100.4%.該方法簡便、靈敏、結果可靠,兩種糖都得到瞭較好的分離,適用于鮮食葡萄果實中糖分的分析.
이용고효액상색보법측정선식포도채후저장과정중당분적변화.색보주위Inertsil NH2주,류동상위75%적을정수용액,용시차절광검측기검측불동저장기선식포도과실중적당분.본방법적상대표준편차위0.52%~1.22%,상관계수분별위0.9973화0.9993,가표회수솔위99.81%~100.4%.해방법간편、령민、결과가고,량충당도득도료교호적분리,괄용우선식포도과실중당분적분석.
Determination of saccharide components in table grape was studied by high performance liquid chromatography (HPLC).The HPLC column is Inertsil NH2, 5 μm, 4.6×250 mm,the mobile phase is CH3CN: H2O=75:25, and the detector is series RID-10A refractive index detector.The relative standard deviations are 0.52%~1.22%, and recoveries ranged from 99.81~100.4%, while the linear related coefficients are 0.997 3 and 0.999 3, respectively.The results showed that the samples are separated completely.The method is proved to be simple,rapid and reliable to determine the saccharine components in table grape.