化学分析计量
化學分析計量
화학분석계량
CHEMICAL ANALYSIS AND METERAGE
2013年
5期
27-29
,共3页
周顺珍%龚雪%周国兰%郭灿%郑文莉
週順珍%龔雪%週國蘭%郭燦%鄭文莉
주순진%공설%주국란%곽찬%정문리
茶叶%儿茶素%咖啡碱%高效液相色谱法
茶葉%兒茶素%咖啡堿%高效液相色譜法
다협%인다소%가배감%고효액상색보법
tea%catechins%caffeine%HPLC chromatography
以绿茶为样本,以GB/T 8305-1987水浸出方式作为样品的提取方法,使用C18色谱柱(150 mm×4.6 mm,5μm),以A相(超纯水)、B相(N-N二甲基甲酰胺︰甲醇︰冰乙酸=40︰2︰1.5)为流动相,在最佳梯度洗脱条件下对8种组分进行分离,紫外检测器检测,检测波长为278 nm ,外标法定量。没食子酸、咖啡碱、表没食子儿茶素、儿茶素、表儿茶素、表没食子儿茶素没食子酸酯、没食子基儿茶素没食子酸酯和表儿茶素没食子酸酯8种组分的进样质量分别在0.0243~0.1456,0.2549~1.5296,0.2027~1.2164,0.0182~0.1102,0.1606~0.9634,1.0004~6.0024,0.0182~0.1090,0.2296~1.3774μg范围内与色谱峰面积的线性关系良好(r为0.9910~0.9999);加标回收率为98.60%~100.17%,RSD均小于0.48%(n=3)。对样品进行6次重复测定,与标准方法相比,8种组分测定结果的相对偏差为0.47%~5.55%。该方法简便、快速、准确、稳定、重复性好,可用于茶叶中8种成分的定量分析。
以綠茶為樣本,以GB/T 8305-1987水浸齣方式作為樣品的提取方法,使用C18色譜柱(150 mm×4.6 mm,5μm),以A相(超純水)、B相(N-N二甲基甲酰胺︰甲醇︰冰乙痠=40︰2︰1.5)為流動相,在最佳梯度洗脫條件下對8種組分進行分離,紫外檢測器檢測,檢測波長為278 nm ,外標法定量。沒食子痠、咖啡堿、錶沒食子兒茶素、兒茶素、錶兒茶素、錶沒食子兒茶素沒食子痠酯、沒食子基兒茶素沒食子痠酯和錶兒茶素沒食子痠酯8種組分的進樣質量分彆在0.0243~0.1456,0.2549~1.5296,0.2027~1.2164,0.0182~0.1102,0.1606~0.9634,1.0004~6.0024,0.0182~0.1090,0.2296~1.3774μg範圍內與色譜峰麵積的線性關繫良好(r為0.9910~0.9999);加標迴收率為98.60%~100.17%,RSD均小于0.48%(n=3)。對樣品進行6次重複測定,與標準方法相比,8種組分測定結果的相對偏差為0.47%~5.55%。該方法簡便、快速、準確、穩定、重複性好,可用于茶葉中8種成分的定量分析。
이록다위양본,이GB/T 8305-1987수침출방식작위양품적제취방법,사용C18색보주(150 mm×4.6 mm,5μm),이A상(초순수)、B상(N-N이갑기갑선알︰갑순︰빙을산=40︰2︰1.5)위류동상,재최가제도세탈조건하대8충조분진행분리,자외검측기검측,검측파장위278 nm ,외표법정량。몰식자산、가배감、표몰식자인다소、인다소、표인다소、표몰식자인다소몰식자산지、몰식자기인다소몰식자산지화표인다소몰식자산지8충조분적진양질량분별재0.0243~0.1456,0.2549~1.5296,0.2027~1.2164,0.0182~0.1102,0.1606~0.9634,1.0004~6.0024,0.0182~0.1090,0.2296~1.3774μg범위내여색보봉면적적선성관계량호(r위0.9910~0.9999);가표회수솔위98.60%~100.17%,RSD균소우0.48%(n=3)。대양품진행6차중복측정,여표준방법상비,8충조분측정결과적상대편차위0.47%~5.55%。해방법간편、쾌속、준학、은정、중복성호,가용우다협중8충성분적정량분석。
Water extraction in GB/T 8305-1987 was as the sample pretreatment method, with a C18 column(150 mm×4.6 mm, 5μm), the mobile phase as: phase A of ultra-pure water and phase B of N-N dimethyl formamide-methanol-acetic acid (40︰2︰1.5), 8 components in green tea sample were gradient elution separation, and determined with UV detector at 278 nm. The external standard was adopted for the assay. There was good linearity between the 1ogarithm values and the peak areas of GA, CAF, EGC,+C, EC, EGCG, GCG , ECG and in the ranges of 0.024 3-0.145 6, 0.254 9-1.529 6, 0.202 7-1.216 4, 0.018 2-0.110 2, 0.160 6-0.963 4, 1.000 4-6.002 4, 0.018 2-0.109 0, 0.229 6-1.377 4μg respectively. Recoveries of the eight components were 98.60%-100.17%, RSDs were all below 0.48%(n=3). The samples were measured for 6 times repeatedly, compared with the results by GB/T 8313-2008, the relative deviations were 0.47%-5.55%(n=6). The method is simple, rapid, accurate, stable, reproducible, and suitable for the quantitative analysis of catechins, caffeine and those 8 components.