海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2014年
8期
57-59
,共3页
高效液相色谱法%武夷茶%咖啡因
高效液相色譜法%武夷茶%咖啡因
고효액상색보법%무이다%가배인
HPLC%Tea%Caffeine
目的:采用高效液相色谱法测定8种茶叶中咖啡因的含量。方法采用 Ultimate XB-C18(4.6×250mm,5μm)色谱柱,流动相:乙腈-0.2%磷酸水溶液,梯度洗脱,流速1.0mL· min -1,检测波长为280nm,进样量20μL。结果在所选条件下,样品中待测组分与其它组分分离良好(R>1.5),咖啡因对照品在10~100μg· mL -1质量浓度范围内线性关系良好,r=0.9998;回收率为98.8%~102.5%,RSD=1.6%(n=6)。结论该方法操作简便,结果可靠,适合用于茶叶中咖啡因定量分析。
目的:採用高效液相色譜法測定8種茶葉中咖啡因的含量。方法採用 Ultimate XB-C18(4.6×250mm,5μm)色譜柱,流動相:乙腈-0.2%燐痠水溶液,梯度洗脫,流速1.0mL· min -1,檢測波長為280nm,進樣量20μL。結果在所選條件下,樣品中待測組分與其它組分分離良好(R>1.5),咖啡因對照品在10~100μg· mL -1質量濃度範圍內線性關繫良好,r=0.9998;迴收率為98.8%~102.5%,RSD=1.6%(n=6)。結論該方法操作簡便,結果可靠,適閤用于茶葉中咖啡因定量分析。
목적:채용고효액상색보법측정8충다협중가배인적함량。방법채용 Ultimate XB-C18(4.6×250mm,5μm)색보주,류동상:을정-0.2%린산수용액,제도세탈,류속1.0mL· min -1,검측파장위280nm,진양량20μL。결과재소선조건하,양품중대측조분여기타조분분리량호(R>1.5),가배인대조품재10~100μg· mL -1질량농도범위내선성관계량호,r=0.9998;회수솔위98.8%~102.5%,RSD=1.6%(n=6)。결론해방법조작간편,결과가고,괄합용우다협중가배인정량분석。
OBJECTIVE To analyze the content of CAF in the eight kinds of tea by High-performance Liquid Chromatography.METHODS Using a Ultimate XB-C18 (4.6 ×250mm,5μm) as the chromatographic column, with the moving phase of acetonitrile:0.2%phosphoric acid solution gradient elution ,the velocity of flow was 1.0 mL · min -1 ,the UV detection wavelength was 280 nm,the sample dose was 20μL.RESULTS Under the selected con-dition,the aim ingredient in the samples got an ideal resolution with others (the resolution was above 1.5).Caffeineshowed good linear relationship in the concentration range of 10 ~100μg· mL-1 ,r =0.9998.The recovery rate was98.8% to 102.5%,RSD was 1.6%(n =6).CONCLUSION The method is simple and result is reliable,whichcan be used for quantitative analysis of caffeine in tea.