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西红花中西红花苷-1和西红花苷-2含量测定方法的建立 被引量:25

Establishment of determination method for crocin-Ⅰand crocin-Ⅱin Crocus sativus L.
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摘要 目的:建立西红花中西红花苷-1和西红花苷-2的含量测定方法。方法:采用高效液相色谱法,使用Zorbax C_(18)色谱柱,乙腈和水为流动相梯度洗脱,检测波长440nm,流速1.0mL·min^(-1);同时采用单因素分析的方法,对影响含量测定结果的主要因素如提取溶剂、超声处理时间、提取温度及是否避光等进行考察。结果:西红花苷-1在5.2~165μg·mL^(-1),西红花苷-2在2.7~85μg·mL^(-1)范围均呈良好线性关系,相关系数分别为0.9999和0.9998,平均回收率分别为102.5%和98.2%。西红花样品溶液的制备应在避光、室温条件下,以50%乙醇超声处理30min为宜。结论:按照本法进行西红花供试品溶液的制备和含量测定,结果稳定,重现性好,可用于西红花中西红花苷-1和西红花苷-2的含量测定。 Objective: To develop a method for the determination of crocin - Ⅰ and crocin - Ⅱ in stigma of saffron. Method :An HPLC method was applied with a Zorbax C18 column by gradient elution using acetonitrile and water. The detection wavelength was 440 nm and the flow rate was 1.0 mL ·min^-1; A single factor analysis method was used to evaluate the influence of sample processing conditions, Such as extraction solvents;ultrasonic temperature and time;and whether in the sade;etc. , on the results of content determination. Results:The calibration curve was linear over the concentration range of 5.2 - 165μg· mL^-1 (r =0. 9999)for crocin - Ⅰ and 2.7 - 85 μg·mL^-1 (r =0. 9998)for crocin - Ⅱ. The average recovery of crocin - Ⅰ was 102. 5% and that of crocin - Ⅱ was 98.2%. The sample should be extracted by uhrasonator with 50% ethanol for 30 min, under the room temperature in the shade. Conelusion:A stable and repeatable result can be obtained by the method to prepare sample solution and HPLC conditions. This method can be used for the determination of crocin - Ⅰ and crocin -Ⅱ in stigma of saffron.
出处 《药物分析杂志》 CAS CSCD 北大核心 2006年第9期1270-1273,共4页 Chinese Journal of Pharmaceutical Analysis
基金 国家"十五"重大科技专项(2001BA701A61) 上海科委中药现代化专项(03D219547 03D219532)资助
关键词 西红花 西红花苷-1 西红花苷-2 高效液相色谱法 stigma of saffron crocin - Ⅰ crocin - Ⅱ HPLC
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