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机构地区:[1]江南大学工业生物技术教育部重点实验室,江南大学生物工程学院无锡214036
出 处:《分析化学》2006年第U09期155-157,共3页Chinese Journal of Analytical Chemistry
基 金:江苏省2004农业科技攻关(No.BE2004305)资助项目
摘 要:根据银杏酚酸在紫外光激发下能产生荧光的性质,建立了检测银杏酚酸的荧光分光光度法。以80%乙醇80℃回流8h提取银杏外种皮,提取液经硅胶柱层析后得酚酸样品。以白果酸为标样,激发波长345nm、发射波长420nm测定银杏酚酸。线性回归方程为,y=2.5024x+0.4152;线性范围为0.50~100mg/L,相关系数r=0.9922,相对标准偏差2.6%;检出限0.11mg/L。A fluorescence spectrophotometry for determination was extracted with 80% ethanol by continuous thermal reflux of ginkgolic acids was established. The sample from Exopleura of Ginkgo biloba at 80℃ for 8 hours and the extract was purified by silica gel column chromatography. Total ginkgolic acids was determined by spectrofluorometry with ginkgolic acid as standard reference at λex = 345 nm and λem = 420 nm. The linearity relationship is y = 2.5024x + 0.4152, with correlative coefficient of 0.9922, relative standard deviation (RSD) of 2.6% and detection limit of 0.114 mg/L. Influences of pH and the dissolved impurities were discussed. The results obtained by this method agreed with those by the high performance liquid chromatography with fluorescence detection(FLD).
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