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作 者:杨东顺[1] 王莉丽 马芙蓉[1] 叶艳萍[1] 毕亚楠 汪禄祥[1] YANG Dong-Shun;WANG Li-Li;MA Fu-Rong;YE Yan-Ping;BI Ya-Nan;WANG Lu-Xiang(Institute of Quality Standard and Testing Technology of Yunnan Academy of Agricultural Sciences,Kunming 650205,China)
机构地区:[1]云南省农业科学院质量标准与检测技术研究所,昆明650205
出 处:《食品安全质量检测学报》2020年第19期7052-7056,共5页Journal of Food Safety and Quality
基 金:云南省农产品质量安全检测平台(2014DA001)。
摘 要:目的建立酶联免疫吸附法测定铁皮石斛中黄曲霉毒素B1(afatoxin B1, AFB1)的分析方法,并研究酶联免疫吸附法(enzyme-linkedimmunosorbentassay,ELISA)和高效液相色谱法(highperformanceliquid chromatography, HPLC)测定云南铁皮石斛中AFB1的结果差异性。方法用甲醇+水溶液(50+50, V/V)提取石斛中AFB1,采用酶联免疫吸附法和高效液相色谱法同时检测云南铁皮石斛(铁皮枫斗)中AFB1,进行准确性、精密度和回收率等方法学实验,比较2种方法的差异性。结果 ELISA法在测定范围内AFB1与其对应的吸光度值之间呈良好的线性关系,回归方程Y=-34.798X+18.134,相关系数r2为0.9967;添加1.0、4.0、10.0μg/kg3个浓度的平均加标回收率为85.3%~94.7%,相对标准偏差为2.57%~4.88%。2种方法的结果符合率为93.2%~117%,相对标准偏差均小于10%。结论 ELISA法具有操作简单、检测速度快、灵敏、特异性好等优点,可同时检测大批量样品中AFB1的含量。Objective To establish a method for the determination of aflatoxin B1 in Dendrobium candidum of Yunnan province by enzyme-linked immunosorbent assay(ELISA) and to study the difference between ELISA and high performance liquid chromatography(HPLC) for the determination of AFB1 in Dendrobium candidum from Yunnan province. Methods Aflatoxin B1(AFB1) was extracted from Dendrobium candidum with methanol and aqueous solution(50+50, V/V). AFB1 in Dendrobium candidum was detected by ELISA and HPLC, and the accuracy, precision and recovery rate of aflatoxin B1 in Dendrobium candidum were compared. Results There was a good linear relationship between AFB1 and its corresponding absorbance value in the detection range of ELISA. The regression equation was Y=-34.798 X+18.134, and the correlation coefficient r2 was 0.9967. The average recoveries and relative standard deviations were 85.3%-94.7% and 2.57%-4.88% with the addition standard of 1.0, 4.0 and 10.0μg/kg. The coincidence rates of ELISA and HPLC were 93.2%-117%, and the relative standard deviations were less than 10%. Conclusion ELISA has the advantages of simple operation, fast detection speed, sensitivity and good specificity. It can simultaneously detect the content of AFB1 in a large number of samples.
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