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液相色谱法测定婴儿配方奶粉中维生素K1的反式和顺式异构体

Liquid chromatographic determination of vitamin K1 trans- and cis-isomers in infant formula.

作者信息

Hwang S M

出版信息

J Assoc Off Anal Chem. 1985 Jul-Aug;68(4):684-9.

PMID:4030639
Abstract

The normal phase liquid chromatographic (LC) method for determination of trans- and cis-isomers of vitamin K1 (phylloquinone) in infant formula described here uses an Apex silica column, isocratic elution, and UV absorption detection at 254 nm. Vitamin K1 is extracted quantitatively from the product matrix by pretreating the as-fed liquid with concentrated ammonium hydroxide and methanol, and then extracting it with a 2:1 mixture of dichloromethane and isooctane. The extract is cleaned up by silica open-column chromatography and concentrated for LC analysis. For trans-vitamin K1, the method precision is less than or equal to 3.3% RSD (relative standard deviation), and the spike recovery is 98 +/- 4%. For cis-vitamin K1, the precision is less than or equal to 12% RSD, determined at levels near the detection limit, and the spike recovery is 95 +/- 9%. The detection limit is 0.3 ng for both isomers at signal/noise = 3.

摘要

本文所述的用于测定婴儿配方奶粉中维生素K1(叶绿醌)反式和顺式异构体的正相液相色谱(LC)方法,使用Apex硅胶柱、等度洗脱,并在254 nm处进行紫外吸收检测。通过用浓氢氧化铵和甲醇对原样液体进行预处理,然后用二氯甲烷和异辛烷的2:1混合物进行萃取,从产品基质中定量提取维生素K1。提取物通过硅胶开放柱色谱进行净化,并浓缩用于LC分析。对于反式维生素K1,该方法的精密度小于或等于3.3%相对标准偏差(RSD),加标回收率为98±4%。对于顺式维生素K1,在接近检测限的水平下测定,精密度小于或等于12% RSD,加标回收率为95±9%。两种异构体在信噪比=3时的检测限均为0.3 ng。

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