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Determination of Vitamin D in Infant Milk Powder by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry with Isotopes Dilution

Wanqin Chen

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Abstract

In order to establish a reliable method for quantitative analysis of vitamin D in infant milk powder,a ultra performance liquid chromatography-tandem mass spectrometry(UPLC/MS/MS) with isotopes dilution method was developed.The samples were saponifed with KOH and extracted by pentane-ethyl ether solution(V(pentane)∶V(ethyl ether)=4∶1).The target analytes were separated on the Waters T3 column with gradient elution using methanol and water(containing 2 mmol/L ammonium formate for both) as mobile phase.The identification and quantification were achieved by using electrospray ionization in positive ion mode and with multiple reaction monitoring.Internal standard method was used to determine the results.The linear range of the calibration curve was 5—150 μg/L.The limit of detection(LOD) of the method was 1.5 μg/kg,and the limit of quantitation(LOQ) was 5.0 μg/kg.The recoveries of the method were in the range of 97.0%—104.7% and 92.7%—108.0% for vitamin D2 and vitamin D3 respectively.The relative standard deviations(RSD) of intra-day and inter-day were less than 10%.The simply,rapid,accurate and sensitive method can be applied to determine the vitamin D in infant milk powder.

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What this paper is about

In order to establish a reliable method for quantitative analysis of vitamin D in infant milk powder,a ultra performance liquid chromatography-tandem mass spectrometry(UPLC/MS/MS) with isotopes dilution method was developed.The samples were saponifed with KOH and extracted by pentane-ethyl ether solution(V(pentane)∶V(ethyl ether)=4∶1).The target analytes were separated on the Waters T3 column with gradient elution using methanol and water(containing 2 mmol/L ammonium formate for both) as mobile phase.The identification and quantification were achieved by using electrospray ionization in positive ion mode and with multiple reaction monitoring.Internal standard method was used to determine the results.The linear range of the calibration curve was 5—150 μg/L.The limit of detection(LOD) of the method was 1.5 μg/kg,and the limit of quantitation(LOQ) was 5.0 μg/kg.The recoveries of the method were in the range of 97.0%—104.7% and 92.7%—108.0% for vitamin D2 and vitamin D3 respectively.The relative standard deviations(RSD) of intra-day and inter-day were less than 10%.The simply,rapid,accurate and sensitive method can be applied to determine the vitamin D in infant milk powder.

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Available abstract

In order to establish a reliable method for quantitative analysis of vitamin D in infant milk powder,a ultra performance liquid chromatography-tandem mass spectrometry(UPLC/MS/MS) with isotopes dilution method was developed.The samples were saponifed with KOH and extracted by pentane-ethyl ether solution(V(pentane)∶V(ethyl ether)=4∶1).The target analytes were separated on the Waters T3 column with gradient elution using methanol and water(containing 2 mmol/L ammonium formate for both) as mobile phase.The identification and quantification were achieved by using electrospray ionization in positive ion mode and with multiple reaction monitoring.Internal standard method was used to determine the results.The linear range of the calibration curve was 5—150 μg/L.The limit of detection(LOD) of the method was 1.5 μg/kg,and the limit of quantitation(LOQ) was 5.0 μg/kg.The recoveries of the method were in the range of 97.0%—104.7% and 92.7%—108.0% for vitamin D2 and vitamin D3 respectively.The relative standard deviations(RSD) of intra-day and inter-day were less than 10%.The simply,rapid,accurate and sensitive method can be applied to determine the vitamin D in infant milk powder.

Key concepts: Chemistry, Chromatography, Ammonium formate, Isotope dilution, Detection limit, Selected reaction monitoring, Mass spectrometry, Electrospray ionization

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