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刊物信息

期刊名称:药物分析杂志
主管单位:中国科学技术协会
主办单位:中国药学会
承办:中国食品药品检定研究院
主编:金少鸿
地址:北京天坛西里2号
邮政编码:100050
电话:010-67012819,67058427
电子邮箱:ywfx@nicpbp.org.cn
国际标准刊号:ISSN 0254-1793
国内统一刊号:CN 11-2224/R
邮发代号:2-237
 

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超临界流体色谱法测定蛋黄卵磷脂中的8种磷脂组分

Determination of eight phospholipid components in egg yolk lecithin by supercritical fluid chromatography

分类号:
出版年·卷·期(页码):2016,36 (2):0-0
DOI: 10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------

目的:建立超临界流体色谱法分离并测定蛋黄卵磷脂中的三棕榈酸甘油酯(TG)、胆固醇(CH)、磷脂酰乙醇胺(PE)、溶血磷脂酰乙醇胺(LPE)、磷脂酰肌醇(PI)、磷脂酰胆碱(PC)、鞘磷脂(SM)、溶血磷脂酰胆碱(LPC)8种磷脂组分。方法:采用Zorbax Silica色谱柱(250 mm×4.6 mm,5 μm)与LiChrosphere100 Diol色谱柱(250 mm×4 mm,5 μm)串联,以二氧化碳为流动相A,甲醇-氨水(100:0.5)为流动相B,进行梯度洗脱,流速为2.3 mL·min-1,柱温为30℃,进样量为5 μL,二氧化碳补偿液(甲醇)流速为0.2mL·min-1,蒸发光散射检测器检测,漂移管温度为90℃,雾化气流速为1.2 L·min-1结果:8种磷脂组分分离完全,且峰面积与浓度的双对数线性关系良好,日内精密度RSD为0.2%~2.0%,日间精密度RSD为0.5%~2.0%,检测限为0.137~0.584 μg,定量限为0.273~1.169 μg,加样回收率为97.1%~100.6%,RSD为1.1%~2.7%,测得3批蛋黄卵磷脂中的TG为1.6%~1.8%,CH为0.4%~0.5%,PE为7.8%~8.9%,LPE为0.7%~0.9%,PI为0.9%~1.1%,PC为79.1%~83.0%,SM为1.4%~1.5%,LPC为1.6%~1.7%。结论:本文建立的方法可用于蛋黄卵磷脂的质量控制。

-----英文摘要:---------------------------------------------------------------------------------------

Objective:To establish a supercritical fluid chromatography method for separation and determination of glycerol tripalmitatec(TG),cholesterol(CH),photidylethanolamine(PE),lysophosphatidyl ethanolamine (LPE),phophotidyl inositol(PI),phosphotidylcholine(PC),sphingomyelin(SM)and lysophosphatidyl choline (LPC)in egg yolk lecithin.Methods:A Zorbax Silica column(250 mm×4.6 mm,5 μm)and a LiChrosphere 100 Diol column(250 mm×4 mm,5 μm)in series were used with the mobile phase A of carbon dioxide and the mobile phase B of methanol-ammonia solution(100:0.5)by gradient elution.The flow rate was 2.3 mL·min-1,and the column temperature was controlled at 30℃.The injection volume was 5 μL,and the flow rate of carbon dioxide makeup(methanol)was 0.2 mL·min-1.The samples were detected by evaporative light scattering detector with drift tube temperature at 90℃ and a flow of atomizing gas at 1.2 L·min-1.Results:Eight phospholipid components were separated completely.The double logarithm linear relationship of peak area and corresponding concentration was good.Within-day and intra-day precision of the method were 0.2%-2.0% and 0.5%-2.0%,respectively.The limit of detection was 0.137-0.584 μg,and limit of quantification was 0.273-1.169 μg.The spiked sample average recoveries were 97.1%-100.6%,and the RSD was 1.1%-2.7%.Eight phospholipid components were determined in 3 batch of egg yolk lecithin.TG were 1.6%-1.8%,CH were 0.4%-0.5%,PE was 7.8%-8.9%,LPE was 0.7%-0.9%,PI was 0.9%-1.1%,PC were 79.1%-83.0%,SM was 1.4%-1.5%,and LPC were 1.6%-1.7%,respectively.Conclusions:The proposed method is proved method validation, and thus can be used to control the quality of egg yolk lecithin.

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