周提军,王莎,李兵,荒井裕子,城田修.基于柱切换技术的高压液相色谱法检测奶粉中的维生素D[J].食品安全质量检测学报,2013,4(2):467-471
基于柱切换技术的高压液相色谱法检测奶粉中的维生素D
Detection of vitamin D in milk powder by HPLC based on column-switching system
投稿时间:2012-11-09  修订日期:2012-12-28
DOI:
中文关键词:  阀切换  维生素D  高压液相色谱法
英文关键词:column-switching  vitamin D  high pressure chromatography (HPLC)
基金项目:
作者单位
周提军 资生堂中国投资有限公司先端科学事业推进部应用技术中心 
王莎 资生堂中国投资有限公司先端科学事业推进部应用技术中心 
李兵 资生堂中国投资有限公司先端科学事业推进部应用技术中心 
荒井裕子 资生堂中国投资有限公司先端科学事业推进部应用技术中心 
城田修 资生堂中国投资有限公司先端科学事业推进部应用技术中心 
AuthorInstitution
ZHOU Ti-Jun Advanced Science and Business Promontion Division Applied Technology Center of Shiseido(China) Investment Co., Ltd. 
WANG Sha Advanced Science and Business Promontion Division Applied Technology Center of Shiseido(China) Investment Co., Ltd. 
LI Bing Advanced Science and Business Promontion Division Applied Technology Center of Shiseido(China) Investment Co., Ltd. 
HUANG JING Yu-Zi Advanced Science and Business Promontion Division Applied Technology Center of Shiseido(China) Investment Co., Ltd. 
CHENG Tian-Xiu Advanced Science and Business Promontion Division Applied Technology Center of Shiseido(China) Investment Co., Ltd. 
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中文摘要:
      目的 建立奶粉中维生素D的柱切换式高压液相色谱分析方法。方法 奶粉样品经过皂化处理、石油醚提取、脱水浓缩后, 用柱切换式高压液相色谱仪进行检测。结果 维生素D3在0.2~1.0 ?g/mL范围内线性关系良好, 回归方程Y=1.74181e?006X?0.00662911, 相关系数r=0.9956, 检出限为0.01 ?g/mL, 定量限为0.2 mg/kg, RSD为2.12%, 平均回收率为 96.8%。结论 该方法简单、快速、准确, 为复杂基质食品中低含量物质的检测提供一定参考。
英文摘要:
      Objective To establish a method for the determination of vitamin D in milk powder by high pressure chromatography based on column-switching methods. Methods After saponification treatment, milk powder was extracted with petroleum ether. The extract was dehydrated with anhydrous sodium sulfate, concentrated, and analyzed by HPLC. Results The method showed a good linearity over the range of 0.2~1 μg/mL for vitamin D with r=0.9956. The linear equations was Y =1.74181e-006X-0.00662911 and the average recoveries were 96.8% with the relative standard deviations(RSDs)of 2.12%. The LOD and LOQ were 0.01 μg/mL and 0.2 mg/kg, respectively. Conclusion The method is simply, rapid and accurate, and it provides a reference for the detection of trace substance in complex matrix.
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