张喜金,魏鲜娥,陈彩云,蔡伟江,黎小兰,蔡斯耿.顶空气相色谱-质谱法测定低取代羟丙纤维素中羟丙氧基的含量[J].食品安全质量检测学报,2017,8(10):4065-4070
顶空气相色谱-质谱法测定低取代羟丙纤维素中羟丙氧基的含量
Determination of hydroxypropoxy in low substituted hydroxypropyl cellulose by headspace gas chromatography-mass spectrometry
投稿时间:2017-07-12  修订日期:2017-09-30
DOI:
中文关键词:  低取代羟丙纤维素  气相色谱-质谱法  羟丙氧基
英文关键词:low substituted hydroxypropyl cellulose  gas chromatography-mass spectrometry  hydroxypropoxy
基金项目:
作者单位
张喜金 汤臣倍健股份有限公司 
魏鲜娥 汤臣倍健股份有限公司 
陈彩云 汤臣倍健股份有限公司 
蔡伟江 汤臣倍健股份有限公司 
黎小兰 汤臣倍健股份有限公司 
蔡斯耿 汤臣倍健股份有限公司 
AuthorInstitution
ZHANG Xi-Jin By-Health Co., Ltd 
WEI Xian-E By-Health Co., Ltd 
CHEN Cai-Yun By-Health Co., Ltd 
CAI Wei-Jiang By-Health Co., Ltd 
LI Xiao-Lan By-Health Co., Ltd 
CAI Si-Geng By-Health Co., Ltd 
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中文摘要:
      目的 建立顶空气相色谱-质谱法(gas chromatography-mass spectrometry, GC-MS)测定低取代羟丙纤维素中羟丙氧基的含量。方法 样品在顶空瓶中与氢碘酸反应, 使羟丙氧基转为2-碘丙烷, 反应结束后加碱液中和过量的氢碘酸防止腐蚀进样器和色谱柱, 随后顶空进样, 以HP-5MS毛细管柱分离, GC-MS选择离子检测模式测定。结果 羟丙氧基的浓度在0.6435~17.26025 mg/mL的范围内线性关系良好, 相关系数r>0.999; 此方法的检出限(S/N=3)为0.039 μg/mL, 定量限(S/N=10)为0.13 μg/mL; 在不同添加水平下, 方法的平均回收率为99.4%, 相对标准偏差为1.3%(n=3)。结论 该方法简便、快速、灵敏、准确, 适合羟丙氧基定性和定量测定。
英文摘要:
      Objective To establish a method for determination of hydroxypropoxy in low substituted hydroxypropyl cellulose (L-HPC) by head space gas chromatography-mass spectrometry (GC-MS). Methods The sample was reacted with the hydrogen iodide in headspace bottle, and the hydroxypropyl was converted to 2-iodopropane. After the reaction, excess hydrogen iodate was neutralized with adding lye to prevent corrosion of the sampler and chromatographic column. Then the samples were injected and HP-5MS capillary column was used for separation, and the selected ion detection mode of GC-MS was used for determination. Results Hydroxypropoxy had a good linear relationship in the range of 0.6435~17.26025 mg/mL, and the correlation coefficient was larger than 0.999. The limit of detection (S/N=3) was 0.039 μg/mL, and limit of quantitation (S/N=10) was 0.13 μg/mL. The average recovery of the method at different spiked levels was 99.4%, with the relative standard deviations of 1.3% (n=3). Conclusion The method is simple, rapid, sensitive and accurate, which is suitable for the qualitative and quantitative determination of hydroxypropyl.
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