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植物精油微粉中肉桂醛含量超高效液相色谱测定OA北大核心CSTPCD

Determination of Cinnamaldehyde in Plant Essential Oil Powder by UPLC

中文摘要英文摘要

建立了检测植物精油微粉中肉桂醛含量的超高效液相色谱法.采用CORTECS® C18色谱柱,以乙腈-水(42∶58)为流动相,流速0.3 mL/min,波长280 nm,柱温为30 ℃,进样量0.6 μL.结果表明,肉桂醛色谱峰峰形良好,在1.0~200.0 μg/mL范围内线性关系良好(R2为0.999 9).检测限为0.5 μg/mL.精密度和稳定性考察结果相对标准偏差均小于2.0%.加样回收率在96.76%~102.66%之间,符合方法学要求.采用上述方法进行了 6批植物精油包被产品的检测,肉桂醛含量均符合要求.此方法具有检测限低,精密度和准确度高,分析快速等特点.

The aim of this study was to establish a UPLC method for determination of cinnamaldehyde in plant essential oil powder.The elution was performed by using CORTECS® C18 column and using acetoni-trile-water(42:58)as mobile phase.The flow rate was set at 0.3 mL/min.The detection wavelength was 280 nm.The column temperature was 30 ℃ and the injection volume was 0.6 μL.The results showed that cinnamaldehyde could be separated completely and the linear relationship was good(R2=0.999 9)in the range of 1.0-200.0 μg/mL.The limit of detection was 0.5 μg/mL.The relative standard deviations for preci-sion and stability assessment results were both less than 2.0%.The average recoveries of cinnamaldehyde were 97.95%-101.71%.All of them were in accordance with the requirements of the methodology.The rela-tive contents of cinnamaldehyde in 6 samples were in accordance with the requirements.This method is characterized by low detection limit,high precision and accuracy,and rapid analysis.

黎乃添;陆泳良;雍燕;袁富威;赵敏端

广东温氏大华农生物科技有限公司,广东云浮 527400

畜牧业

植物精油包被制剂肉桂醛超高液相色谱法

plant essential oilcinnamomum cassiacinnamaldehydeUPLC

《动物医学进展》 2024 (007)

38-42 / 5

云浮市科技计划项目(S2021020101);温氏科研基金项目(DHN20230210JKYZYY002)

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