Lei Meikang, Peng Fang, Ding Tao, Zhu Zitong, Xu Jiawen, Wu Xiaoqin
Se Pu. 2015 Jan;33(1):65-7. doi: 10.3724/sp.j.1123.2014.08022.
A method based on solid phase extraction and ultra performance liquid chromatography coupled with tandem mass spectrometry (SPE-UPLC-MS/MS) has been proposed for the determination of wilforine residue in honey. After the sample was dissolved with water, concentrated and purified by an HLB solid phase extraction cartridge, the UPLC separation was performed on a Hypersil GOLD C18 column (50 mm x 2.1 mm, 1.9 microm) utilizing a gradient elution program of methanol (containing 0.15% formic acid) and water as mobile phases at a flow rate of 0. 25 mL/min. The determination was carried out with electrospray ion source in the positive mode (ESI) and multiple reaction monitoring (MRM) mode. The mass concentration of wilforine in the range of 0.01-2 microg/L was linearly correlated with the peak area, and the correlation coefficients was greater than 0.998. The limit of quantification (S/N>10) for wilforine was 0.01 microg/kg. The recoveries were 76.1% to 96.2% in the spiked levels of 0.01, 0.05 and 0.5 microg/kg with the relative standard deviations (RSD, n=6) lower than 10%. The results indicate that the method is rapid, sensitive and accurate, and can be applied for the qualitative and quantitative analysis of wilforine in honey.
提出了一种基于固相萃取-超高效液相色谱-串联质谱法(SPE-UPLC-MS/MS)测定蜂蜜中吴茱萸次碱残留量的方法。样品用水溶解后,通过HLB固相萃取小柱进行浓缩和净化,然后在Hypersil GOLD C18柱(50 mm×2.1 mm,1.9μm)上进行UPLC分离,以甲醇(含0.15%甲酸)和水为流动相,采用梯度洗脱程序,流速为0.25 mL/min。采用电喷雾离子源正离子模式(ESI)和多反应监测(MRM)模式进行测定。吴茱萸次碱质量浓度在0.01~2μg/L范围内与峰面积呈线性关系,相关系数大于0.998。吴茱萸次碱的定量限(S/N>10)为0.01μg/kg。在0.01、0.05和0.5μg/kg加标水平下,回收率为76.1%~96.2%,相对标准偏差(RSD,n=6)低于10%。结果表明,该方法快速、灵敏、准确,可用于蜂蜜中吴茱萸次碱的定性和定量分析。