Shen Chongyu, Guo Siyan, Ding Tao, Liu Yun, Chen Lei, Fei Xiaoqing, Zhang Rui, Wu Bin, Shen Weijian, Chen Lei, Zhang Feng, Feng Feng, Deng Xiaojun, Yi Xionghai, Yang Gongjun, Chen Guoqiang
Animal, Plant and Food Inspection Center, Jiangsu Entry-Exit Inspection and Quarantine Bureau, Nanjing 210001, China.
College of Pharmacy, China Pharmaceutical University, Nanjing 211198, China.
Se Pu. 2017 Oct 8;35(10):1068-1072. doi: 10.3724/SP.J.1123.2017.07009.
A method for the determination of characteristic compound 3,5-dimethoxybenzoate-4-diglucoside (leptosperin) in manuka honey was developed by automatic on-line solid phase extraction-liquid chromatography-high resolution mass spectrometry (SPE-LC-HRMS). The samples were separated on a Dikma Diamonsil Plus C column (150 mm×4.6 mm, 5 μm) using the mobile phases of 0.1% (v/v) formic acid aqueous solution and acetonitrile with gradient elution. The compound was detected with negative electrospray ionization (ESI) in Target-MS mode. The results showed that the linear range was 0.5-100.0 mg/L, the correlation coefficient was 0.9993. The limit of detection (LOD, ≥ 3) and limit of quantification (LOQ, ≥ 10) of the method was 3 mg/kg and 10 mg/kg, respectively. The recoveries at the spiked levels of 50.0, 100.0, 200.0 mg/kg (10.0, 20.0, 50.0 mg/kg in black locust samples) were in the range of 82.0%-95.2% with the relative standard deviations ranging from 2.7% to 9.7% (=6). The proposed method was applied to 95 mature honey samples from hives in New Zealand including 12 different kinds and 50 commercial honey samples from four different countries. The method is fast, sensitive and accurate to provide technical support to solve the judgment of the manuka honey imported from New Zealand.
建立了一种采用自动在线固相萃取-液相色谱-高分辨率质谱法(SPE-LC-HRMS)测定麦卢卡蜂蜜中特征化合物3,5-二甲氧基苯甲酸-4-二葡萄糖苷(细籽素)的方法。样品在迪马钻石plus C柱(150 mm×4.6 mm,5μm)上分离,流动相为0.1%(v/v)甲酸水溶液和乙腈,采用梯度洗脱。该化合物在目标质谱模式下采用负电喷雾电离(ESI)进行检测。结果表明,线性范围为0.5-100.0 mg/L,相关系数为0.9993。该方法的检测限(LOD,≥3)和定量限(LOQ,≥10)分别为3 mg/kg和10 mg/kg。在50.0、100.0、200.0 mg/kg(刺槐样品中为10.0、20.0、50.0 mg/kg)的加标水平下,回收率在82.0%-95.2%之间,相对标准偏差在2.7%-9.7%之间(n=6)。该方法应用于来自新西兰蜂巢的95个成熟蜂蜜样品,包括12种不同种类,以及来自四个不同国家的50个商业蜂蜜样品。该方法快速、灵敏、准确,为解决新西兰进口麦卢卡蜂蜜的判定提供了技术支持。