Horie Masakazu, Takegami Harumi, Toya Kazuo, Kikuchi Yoshinori, Nakazawa Hiroyuki
Saitama Prefectural Institute of Public Health: 639-1, Kamiokubo, Sakura-ku, Saitama 338-0824, Japan.
Shokuhin Eiseigaku Zasshi. 2003 Jun;44(3):150-4. doi: 10.3358/shokueishi.44.150.
A simple and reliable method using liquid chromatography-electrospray ionization-mass spectrometry (LC/ESI-MS) has been developed for the determination of the macrolide antibiotics spiramycin and tilmicosin in meat and fish. The drugs were extracted from meat and fish with 0.2% metaphosphoric acid-methanol (6:4), and the extracts were cleaned up on an Oasis HLB cartridge (60 mg). Positive ionization produced the molecular related ions, (M + 2H)2+, at m/z 350.2, 422.3 and 435.3 for neospiramycin I, spiramycin I and tilmicosin, respectively. The LC separation was performed on a Capcell Pak MG-C18 column (150 x 2 mm i.d.) with a gradient system of 0.02% formic acid-acetonitrile as the mobile phase at a flow rate of 0.2 mL/min. The molecular-related ions of the drugs were very clear under this condition. The calibration graph for each drug was rectilinear from 0.05 to 5 ng with selected ion monitoring (SIM). The recoveries of the drugs from meat and fish fortified at the level of 0.2 microgram/g was 73.2-89.2%, with high precision. The limits of detection of the drugs in meat and fish were 0.01 microgram/g.
已开发出一种使用液相色谱 - 电喷雾电离 - 质谱联用(LC/ESI-MS)的简单可靠方法,用于测定肉类和鱼类中的大环内酯类抗生素螺旋霉素和替米考星。用0.2%偏磷酸 - 甲醇(6:4)从肉类和鱼类中提取药物,提取物在Oasis HLB柱(60 mg)上进行净化处理。正离子模式下,新螺旋霉素I、螺旋霉素I和替米考星分别在m/z 350.2、422.3和435.3处产生分子相关离子(M + 2H)2+。液相色谱分离在Capcell Pak MG-C18柱(150×2 mm内径)上进行,以0.02%甲酸 - 乙腈为流动相,采用梯度洗脱系统,流速为0.2 mL/min。在此条件下,药物的分子相关离子非常清晰。在选择离子监测(SIM)模式下,每种药物的校准曲线在0.05至5 ng范围内呈线性。在肉类和鱼类中添加水平为0.2微克/克时,药物的回收率为73.2 - 89.2%,精密度高。肉类和鱼类中药物的检测限为0.01微克/克。