Pan Yingyu, Xu Qian, Kang Xuejun, Zhang Jianxin
Department of Nutrition and Food Hygiene, School of Public Health, Southeast University, Nanjing 210009, China.
Se Pu. 2005 Nov;23(6):577-80.
A high performance liquid chromatographic method with fluorescence detection for the determination of chloramphenicol (CAP) residues in milk was developed. Although CAP itself is non-fluorescent the aromatic nitro group of CAP could be reduced to aromatic primary amino group and fluorescamine can be used as a selective reagent for primary amines. Therefore, the CAP was derivatized with fluorescamine prior to injection in this project. The HPLC method was performed on a Diamond C18 column (250 mm x 4.6 mm i. d., 4.0 microm) with the mobile phase composed of sodium acetate buffer (0.02 mol/L, pH 6.0) -acetonitrile-tetrahydrofuran (76: 16: 8, v/v/v). The flow rate of the mobile phase was set at 1.0 mL/min, and the column was maintained at 40 degrees C. Analytes were detected by a fluorescence detector at 410 nm excitation and 508 nm emission wavelength. The standard curve was linear in the range from 0.4 microg/L to 800 microg/L. The limit of detection (LOD) was 0.2 microg/L, and the limit of quantitation (LOQ) was 0.4 microg/L. Overall recoveries were between 66.6% and 92.8% with relative standard deviations between 4.5% and 9.4%. The procedure provides a rapid, reliable and sensitive method for the determination of CAP in milk.
建立了一种带荧光检测的高效液相色谱法,用于测定牛奶中的氯霉素(CAP)残留量。虽然氯霉素本身无荧光,但氯霉素的芳香硝基可被还原为芳香伯氨基,而荧光胺可作为伯胺的选择性试剂。因此,在本项目中,氯霉素在进样前用荧光胺进行衍生化。高效液相色谱法在Diamond C18柱(250 mm×4.6 mm内径,4.0μm)上进行,流动相由醋酸钠缓冲液(0.02 mol/L,pH 6.0)-乙腈-四氢呋喃(76:16:8,v/v/v)组成。流动相流速设定为1.0 mL/min,柱温保持在40℃。通过荧光检测器在激发波长410 nm和发射波长508 nm下检测分析物。标准曲线在0.4μg/L至800μg/L范围内呈线性。检测限(LOD)为0.2μg/L,定量限(LOQ)为0.4μg/L。总体回收率在66.6%至92.8%之间,相对标准偏差在4.5%至9.4%之间。该方法为牛奶中氯霉素的测定提供了一种快速、可靠且灵敏的方法。