Oliveira Regina V, De Pietro Angela C, Cass Quezia B
Departamento de Química, Universidade Federal de São Carlos, Caixa Postal 676, São Carlos, 13565-905 SP, Brazil.
Talanta. 2007 Feb 28;71(3):1233-8. doi: 10.1016/j.talanta.2006.06.024. Epub 2006 Jul 25.
A multidimensional, selective and precise high performance liquid chromatography (HPLC) method based on direct injection of biological samples has been developed for the determination of cephalexin in skimmed and whole bovine milk. The cephalosporin antibiotic was extracted from bovine milk using an octyl restricted access medium bovine serum albumin column (C(8)-RAM-BSA) and analyzed on an octadecyl column using phosphate buffer (pH 7.5, 0.01M): ACN (92:8, v/v) and ultraviolet detection at 260nm. The calibration graph was linear in the concentration range of 25-1600ng/mL and this is in accordance with the tolerance level of 100ng/mL set by the FDA (Food and Drug Administration) and EU (European Union) for cephalexin as residue in bovine milk. The intra- and inter-day coefficients of variation for the replicate analysis at the quality control levels were less than 15% while the transfer efficiency was in the range of 90.2-92.3%. The limits of detection and quantification were 10 and 20ng/mL, respectively.
已开发出一种基于直接进样生物样品的多维、选择性和精确的高效液相色谱(HPLC)方法,用于测定脱脂和全脂牛奶中的头孢氨苄。使用辛基受限介质牛血清白蛋白柱(C(8)-RAM-BSA)从牛奶中提取头孢菌素抗生素,并在十八烷基柱上用磷酸盐缓冲液(pH 7.5,0.01M):乙腈(92:8,v/v)进行分析,在260nm处进行紫外检测。校准曲线在25 - 1600ng/mL的浓度范围内呈线性,这与美国食品药品监督管理局(FDA)和欧盟(EU)规定的牛奶中头孢氨苄残留耐受水平100ng/mL相符。质量控制水平下重复分析的日内和日间变异系数小于15%,而转移效率在90.2 - 92.3%范围内。检测限和定量限分别为10和20ng/mL。