猪血浆中去呋喃甲酰基头孢噻呋浓度的HPLC测定  

Determination of desfuroylceftiofur in pig plasma by HPLC

作　　者：李长流[1] 俞道进[1] 马玉芳[1] 李健[1] 徐敏祥[1] 杨志民[1] 黄一帆[1] 

机构地区：[1]福建农林大学动物保健研究所,福建福州350002

出　　处：《福建农林大学学报（自然科学版）》2010年第1期58-62,共5页Journal of Fujian Agriculture and Forestry University:Natural Science Edition

摘　　要：建立了测定猪血浆中去呋喃甲酰基头孢噻呋(DFC)的高效液相色谱法(HPLC).血浆样品经DTE-磷酸缓冲液提取,过SPE小柱净化浓缩,甲醇洗脱,用XDB-C18色谱柱分离,流动相由乙腈(A)和0.1%三氟乙酸水溶液(B)组成.采用梯度洗脱:0 min为12%A和88%B,15 min为18%A和82%B,18 min为12%A和88%B,平衡至20 min.流速0.8 mL.min-1,波长266 nm.以DFC峰面积定量,浓度在0.25-40.0μg.mL-1时,其峰面积与浓度呈良好的线性关系,r2=0.9987,平均回收率为82.1%-87.4%,其日内和日间变异系数(RSD)分别为5.04%-8.58%和6.83%-9.34%.该方法适用于血浆中DFC的浓度测定和药代动力学研究.High performance liquid chromatography（HPLC） was established to determine desfuroylceftiofur（DFC） in pig plasma.Plasma sample was extracted with dithioerythritol-phosphate buffer,then concentrated and purified by SPE course and eluted with methanol.Chromatographic separation was carried out on a XDB-C18 chromatographic column,the mobile phases consisted of acetonitrile（A） and 0.1% trifluoroacetic acid solution（B）.A gradient elution procedure was performed： 12%A and 88%B at 0 min,18%A and 82%B at 15 min,12%A and 88%B at 18 min,then balanced to 20 min.The flow rate was 0.8 mL·min-1,the wave length of DAD detector was 266 nm.The determination was quantitated according to peak area of DFC.The calibration curve was linear in the range of 0.25-40.0 μg·mL^-12=0.9987）,and the average recovery was 82.1%-87.4%,relative standard deviations（RSD） of inter-day and intra-day were 5.04%-8.58% and 6.83%-9.34%,respectively.The method could be applied to the concentration determination of DFC in plasma and pharmacokinetics research.

关 键 词：去呋喃甲酰基头孢噻呋 血浆浓度 高效液相色谱法 

分 类 号：S859.7[农业科学—临床兽医学]