期刊文献+

阿莫西林在牛肉中残留的高效液相色谱检测及分析 被引量:12

Determination and Analys of Amoxicillin Residue in Beeves with RP-HPLC
下载PDF
导出
摘要 建立了反相高效液相色谱分析牛肉样品中阿莫西林残留量的方法。对动物组织样品采用磷酸盐缓冲溶液提取、三氯乙酸沉淀蛋白、固相萃取净化和富集。研究了样品在C18柱上的保留行为和阿莫西林的特征谱图。待测物用高效液相色谱法分离,外标定法定量分析,标准曲线的线性良好,相关系数为0.99934,线性范围为5.0~500.0μg/L。动物组织样品中阿莫西林的加标回收率为77.3%~97.4%,相对标准偏差为1.2%~13.5%,最低检出限低于10μg/kg。该分析方法具有良好的重现性。 A reversed-phase high performance liquid chromatographic method (RP-HPLC) has been developed for the determination of amoxicillin residue in beeves. Beeves were extracted with phosphate buffer, precipitated the proteins with trichioroacetic acid (TCA) solution, and purified and enriched by solid phase extraction (SPE). The retention results on a C18 column and the chromatography conditions of amoxiciUin were investigated, The samples were separated by RP-HPLC and quantified with external standard calibration curves.There are good linear correlations with the correlation coefficient as 0.99934 between the peak areas and concentrations of amoxicillin .The dynamic linear range is 5.0-500 μg/ml. The average recoveries of amoxicillin in spiked animal tissues range from 77.3 % to 97.4 %, and the relative standard deviations are between 1.2% and 13.5%. The limit of detection is below 10 μg/kg. The relative standard deviations of intra-assay and inter-assay are both within 10%. Tiffs analysis method shows good recurrence.
作者 于桂阳
出处 《食品科学》 CAS CSCD 北大核心 2008年第4期332-334,共3页 Food Science
关键词 高效液相色谱 固体萃取 阿莫西林 残留量 牛肉 HPLC. solid phase extraction amoxicillin residue beeves
  • 相关文献

参考文献6

  • 1武晋孝,李淑琴,柴桂珍,宋艳红.高效液相色谱法测定复方阿莫西林各组分含量[J].兽药与饲料添加剂,2003,8(6):30-31. 被引量:2
  • 2刘媛,丁岚,谢孟峡,刘素英,杨清峰,单吉浩.动物组织中阿莫西林残留的液相色谱分析方法研究[J].色谱,2003,21(6):541-544. 被引量:27
  • 3JOSE A M, JUAAN R, JOSE M L, et al. Determination of amoxicillin and cephalexin in mixtures by second-derivative spectrophotometry[J]. Analyst, 1990, 115(8): 1117-1119.
  • 4中华人民共和国农业部公告第235号动物性食品中兽药最高残留限量[S].
  • 5傅若农.色谱分析概论[M].北京:化学工业出版社,2002.123-124.
  • 6SHAKOOR O, TAYLOR R B, MOODY R R. Analysis of amoxicillin in capsules and oral suspensions by high performance liquid chromatography [J]. Analyst, 1995, 120(8): 2191-2194.

二级参考文献19

  • 1[1]Chin G J, Marx J. Science, 1994, 264: 359
  • 2[2]Begley S. Newsweek, 1994, 28(3): 47
  • 3[3]Moats W A. J Chromatogr, 1992, 693: 15
  • 4[4]Senyk G F, Davison J H, Brown M M, Hallstead E R, Sherban J W. J Food Prot, 1990, 53: 158
  • 5[5]Schermerhorn P G, Ngoh M A, Chu P S, Righter H F. FDA Forum on Regulatory Sciences. Washington DC: [s.n.], 1985. Abstract A27
  • 6[6]Wiese B, Martin K. J Pharm Biomed Anal, 1989, 7: 95
  • 7[7]DePaolis A M, Katz S E, Rosen J D. J Agric Food Chem, 1977, 25: 1 112
  • 8[8]Munns R K, Shimoda W, Roybal J E, Vieira C. J Assoc Off Anal Chem, 1985, 68: 968
  • 9[9]Wang Chao, Li Shujuan. Chinese Journal of Instrumental Analysis, 2000, 19(6): 72王超, 李淑娟. 分析测试学报, 2000, 19(6): 72
  • 10[10]Sorensen L K, Snor L K, Elkaer T, Hansen H. J Chromatogr B, 1999, 734: 307

共引文献28

同被引文献123

引证文献12

二级引证文献37

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部