马俊琴,于小慧,贾翠玲,吕运开.分子印迹杂化介孔硅胶材料的制备及固相萃取-高效液相色谱法测定鳕鱼中氟喹诺酮类兽药残留[J].食品安全质量检测学报,2018,9(3):540-546
分子印迹杂化介孔硅胶材料的制备及固相萃取-高效液相色谱法测定鳕鱼中氟喹诺酮类兽药残留
Preparation of molecularly imprinted hybrid mesoporous silica materials for determination of fluoroquinolone veterinary drug residues in codfish by solid-phase extraction-high performance liquid chromatography
投稿时间:2017-12-14  修订日期:2018-01-19
DOI:
中文关键词:  分子印迹介孔硅胶材料  固相萃取  鳕鱼  氟喹诺酮类药物
英文关键词:molecularly imprinted mesoporous silicamaterials  solid-phase extraction  codfish  fluoroquinolones
基金项目:国家自然科学基金项目(21375032)、河北省自然科学基金项目(B2016201213)
作者单位
马俊琴 河北大学化学与环境科学学院 
于小慧 河北大学化学与环境科学学院 
贾翠玲 河北大学化学与环境科学学院 
吕运开 河北大学化学与环境科学学院 
AuthorInstitution
MA Jun-Qin College of Chemistry and Environmental Science,Hebei University 
YU Xiao-Hui College of Chemistry and Environmental Science, Hebei University 
JIA Cui-Lin College of Chemistry and Environmental Science,Hebei University 
LV Yun-Kai College of Chemistry and Environmental Science,Hebei University 
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中文摘要:
      目的 建立一种分子印迹介孔硅胶材料的制备方法, 并用于鳕鱼中氟喹诺酮类药物残留的选择性富集。方法 采用分子印迹技术和共缩聚法合成了苯基和氨基功能化的新型分子印迹杂化介孔硅胶材料。在最佳条件下, 采用固相萃取-高效液相色谱法测定鳕鱼中氧氟沙星、洛美沙星和沙拉沙星3种氟喹诺酮类药物残留。结果 在最佳固相萃取条件下, 获得了较高的富集倍数(8.56)。在鱼样中, 添加0.05、0.10和0.50 mg/kg的方法回收率为79.2%~95.2%, 相对标准偏差为2.2%~4.9%, 方法检出限(S/N=3)和定量限(S/N=10)分别为6.82~14.45 mg/kg和22.73~48.45 mg/kg。结论 该样品处理方法选择性好、简单、快速, 可用于鳕鱼中氟喹诺酮类药物残留的分离检测。
英文摘要:
      Objective To establish a preparation method of molecularly imprinted mesoporous silica material for selective enrichment of fluoroquinolones drug residues in codfish. Methods A new type of molecularly imprinted hybrid mesoporous silica material based on phenyl-and amino-siloxane was synthesized by the molecular imprinting technique and co-condensation method. Under the optimal condition, the ofloxacin, lomefloxacin and sarafloxacin residues in codfish were determined by solid-phase extraction coupled with high performance liquid chromatography. Results An enrichment factor of 8.56 was obtained under optimum on-line solid phase extraction conditions. The recoveries of fluoroquinolones in fish samplesat 0.05, 0.10 and 0.50 mg/kg were in the range of 79.2%~95.2% with the relative standard deviation (RSD) of 2.2%~4.9%. The limit of detection (S/N=3) and limit of quantitation (S/N=10) of the proposed method were 6.82~14.45 mg/kg and 22.73~48.45 mg/kg, respectively. Conclusion The sample treatment method is selective, simple and rapid, which can be used for the separation and detection of fluoroquinolones in codfish samples.
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