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作 者:朱华玲[1] 陆亚春[1] 王卫平[1] 王爱军[2] 陈建荣[2]
机构地区:[1]浙江师范大学化学与生命科学学院,浙江金华321004 [2]浙江师范大学地理与环境科学学院,浙江金华321004
出 处:《浙江师范大学学报(自然科学版)》2014年第1期69-75,共7页Journal of Zhejiang Normal University:Natural Sciences
基 金:国家自然科学基金资助项目(20805011);浙江师范大学博士科研启动基金资助项目(ZC304007104)
摘 要:建立了固相萃取-毛细管电泳联用测定河水水样中四环素类抗生素残留的分析方法.以有序介孔炭(OMC)作为固相萃取吸附剂,考察了有序介孔炭对四环素类抗生素(四环素、土霉素和多西环素)的吸附性能,探讨了影响固相萃取效率的因素,得到最佳萃取条件为:水样2.00 mL(pH 10.0),有序介孔炭5.0 mg,V(甲醇)∶V(乙腈)=1∶1的洗脱液4.00 mL,洗脱速度0.7 mL/min,此时富集倍数达50倍.在最佳的毛细管电泳分离条件下,各组分含量在3 000~11 000 μg/L呈良好的线性关系,且各组分峰面积的日内相对标准偏差低于8.5%(n=5).四环素、土霉素和多西环素的最低检测限和平均回收率分别为1.96~2.14 μg/mL和46.7%~93.6%.研究表明,有序介孔炭可作为环境样品中多西环素和土霉素的高效吸附材料.A solid-phase extraction (SPE)-capillary electrophoresis method tion of tetracyclines residues in surface water. It was aimed to evaluate the was developed for the determina- adsorption specificity of ordered mesoporous carbon (OMC) as solid phase extraction (SPE ) adsorbents with tetracychnes (tetracycline, oxy- tetracycline and doxycyctine) as model analytes. The parameters affecting the adsorption efficiency were inves- tigated in detail. The optimal extraction conditions were showed as follows: 2.00 mL water sample ( pH 10.0 ) , 5 mg OMC as adsorbent, 4.00 mL mixture of methanol and acetonitrile ( VMeOH : VACN = 1 : 1 ) as elu- ent at a speed of 13.7 mL · min^-1, enrichment factors of actual water sample were 50. Combined with optimal separation conditions of capillary electrophoresis, the linear range of the analytes varied from 3 000 to 11 000 μg · L^- 1, and relative standard deviations of peak area of each component were less than 8.5 % ( n = 5 ) in- tra-day analyses. The limits of detection and the average recovery ( for tetracycline, oxytetracycline and doxy- cycline) were in the range of 1.96 - 2.14 μg · mL^-1 and 46.7% - 93.6%, respectively. It demonstrated that OMC was a potential adsorbing material in preconeentrating doxyeyeline and oxytetraeycline from environ- mental samples.
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