色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
3期
294-298
,共5页
固相萃取%高效液相色谱%磺胺%猪肉%鸡肉%多壁碳纳米管
固相萃取%高效液相色譜%磺胺%豬肉%鷄肉%多壁碳納米管
고상췌취%고효액상색보%광알%저육%계육%다벽탄납미관
solid-phase extraction(SPE)%high performance liquid chromatography-ultraviolet detection( HPLC-UV)%sulfonamides( SAs)%pork%chicken%multi-walled carbon nanotubes (MWCNTs)
建立了多壁碳纳米管为吸附剂的固相萃取净化-高效液相色谱-紫外检测测定猪肉和鸡肉中多种磺胺类药物多残留的方法。样品采用乙腈提取,多壁碳纳米管固相萃取净化,NaH2PO4缓冲溶液(pH5.5~6.0)溶解上样,5%(v/v)丙酮-正己烷淋洗,丙酮-二氯甲烷(1:1,v/v)洗脱。色谱分离以50mmol/LNaH2PO4-乙腈(7:3,v/v)为流动相,方法的线性范围为0.01~1.00mg/L,线性相关系数大于0.998,检出限(LOD)为0.003mg/L,定量限(LOQ)为0.01mg/L。在0.02~0.2mg/kg添加范围内,9种磺胺类药物的回收率高于70%,RSD低于8%,表明多壁碳纳米管对磺胺类药物具有较强的吸附富集能力。该方法简便、准确可用于动物组织及产品中磺胺药物残留的检测。
建立瞭多壁碳納米管為吸附劑的固相萃取淨化-高效液相色譜-紫外檢測測定豬肉和鷄肉中多種磺胺類藥物多殘留的方法。樣品採用乙腈提取,多壁碳納米管固相萃取淨化,NaH2PO4緩遲溶液(pH5.5~6.0)溶解上樣,5%(v/v)丙酮-正己烷淋洗,丙酮-二氯甲烷(1:1,v/v)洗脫。色譜分離以50mmol/LNaH2PO4-乙腈(7:3,v/v)為流動相,方法的線性範圍為0.01~1.00mg/L,線性相關繫數大于0.998,檢齣限(LOD)為0.003mg/L,定量限(LOQ)為0.01mg/L。在0.02~0.2mg/kg添加範圍內,9種磺胺類藥物的迴收率高于70%,RSD低于8%,錶明多壁碳納米管對磺胺類藥物具有較彊的吸附富集能力。該方法簡便、準確可用于動物組織及產品中磺胺藥物殘留的檢測。
건립료다벽탄납미관위흡부제적고상췌취정화-고효액상색보-자외검측측정저육화계육중다충광알류약물다잔류적방법。양품채용을정제취,다벽탄납미관고상췌취정화,NaH2PO4완충용액(pH5.5~6.0)용해상양,5%(v/v)병동-정기완림세,병동-이록갑완(1:1,v/v)세탈。색보분리이50mmol/LNaH2PO4-을정(7:3,v/v)위류동상,방법적선성범위위0.01~1.00mg/L,선성상관계수대우0.998,검출한(LOD)위0.003mg/L,정량한(LOQ)위0.01mg/L。재0.02~0.2mg/kg첨가범위내,9충광알류약물적회수솔고우70%,RSD저우8%,표명다벽탄납미관대광알류약물구유교강적흡부부집능력。해방법간편、준학가용우동물조직급산품중광알약물잔류적검측。
A multi-residue analytical method based on solid-phase extraction(SPE)with multi-walled carbon nanotubes(MWCNTs)as sorbent was developed. The determination of the sul-fonamides(SAs)in pork and chicken was carried out by high performance liquid chromatogra-phy-ultraviolet detection( HPLC-UV). The clean-up conditions were optimized. The analytes were extracted by acetonitril and cleaned-up by MWCNTs SPE cartridge. The extract was re-dissolved with the Na 2 HPO 4 buffer( pH 5. 5- 6. 0)for loading,and was washed with acetone-hexane(5 :95,v / v),then eluted with acetone-dichloromethane(1 :1,v / v)from the column. The mobile phase used in the chromatographic separation consisted of a binary mixture of ace-tonitrile and 50 mmol / L NaH 2 PO 4 with the volume ratio of 7 :3. A wide linear range was 0. 01-1. 00 mg / L with the correlation coefficients above 0. 998. The limits of detection(S / N = 3)were 0. 003 mg / L,and the limits of quantification(S / N = 10)were 0. 01 mg / L. The average recover-ies were over 70% for the nine SAs in the spiked range of 0. 02-0. 2 mg / kg,with the relative standard deviations( RSDs)lower than 8% . This study indicated that the MWCNTs SPE car-tridge is efficient for the clean-up of the SAs in animal tissues or products,and the method is simple,accurate and suitable for the quantification of the SAs residues.