热带农业科学
熱帶農業科學
열대농업과학
CHINESE JOURNAL OF TROPICAL AGRICULTURE
2014年
4期
77-82
,共6页
丁晨红%骆冲%邓义才%王富华%王刚%叶倩%梁应坤
丁晨紅%駱遲%鄧義纔%王富華%王剛%葉倩%樑應坤
정신홍%락충%산의재%왕부화%왕강%협천%량응곤
分散固相萃取%反相高效液相色谱法%荧光检测%氨基甲酸酯%农药残留
分散固相萃取%反相高效液相色譜法%熒光檢測%氨基甲痠酯%農藥殘留
분산고상췌취%반상고효액상색보법%형광검측%안기갑산지%농약잔류
dispersive solid phase extraction%reverse phases high performance liquid chromatography (RP-HPLC)%fluorescence detector (FLD)%carbamate pesticides%pesticide residues
建立分散固相萃取-反相高效液相色谱同时测定蔬菜和水果中10种氨基甲酸酯类农药(涕灭威,涕灭威砜,涕灭威亚砜,克百威,3-羟基克百威,灭多威,甲萘威,异丙威,速灭威,仲丁威)残留的分析方法。样品经乙腈提取, PSA分散固相萃取净化,液相色谱柱后衍生分离,荧光检测(姿ex=330 nm,姿em=465 nm)测定,外标法定量。10种农药在0.005~0.50 mg/L范围内线性关系良好;检出限在0.004~0.008 mg/L;平均加标回收率在75.6%~112.3%,相对标准偏差(RSD)在0.8%~10.2%。该方法具有快速、灵敏、准确、重现性好以及操作简单等特点,适合日常大批量蔬菜和水果样品中10种氨基甲酸酯类农药残留的测定。
建立分散固相萃取-反相高效液相色譜同時測定蔬菜和水果中10種氨基甲痠酯類農藥(涕滅威,涕滅威砜,涕滅威亞砜,剋百威,3-羥基剋百威,滅多威,甲萘威,異丙威,速滅威,仲丁威)殘留的分析方法。樣品經乙腈提取, PSA分散固相萃取淨化,液相色譜柱後衍生分離,熒光檢測(姿ex=330 nm,姿em=465 nm)測定,外標法定量。10種農藥在0.005~0.50 mg/L範圍內線性關繫良好;檢齣限在0.004~0.008 mg/L;平均加標迴收率在75.6%~112.3%,相對標準偏差(RSD)在0.8%~10.2%。該方法具有快速、靈敏、準確、重現性好以及操作簡單等特點,適閤日常大批量蔬菜和水果樣品中10種氨基甲痠酯類農藥殘留的測定。
건립분산고상췌취-반상고효액상색보동시측정소채화수과중10충안기갑산지류농약(체멸위,체멸위풍,체멸위아풍,극백위,3-간기극백위,멸다위,갑내위,이병위,속멸위,중정위)잔류적분석방법。양품경을정제취, PSA분산고상췌취정화,액상색보주후연생분리,형광검측(자ex=330 nm,자em=465 nm)측정,외표법정량。10충농약재0.005~0.50 mg/L범위내선성관계량호;검출한재0.004~0.008 mg/L;평균가표회수솔재75.6%~112.3%,상대표준편차(RSD)재0.8%~10.2%。해방법구유쾌속、령민、준학、중현성호이급조작간단등특점,괄합일상대비량소채화수과양품중10충안기갑산지류농약잔류적측정。
Developed a method for the simultaneous determination of ten pesticide residues including aldicarb, aldicarb sulfone, aldicarb sulfoxide, methomyl, carbofuran, 3-hydroxycarbofuran, carbaryl,isoprocarb, metolcarb, fenobucarb in vegetables and fruits by Dispersive solid-phase extraction cleanup and Phase High Performance Liquid Chromatography-Fluorescence Detector (HPLC-FLD). The sample was extracted by acetonitrile and purified by Primary-secondary amine (PSA) dispersive solid phase extraction. The collected solution was analyzed by HPLC-FLD with post-column derivation and quantified by external standard method. The wavelengths were set at 330 nm and 465 nm. The results indicated that the calibration curves of the ten pesticides showed good linear relationship in the concentration of 0.005~0.50 mg/L with correlation coefficients greater than 0.999. The detection limits ranged from 0.004~0.008 mg/L. The recoveries ranged from 75.6%~112.3%with the relative standard deviation (RSD) range of 0.8%~10.2%. The method was simple, rapid, sensitive, accurate, and was suitable for the determination of the above 10 pesticide residues in fruits and vegetables.