福州大学学报(自然科学版)
福州大學學報(自然科學版)
복주대학학보(자연과학판)
JOURNAL OF FUZHOU UNIVERSITY(NATURAL SCIENCE EDITION)
2015年
4期
554-559
,共6页
卢巧梅%张文敏%黄川辉%卢明华%励建荣%张兰
盧巧梅%張文敏%黃川輝%盧明華%勵建榮%張蘭
로교매%장문민%황천휘%로명화%려건영%장란
悬浮固化液相微萃取%高效液相色谱%液相微萃取%生长素
懸浮固化液相微萃取%高效液相色譜%液相微萃取%生長素
현부고화액상미췌취%고효액상색보%액상미췌취%생장소
solidified floating organic drop microextraction%high -performance liquid chromatogra-phy%liquid phase microextraction%auxin
建立基于悬浮固化液相微萃取预处理的高效液相色谱-荧光检测法( SFODME-HPLC-FLD)用于两种植物生长素(吲哚丙酸和吲哚丁酸)的分析.实验考察各因素对萃取过程的影响,确定最佳条件:50μL十二醇(纯)为萃取剂,20.0 mL样品溶液(pH 3.0)、0.25 g· mL-1 NaCl、26℃、1800 r· min-1条件下萃取10 min.结果表明, SFODME技术重现性好、灵敏度高,相对标准偏差小于8.66%,检测限为0.01 ng· mL-1,线性范围为0.02~60 ng· mL-1,加标回收率大于84.3%.方法快速、稳定、环境友好,适用于实际样品的检测.
建立基于懸浮固化液相微萃取預處理的高效液相色譜-熒光檢測法( SFODME-HPLC-FLD)用于兩種植物生長素(吲哚丙痠和吲哚丁痠)的分析.實驗攷察各因素對萃取過程的影響,確定最佳條件:50μL十二醇(純)為萃取劑,20.0 mL樣品溶液(pH 3.0)、0.25 g· mL-1 NaCl、26℃、1800 r· min-1條件下萃取10 min.結果錶明, SFODME技術重現性好、靈敏度高,相對標準偏差小于8.66%,檢測限為0.01 ng· mL-1,線性範圍為0.02~60 ng· mL-1,加標迴收率大于84.3%.方法快速、穩定、環境友好,適用于實際樣品的檢測.
건립기우현부고화액상미췌취예처리적고효액상색보-형광검측법( SFODME-HPLC-FLD)용우량충식물생장소(신타병산화신타정산)적분석.실험고찰각인소대췌취과정적영향,학정최가조건:50μL십이순(순)위췌취제,20.0 mL양품용액(pH 3.0)、0.25 g· mL-1 NaCl、26℃、1800 r· min-1조건하췌취10 min.결과표명, SFODME기술중현성호、령민도고,상대표준편차소우8.66%,검측한위0.01 ng· mL-1,선성범위위0.02~60 ng· mL-1,가표회수솔대우84.3%.방법쾌속、은정、배경우호,괄용우실제양품적검측.
Determination of two anxins ( indole propionic acid and indole butyric acid) by solidifica-tion of floated organic drop microextraction with high -performance liquid chromatography-fluores-cence detection ( SFODME-HPLC-FLD) was established.The experimental conditions affecting the extraction process were optimized.The optimal conditions of SFODME were as follows:50μL dode-canol as extraction solvent, 20.0 mL sample solution with pH 3.0 and 0.25 g · mL-1 NaCl.The above solution was extracted for 10 min at temperature of 26 ℃ and centrifugation speed of 1 800 r· min-1 .Results showed that this SFODME approach had high sensitivity and good reproducibility, with relative standard deviations lower than 8.66%.Its linear range was 0.02~60 ng· mL-1 , with the limit of detection of 0.01 ng · mL-1 and the recoveries larger than 84.3%.This method was rapid, stable and environmentally benign, and it can be applied to real sample analysis.