以离子对试剂作流动相,采用离子对抑制电导检测法同时测定植物中残留的矮壮素和缩节胺.简单处理后的样品经过Dionex IonPac NG1保护柱和NS1分离柱,在流速为1.00 mL/min、淋洗液为1.00 mmol/L九氟戊酸(作为离子对试剂)-7%(体积分数,下同)乙腈时等度洗脱分离,能够快速稳定出峰,且被测物与其他干扰离子充分分离.矮壮素和缩节胺的检出限分别为0.154 6和0.171 4 mg/L,在1~100 mg/L范围内具有良好的线性关系和重现性.对实际样品进行测定,矮壮素和缩节胺的回收率范围分别为96.06%~104.6%和98.53%~103.7%,相对标准偏差小于3%.该方法分析结果令人满意,可以满足矮壮素和缩节胺常规的定性、定量分析需求.
参考文献
[1] | Wang Q M,Guo D P.Plant Hormone and Vegetable Growing Development.Beijing:Agricultural Press of China(汪俏梅,郭得平.植物激素与蔬菜的生长发育.北京:中国农业出版社),2001:97 |
[2] | Tafuri F,Businelli M,Giusquiani P L.Analyst,1970,95:675 |
[3] | Zhao Y X,song G L,Zhang J,et al.Chinese Journal of Health Laboratory Technology(赵永信,宋国良,张晶.等.中国卫生检验杂志),2008,18(6):1064 |
[4] | Karasali H,loannou S.Bull Environ Contam Toicol,2009,83:636 |
[5] | Riediker S,Obrist H,Varga N,et al.J Chromatogr A,2002,966(1):15 |
[6] | Wang J H,Lu X Y,Huang M,et al.Chinese Journal of Analyrical Chemistry(王金花,卢晓宇,黄梅,等.分析化学),2007,35(10):1509 |
[7] | Esparza X,Moyano E,Galceran M T.J Chromatogr A,2009.1216:4402 |
[8] | Henriksen T,Juhler R K,Brandt G.et al.J Chromatogr A,2009,1216:2504 |
[9] | Zhou Y M,Han Y,Tian H Z,et al.Journal of Instrumental Analysis(周艳明,韩瑜,田宏哲,等.分析测试学报),2009,28(10):1206 |
[10] | Quintas G,Garrigues S,Pastor A,et al.Vibrational Spectroscopy,2004,06:41 |
[11] | Peeters M C,Defloor I,Coosemans J,et al.J Chromatogr A,2001,920:255 |
[12] | Fegert A,Schepers U,Schwarz B.Fresenius J Anal Chem,1991,339:441 |
[13] | Zhu Y.Theory and Application of Ion Chromatography.Hangzhou:Zhejiang University Press(朱岩.离子色谱原理及其应用.杭州:浙江大学出版社),2002:10 |
[14] | Huang C Q,Wang L L,Chen Y J,et al.Chinese Journal of Analytical Chemistry(黄超群,王丽丽,陈永菁,等.分析化学),2006,34:1641 |
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