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采用高效液相色谱-紫外法和液相色谱-串联质谱法同时测定大米中的 orysastrobin 及其异构体。

Simultaneous determination of orysastrobin and its isomers in rice using HPLC-UV and LC-MS/MS.

机构信息

Food Standards Division, Korea Food and Drug Administration, 187 Osongsaengmyeong2-ro, Gangoe-Myeon, Cheongwon-gun, Chungcheongbuk-do 363-951, Republic of Korea.

出版信息

J Agric Food Chem. 2011 Oct 26;59(20):10826-30. doi: 10.1021/jf202228p. Epub 2011 Oct 4.

Abstract

Orysastrobin is a new strobilurin-type fungicide to control leaf and panicle blast and sheath blight in rice. An analytical method was developed to determine the residues of orysastrobin and its two isomers, the main metabolite F001 and the major impurity F033, in hulled rice by the use of high-performance liquid chromatography with ultraviolet photometry (HPLC-UV) and liquid chromatography with tandem mass spectrometry (LC-MS/MS). All compounds were extracted with acetone from hulled rice samples. The extract was diluted with saline water, and an extraction step using dichloromethane/n-hexane partition was used to recover analytes from the aqueous phase. An n-hexane/acetonitrile partition and Florisil column chromatography were employed to further remove interfering coextractives prior to instrumental analysis. An octadecylsilyl column was successfully applied to identify orysastrobin and its isomers in sample extracts. Net recovery rates of orysastrobin, F001, and F033 from fortified samples ranged from 80.6 to 114.8% using HPLC-UV and LC-MS/MS. Relative standard deviations for the analytical methods were all <20%, and the quantification limits of the method were in the 0.002-0.02 mg/kg range. The proposed methods were reproducible and sufficiently accurate to evaluate the terminal residue of orysastrobin and its isomers in rice.

摘要

抑霉唑是一种新型的噻二唑类杀菌剂,用于防治水稻的叶瘟和穗瘟以及纹枯病。建立了一种用高效液相色谱-紫外分光光度法(HPLC-UV)和液相色谱-串联质谱法(LC-MS/MS)测定糙米中抑霉唑及其两种同分异构体、主要代谢物 F001 和主要杂质 F033 残留量的分析方法。所有化合物均用丙酮从糙米样品中提取。用盐水稀释提取物,然后用二氯甲烷/正己烷分配步骤从水相回收分析物。用正己烷/乙腈分配和 Florisil 柱层析进一步去除仪器分析前的干扰共提物。在样品提取物中,成功地应用十八烷基硅烷柱来鉴定抑霉唑及其同分异构体。用 HPLC-UV 和 LC-MS/MS 测定添加的抑霉唑、F001 和 F033 的回收率在 80.6%至 114.8%之间。分析方法的相对标准偏差均<20%,方法的定量限在 0.002-0.02mg/kg 范围内。所提出的方法重现性好,准确度足以评估抑霉唑及其异构体在水稻中的最终残留量。

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