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Simultaneous determination of florfenicol, its metabolite and three fluoroquinolone residues in poultry muscles via high-performance liquid chromatography with fluorescence detection

文献类型: 外文期刊

作者: Hong, Lu 1 ; Liu, Yun 3 ; Guo, Yawen 1 ; Gao, Pengfei 2 ; Ding, Hao 2 ; Xu, Junjie 1 ; Xie, Xing 5 ; Xie, Kaizhou 1 ;

作者机构: 1.Yangzhou Univ, Coll Anim Sci & Technol, Yangzhou 225009, Jiangsu, Peoples R China

2.Yangzhou Univ, Joint Int Res Lab Agr & Agriprod Safety, Yangzhou 225009, Jiangsu, Peoples R China

3.Jiangsu Lushui Qingshan Inspect & Testing Technol, Lianyungang 222000, Peoples R China

4.Yangzhou Univ, Coll Vet Med, Yangzhou 225009, Jiangsu, Peoples R China

5.Jiangsu Acad Agr Sci, Inst Vet Med, Key Lab Vet Bioprod Engn, Minist Agr & Rural Affairs, Nanjing 210014, Peoples R China

关键词: Poultry muscles; Florfenicol; Fluoroquinolones; LLE; HPLC-FLD

期刊名称:MICROCHEMICAL JOURNAL ( 影响因子:5.1; 五年影响因子:4.7 )

ISSN: 0026-265X

年卷期: 2024 年 207 卷

页码:

收录情况: SCI

摘要: A high-performance liquid chromatography with fluorescence detection (HPLC-FLD) procedure was developed and refined to detect florfenicol (FF), its metabolite florfenicol amine (FFA), and three fluoroquinolone (FQ) residues present in poultry muscles concurrently. Sample pretreatment was conducted through liquid-liquid extraction (LLE). Ethylenediaminetetraacetic acid (EDTA), 90 % acetonitrile and acetonitrile were used as extraction solvents. The stationary phase employed was an XBridge BEH C18 column (5 mu m, 4.6 mm x 150 mm), and the mobile phase consisted of a 0.01 mol/L solution of sodium dihydrogen phosphate and acetonitrile (65:35, V/V); the former contained 0.005 mol/L sodium dodecyl sulfate and 0.1 % triethylamine (pH adjusted to 4.8 with phosphoric acid). The limits of detection (LODs) and limits of quantification (LOQs) were 0.03-1.5 mu g/ kg and 0.1-5.0 mu g/kg, respectively. The linear relationships were satisfactory within the corresponding concentration ranges, with determination coefficients (R-2) >= 0.9997. The mean recoveries ranged from 70.34 to 94.98 %, and the intraday relative standard deviations (RSDs) and interday RSDs were 1.46-6.24 % and 1.60-7.31 %, respectively. This verified method is applicable and reliable for analyzing actual samples.

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