液相色谱-串联质谱法研究氟噻草胺在大鼠体内组织中的分布行为
投稿时间:2018-08-26      点此下载全文 HTML
引用本文:罗雪琪,余洋,来庆娜,等.液相色谱-串联质谱法研究氟噻草胺在大鼠体内组织中的分布行为[J].农药学学报,2019,21(4):506-513.
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作者单位E-mail
罗雪琪 沈阳化工研究院有限公司 安全评价中心, 沈阳 110141  
余洋 沈阳化工研究院有限公司 安全评价中心, 沈阳 110141  
来庆娜 沈阳药科大学 药学院, 沈阳 110016  
林立红 沈阳化工研究院有限公司 安全评价中心, 沈阳 110141 linlihong@sinochem.com 
李晓磊 沈阳化工研究院有限公司 安全评价中心, 沈阳 110141  
李娜 沈阳化工研究院有限公司 安全评价中心, 沈阳 110141  
郑鸿薇 沈阳化工大学 应用化学学院, 沈阳 110020  
基金项目:“十三五”国家重点研发计划项目(2016YFD0300708)
中文摘要:建立了大鼠组织中氟噻草胺的液相色谱-串联质谱(LC-MS/MS)分析方法,并对其经灌胃给药后在大鼠体内各组织中的分布行为进行了研究。大鼠组织样品经乙腈提取后,采用LC-MS/MS法测定。色谱柱为Phenomenex反向C18色谱柱(50 mm×4.6 mm,5 μm),以体积分数为72%乙腈水溶液(含体积分数为0.1%甲酸)为流动相,等度洗脱,流速0.6 mL/min。质谱采用电喷雾离子源(ESI)及多重反应监测(MRM)模式,定量离子对为m/z 364.1/194.2。大鼠心、肝、脾、肺、肾、脑、肌肉、睾丸和脂肪在0.002~0.1 mg/L范围内,大肠、小肠和胃在0.10~10 mg/L范围内,氟噻草胺的质量浓度与对应的峰面积间线性关系良好(r > 0.99)。质控样品的相对标准偏差均小于11%,基质效应在94.5%~95.6%之间,提取回收率在96%~107%之间,稳定性在95%~104%之间,均符合方法学要求。经单次灌胃给予氟噻草胺400 mg/kg后,其主要分布于大鼠的胃、大肠、小肠和肺中,各组织浓度达峰值后,随着时间延长均可从体内消除。表明氟噻草胺在动物体内分布广泛且降解迅速。本研究建立了一种可用于测定大鼠组织中氟噻草胺浓度的高效、专属、灵敏的LC-MS/MS方法,进而阐明了氟噻草胺的组织分布行为。
中文关键词:液相色谱-串联质谱(LC-MS/MS)  氟噻草胺  大鼠  组织分布  安全评价
 
Tissue distribution of flufenacet in rats determined by liquid chromatography-tandem mass spectrometry
Abstract:A method using liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed for the determination of flufenacet in rat tissues and the investigation of the tissues distribution behavior of test item in rats after intragastric administration. Rat tissue homogenate was extracted withacetonitrile and analyzed by LC-MS/MS. Chromatographic separation was performed on a Phenomenex reverse C18 (50 mm×4.6 mm, 5 μm) column at a flow rate of 0.6 mL/min with iscratic elution. The mobile phase was 72% acetonitrile/water solution (containing 0.1% formic acid). Electrospray ionization (ESI) with a positive-ion and multiple reaction monitoring mode was used. Quantitative ion pair was 364.1/194.2. The linear ranges of flufenacet in heart, liver, spleen, lung, kidney, brain, muscle, testis and fat were all ranged from 0.002 to 0.1 mg/L. The linear ranges of flufenacet in large intestine, small intestine and stomach were in the range of 0.10-10 mg/L. The correlation coefficient between the mass concentration of flufenacet and the corresponding peak area was good (r > 0.99). The precision of this method for QC samples was less than 11%. The matrix effect was in the range of 94.5%-95.6%. The recovery was in 96%-107%, and the stability was in 95%-104%. All these parameters met the requirements of methodology. The experimental results of tissue distribution of flufenacet showed that flufenacet was widely and rapidly distributed in rats after the gavage of 400 mg/kg flufenacet. Flufenacet mainly distributed in large intestine, small intestine, stomach and lung. And after the concentration of each tissue reached the peak, flufenacet could be eliminated in all tissues. An efficient, specific and sensitive LC-MS/MS method was established, and this validated method could be used in the analysis of flufenacet in rat tissues to realize the tissue distribution behaviors.
Key words:liquid chromatography-tandem mass spectrometry  flufenacet  rat  tissue distribution  safety evaluation
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