首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development of an automated on-line pre-column derivatization procedure for sensitive determination of histamine in food with high-performance liquid chromatography-fluorescence detection
【24h】

Development of an automated on-line pre-column derivatization procedure for sensitive determination of histamine in food with high-performance liquid chromatography-fluorescence detection

机译:高效液相色谱-荧光检测法开发用于食品中组胺灵敏测定的自动在线柱前衍生程序

获取原文
获取原文并翻译 | 示例
           

摘要

An improved sensitive method was developed and validated for the determination of histamine in food samples by using automated on-line pre-column derivatization coupled with high performance liquid chromatography and fluorescence detection (HPLC-FLD). o-Phthaldialdehyde (OPA) was adopted as derivatization reagent, and a "sandwich" (OPA+ histamine + OPA) aspiration mode for the automated online pre-column derivatization was found to efficiently enhance the method sensitivity and precision. Histamine in food samples was efficiently extracted with a methanol-phosphate buffer solution (50:50, v/v) at 60 degrees C for 30 min, and purified with Waters Oasis MCX solid-phase extraction (SPE) cartridge. The limit of quantification for this method is 0.2 mg/kg, which is very sensitive for histamine determination. With the "sandwich" injection program, 3.7% of relative standard deviation (RSD) was achieved by five replicative determinations of a sample blank spiked with 0.25 mg/kg histamine standard. Histamine in food samples such as fumitory skipjack and mackerel was analyzed with relative recoveries over 95% at spiking level of 150 mg/kg, as well as canned tuna fish and cheese with relative recoveries up to 98% at spiking levels of 0.50 and 5.0 mg/kg, respectively. The proposed method was validated with a sample from the Food Analysis Performance Assessment Scheme (FAPAS) as a standard certified material; and the results (140 +/- 6 mg/kg) agreed well with the assigned value (139 mg/kg).
机译:通过使用自动在线柱前衍生化结合高效液相色谱和荧光检测(HPLC-FLD),开发了一种改进的灵敏方法并验证了该方法用于食品样品中组胺的测定。采用邻苯二甲醛(OPA)作为衍生试剂,发现用于在线自动柱前衍生的“三明治”(OPA +组胺+ OPA)抽吸模式有效地提高了方法的灵敏度和精密度。食品样品中的组胺可在60摄氏度下用磷酸甲醇缓冲溶液(50:50,v / v)有效提取30分钟,并用Waters Oasis MCX固相萃取(SPE)柱纯化。该方法的定量限为0.2 mg / kg,对组胺的测定非常敏感。在“三明治”注射程序中,通过对0.25 mg / kg组胺标准品加标的空白样品进行五次重复测定,可实现相对标准偏差(RSD)的3.7%。对食品样品中的组胺进行了分析,例如在skip鱼和鲭鱼的加标水平为150 mg / kg时,相对回收率超过95%;在吞拿水平为0.50和5.0 mg时,罐装吞拿鱼和奶酪的相对回收率高达98%。 / kg。食品分析绩效评估计划(FAPAS)的样品作为标准认证材料对提出的方法进行了验证;结果(140 +/- 6 mg / kg)与指定值(139 mg / kg)很好地吻合。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号