• EI
  • Scopus
  • 中国科技期刊卓越行动计划项目资助期刊
  • 北大核心期刊
  • DOAJ
  • EBSCO
  • 中国核心学术期刊RCCSE A+
  • 中国精品科技期刊
  • JST China
  • FSTA
  • 中国农林核心期刊
  • 中国科技核心期刊CSTPCD
  • CA
  • WJCI
  • 食品科学与工程领域高质量科技期刊分级目录第一方阵T1
中国精品科技期刊2020
郭翔. 毛细管电泳-色谱联用法(CEC-LIF)检测运动营养品中α2-受体激动剂[J]. 食品工业科技, 2020, 41(7): 197-202. DOI: 10.13386/j.issn1002-0306.2020.07.033
引用本文: 郭翔. 毛细管电泳-色谱联用法(CEC-LIF)检测运动营养品中α2-受体激动剂[J]. 食品工业科技, 2020, 41(7): 197-202. DOI: 10.13386/j.issn1002-0306.2020.07.033
GUO Xiang. Determination of α2-Receptor Agonists in Sports Nutrients by CEC-LIF[J]. Science and Technology of Food Industry, 2020, 41(7): 197-202. DOI: 10.13386/j.issn1002-0306.2020.07.033
Citation: GUO Xiang. Determination of α2-Receptor Agonists in Sports Nutrients by CEC-LIF[J]. Science and Technology of Food Industry, 2020, 41(7): 197-202. DOI: 10.13386/j.issn1002-0306.2020.07.033

毛细管电泳-色谱联用法(CEC-LIF)检测运动营养品中α2-受体激动剂

Determination of α2-Receptor Agonists in Sports Nutrients by CEC-LIF

  • 摘要: 建立一种毛细管电泳-色谱联用法检测运动营养品中赛拉嗪、右美托咪啶、胍那苄等3种α2-受体激动剂的分析方法。本研究结合激光诱导荧光技术,以1.0 mmol/L的4-氟-7-硝基-2,1,3-苯并呋咱为衍生剂,在pH8.9、衍生温度60℃、衍生反应30 min。所得衍生产物以乙腈-磷酸钾(10 mmol/L)(55:45,v/v)为流动相,经苯基毛细管色谱填充柱进行分离后检测。结果表明,3种α2-受体激动剂能在1.0~20.0 ng/mL浓度范围内线性良好,相关系数R2为0.995~0.999,检出限均为5.0 μg/kg,定量限均为16.0 μg/kg,加标回收率达到80.5%~93.4%。本方法前处理操作简单、灵敏,为运动营养品中α2-受体激动剂分离分析提供了新手段。

     

    Abstract: A capillary electrophoresis-chromatography method was developed for the determination of serazine,dexmedetomidine and guanabenz in sports nutrients. This study combines laser-induced fluorescence technology and prepared with 1.0 mmol/L 4-fluoro-7-nitro-2,1,3-benzofurazan(NBD-F)as derivative agent at pH8.9,derivation temperature 60℃,and derivatization reaction for 30 minutes. Acetonitrile-potassium phosphate(10 mmol/L)(55:45,v/v)was used as mobile phase for the separation and determination of the derivatives by phenyl capillary column. The results showed that the linearity of three α2-receptor agonists was good in the concentration range of 1.0~20.0 ng/mL. The correlation coefficient R2 was 0.995~0.999,the detection limit was 5.0 ug/kg,the quantitative limit was 16.0 ug/kg,and the recovery rate was 80.5%~93.4%. This method is simple and sensitive,and provides a new method for the separation and analysis of three α2-receptor agonists in sports nutrients.

     

/

返回文章
返回