期刊文献+

胶束电动毛细管色谱法测定板蓝根中苯甲酸、水杨酸和邻氨基苯甲酸 被引量:3

Determination of Benzoic Acid,Salicylic Acid and o-Aminobenzoic Acid in Radix Isatidis by Micellar Electrokinetic Capillary Chromatography
下载PDF
导出
摘要 采用胶束电动毛细管色谱法对板蓝根中芳香酸类化合物苯甲酸、水杨酸和邻氨基苯甲酸进行了分离测定。电泳介质(pH 9.8)为20 mmol.L-1硼砂、30 mmol.L-1十二烷基硫酸钠、2 mmol.L-1β-环糊精和4%(体积分数)甲醇组成的混合溶液,以对-羟基苯甲酸为内标,分离电压为16 kV,检测波长为250 nm。在优化的试验条件下,苯甲酸、水杨酸和邻氨基苯甲酸的线性范围分别为40~240 mg.L-1,64~320 mg.L-1和40~400 mg.L-1,检出限(3S/N)依次为0.64,1.08,1.36 mg.L-1。应用此方法分析了板蓝根样品,测定回收率在93.3%~104.2%之间。 Micellar electrokinetic capillary chromatography (MECC) was applied to the separation and determination of aromatic acids, including benzoic acid, salicylic acid and o-aminobenzoic acid, in Radiz Isatldis. A mixed buffer solution of pH 9.8 containing 20 mmol · L ^-1 borate, 30 mmol ·L ^-1 SDS, 2 mmol· L ^-1 β-CD and 4% (by vol. ) methanol was used as the electrophoretic medium, p-Hydroxybenzoic acid was chosen as internal standard. Separation voltage applied was 16 kV and wavelength of detection was taken at 250 nm. Under the optimum conditions, linearity ranges of benzoic acid, salicylic acid and o aminobenzoic acid found were between 40- 240, 64-320 and 40-400 mg · L^-1 , with detection limits (3S/N) of 0. 64, 1.08, 1.36 mg · L^-1 respectively. The proposed method was used in the analysis of sample of Radix Isatidis, giving values of recovery in the range of 93.3%-104. 20%.
出处 《理化检验(化学分册)》 CAS CSCD 北大核心 2012年第4期392-395,共4页 Physical Testing and Chemical Analysis(Part B:Chemical Analysis)
基金 陕西省教育厅科研计划项目资助(11JK0656) 国家自然科学基金资助项目(20975081)
关键词 胶束电动毛细管色谱法 板蓝根 苯甲酸 水杨酸 邻氨基苯甲酸 Micellar electrokinetic capillary chromatography (MECC) Radiac Isatidis Benzoic acid Salicylic acid o-Aminobenzoic acid
  • 相关文献

参考文献13

二级参考文献33

共引文献134

同被引文献30

  • 1李晓静,陈桂鸾,徐远金.胶束电动毛细管色谱法分析性激素[J].广西科学院学报,2006,22(z1):463-465. 被引量:2
  • 2杨若明,张经华,蓝叶芬.固相萃取-毛细管电泳法测定麋鹿茸中的性激素[J].现代仪器,2005,11(1):25-27. 被引量:11
  • 3胡耀铭,陈正夫.化学衍生化/GC/MS鉴定焦化废水中羧酸化合物[J].环境监测管理与技术,1995,7(1):32-33. 被引量:5
  • 4傅若农.近年国内固相萃取-色谱分析的进展[J].分析试验室,2007,26(2):100-122. 被引量:78
  • 5Heli S, Tuulikki S L, Matej O. Capillary electrophoresis with UV detection and mass spectrometry in method development for profiling metabo- lites of steroid hormone metabolism [ J ]. J Chromatogr B,2008,871 ( 2 ) :375-382.
  • 6Watanabe E, Kubo H, Kanzaki Y, et al. Immunoassay based on a polyclonal antibody for sex steriod hormones produced by a heterogeneous hap- ten-conjugated immunogen : Estimation of its potentiality and antibody characteristics [ J ]. Anal Chim Acta,2010,658 ( 1 ) :56-62.
  • 7Tort N, Salvador J P, Marco M P. Multiplexed immunoassay to detect anabolic androgenic steroids in human serum [ J ]. Anal Bioanal Chem, 2012,403 (5) : 1361-1371.
  • 8Nara S, Tripathi V, Chaube S K, et al. Influence of hydrophobie and hydrophilic spacer-containing enzyme conjugates on functional parameters of steroid immunoassay[ J]. Anal Biochem,2008,373 ( 1 ) : 18-25.
  • 9Zou Yan, Li anhua, Jin Hua, et al. Determination of estrogens in human urine by high-performance liquid chromatography/diode array detec- tion with ultrasound-assisted cloud-point extraction[J]. Anal Biochem ,2012,421 (2) :378-384.
  • 10Yang Lihua, Luan Tiangang, Lan Chongyu. Solid-phase microextraction with on-fiber silylation for simultaneous determinations of endocrine dis- ruptlng chemicals and steroid hormones by gas chromatography-mass sepectrometry [J] J Chromatogr A ,2006,1104 (1/2) :23-32.

引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部