期刊文献+

磺基水杨酸-铁(Ⅲ)显色体系间接测定左旋多巴的研究 被引量:3

Study on the Indirectly Determination of Levodopa by Sulfosalicylic Acid-iron(Ⅲ) Color Reaction System
下载PDF
导出
摘要 磺基水杨酸与Fe(Ⅲ)在pH=2.00~3.00的溶液中形成紫红色磺基水杨酸合铁(Ⅲ)配离子,左旋多巴的还原性,可将Fe(Ⅲ)定量还原为Fe(Ⅱ),使Fe(Ⅲ)-磺基水杨酸体系的颜色褪去,其吸光度降低值与左旋多巴含量在一定范围内呈良好的线性关系,据此提出了基于Fe(Ⅲ)-磺基水杨酸显色体系间接分光光度法测定左旋多巴含量的新方法。对实验条件进行了研究和选择。方法线性范围为4.0×10-7~2.0×10-5mol/L,检出限为3.1×10-7mol/L,回收率为98.0%~101.0%。该方法简单、快速、灵敏,用于片剂中左旋多巴的测定,结果满意。 The sulfosalicylic acid and Fe(Ⅲ) could form a purple-red complex in pH=2.00~3.00 solution,the reducing nature of levodopa could reduce Fe(Ⅲ) to Fe(Ⅱ),thus the absorbance of the Fe(Ⅲ)-sulfosalicylic system decreased.The absorbance reduction of Fe(Ⅲ)-sulfosalicylic system and the contents of levodopa appeared linear relationships.A new method for the indirectly determination of levodopa has been developed based on the characteristic.Different conditions affecting the absorbance were studied and optimized.Under the optimum experimental conditions,the linear range was 4.0×10-7~2.0×10-5mol/L,the detection limit for levodopa was 3.1×10-7mol/L and the recoveries were 98.0%-101.0%.The method was simple,accurate and sensitive,and has been used to determine the levodopa in tablets with satisfactory results.
出处 《延安大学学报(自然科学版)》 2011年第1期47-49,共3页 Journal of Yan'an University:Natural Science Edition
基金 陕西省教育厅专项科研基金资助课题(09JK821) 延安市科技局科技计划项目(2008ks-20) 延安大学大学生科技创新训练计划项目
关键词 分光光度法 左旋多巴 磺基水杨酸 显色体系 spectrophotometry levodopa Fe sulfosalicylic acid color reaction
  • 相关文献

参考文献7

二级参考文献55

  • 1吕元琦,邬春华,袁倬斌.毛细管电泳法测定美多芭片剂中的左旋多巴和羟苄丝肼[J].化学试剂,2004,26(4):217-219. 被引量:3
  • 2于民,张扬达.左旋多巴治疗并发症的研究进展及治疗对策[J].国外医学(神经病学.神经外科学分册),1996,23(5):233-236. 被引量:2
  • 3[3]Nagaraja P,Vasantha RA,Sunitha KR.A sensitive and selective spectrophotometric estimation of catechol derivatives in pharmaceutical preparations[J].Talanta,2001,55(6):1039-1046.
  • 4[4]Damiani PC,Moschetti AC,Rovetto AJ,et al.Design and optimization of a chemo-metrics-assisted spectrophotometric method for the simultaneous determination of levodopa and carbidopa in pharmaceutical products[J].Anal Chim Acta,2005,543(1/2):192-198.
  • 5[5]Tait RJ,Finnin BC,Reed BL.A study of irreversible electrode processes under steady-state flowing solution conditions with a microelectrode based scanning electrochemical detector[J].Anal Chim Acta,1996,324(1):1-11.
  • 6[6]WoodAT,HallMR.Reversed-phase high-performance liquid chromatography of catecholamines and indoleamines using a simple gradient solvent system and native fluorescence detection[J].J Chromatogr B Biomed Sci Appl,2000,744(1):221-225.
  • 7[7]Neves HJC,Morais ZB.HPLC assay of underivalized free amino acids with column switching and evaporative light-scattering detection[J].J High Resolut Chromatogr,1997,20(2):115-118.
  • 8[8]Fanali S,Pucci V,Sabbioni C,et al.Quality control of benserazide-levodopa and carbidopa-levodopa tablets by capillary zone electrophoresis[J].Electrophoresis,2000,21(12):2431-2437.
  • 9[9]Lee JH,Choi OK,Jung HS,et al.Capillary electrophoresis of nonprotein and protein amino acids without derivalization[J].Electrophoresis,2000,21(5):930-934.
  • 10[10]Chen XF,Zhang JY,Zhai HL,et al.Determination of levodopa by capillary zone electrophoresis using an acidic phosphate buffer and its application in the analysis of beans[J].Food Chem,2005,92(2):381-386.

共引文献22

同被引文献31

引证文献3

二级引证文献6

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