Photometric Determination of Captopril in Its Tablets Based on Reductive Color-Fading of Fe(Ⅲ)-Tiron Complex
摘 要
卡托普利分子中的巯基(-SH)能还原三价铁至二价状态,试验发现铁(Ⅲ)与钛铁试剂络合物的色泽由于卡托普利的存在而出现消褪。确定了铁(Ⅲ)与钛铁试剂的反应条件:于25 mL的容量瓶中依次加入0.250 0 g·L-1铁(Ⅲ)溶液2.20 mL,6.25 g·L-1钛铁试剂溶液0.6 mL及pH 3.0 Clark-Lubs缓冲溶液10.0 mL,加水定容,于80 ℃水浴中加热20 min使显色完全。在其吸收峰670 nm处测量吸光度A1。在此反应体系中加入不同浓度的卡托普利标准溶液,按相同步骤操作并测得其吸光度A2,结果表明:A1与A2之差(ΔA)与卡托普利的质量浓度在0.012~0.036 g·L-1范围内呈线性关系。将此方法应用于卡托普利片剂中卡托普利含量的测定,所得测定值与用药典法测定的结果相符。
Abstract
It was shown that the -SH group in molecules of captopril (CTPR) exhibits the property of reduction of Fe(Ⅲ) to Fe(Ⅱ), and that the color of complex formed between Fe(Ⅲ) and tiron is extincted by the presence of CTPR. Conditions for color reaction between Fe(Ⅲ) and tiron were taken as follows: in a 25 mL volumetric flask, 2.20 mL of 0.250 0 g·L-1 Fe(Ⅲ) solution, 0.6 mL of 6.25 g·L-1 tiron solution and 10.0 mL of Clark-Lubs buffer solution of pH 3.0 were added and water was added to make up the volume to 25 mL. The reaction mixture was heated in water bath at 80 ℃ for 20 min for completion of the color reaction. After cooling absorbance (A1) of the solution is measured at its absorption maximum of 670 nm. Standard solutions of CTPR with various concentrations were added to solutions of the color reaction system described above and operated in the same way. Values of absorbance (A2) were measured, and linear relationship between values of ΔA(A1-A2) and mass concentration of CTPR was kept in the range of 0.012-0.036 g·L-1. The above procedure was applied to determination of CTPR in its tablets, giving results in consistency with the values found by the method of pharmacopoeia.
中图分类号 O657.3
所属栏目 工作简报
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收稿日期 2013/6/22
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备注涂常青(1970-),女,广东平远人,教授,硕士,研究方向为药物分析。
引用该论文: TU Chang-qing,WEN Xin-rong,GUO Chun-yan. Photometric Determination of Captopril in Its Tablets Based on Reductive Color-Fading of Fe(Ⅲ)-Tiron Complex[J]. Physical Testing and Chemical Analysis part B:Chemical Analysis, 2014, 50(8): 1018~1020
涂常青,温欣荣,郭春燕. 光度法测定药物中卡托普利的含量——基于对铁(Ⅲ)-钛铁试剂络合物的还原褪色反应[J]. 理化检验-化学分册, 2014, 50(8): 1018~1020
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参考文献
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【4】李克,谭力,闫卫利.RP-HPLC测定人血浆中卡托普利[J].中国药学杂志, 1995,30(12):740-742.
【5】ENSAFI A A, ARABZADEH A. A new sensor for electrochemical determination of captopril using chlorpromazine as a mediator at a glassy carbon electrode[J]. J Anal Chem, 2012,67(5):486-496.
【6】ZIYATDINOVA G K, BUDNIKOV G K, POGOREL'TSEV V I. Determination of captopril in pharmaceutical forms by stripping voltammetry[J]. J Anal Chem, 2006,61(8):798-800.
【7】谢志海,张志红.单扫描示波极谱法测定药物中的卡托普利[J].分析化学, 2003,31(10):1195-1198.
【8】AHMED O A. Simultaneous CE determination of captopril and indapamide in pharmaceuticals and human plasma[J]. Chromatographia, 2008,68(5/6):437-442.
【9】SOROURADDIN M H, IRANIFAM M, NABIYYI A I. A novel captopril chemiluminescence system for determination of copper(Ⅱ) in human hair and cereal flours[J]. J Fluoresc, 2009,19:575-581.
【10】刘传华,刘师莲,陈沪宁,等.气相色谱法测定卡托普利含量[J].色谱, 1998,16(1):82-83.
【11】KUSMIEREK K, BALD E. A simple liquid chromatography method for the determination of captopril in urine[J]. Chromatographia, 2007,66(1/2):71-74.
【12】韩加怡,陈雪帆,杨伟峰,等.LC-MS/MS测定人血浆中卡托普利的浓度及其药动学研究[J].药物分析杂志, 2007,27(8):1200-1204.
【13】肇丽梅,胡立刚,姜瑶,等.液相色谱-串联质谱法测定人血浆中卡托普利的浓度[J].分析化学, 2006,34(11):1599-1602.
【14】李亚荣,郎惠云,谭峰,等.流动注射在线过滤稀释原子吸收法测定药物制剂中卡托普利[J].分析化学, 2002,30(2):165-168.
【15】PARASKEVAS D T, DEMETRIUS G T, ANASTASIOS E, et al. Flow and sequential injection manifolds for the spectrophotometric determination of captopril based on its oxidation by Fe(Ⅲ)[J]. Microchim Acta, 2003,142:55-62.
【16】常文保,李克安.简明分析化学手册[M].北京:北京大学出版社, 1981.
【17】国家药典委员会.中华人民共和国药典(二部)[M].北京:化学工业出版社, 2005.
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