UV-SPECTROPHOTOMETRIC DETERMINATION OF LOMEFLOXACIN CONTENT IN DRUG CAPSULES BY THE TERNARY REACTION SYSTEM AMONG LOMEFLOXACIN,ALIZARIN AND LANTHANUM
摘 要
应用洛美沙星(LMX)-茜素-镧形成的三元化合物,在紫外光区有明显的吸收,最大吸收波长为286 nm,在0.7~12 mg·L-1范围内服从比耳定律.其摩尔吸光系数为4.2×104L·mol-1·cm-1.应用此方法分析了洛美沙星胶囊中LMX的含量,所得结果与文献<参考文献原文>方法的结果一致.测定结果的平均RSD值为0.95%,回收率的平均值为101.1%.加入反应物的次序对测定结果有影响,必须按照先加洛美沙星,其次茜素,最后加镧的顺序.反应物的最佳摩尔比为1∶1∶2(洛美沙星∶茜素∶镧),以氯仿作为溶剂.反应的温度和时间对测定结果影响不明显.反应产物在2 h内稳定.
Abstract
Based on the absorption behavior of the ternary complex formed among lomefloxacin,alizarin and lanthanum in the ultra-violet band with its absorption maxima at 286 nm,an UV-spectrophotometric method for the determination of lomefloxacin was proposed.Linear relationship between the absorbance and concentration of lemofloxacin was found in the range of 0.7-12 mg·L-1,with molar absorptivity of 4.2×104L·mol-1·cm-1.As shown by experimental results,the addition of reagents should be in the order of adding firstly alizarin solution to the sample solution containing lomefloxacin,and then adding the La(Ⅲ) solution.The mole ratio of the ternary complex was found to be [lomefloxacin∶alizarin∶La(Ⅲ)] 1 to 1 to 2.Chloroform was used as solvent to remove excess of alizarin by extraction.The ternary complex was stable within 2 h.Temperatures within the range of 20-70 ℃ were tolerable for the complexing reaction.In the analysis of a sample of lomefloxacin capsules,the results obtained by this method were found in consistency with the labelled value and also with the results obtained by the method given in literature<参考文献原文>,Average values of RSD′s was 0.95% and of recovery was 101.1%.
中图分类号 O657.3
所属栏目 工作简报
基金项目 上海市教委自然科学基金资助课题(No.03HK13)
收稿日期 2005/1/12
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备注祝优珍(1954-),女,浙江人,副教授 ,从事分析化学教学和科研工作.
引用该论文: ZHU You-zhen,YAN Yi-jun,XU Li-ying. UV-SPECTROPHOTOMETRIC DETERMINATION OF LOMEFLOXACIN CONTENT IN DRUG CAPSULES BY THE TERNARY REACTION SYSTEM AMONG LOMEFLOXACIN,ALIZARIN AND LANTHANUM[J]. Physical Testing and Chemical Analysis part B:Chemical Analysis, 2006, 42(12): 1034~1036
祝优珍,严怡君,徐莉英. 洛美沙星-茜素-镧三元体系光度测定洛美沙星胶囊含量[J]. 理化检验-化学分册, 2006, 42(12): 1034~1036
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参考文献
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【15】周静,晋卫军,杜黎明.洛美沙星在酸性介质中的紫外光谱性质的研究及应用[J].山西师范大学学报:自然科学版,2001,15(4):43-45.
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【4】杜黎明,许庆琴,曹玺珉,等.胶束增稳荷移反应紫外分光光度法测定洛美沙星[J].分析化学,2003,31(1):44-47.
【5】谭峰,郎惠云,李媛.萃取分光光度法测定盐酸洛美沙星[J].分析化学,2001,29(5):561-564.
【6】陈学锋,徐新元.差示紫外分光光度法测定盐酸洛美沙星胶囊的含量[J].辽宁药物与临床杂志,2001,4(4):171-172.
【7】张若燕,欧阳晓玫.荧光分光光度法测定洛美沙星注射液及胶囊的含量[J].中国药房,2002,13(1):45-46.
【8】冯琳,储秋萍,邵志高.荧光分光光度法测定盐酸洛美沙星胶囊含量[J].中国抗生素杂志,1996,21(1):17-19.
【9】李媛,郎惠云,谢志海.间接原子吸收法测定药物中盐酸洛美沙星含量[J].西北大学学报:自然科学报,2000,30(1):39-42.
【10】王君耀,刘放.RP-HPLC测定盐酸洛美沙星及其制剂的含量[J].华西药学杂志,2002,17(2):135-136.
【11】李建晴,冯小花,双少敏,等.7种喹诺酮类药物的光谱研究[J].分析化学,2003,31(1):19-23.
【12】赵慧春,金林培.镧系离子与氟喹诺酮类药物配合物的光化学敏化发光及其应用[J].中国科学基金,2001(1):54-56.
【13】周万斌,王玉华,马文莲.氧氟沙星与茜素的显色反应研究[J].锦州医学院学报,1999,20(6):7-8.
【14】李华侃,柳越,王玉华,等.氟哌酸与茜素的显色反应及其应用[J].锦州医学院学报,1998,19(6);7-9.
【15】周静,晋卫军,杜黎明.洛美沙星在酸性介质中的紫外光谱性质的研究及应用[J].山西师范大学学报:自然科学版,2001,15(4):43-45.
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