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作 者:张淑芳[1,2] 李怀娜[1,2] 张冬梅 周奇志[1,2]
机构地区:[1]曲阜师范大学化学系 [2]山东威海市药品检验所
出 处:《光谱学与光谱分析》1998年第4期488-491,共4页Spectroscopy and Spectral Analysis
摘 要:本文建立了以0.1mol/LHCl为介质,采用三阶导数光谱法,同时测定甲硝唑和维生素B6的新方法。方法检测限为0.81μg/mL甲硝唑和0.16μg/mL维生素B6。二者测定的线性范围均为1.6~22.4μg/mL,直接用于复方甲硝唑片剂中甲硝唑和维生素B6的测定。两种物质的测定变异系数分别小于2.26和2.60%,回收率分别为93~102%和99~101%。A new method for simultaneous determination of metronidazolum and vitamin B6 was established by the third derivative spectrophotometry in 0.1mol/L HCl solution.The detection limits were 0.81μg/mL for metronidazolum and 0.16μg/mL for vitamin B.6.The linear range of determination was 1.6~22.4μg/mL for both metronidazolum and vitamin B.6.This method has been applied to the determination of metronidazolum and vitamin B6 in tabellae metronidazoli compositae with satisfactory results.The coefficients of variation are below 2.26 and 2.65% and the recoveries are 93—102% and 99—101% for metronidazolum and vitamin B6,respectively.
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