首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of minocycline by oxidative coupling and diazocoupling reactions in pharmaceutical formulations.
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Determination of minocycline by oxidative coupling and diazocoupling reactions in pharmaceutical formulations.

机译:通过药物制剂中的氧化偶合和重氮偶合反应测定米诺环素。

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摘要

Simple and sensitive spectrophotometric methods (M(1)-M(4)) by the application of oxidative coupling and diazocoupling reactions for the assay of minocycline (MC) in pure form and pharmaceutical formulations have been described. Methods M(1) and M(2) involve the oxidative coupling reactions of MC with 3-methyl-2-benzothiozolinone hydrazone (MBTH) (method M(1), lambda(max) 440 nm) or 4-aminophenazone (4-AP) (method M(2), lambda(max) 520 nm) in the presence of periodate. Methods M(3) and M(4) are based on the formation of diazocoupling products of MC with diazotised p-nitroaniline (DPNA) (method M(3), lambda(max) 420 nm) or diazotised sulfanilic acid (DSAC) (method M(4), lambda(max) 420 nm). Regression analysis of Beer's law plot showed good correlation in the concentration range of 8-48, 20-120, 4-20 and 8-40 &mgr;g ml(-1) for methods A, B, C and D, respectively. The molar absorptivities fell within the range of 2.23x10(3)-1.51x10(4) l mol(-1) cm(-1).The recoveries range from 99.02 to 100.61%.
机译:简单和灵敏的分光光度法(M(1)-M(4))通过应用氧化偶合和重氮偶合反应测定米诺环素(MC)的纯净形式和药物制剂,已得到描述。方法M(1)和M(2)涉及MC与3-甲基-2-苯并噻唑啉酮(MBTH)(方法M(1),λ(最大)440 nm)或4-氨基酚(4-的氧化偶联反应AP)(方法M(2),λ(最大)520 nm)在高碘酸盐的存在下。方法M(3)和M(4)基于MC与重氮化对硝基苯胺(DPNA)(方法M(3),λ(最大)420 nm)或重氮化磺胺酸(DSAC)的重氮偶联产物的形成(方法M(4),λ(最大)420 nm)。比尔定律图的回归分析显示,方法A,B,C和D的浓度范围分别为8-48、20-120、4-20和8-40 mg·g(-1),具有良好的相关性。摩尔吸收率在2.23x10(3)-1.51x10(4)l mol(-1)cm(-1)范围内。回收率范围为99.02%至100.61%。

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