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通过与对二甲氨基肉桂醛反应分光光度法测定异卡波肼原料药和片剂。

Spectrophotometric determination of isocarboxazid bulk drug and tablets by reaction with p-dimethylaminocinnamaldehyde.

作者信息

el-Kommos M E

机构信息

University of Assiut, Faculty of Pharmacy, Pharmaceutical Chemistry Department, Egypt.

出版信息

J Assoc Off Anal Chem. 1988 Nov-Dec;71(6):1134-6.

PMID:3240968
Abstract

A spectrophotometric method is described for the determination of isocarboxazid. The method is based on the reaction of the drug with p-dimethylaminocinnamaldehyde in the presence of trichloroacetic acid in a methanolic medium to produce a very intense red chromophore (lambda max = 500 nm, Emax = 1.05 x 10(5]. The reaction is proposed to proceed via electrophilic attack at the C-4 position of the isoxazole nucleus. Job's plot indicated a 1:1 drug-to-reagent ratio. Regression analysis of Beer's plot showed excellent correlation (r = 0.9996) in the concentration range 0.25-2.10 micrograms isocarboxazid/mL. The developed color is stable for at least 12 h. Results of analyses of bulk drug and tablets by the proposed method are comparable to those for USP XXI methods.

摘要

描述了一种测定异卡波肼的分光光度法。该方法基于药物在甲醇介质中与对二甲氨基肉桂醛在三氯乙酸存在下反应生成非常强烈的红色发色团(最大吸收波长λmax = 500 nm,最大吸光度Emax = 1.05×10⁵)。该反应被认为是通过亲电进攻异恶唑核的C-4位进行的。乔布氏曲线表明药物与试剂的比例为1:1。比尔定律曲线的回归分析表明,在异卡波肼浓度为0.25 - 2.10微克/毫升的范围内具有良好的相关性(r = 0.9996)。显色至少稳定12小时。用所提出的方法对原料药和片剂进行分析的结果与美国药典第二十一版方法的结果相当。

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