Ion-Pair Complex of Trimethoprim with Alizarin Yellow and its Determination and Extraction by LLE and DLLME

Araf I. Jabbar, Mohammed Z. Thani, Ali I. Khaleel
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Abstract

For the analysis of trimethoprim medication in its pure form and pharmaceutical formulations, precise and accurate microextraction techniques with UV-Vis measurement have been developed and confirmed. In this study, LLE and DLLME procedures were utilized for the separation, pre-concentration, and evaluation of trimethoprim in pure form and pharmaceutical preparations by UV-Vis spectroscopy at 390 nm. The method was validated and applied to the evaluation of trimethoprim in pharmaceutical formulations. Several experimental factors containing the type of dispersive and extraction solvents and their volumes, pH, temperature, and centrifuging time were carried out. Under the ideal conditions, the procedures were linear in the range of 2–45 and 1-10 mg/L, with a coefficient of determination (R2) of 0.9961 and 0.9992 for LLE and DLLME, respectively. The limit of detection (LOD) was 1.52 and 0.21 mg/L. Recovery of the target analyte in pharmaceutical formulations was 99.3%-104.9%.
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甲氧苄啶与茜素黄的离子对配合物及其液相色谱法和液相色谱法的测定与提取
为了分析甲氧苄氨嘧啶药物的纯形式和药物配方,已经开发并确认了精确和准确的紫外可见微提取技术。在本研究中,采用LLE和DLLME方法对甲氧苄啶纯品和药物制剂进行分离、预富集和390 nm紫外可见光谱评价。验证了该方法的有效性,并将其应用于复方甲氧苄啶的质量评价。考察了分散溶剂和萃取溶剂的种类及其体积、pH、温度和离心时间等实验因素。在理想条件下,LLE和DLLME在2 ~ 45和1 ~ 10 mg/L范围内呈线性关系,决定系数(R2)分别为0.9961和0.9992。检出限分别为1.52和0.21 mg/L。目的分析物在制剂中的回收率为99.3% ~ 104.9%。
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