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首页> 外文期刊>Current Analytical Chemistry >Automated Fluorimetric Assay for Baclofen After On-line Derivatization with o-phthalaldehyde Based on the Sequential Injection Principle
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Automated Fluorimetric Assay for Baclofen After On-line Derivatization with o-phthalaldehyde Based on the Sequential Injection Principle

机译:基于顺序进样原理的邻苯二甲醛在线衍生化后巴氯芬的自动化荧光分析

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摘要

In the present study we report the first automated flow-based derivatization method for the determination of the anti-spastic active pharmaceutical ingredient baclofen. The analyte reacts on-line with o-phthalaldehyde in the presence of N-acetylcysteine in a sequential injection manifold to form a highly fluorescent derivative (340 / 455 nm). The various instrumental (flow rate, volumes of sample and reagents, length of reaction coil) and chemical (pH, amount concentrations of the reagents) variables were carefully investigated. The analytical performance of the proposed method included linearity (5 - 150 % or 1 - 30 mg L~(-1) baclofen), limits of detection (60 μg L~(-1)) and quantification (200 μg L~(-1)), accuracy, precision and selectivity. Analytical applications involved assay, content uniformity and dissolution studies of baclofen-containing formulations at a sampling throughput of 35-40 h~(-1).
机译:在本研究中,我们报告了第一种基于流动的自动化衍生方法,用于测定抗痉挛性活性药物成分巴氯芬。在顺序进样歧管中,在N-乙酰基半胱氨酸存在下,分析物与邻苯二甲醛在线反应,形成高荧光衍生物(340/455 nm)。仔细研究了各种仪器(流速,样品和试剂的体积,反应盘管的长度)和化学(pH,试剂的浓度)变量。该方法的分析性能包括线性度(5-150 mg L〜(-1)baclofen),检测限(60μgL〜(-1))和定量分析(200μgL〜(-1) 1)),准确性,精确度和选择性。分析应用涉及以35-40 h〜(-1)的采样量对含巴氯芬的制剂进行测定,含量均匀性和溶出度研究。

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