首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Isoindole based fluorophore for the sensitive fluorimetric determination of isobutyl gamma aminobutyric acid
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Isoindole based fluorophore for the sensitive fluorimetric determination of isobutyl gamma aminobutyric acid

机译:基于异吲哚的荧光团,用于敏感的荧光测定异丁基γ氨基丁酸

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摘要

The present work deals with the development and validation of a selective and highly sensitive spectrofluorimetric method for determination of 3-isobutyl gamma amino butyric acid (3-isobutyl GABA). The drug is selectively condensed with o-phthalaldehyde in presence of 2-mercaptoethanol to form a highly fluorescent isoindole derivative. The fluorescent intensity of the obtained fluorophore was monitored at 431 nm (lambda(ex)= 335 nm). The influence of reaction conditions was investigated in order to enhance the sensitivity of the proposed procedure. At the optimized reaction condition the fluorescence intensity was found to be in linear relationship with drug concentration in the range of 0.025 0.125 mu g ml(-1). The quantitation and detection limits were 15.5 and 4.6 ng ml(-1), respectively. The guidelines of the International Conference on Harmonization (ICH) were followed in order to validate the suggested procedure. The developed method was employed for the analysis of pharmaceutical preparations containing the cited drug. The obtained data were compared with those from the reported method. Good agreement was found between both methods in respect to the accuracy and precision. Moreover, the proposed method utilizes low cost reagents, and has high sensitivity. These advantages give the method the ability to be a good alternative for determination of cited drug in routine analysis.
机译:本作工作涉及一种选择性和高灵敏度的光谱氟化物方法的开发和验证,用于测定3-异丁基γ氨基丁酸(3-异丁基GABA)。用2-巯基乙醇存在于2-巯基乙醇中选择性地凝聚用O-酞甲醛,以形成高荧光异吲哚衍生物。将所得荧光团的荧光强度以431nm监测(λ(λ)= 335nm)。研究了反应条件的影响,以提高所提出的程序的敏感性。在优化的反应条件下,发现荧光强度与药物浓度的线性关系,在0.025 0.125mm g ml(-1)的范围内。定量和检测限分别为15.5和4.6ng ml(-1)。遵循国际协调会议(ICH)会议的指导方案,以验证建议的程序。研制方法用于分析含有所引用的药物的药物制剂。将获得的数据与来自报告方法的数据进行比较。两种方法都发现了对准确性和精度之间的良好协议。此外,该方法利用低成本试剂,具有高灵敏度。这些优点使方法能够成为常规分析中被引用的药物测定的良好替代方案。

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