首页> 外文期刊>Journal of drug research. >Fluorescence Spectral Behaviour of Amlodipine Besylate and Dobutamine Hydrochloride and their Determination in Dosage Forms and Spiked Plasma.
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Fluorescence Spectral Behaviour of Amlodipine Besylate and Dobutamine Hydrochloride and their Determination in Dosage Forms and Spiked Plasma.

机译:苯磺酸氨氯地平和盐酸多巴酚丁胺的荧光光谱行为及其在剂型和加标血浆中的测定。

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摘要

The present work describes sensitive, simple and validated fluorimetric methods for the determination of Amlodipine besylate (AM) and Dobutamine Hydrochloride (DO). The methods depend on measurement of native fluorescence intensity of both drugs at lambda_(emission)450nm, and 310nm using lambda_(excitation) 360nm and 272nm for both drugs. The fluorescence spectral properties of AM and DO was also achieved in presence of different surfactants, B-cyclodextrin and some metal ions. Quantum yield, formation constant (K) and free energy changes (A G) values were calculated, for all the suggested methods under the optimum condition and experimental parameters. Linear relationships and good correlation coefficients (0.9995-0.9999) were found between fluorescence intensity, and the concentration ranges of the investigated drugs. No interference was observed when the methods were applied in the presence of co- administrated and common drugs. Moreover the methods can be used as stability indicating methods for AM. The results obtained were statistically comparable with those obtained by official methods. The proposed methods were successfully applied to the determination of AM and DO in bulk powder, dosage forms, and spiked human plasma. The validity of the methods was assessed according to USP guidelines and also by applying the standard addition technique.
机译:本工作描述了测定苯磺酸氨氯地平(AM)和盐酸多巴酚丁胺(DO)的灵敏,简单且经过验证的荧光法。该方法取决于两种药物在λ(发射)450nm和310nm处使用λ(激发)360nm和272nm的天然荧光强度的测量。在不同的表面活性剂,B-环糊精和一些金属离子的存在下,也获得了AM和DO的荧光光谱特性。对于所有建议的方法,在最佳条件和实验参数下,计算了量子产率,形成常数(K)和自由能变化(AG)值。在荧光强度和所研究药物的浓度范围之间发现线性关系和良好的相关系数(0.9995-0.9999)。当在共同给药和普通药物存在下应用该方法时,未观察到干扰。此外,该方法可用作AM的稳定性指示方法。所获得的结果与通过官方方法获得的结果在统计学上可比。所提出的方法已成功应用于散装粉末,剂型和加标人体血浆中AM和DO的测定。该方法的有效性根据USP指南以及通过应用标准添加技术进行评估。

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