Spectrofluorimetric Estimation of Some Sulfhydryl – Containing Drugs by Demasking Reaction of the Palladium Chelate of 8-Hydroxyquinoline-5-Sulfonic Acid

Haggag Rs, Belal Sf, Hewala, ElRouby Oa
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引用次数: 1

Abstract

A simple and sensitive spectrofluorimetric method has been developed for the determination of some selected sulfhydryl–containing drugs namely Acetylcysteine (ACS), Captopril (CAP) and Mesna (MSN). The method is based on the interaction of the drugs with potassium (5-sulfoxino) palladium II in alkaline medium in presence of magnesium ions, where the sulfhydryl group combines with palladium from the non-fluorescent potassium bis (5-sulfoxino) palladium II. The resulting 8-hydroxy-5-quinoline sulfonic acid coordinates with magnesium to form the fluorescent chelate that is a measure of the amount of sulfhydrl containing drug analyzed. The fluorescence intensity was measured at an emission wavelength of 485 nm, by excitation at 345 nm. All the experimental parameters affecting the reaction were studied and optimized. The proposed method was applicable over the concentration range of 0.04-0.44 μg/mL for the three drugs and was applied for their determination in bulk form and in pharmaceutical preparations without interference from common excipients. The assay results were statistically compared with those obtained from previously reported methods where no significant difference was found between them. The selectivity and the stability-indicating aspect of the proposed method were confirmed by preparing the disulphides of the studied drugs and applying the reaction to the parent drugs in presence of their disulphides where no interference was detected from these related substances. By virtue of its high sensitivity, the proposed method was also extended to analyze the drugs in spiked human plasma and urine.
8-羟基喹啉-5-磺酸钯螯合物掩膜反应荧光光谱法测定某些含巯基药物
建立了一种简单、灵敏的含巯基药物乙酰半胱氨酸(ACS)、卡托普利(CAP)和美斯那(MSN)的荧光光谱测定方法。该方法是基于药物与钾(5-亚砜)钯II在镁离子存在的碱性介质中的相互作用,其中巯基与非荧光双(5-亚砜)钯II中的钯结合。由此产生的8-羟基-5-喹啉磺酸与镁配合形成荧光螯合物,这是对含巯基药物分析量的测量。在发射波长为485 nm,激发波长为345 nm处测量荧光强度。对影响反应的实验参数进行了研究和优化。该方法适用于3种药物在0.04 ~ 0.44 μg/mL的浓度范围内,适用于原料药和制剂中三种药物的测定,不受常用辅料的干扰。测定结果与以前报道的方法进行了统计比较,发现它们之间没有显着差异。通过制备所研究药物的二硫化物,并在母体药物的二硫化物存在的情况下将反应应用于母体药物,并且没有检测到这些相关物质的干扰,从而证实了所提出方法的选择性和稳定性。该方法具有较高的灵敏度,可应用于人血浆和尿液中药物的分析。
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