铈氧化法测定某些抗病毒药物的简单荧光法(ⅳ)

Ibrahim A. Darwish , Alaa S. Khedr , Hassan F. Askal , Ramadan M. Mahmoud
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引用次数: 53

摘要

建立了一种简便、灵敏的测定抗病毒药物利巴韦林、阿昔洛韦和盐酸金刚烷胺的荧光法。该方法是基于高氯酸存在下铈(IV)氧化这些药物,随后监测诱导的铈(III)在λ激发255和λ发射355 nm处的荧光。对铈(IV)浓度、酸介质种类和浓度、反应时间、温度、稀释溶剂等影响反应条件的因素进行了仔细的研究和优化。在最佳条件下,相对荧光强度与药物浓度在50 ~ 1400 ng ml-1范围内呈良好的线性关系,相关系数为0.9978 ~ 0.9996。检测限为20 ~ 49 ng ml-1,定量限为62 ~ 160 ng ml-1。该方法的精密度令人满意;相对标准偏差不超过1.58%。在剂型中通常存在的赋形剂没有观察到干扰。该方法成功地应用于所研究药物的纯剂型和制剂剂型的分析,具有良好的准确度和精密度;回收率为99.2% ~ 101.2±0.48 ~ 1.30%。所提出的荧光法所得结果与美国药典中规定的官方方法所得结果相当。
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Simple fluorimetric method for determination of certain antiviral drugs via their oxidation with cerium (IV)

A simple and sensitive fluorimetric method for determination of antiviral drugs: ribavirin, acyclovir, and amantadine hydrochloride has been developed. The method was based on the oxidation of these drugs by cerium(IV) in presence of perchloric acid and subsequent monitoring the fluorescence of the induced cerium(III) at λexcitation 255 and λemission 355 nm. Different variables affecting the reaction conditions such as the concentrations of cerium(IV), type and concentration of acid medium, reaction time, temperature, and the diluting solvents were carefully studied and optimized. Under the optimum conditions, linear relationships with good correlation coefficients (0.9978–0.9996) were found between the relative fluorescence intensity and the concentrations of the investigated drugs in the range of 50–1400 ng ml–1. The assay limits of detection and quantitation were 20–49, and 62–160 ng ml–1, respectively. The precision of the method was satisfactory; the values of relative standard deviations did not exceed 1.58%. No interference could be observed from the excipients commonly present in dosage forms. The proposed method was successfully applied to the analysis of the investigated drugs in pure and pharmaceutical dosage forms with good accuracy and precision; the recovery percentages ranged from 99.2 to 101.2 ± 0.48–1.30%. The results obtained by the proposed fluorimetric method were comparable with those obtained by the official method stated in the United States Pharmacopoeia.

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