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Development and validation of a new spectrofluorimetric method for the determination of some beta-blockers through fluorescence quenching of eosin Y. Application to content uniformity test

机译:开发和验证一种新的荧光光谱法,通过曙红Y的荧光猝灭测定某些β-受体阻滞剂。在含量均匀性测试中的应用

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A simple, rapid, sensitive and economic spectrofluorimetric method has been developed and validated for determination of some β-adrenergic blocking agents namely; betaxolol hydrochloride (BTX), carvedilol (CAR), labetalol hydrochloride (LBT), nebivolol hydrochloride (NEB) and propranolol hydrochloride (PRO). The method is based on the quenching effect of the cited drugs on the fluorescence intensity of eosin Y at pH 3.4 (acetate buffer). The fluorescence quenching is due to the formation of an ion-pair complex and was measured without extraction at 545 nm (λex. 301.5 nm). The factors affecting the formation of the ion-pair complex were carefully studied and optimized. Under the optimal conditions, the linear ranges for the relationship between the fluorescence quenching value and the concentration of the investigated drugs were 100-2500, 150-2500 and 50-2250 ng mL-1 for (BTX, CAR), (LBT, NEB) and (PRO) respectively. The method was validated according to ICH guidelines and was applied for determination of the cited drugs in pharmaceutical dosage forms with excellent recoveries. In addition, content uniformity testing of some commercial dosage forms was checked by the proposed method.
机译:已经开发了一种简单,快速,灵敏且经济的分光荧光法,并已成功用于测定某些β-肾上腺素阻断剂。盐酸倍他洛尔(BTX),卡维地洛(CAR),拉贝洛尔(LBT),盐酸奈比洛尔(NEB)和盐酸普萘洛尔(PRO)。该方法基于所引用药物在pH 3.4(醋酸盐缓冲液)下对曙红Y荧光强度的猝灭作用。荧光猝灭归因于离子对络合物的形成,并且在没有提取的情况下在545 nm(λex。301.5 nm)处进行了测量。仔细研究和优化了影响离子对络合物形成的因素。在最佳条件下,(BTX,CAR),(LBT,NEB)的荧光猝灭值与所研究药物浓度之间的关系的线性范围为100-2500、150-2500和50-2250 ng mL-1 )和(PRO)。该方法已按照ICH指南进行了验证,并用于测定具有良好回收率的药物剂型中的被引药物。此外,通过所提出的方法检查了一些商业剂型的含量均匀性测试。

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