Marques Karine L, Santos João L M, Lima José L F C
REQUIMTE, Departamento de Química-Física, Faculdade de Farmácia (UP), 4050 Porto, Portugal.
J Pharm Biomed Anal. 2005 Oct 4;39(5):886-91. doi: 10.1016/j.jpba.2005.04.027. Epub 2005 Jun 2.
In this work, a fully automated analytical methodology for the chemiluminometric determination of propranolol hydrochloride in pharmaceutical preparations is proposed. The developed procedure was based on the oxidation of propranolol by potassium permanganate in acidic medium and was implemented in a multicommutated flow system. The combined automated actuation of syringe pumps and two-way solenoid valves, under computer control, assured a high versatility in terms of sample and reagent manipulation and an effective run-time control of all analytical parameters, including a time-based insertion that enabled a significant solutions saving and the exploitation of different strategies for sample/reagent mixing. The calibration graph was linear over the range 20-150 mg l(-1) of propranolol hydrochloride with a relative standard deviation lower than 1.6% (n = 7). The results were in agreement with those obtained by the reference procedure with a relative deviation between -3.8 and 3.7% and a sampling rate of about 27 samples h(-1).
在本研究中,提出了一种用于药物制剂中盐酸普萘洛尔化学发光测定的全自动分析方法。所开发的方法基于在酸性介质中高锰酸钾对盐酸普萘洛尔的氧化,并在多通道流动系统中实现。在计算机控制下,注射泵和二位电磁阀的联合自动驱动确保了在样品和试剂操作方面具有高度的通用性,以及对所有分析参数的有效运行时间控制,包括基于时间的进样,这能够显著节省溶液并采用不同的样品/试剂混合策略。盐酸普萘洛尔校准曲线在20 - 150 mg l(-1)范围内呈线性,相对标准偏差低于1.6%(n = 7)。结果与参考方法所得结果一致,相对偏差在 - 3.8%至3.7%之间,采样速率约为27个样品 h(-1)。