Lima J L, Montenegro M C, Sales M G
CEQUP/Departamento de Química-Física, Faculdade de Farmácia, R. Anibal Cunha, Porto, Portugal.
J Pharm Biomed Anal. 1996 Jun;14(8-10):931-8. doi: 10.1016/0731-7085(95)01710-0.
The construction and evaluation of tripelennamine conventionally-shaped ion-selective electrodes and tubular detectors for the determination of this compound in pharmaceutical formulations are described. Electrodes with conventional configuration have been constructed without an internal reference solution, using several types of immobilized ionic sensors in PVC. The different electrode membranes were prepared by using tripelennamine tetraphenylborate as ionic-exchanger, dissolved in 2-nitrophenyl octyl ether (type A), dibutylphthalate (type B) and bis-(2-ethylhexyl)sebacate (type C) as plasticizer solvents. The general working characteristics of the different types of conventional electrodes were evaluated in tripelennamine solutions, with adjusted ionic strength, showing a linear response in the concentration range of about 4 x 10(-5) - 1 x 10(-1) M and a slope near the theoretical value. The electrodes presented a fast response (> 20 s) and a high reproducibility (> or = 0.2 mV per day). The electrode selectivity in the presence of some interferents, such as sodium, potassium, lithium, ammonium, chlorpheniramine, diphenydramine, promethazine, meclizine and pentazocine, was good, particularly for those whose sensor membrane was prepared with tripelennamine tetraphenylborate dissolved in 2-nitrophenyl octyl ether (type A). Tubular detectors were also prepared using the same sensor membrane and were evaluated in a low-dispersion flow-injection manifold. Under these conditions the detectors presented response characteristics similar to those of the corresponding conventionally-shaped electrodes. The analysis of different pharmaceutical forms (creams, syrups and gels) gave good results with mean recoveries of 99.8-100.6% when the experiments were conducted by direct potentiometry and 99.9-100.4% where the same determinations were conducted by flow-injection analysis with tubular detectors.
本文描述了用于测定药物制剂中曲吡那敏的传统形状离子选择电极和管状检测器的构建与评估。已构建了无内部参比溶液的传统构型电极,在聚氯乙烯(PVC)中使用了几种类型的固定化离子传感器。通过使用四苯基硼酸曲吡那敏作为离子交换剂,溶解在2-硝基苯基辛醚(A型)、邻苯二甲酸二丁酯(B型)和癸二酸二(2-乙基己基)酯(C型)作为增塑剂溶剂中来制备不同的电极膜。在离子强度已调整的曲吡那敏溶液中评估了不同类型传统电极的一般工作特性,结果表明在约4×10⁻⁵ - 1×10⁻¹ M的浓度范围内呈线性响应,斜率接近理论值。这些电极响应快速(> 20 s)且重现性高(>或 = 0.2 mV/天)。在存在一些干扰物(如钠、钾、锂、铵、氯苯那敏、苯海拉明、异丙嗪、美克洛嗪和喷他佐辛)的情况下,电极的选择性良好,特别是对于那些其传感膜是用溶解在2-硝基苯基辛醚中的四苯基硼酸曲吡那敏制备的电极(A型)。还使用相同的传感膜制备了管状检测器,并在低分散流动注射歧管中进行了评估。在这些条件下,检测器呈现出与相应传统形状电极相似的响应特性。当通过直接电位法进行实验时,对不同药物剂型(乳膏、糖浆和凝胶)的分析结果良好,平均回收率为99.8 - 100.6%;当使用管状检测器通过流动注射分析进行相同测定时,平均回收率为99.9 - 100.4%。