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Determination of diclofenac in pharmaceuticals using a metalloporphyrin-based selective electrode

机译:使用基于金属卟啉的选择性电极的药物中双氯芬酸的测定

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The construction and the potentiometric response characteristics of a new diclofenac-selective electrode based on rhodium(III)tetraphenylporphyrin (Rh(III)TPP-Cl) as an ionophore are presented. The ionophore was incorporated into a PVC matrix. The effect of lipophilic cationic and anionic additives on the potentiometric response was investigated. The best results were obtained for the membrane having the cationic additive trioctylmethylammonium chloride (TOMACl) added. The corresponding sensor exhibited a near-Nernstian response to diclofenac in the concentration range 5×10~(-6)-1×10~(-2) M with a slope of -59.4mV per concentration decade in a buffer solution of pH 7.1. The selectivity of the sensor relative to a lot of organic and inorganic anions is also reported. This electrode was applied for the direct determination of diclofenac in pharmaceutical formulations and the results were compared with those provided by the HPLC reference method.
机译:介绍了基于铑(III)四苯基卟啉(RH(III)TPP-CL)作为离子载体的新型双氯芬酸选择电极的结构和电位响应特征。将离子载体掺入PVC基质中。研究了亲脂性阳离子和阴离子添加剂对电位响应的影响。为加入阳离子添加剂三乙基甲基甲基甲基铵(TOMACL)的膜获得了最佳结果。相应的传感器在浓度范围5×10〜(-6)-1×10〜(-2)m中对双峰的反应表现出在5×10〜(-6)-1×10〜(-2)m中,在pH7.1的缓冲溶液中每浓度为-59.4mV的斜率。 。还报道了传感器相对于大量有机和无机阴离子的选择性。该电极用于直接测定药物制剂中的双氯芬酸,并将结果与​​通过HPLC参考方法提供的结果进行比较。

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