Lourenção Bruna Cláudia, Medeiros Roberta Antigo, Rocha-Filho Romeu C, Mazo Luiz Henrique, Fatibello-Filho Orlando
Instituto de Química de São Carlos, Universidade de São Paulo, C.P. 780, 13560-970 São Carlos, SP, Brazil.
Talanta. 2009 May 15;78(3):748-52. doi: 10.1016/j.talanta.2008.12.040. Epub 2008 Dec 30.
A simple and highly selective electrochemical method was developed for the single or simultaneous determination of paracetamol (N-acetyl-p-aminophenol, acetaminophen) and caffeine (3,7-dihydro-1,3,7-trimethyl-1H-purine-2,6-dione) in aqueous media (acetate buffer, pH 4.5) on a boron-doped diamond (BDD) electrode using square wave voltammetry (SWV) or differential pulse voltammetry (DPV). Using DPV with the cathodically pre-treated BDD electrode, a separation of about 550 mV between the peak oxidation potentials of paracetamol and caffeine present in binary mixtures was obtained. The calibration curves for the simultaneous determination of paracetamol and caffeine showed an excellent linear response, ranging from 5.0 x 10(-7)mol L(-1) to 8.3 x 10(-5)mol L(-1) for both compounds. The detection limits for the simultaneous determination of paracetamol and caffeine were 4.9 x 10(-7)mol L(-1) and 3.5 x 10(-8)mol L(-1), respectively. The proposed method was successfully applied in the simultaneous determination of paracetamol and caffeine in several pharmaceutical formulations (tablets), with results similar to those obtained using a high-performance liquid chromatography method (at 95% confidence level).
开发了一种简单且高度选择性的电化学方法,用于在硼掺杂金刚石(BDD)电极上,采用方波伏安法(SWV)或差分脉冲伏安法(DPV),在水介质(pH 4.5的醋酸盐缓冲液)中单独或同时测定对乙酰氨基酚(N - 乙酰 - 对氨基酚,扑热息痛)和咖啡因(3,7 - 二氢 - 1,3,7 - 三甲基 - 1H - 嘌呤 - 2,6 - 二酮)。使用经阴极预处理的BDD电极进行DPV时,二元混合物中对乙酰氨基酚和咖啡因的氧化峰电位之间可获得约550 mV的分离度。同时测定对乙酰氨基酚和咖啡因的校准曲线显示出优异的线性响应,两种化合物的线性范围均为5.0×10⁻⁷ mol L⁻¹至8.3×10⁻⁵ mol L⁻¹。同时测定对乙酰氨基酚和咖啡因的检测限分别为4.9×10⁻⁷ mol L⁻¹和3.5×10⁻⁸ mol L⁻¹。所提出的方法成功应用于几种药物制剂(片剂)中对乙酰氨基酚和咖啡因的同时测定,结果与使用高效液相色谱法获得的结果相似(在95%置信水平)。