Dogan-Topal Burcu, Uslu Bengi, Ozkan Sibel A
Ankara University, Faculty of Pharmacy, Department of Analytical Chemistry, 06100, Tandogan, Ankara, Turkey.
Biosens Bioelectron. 2009 Apr 15;24(8):2358-64. doi: 10.1016/j.bios.2008.12.005. Epub 2008 Dec 9.
The interaction of Efavirenz (EFV) with fish sperm dsDNA immobilized onto pencil graphite electrode (PGE) has been studied by using differential pulse voltammetric technique using an electrochemical DNA biosensor. The guanine signal was lower with (double stranded-DNA) dsDNA-treated PGE than the untreated electrode after the interaction with EFV occurred. The changes in the experimental parameters such as the accumulation time and the concentration of EFV were also studied. All necessary parameters such as sensitivity, selectivity, accuracy and precision were calculated. In addition, the detection and determination limits, reproducibility and applicability of the analysis to pharmaceutical dosage forms were also investigated. These results showed that this DNA biosensor could be used for the sensitive, rapid simple and cost effective detection and determination of EFV-dsDNA interaction. The linearity was between 2 and 24 ppm of EFV concentration on guanine signal decreasing curve. EFV showed an irreversible oxidation behavior at all investigated pH values. This oxidation step was adsorption controlled on PGE. Hence, differential pulse adsorptive stripping (AdsDPV) voltammetric method was developed for the determination of EFV. Accumulation time and potential were optimized. Under these conditions, the current showed a linear dependence with concentration in the range between 0.018 and 2.56 ppm. Both determination methods were fully validated and applied for the analysis of EFV pharmaceutical dosage form.
采用电化学DNA生物传感器,运用差分脉冲伏安法研究了依非韦伦(EFV)与固定在铅笔石墨电极(PGE)上的鱼精双链DNA(dsDNA)的相互作用。与EFV相互作用后,经dsDNA处理的PGE上鸟嘌呤信号低于未处理电极上的信号。还研究了诸如富集时间和EFV浓度等实验参数的变化。计算了灵敏度、选择性、准确度和精密度等所有必要参数。此外,还研究了检测限、测定限、重现性以及该分析方法对药物剂型的适用性。这些结果表明,这种DNA生物传感器可用于灵敏、快速、简单且经济高效地检测和测定EFV与dsDNA的相互作用。在鸟嘌呤信号降低曲线上,EFV浓度在2至24 ppm之间呈线性关系。在所有研究的pH值下,EFV均表现出不可逆的氧化行为。此氧化步骤在PGE上受吸附控制。因此,开发了差分脉冲吸附溶出伏安法(AdsDPV)来测定EFV。对富集时间和电位进行了优化。在这些条件下,电流与浓度在0.018至2.56 ppm范围内呈线性关系。两种测定方法均经过充分验证,并应用于EFV药物剂型的分析。