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Enzymatic and Nonenzymatic Electrochemical Interactionof Abiraterone (Antiprostate Cancer Drug) with Multiwalled CarbonNanotube Bioelectrodes

机译:酶和非酶电化学相互作用壁碳的阿比特龙(抗前列腺癌药物)的研究纳米管生物电极

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摘要

Unexplored electrochemical behavior of abiraterone, a recent and widely used prostate cancer drug, in interaction with cytochrome P450 3A4 (CYP3A4) enzyme and multiwalled carbon nanotubes (MWCNTs) is investigated in this work. The results reported in this work are significant for personalized medicine and point-of-care chemical treatment, especially to improve the life expectancy and quality of life of patients with prostate-cancer. To this purpose, enzymatic and nonenzymatic electrochemical biosensors were developed and characterized with different concentrations of abiraterone. Nonenzymatic biosensors were functionalized with MWCNTs as a catalyst for signal enhancement, while enzymatic biosensors have been obtained with CYP3A4 protein immobilized on MWCNTs as recognition biomolecule. Enzymatic electrochemical experiments demonstrated an inhibition effect on the CYP3A4, clearly observed as a diminished electrocatalytic activity of the enzyme. Electrochemical responses of nonenzymatic biosensors clearly demonstrated the direct electroactivity of abiraterone when reacting with MWCNT as well as an electrode-foulingeffect.
机译:在这项工作中,研究了一种新近广泛使用的前列腺癌药物阿比特龙与细胞色素P450 3A4(CYP3A4)酶和多壁碳纳米管(MWCNTs)相互作用的未探索的电化学行为。这项工作报告的结果对于个性化医学和即时护理化学治疗具有重要意义,特别是对于提高前列腺癌患者的预期寿命和生活质量而言。为此,开发了酶促和非酶促电化学生物传感器,并用不同浓度的阿比特龙进行了表征。非酶生物传感器功能化了碳纳米管作为信号增强的催化剂,而酶生物传感器已经获得了CYP3A4蛋白固定在碳纳米管上作为识别生物分子。酶促电化学实验表明对CYP3A4有抑制作用,清楚地观察到该酶的电催化活性降低。非酶生物传感器的电化学反应清楚地证明了阿比特龙与MWCNT反应时的直接电活性以及电极结垢影响。

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