Circuits design and nano-structured electrodes for drugs monitoring in personalized therapy

S. Carrara, A. Cavallini, G. De Micheli, V. Shumyantseva, A. Archakov, J. Olivo, L. Benini
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引用次数: 5

Abstract

Drug development and personalized therapy require accurate and frequent monitoring of the metabolic response by living tissues to treatments. In case of high risk side effects, e.g. therapies with interfering anti-cancer molecule cocktails, direct monitoring of the patientpsilas drugs metabolism is essential as the metabolic pathways efficacy is highly variable on a patient-by-patient basis. Currently, there are no fully mature point-of-care bio-sensing systems for drugs metabolism monitoring directly in blood. The aim of the paper is to investigate solutions to develop point-of-care systems for drugs monitoring in personalized therapy. P450 enzymes are the considered probe molecules as they are key proteins directly involved in drugs metabolism of humans. Sensitivity improvement is ensured by means of enzyme integration onto electrodes structured with carbon nanotubes. Component Off-The-Shelf (COTS) based circuits design is investigated toward bio-chip development. Results show that the proposed circuitry is suitable for the aim and confirm that nanotubes are detection enhancers.
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个性化治疗中药物监测的电路设计和纳米结构电极
药物开发和个性化治疗需要准确和频繁地监测活组织对治疗的代谢反应。在高风险副作用的情况下,例如使用干扰抗癌分子鸡尾酒治疗,直接监测患者体内药物代谢是必不可少的,因为代谢途径的功效在每个患者的基础上都是高度可变的。目前,还没有完全成熟的即时生物传感系统用于直接监测血液中的药物代谢。本文的目的是研究解决方案,以开发点护理系统的药物监测个性化治疗。P450酶是直接参与人体药物代谢的关键蛋白,被认为是探针分子。通过将酶整合到碳纳米管结构的电极上,确保了灵敏度的提高。研究了面向生物芯片开发的基于元器件现货(COTS)的电路设计。实验结果表明,所提出的电路符合目标,并证实了纳米管是检测增强器。
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