Docherty Niamh, Macdonald Daniel, Gordon Alisdair, Dobrea Alexandra, Mani Veerappan, Fu Ying, Pang Susan, Jimenez Melanie, Corrigan Damion K
Centre for Advanced Measurement Science and Health Translation, Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, G1 1XL, UK.
Wolfson Centre, Department of Biomedical Engineering, University of Strathclyde, Glasgow, G4 0NS, UK.
Chem Commun (Camb). 2025 Aug 15. doi: 10.1039/d5cc02322j.
Extensive academic attention has been given to showcasing the potential high-level analytical performance of electrochemical and microfluidic diagnostic platforms across a range of target analytes and disease areas. Despite this high volume of research and proof of concept demonstrations for feasible technology platforms, electrochemical biosensors have not yet realised their full commercial potential, given the well-known advantages of low cost, high analytical sensitivity, ease of multiplexing, compatibility with mass manufacturing techniques and seamless connection to smartphones. This is often not because of limitations in analytical performance, but due to challenges in translating laboratory devices into usable, scalable, and accessible systems. Many commercialised point of care (POC) platforms have struggled to integrate effectively into real-world, low-resource clinical environments, underscoring the need for more holistic development strategies. After providing some background on state-of-the-art developments, this article offers a perspective on the major barriers to successful translation for academic research teams through a discussion of the key elements of the biosensor development and translation process. This feature article highlights the importance of the voice of the user, and the iterative research and development process which cycles through stages of innovation, user requirement consideration, analytical performance determination and ensuring the platform is accessible in a POC format. Recent advances in electrode fabrication, 3D printing, and laser ablation empower academic teams to rapidly prototype for practical application. The article intends to serve as a useful guide for those initiating new fundamental electrochemical sensing studies, highlighting recent literature and recommending steps that academic teams can take at the beginning of projects to maximise the chances of future translational success.
学术界广泛关注展示电化学和微流控诊断平台在一系列目标分析物和疾病领域的潜在高水平分析性能。尽管针对可行技术平台进行了大量研究和概念验证演示,但考虑到低成本、高分析灵敏度、易于多路复用、与大规模制造技术的兼容性以及与智能手机的无缝连接等众所周知的优势,电化学生物传感器尚未充分实现其商业潜力。这往往不是因为分析性能的限制,而是由于将实验室设备转化为可用、可扩展且可及的系统面临挑战。许多商业化的即时检测(POC)平台难以有效融入现实世界、资源匮乏的临床环境,这凸显了更全面发展策略的必要性。在介绍了一些最新进展的背景之后,本文通过讨论生物传感器开发和转化过程的关键要素,对学术研究团队成功转化的主要障碍提出了一种观点。这篇专题文章强调了用户声音的重要性,以及通过创新、用户需求考虑、分析性能确定以及确保平台以POC形式可及等阶段循环的迭代研发过程。电极制造、3D打印和激光烧蚀的最新进展使学术团队能够快速制作实际应用的原型。本文旨在为那些启动新的基础电化学传感研究的人员提供有用的指导,突出近期文献并推荐学术团队在项目开始时可以采取的步骤,以最大限度地提高未来转化成功的机会。