Real-time measurement of tumour hypoxia using an implantable microfabricated oxygen sensor

Jamie R. K. Marland(National Microelectronics Institute), Mark Gray(Roslin Institute), Camelia Dunare(National Microelectronics Institute), Ewen O. Blair(National Microelectronics Institute), Andreas Tsiamis(University of Edinburgh), P. J. Sullivan(National Microelectronics Institute), Eva González‐Fernández(University of Edinburgh), Stephen N. Greenhalgh(Roslin Institute), Rachael Gregson(University of Edinburgh), R. Eddie Clutton(Roslin Institute), Magdalena Parys(University of Edinburgh), Alex Dyson(University College London), Mervyn Singer(Bury College), Ian Kunkler(Edinburgh Cancer Research), Mark A. Potter(Western General Hospital), Srinjoy Mitra(University of Edinburgh), Jonathan G. Terry(University of Edinburgh), Stewart Smith(University of Edinburgh), Andrew R. Mount(University of Edinburgh), Ian Underwood(University of Edinburgh), A.J. Walton(University of Edinburgh), David J. Argyle, Alan F. Murray(University of Edinburgh)
Sensing and Bio-Sensing Research
August 11, 2020
Cited by 45Open Access
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Abstract

Hypoxia commonly occurs within tumours and is a major cause of radiotherapy resistance. Clinical outcomes could be improved by locating and selectively increasing the dose delivered to hypoxic regions. Here we describe a miniature implantable sensor for real-time monitoring of tissue oxygenation that could enable this novel treatment approach to be implemented. The sensor uses a solid-state electrochemical cell that was microfabricated at wafer level on a silicon substrate, and includes an integrated reference electrode and electrolyte membrane. It gave a linear response to oxygen concentration, and was unaffected by sterilisation and irradiation, but showed susceptibility to biofouling. Oxygen selectivity was also evaluated against various clinically relevant electroactive compounds. We investigated its robustness and functionality under realistic clinical conditions using a sheep model of lung cancer. The sensor remained functional following CT-guided tumour implantation, and was sufficiently sensitive to track acute changes in oxygenation within tumour tissue.


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