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

Marland, Jamie R.K. and Gray, Mark E. and Dunare, Camelia and Blair, Ewen O. and Tsiamis, Andreas and Sullivan, Paul and González-Fernández, Eva and Greenhalgh, Stephen N. and Gregson, Rachael and Clutton, R. Eddie and Parys, Magdalena M. and Dyson, Alex and Singer, Mervyn and Kunkler, Ian H. and Potter, Mark A. and Mitra, Srinjoy and Terry, Jonathan G. and Smith, Stewart and Mount, Andrew R. and Underwood, Ian and Walton, Anthony J. and Argyle, David J. and Murray, Alan F. (2020) Real-time measurement of tumour hypoxia using an implantable microfabricated oxygen sensor. Sensing and Bio-Sensing Research, 30. 100375. (https://doi.org/10.1016/j.sbsr.2020.100375)

[thumbnail of Marland-etal-SBR-2020-Real-time-measurement-of-tumour-hypoxia-using-an-implantable-microfabricated-oxygen-sensor]
Preview
Text. Filename: Marland_etal_SBR_2020_Real_time_measurement_of_tumour_hypoxia_using_an_implantable_microfabricated_oxygen_sensor.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo

Download (3MB)| Preview

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.

ORCID iDs

Marland, Jamie R.K., Gray, Mark E., Dunare, Camelia, Blair, Ewen O. ORCID logoORCID: https://orcid.org/0000-0002-1887-8001, Tsiamis, Andreas, Sullivan, Paul, González-Fernández, Eva, Greenhalgh, Stephen N., Gregson, Rachael, Clutton, R. Eddie, Parys, Magdalena M., Dyson, Alex, Singer, Mervyn, Kunkler, Ian H., Potter, Mark A., Mitra, Srinjoy, Terry, Jonathan G., Smith, Stewart, Mount, Andrew R., Underwood, Ian, Walton, Anthony J., Argyle, David J. and Murray, Alan F.;