“…The potential limitation of providing data from one site and not providing information on oxygen distribution in the entire tissue may be mitigated using multiple implants to assess heterogeneity of oxygen (57,62), or by combining EPR oximetry with volumetric methods of oxygen assessment (63)(64)(65). The operational frequency, approximately 1,150 MHz, of the current EPR scanner limits the use of the OxyChip to superficial tumors; however, this limitation can be overcome using implantable resonators containing OxyChip-like sensors (66,67) or low-frequency and pulse EPR methods (68)(69)(70)(71). Potential improvements in the future could also include the use of other clinical imaging modalities in addition to ultrasound, e.g., CT or PET, to improve both the precision of implantation and visualization of the implant in the tumor during treatment and pO 2 measurements (72).…”