epr oximetry
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2021 ◽  
Vol 11 ◽  
Author(s):  
Philip E. Schaner ◽  
Benjamin B. Williams ◽  
Eunice Y. Chen ◽  
Jason R. Pettus ◽  
Wilson A. Schreiber ◽  
...  

ObjectiveThe overall objective of this clinical study was to validate an implantable oxygen sensor, called the ‘OxyChip’, as a clinically feasible technology that would allow individualized tumor-oxygen assessments in cancer patients prior to and during hypoxia-modification interventions such as hyperoxygen breathing.MethodsPatients with any solid tumor at ≤3-cm depth from the skin-surface scheduled to undergo surgical resection (with or without neoadjuvant therapy) were considered eligible for the study. The OxyChip was implanted in the tumor and subsequently removed during standard-of-care surgery. Partial pressure of oxygen (pO2) at the implant location was assessed using electron paramagnetic resonance (EPR) oximetry.ResultsTwenty-three cancer patients underwent OxyChip implantation in their tumors. Six patients received neoadjuvant therapy while the OxyChip was implanted. Median implant duration was 30 days (range 4–128 days). Forty-five successful oxygen measurements were made in 15 patients. Baseline pO2 values were variable with overall median 15.7 mmHg (range 0.6–73.1 mmHg); 33% of the values were below 10 mmHg. After hyperoxygenation, the overall median pO2 was 31.8 mmHg (range 1.5–144.6 mmHg). In 83% of the measurements, there was a statistically significant (p ≤ 0.05) response to hyperoxygenation.ConclusionsMeasurement of baseline pO2 and response to hyperoxygenation using EPR oximetry with the OxyChip is clinically feasible in a variety of tumor types. Tumor oxygen at baseline differed significantly among patients. Although most tumors responded to a hyperoxygenation intervention, some were non-responders. These data demonstrated the need for individualized assessment of tumor oxygenation in the context of planned hyperoxygenation interventions to optimize clinical outcomes.


Author(s):  
Paul W. Buehler ◽  
Ann Barry Flood ◽  
Harold M. Swartz

Author(s):  
Eunice Y. Chen ◽  
Dan Tse ◽  
Huagang Hou ◽  
Wilson A. Schreiber ◽  
Philip E. Schaner ◽  
...  
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2021 ◽  
Vol 22 (9) ◽  
pp. 4465
Author(s):  
Krystian Mokrzynski ◽  
Shosuke Ito ◽  
Kazumasa Wakamatsu ◽  
Theodore G. Camenish ◽  
Tadeusz Sarna ◽  
...  

Photoreactivity of melanin has become a major focus of research due to the postulated involvement of the pigment in UVA-induced melanoma. However, most of the hitherto studies were carried out using synthetic melanin models. Thus, photoreactivity of natural melanins is yet to be systematically analyzed. Here, we examined the photoreactive properties of natural melanins isolated from hair samples obtained from donors of different skin phototypes (I, II, III, and V). X-band and W-band electron paramagnetic resonance (EPR) spectroscopy was used to examine the paramagnetic properties of the pigments. Alkaline hydrogen peroxide degradation and hydroiodic acid hydrolysis were used to determine the chemical composition of the melanins. EPR oximetry and spin trapping were used to examine the oxygen photoconsumption and photo-induced formation of superoxide anion, and time-resolved near infrared phosphorescence was employed to determine the singlet oxygen photogeneration by the melanins. The efficiency of superoxide and singlet oxygen photogeneration was related to the chemical composition of the studied melanins. Melanins from blond and chestnut hair (phototypes II and III) exhibited highest photoreactivity of all examined pigments. Moreover, melanins of these phototypes showed highest quantum efficiency of singlet oxygen photogeneration at 332 nm and 365 nm supporting the postulate of the pigment contribution in UVA-induced melanoma.


The Analyst ◽  
2020 ◽  
Vol 145 (14) ◽  
pp. 4964-4971 ◽  
Author(s):  
Xing Wang ◽  
Chao Peng ◽  
Ke He ◽  
Kaiyun Ji ◽  
Xiaoli Tan ◽  
...  

Intracellular delivery of TAM radical CT-03 is achieved using a liposome-based method, enabling simultaneous measurement of the intra/extracellular O2 levels and O2 consumption rates in combination of the extracellular TAM radical CT02-H.


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