Paul H. Gamache
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Paul H. Gamache has a total of 7 co-authors. Here are the top co-authors by number of shared publications:
Douglas R. McCabe
1 shared publicationHasan Parvez
1 shared publicationIan N. Acworth
1 shared publicationRuben Pawellek
University of Würzburg, Institute for Pharmacy and Food Chemistry, 97074 Würzburg, Germany
1 shared publicationSimone Parvez
1 shared publication- Tibor Muellner
Thermo Fisher Scientific, 82110 Germering, Germany
1 shared publication
Latest Publications
- 18 January 2024
- Published by Taylor & Francis
- p. 99-126
The Measurement of Markers of Oxidative Damage, Anti-Oxidants and Related Compounds Using HPLC and Coulometric Array Analysis
The old adage “moderation in all things” is perhaps best demonstrated by the toxicity of pure oxygen. Although it is obvious that oxygen is essential for life (at least for aerobic organisms), breathing pure oxygen at atmospheric pressure for longer than 48 hours will lead to respiratory distress and death (Huber and Drath, 1981). This toxicity is not due entirely to oxygen per se but more to the production of a variety of reactive oxygen species (ROS). Several ROS exist. Diatomic molecular oxygen (O2) readily reacts to form partially reduced species, which are generally short-lived and highly reactive and include the superoxide anion (O2), the hydroperoxyl radical (HO2’) as well as the most reactive species, the hydroxyl free radical (HO’). ROS are produced as part of normal metabolism (e.g. superoxide is formed when xanthine is converted to uric acid by xanthine oxidase) and are also extremely useful (e.g. superoxide and hydrogen peroxide are the major “microbicides” produced by circulating phagocytic leukocytes) (Johnston et al., 1975; Babior, 1978; Colton and Gilbert, 1987; Green et al., 1987). Furthermore, the effectiveness of certain anticancer drugs is also dependent on their ability to produce free radicals (Kehrer, 1993).
- 18 January 2024
- Published by Taylor & Francis
- p. 99-126
The Measurement of Markers of Oxidative Damage, Anti-Oxidants and Related Compounds Using HPLC and Coulometric Array Analysis
The old adage “moderation in all things” is perhaps best demonstrated by the toxicity of pure oxygen. Although it is obvious that oxygen is essential for life (at least for aerobic organisms), breathing pure oxygen at atmospheric pressure for longer than 48 hours will lead to respiratory distress and death (Huber and Drath, 1981). This toxicity is not due entirely to oxygen per se but more to the production of a variety of reactive oxygen species (ROS). Several ROS exist. Diatomic molecular oxygen (O2) readily reacts to form partially reduced species, which are generally short-lived and highly reactive and include the superoxide anion (O2), the hydroperoxyl radical (HO2’) as well as the most reactive species, the hydroxyl free radical (HO’). ROS are produced as part of normal metabolism (e.g. superoxide is formed when xanthine is converted to uric acid by xanthine oxidase) and are also extremely useful (e.g. superoxide and hydrogen peroxide are the major “microbicides” produced by circulating phagocytic leukocytes) (Johnston et al., 1975; Babior, 1978; Colton and Gilbert, 1987; Green et al., 1987). Furthermore, the effectiveness of certain anticancer drugs is also dependent on their ability to produce free radicals (Kehrer, 1993).
- 1 January 2021
- Published by Elsevier in Journal of Chromatography A
- Vol. 1637, 461844
Power function setting in charged aerosol detection for the linearization of detector response – optimization strategies and their application
- 1 January 2021
- Published by Elsevier in Journal of Chromatography A
- Vol. 1637, 461844
Power function setting in charged aerosol detection for the linearization of detector response – optimization strategies and their application