Molecular basis of scavenging effect of zonisamide on hydroxyl radical in vitro
Ken‐ichi Tanaka, Takeshi Nanba, Tomoyuki Furubayashi, Yasuko Noda, Luther James Willmore, Akitane Mori
Abstract
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Ken‐ichi Tanaka, Takeshi Nanba, Tomoyuki Furubayashi, Yasuko Noda, Luther James Willmore, Akitane Mori
Abstract
Open-access reader
Zonisamide (ZNS), a commonly used anticonvulsant, scavenged hydroxyl radicals at a clinically relevant concentration. Reactants of ZNS with hydrogen peroxide and with hydrogen peroxide plus UV irradiation, yielding hydroxyl radicals, were analyzed by the LC/MS technique. Many small fragments were found in the both reactions, suggesting that ZNS was decomposed not only by hydroxyl radicals but also by hydrogen peroxide. Furthermore, mass-fragment-grams showed that m/z: 213 (ZNS itself) was decreased markedly and m/z: 118 (may be a decomposed product by ring cleavage of ZNS) was detected specifically by treatment with hydroxyl radical. These data suggested that ZNS may react directly with free radicals.
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Zonisamide (ZNS), a commonly used anticonvulsant, scavenged hydroxyl radicals at a clinically relevant concentration. Reactants of ZNS with hydrogen peroxide and with hydrogen peroxide plus UV irradiation, yielding hydroxyl radicals, were analyzed by the LC/MS technique. Many small fragments were found in the both reactions, suggesting that ZNS was decomposed not only by hydroxyl radicals but also by hydrogen peroxide. Furthermore, mass-fragment-grams showed that m/z: 213 (ZNS itself) was decreased markedly and m/z: 118 (may be a decomposed product by ring cleavage of ZNS) was detected specifically by treatment with hydroxyl radical. These data suggested that ZNS may react directly with free radicals.
Key concepts: Radical, Chemistry, Hydroxyl radical, Hydrogen peroxide, Scavenging, Photochemistry, Medicinal chemistry, Zonisamide