姜黄素
过氧化氢
化学
抗氧化剂
前药
萘普生
药理学
生物化学
医学
病理
替代医学
作者
Berwin Singh Swami Vetha,Eunkyeong Jung,Joungyoun Noh,Donghyuck Yoo,Changsun Kang,Hyejin Hyeon,Gi-Wook Kim,Gilson Khang,Dongwon Lee
标识
DOI:10.1016/j.nano.2018.11.003
摘要
Curcumin is a major active phenolic component of turmeric and has gained great attention in pharmaceutics due to its potent antioxidant, anti-inflammatory and anticancer activity. Here, we developed poly(oxalate-co-curcumin) (POC) as a hydrogen peroxide (H2O2)-activatable polymeric prodrug of curcumin by incorporating curcumin in the backbone of H2O2-responsive polyoxalate. POC particles effectively scavenged H2O2 and released curcumin in a H2O2-triggered manner. POC particles exhibited excellent antioxidant and anti-inflammatory activity in activated cells. POC particles intravenously administrated into acetaminophen-intoxicated mice remarkably suppressed the level of alanine transaminase and inhibited apoptotic cell death in liver. Interestingly, POC particles could also enhance the ultrasound contrast in the intoxicated liver due to CO2 bubble generation through H2O2-triggered oxidation of peroxalate esters. Given their H2O2-responsiveness and highly potent antioxidant activity, POC particles hold great translational potential as theranostic agents for H2O2-associated diseases.
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