Reactive oxygen species (ROS) play an important role in the pathogenesis of a variety of diseases or pathological processes, including various forms of cancer, type 2 diabetes, atherosclerosis, chronic inflammation, ischemia/reperfusion injury, sepsis, and some neurodegenerative diseases. Mitochondria are a major intracellular source of ROS under pathological conditions and there is increasing interest in the concept of developing mitochondria-targeted antioxidants as therapeutic agents. However many of the most extensively studied compounds fail to localize within the mitochondria or even enter the intracellular environment.
The most common approach to targeting compounds to mitochondria is to exploit the potential gradient of the inner mitochondrial membrane, which causes the matrix side of the membrane to be negatively charged. Due to the electrolysis of the inner membrane, lipophilic cations tend to accumulate within the mitochondrial matrix. As a leader in the field of cellular stress, Creative Bioarray can provide our customers with solutions for the development and evaluation of lipophilic cation-based antioxidants.
Oxidants such as vitamin E, panthenol, and N-acetylcysteine have been shown to reduce mitochondrial oxidative damage, but their effectiveness is limited by the fact that these compounds do not accumulate within the mitochondria.
To develop antioxidants that target mitochondria, we attached antioxidants to lipophilic cations. The lipophilic cations should deliver their attached antioxidants to the mitochondria, thereby preventing mitochondrial oxidative damage.
Antioxidants attached to lipophilic cations accumulate rapidly through isolated mitochondria and intracellular mitochondria. Importantly, due to this selective accumulation, the targeted antioxidants protect mitochondrial function from oxidative damage more effectively than by themselves.
We customize the appropriate synthesis according to the client's target antioxidants (vitamin E, panthenol and N-acetylcysteine, etc.). Accumulation of antioxidants by isolated mitochondria.
Incubate mitochondria with targeted antioxidants to verify their role in preventing oxidative damage and reducing lipid peroxidation (thiobarbituric acid reactive substances) and protein damage (protein carbonyl compounds).
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