Reactive oxygen species (ROS) is known to play a variety of roles at many important event opportunities in vivo. However, overproduction of ROS causes serious adverse side effects in the body. Many drugs have been applied to reduce excessively produced ROS. However, low molecular weight (LMW) antioxidants spread nonspecifically to the whole body and are internalized in healthy cells. Since the organism acquires energy via the mitochondrial electron transport chain, such LMW antioxidants suppress this type of normal redox reaction and cause severe damage to normal organs and the body. In order to improve selective antioxidant properties in vivo, we started to focus on novel design of effective antioxidant drugs. Our concept of drug design is to avoid side effects such as inevitable toxicity of small molecules and to create safe and effective drugs by molecular assembly. To create this concept, we synthesized a redox amphiphilic block copolymer, forms self-assembling nanoparticles in an aqueous media. Our idea is to prevent mitochondrial damage of healthy cells by preventing cellular uptake by self-assembly structure of antioxidant. The nitroxide radical, which is one of the strongest antioxidants, covalently conjugated as a side chain of the hydrophobic segment in the block copolymer were compartmentalized into the solid core of the nano-drug and was named nitroxide radical containing nanoparticles (RNPN). Because RNPN is hardly incorporated into healthy cells, unlike LMW antioxidants, its in vivo toxicity has become extremely low. Since RNPN has pH-sensitive disassembling properties, it collapse at pH-reducing tumors and sites of inflammation. We have confirmed that this particle can be applied for versatile oxidative stress related diseases such as cerebral, renal and myocardial ischemia reperfusion injuries, cerebral hemorrhage, cancer, ulcerative colitis and Alzheimer's disease and it is promising as a novel antioxidant self-assembling nanodrugs.

Self-assembling nanodrugs for novel antioxidant therapeutics

2019 Spring National Meeting

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