Prevent Drug Leakage via the Boronic Acid Glucose-Insensitive Micelle for Alzheimer's Disease Combination Treatment.
Jian RenHaodong HuShaoteng WangYang HeYanhong JiYiran ChenKangna WangHaiyan ZhangYiping ZhaoFengying DaiPublished in: ACS applied materials & interfaces (2022)
Boronic acid (BA) materials have been widely applied to glucose and oxidative stress-sensitive drug delivery for the treatment of cancer, diabetes, and Alzheimer's disease (AD). There are completely various BA-sensitive delivery conditions in different diseases. BA materials in the treatment of diabetes show better performance at a high-glucose environment than normal. In contrast, the concentration of glucose in the brain is much lower than that in the blood of AD patients. Hence, the typical glucose and oxidative stress dual-sensitive BA materials inevitably encounter drug leakage in circulation in AD. Attempts to decrease the glucose-sensitive capacity of BA materials are extremely essential for AD drug delivery. In this study, the epoxy group (electron-donating group) was introduced to increase the p K a values of BA materials by increasing the electron cloud density, and thus, the glucose-insensitive micelle (GIM) was obtained. The treatment effect and the synergism mechanism of the drug-loaded GIM micelle were studied on senescence-accelerated mouse prone 8 mice. This work provided excellent antioxidant drugs (vitamin E succinate, melatonin, and quercetin) and a glucose metabolism drug (insulin) loaded in GIM micelle for AD treatment. The discovery of the combination mechanism is enormously valuable for AD clinical research.
Keyphrases
- drug delivery
- oxidative stress
- type diabetes
- blood glucose
- endothelial cells
- dna damage
- computed tomography
- cancer therapy
- emergency department
- end stage renal disease
- small molecule
- newly diagnosed
- high glucose
- skeletal muscle
- ischemia reperfusion injury
- peritoneal dialysis
- white matter
- cognitive decline
- young adults
- mild cognitive impairment
- wound healing
- high throughput
- drug release