Oral Ionic Liquid for Transdermal Delivery and Obesity Treatment.
Beibei LuChengyu WuJichuan ZhangJianglin ZhangJiaheng ZhangPublished in: ACS biomaterials science & engineering (2023)
Obesity is currently a prerequisite for more than 70% of adults, including chronic obesity and long-term obesity. With the increase of diabetes patients in the world, it is urgent to develop effective oral drugs to replace insulin. However, the gastrointestinal tract is a main obstacle to oral drug preparations. Here, a highly effective oral drug was developed, mainly formulated as an ionic liquid (IL) prepared by l-(-)-carnitine and geranic acid. Density functional theory (DFT) calculations showed that l-(-)-carnitine and geranic acid can exist stably through hydrogen bonding. IL can significantly enhance the transdermal transport of drugs. In vitro study of intestinal permeability showed that particles formed by IL can prevent the absorption of intestinal fat. Compared with the control group, oral administration of IL (10 mL kg -1 ) significantly reduced blood glucose, white adipose tissue in the liver and epididymis, and the expression of SREBP-1c and ACC in IL. Therefore, these results and high-throughput sequencing analysis showed that IL can effectively reduce the intestinal absorption of adipose tissue to reduce blood glucose. IL has good biocompatibility and stability. Therefore, IL has a certain application value in the field of oral drug-delivery carriers, which provides an effective means for the treatment of diabetes and is a potential tool to solve the epidemic of obesity.
Keyphrases
- type diabetes
- insulin resistance
- blood glucose
- adipose tissue
- ionic liquid
- density functional theory
- metabolic syndrome
- glycemic control
- weight loss
- high fat diet induced
- drug delivery
- cardiovascular disease
- weight gain
- emergency department
- room temperature
- molecular dynamics
- climate change
- newly diagnosed
- ejection fraction
- end stage renal disease
- risk assessment
- molecular docking
- skeletal muscle
- adverse drug
- molecular dynamics simulations
- body mass index
- high throughput sequencing
- binding protein
- fatty acid
- drug release