Improved oral delivery of insulin by PLGA nanoparticles coated with 5β-cholanic acid conjugated glycol chitosan.
Weizhi WangChenggong YuFangfang ZhangYuxuan LiBo ZhangJie HuangZhijun ZhangLiang JinPublished in: Biomedical materials (Bristol, England) (2021)
Oral insulin has been regarded as the best alternative to insulin injection in therapy of diabetes because of its convenience and painlessness. However, several obstacles in the gastrointestinal tract, such as gastric acid and enzyme, greatly reduce the bioavailability of oral insulin. Herein, we report design and preparation of poly (d, l-lactic-co-glycolic acid) nanoparticles (PLGA NPs) coated with 5β-cholanic acid modified glycol chitosan (GC-CA) (GC-CA@PLGA NPs) to improve the oral delivery of insulin. The GC-CA@PLGA NPs with the size of (302.73 ± 5.13 nm) and zeta potential of (25.03 ± 0.31 mV) were synthesized using the double-emulsion method. The insulin-loading capacity and encapsulation efficiency were determined to be 5.77 ± 0.58% and 51.99 ± 5.27%, respectively. Compared with GC-modified PLGA NPs (GC@PLGA NPs) and bare PLGA NPs, the GC-CA@PLGA NPs showed excellent stability and uptake by Caco-2 cells after simulated gastric acid digestion. Further experiment suggests good biocompatibility of GC-CA@PLGA NPs, including hemolysis and cytotoxicity. Inin vivoexperiment, the insulin loaded in the GC-CA@PLGA NPs exhibited a long-term and stable release profile for lowering blood glucose and presented 30.43% bioavailability in oral administration. In brief, we have developed an efficient and safe drug delivery system, GC-CA@PLGA NPs, for significantly improved oral administration of insulin, which may find potential application in the treatment of diabetes.
Keyphrases
- drug delivery
- type diabetes
- glycemic control
- drug release
- blood glucose
- oxide nanoparticles
- bone regeneration
- cancer therapy
- gas chromatography
- cardiovascular disease
- mass spectrometry
- adipose tissue
- weight loss
- oxidative stress
- insulin resistance
- photodynamic therapy
- mesenchymal stem cells
- skeletal muscle
- blood pressure
- cell death
- tandem mass spectrometry
- stem cells
- climate change
- liquid chromatography
- wound healing