Diabetes mellitus is one of the major global public health problems. A large body of recent evidence suggests that imbalance in cellular redox status leads to oxidative stress in pancreatic β-cells and promotes the development of diabetes and related complications. Dietary antioxidants, such as curcumin, have been shown to have therapeutic effects in diabetes. However, these antioxidants have poor solubility, permeability and stability in conventional delivery systems, ultimately leading to their poor oral bioavailability.
Solid lipid nanoparticles (SLN) are a novel drug delivery system being developed in recent years, which combines the advantages of drug-containing microemulsions and liposomes as drug carriers, allowing for improved bioavailability, good physiological compatibility, controlled drug release and good targeting.
As a specialist in cellular stress, Creative Bioarray uses solid natural lipids as carriers to encapsulate antioxidants promising for the treatment of diabetes in lipid-like nuclei. This strategy significantly improves the oral bioavailability of antioxidants and provides the basis for the development of antioxidant drugs for the treatment of diabetes.
The prescribed amount of antioxidant, glycerol monostearate and lecithin were dissolved in a certain amount of dichloromethane, and the solvent was recovered under reduced pressure to make the film-forming material form a uniform film on the wall of the flask. Another polysorbate solution was taken and placed in the film-forming flask, and the film was eluted by rotation, and the antioxidant-liposome suspension system was obtained by ultrasonic treatment, and stored at 4℃ for backup.
Determination of antioxidants in liposomal particles by UV spectrophotometry
Determination of drug loading and encapsulation rate
Antioxidant-SLN particle size and zeta potential investigation
Establish mouse models of diabetes or other related diseases. Grouped oral antioxidant/carrier-liposome dosing to assess
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