Oral empagliflozin-loaded tri-layer core-sheath fibers fabricated using tri-axial electrospinning: Enhanced <i>in vitro</i> and <i>in vivo</i> antidiabetic performance
Oluşturanlar
- 1. Marmara Univ, Fac Pharm, Dept Pharmacol, TR-34854 Istanbul, Turkiye
- 2. Marmara Univ, Fac Pharm, Dept Pharmaceut Chem, TR-34854 Istanbul, Turkiye
- 3. Kocaeli Univ, Med Fac, Stem Cell & Gene Therapies Res & Appl Ctr, TR-41380 Kocaeli, Turkiye
- 4. UCL, Royal Free Hosp Campus, UCL Div Surg & Intervent Sci, Rowland Hill St, London NW3 2PF, England
Açıklama
Empagliflozin (EM) was successfully loaded in polycaprolactone/poly (L-lactic acid)/polymethyl methacrylate (PCL/PLA/PMMA) fibers. In the rat beta-cell line (BRIN-BD11), the insulin expression ratio of pancreatic beta-cells was stimulated at high and low glucose by culturing with tri-layer EM-loaded fiber (EMF) for 48 h. The expression ratios of glucokinase and GLUT-2 proteins increased after EMF treatment. According to the in vitro drug release test, 97% of all drug contained in fibers was released in a controlled manner for 24 h. The pharmacokinetic test revealed that the bioavailability was improved similar to 4.8-fold with EMF treatment compared to EM-powder and blood glucose level was effectively controlled for 24 h with EMF. Oral administration of EMF exhibited a better sustainable anti-diabetic activity even in the half-dosage than EM-powder in streptozotocin/nicotinamide-induced T2DM rats. The levels of GLP-1, PPAR-gamma, and insulin were increased while the levels of SGLT-2 and TNF-alpha were decreased with EMF treatment. Also, EMF recovered the histopathological changes in the liver, pancreas, and kidney in T2DM rats and protected pancreatic beta-cells. Consequently, EMF is suggested as an un-precedented and promotive treatment approach for T2DM with a higher bioavailability and better antidiabetic effect compared to conventional dosage forms.
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