Fabrication and Sustained Release of Chlorogenic Acid from Poly(vinyl alcohol)/Poly(γ-glutamic Acid) Blends Electrospun Mats

Autor: R. Torres-Lubian, C. Alvaro-Canche, I. E. Sandova-Herrera, A. De-León, A. Ledezma-Pérez, J. Romero-García
Rok vydání: 2020
Předmět:
Popis: Background: Diabetic foot is a condition that is caused by high levels of glucose in the blood. Poly (γ-glutamic acid) [γ-PGA]/polyvinyl alcohol [PVA] electrospun biopolymers and their use in the release of chlorogenic acid (CGA) is a promising system, thanks to their biocompatibility and the use of (CGA) in the treatment of certain symptoms of diabetic conditions. The use of CGA was reported in 2005 as a capable substance in the treatment of lesions caused by diabetic foot ulcers, thanks to the fact that it has no toxic effects.Methods: In this work, was carried out the bio-synthesis of γ-PGA producing by the Bacillus liqueniformis ATCC-9945a. This material was utilized in the preparation of electrospun nanofibers with solutions of polyvinyl alcohol [PVA] to 10% p/v mixed with γ-PGA to 5 and 10% p/v. These solutions were loaded with chlorogenic acid (CGA) like an active hypoglycemic agent.Results: The morphological analysis shows a size decrease for the fiber with PVA/ γ -PGA, compared to PVA nanofibers; this could be attributed to the hydrogen bonding interactions between γ-PGA and PVA. The use of glutaraldehyde vapors permit the nanofibers crosslinking to maintain a stable structure and allows the CGA release. The in vitro release analysis shows that the PVA membranes reach 28% of delivery after the first 24 hours. Instead of, for the nanofiber mat with PVA blended with γ-PGA at 5% goes up to 57% and nanofiber PVA/γ-PGA at 10% reach to 66% in the same time, the rate constant for release kinetics shows that PVA/γ-PGA at 5% it's higher than the others, being the first in reach the saturation.Conclusions: Biodegradable polymer meshes were fabricated by electrospinning of PVA and PVA/γ-PGA polymer and loaded with CGA. The presence of γ-PGA into PVA solutions increases the in vitro drug release from electrospun fiber mats. The maximal release of CGA was reached at 10% of γ-PGA introduced in the PVA solution, which was 82% release from the electrospun polymer fiber mats. Finally, the use of Peppas and Weibull models indicates the released kinetics of CGA from PVA, PVA/γ-PGA 5, and PVA/γ-PGA 10 electrospun fiber mats are driven by diffusion mechanism.
Databáze: OpenAIRE