by Keyword: enzymatic degradation
Gutierrez, PAH, Colombi, S, Casanovas, J, Resina, L, Sans, J, Engel, E, Enshaei, H, García-Torres, J, Pérez-Madrigal, MM, Alemán, C, (2025). Engineering Poly(lactic Acid)-Based Scaffolds for Abundant, Sustained, and Prolonged Lactate Release Acs Polymers Au ,
Recent studies have revealed that cardiac tissue regeneration is promoted by administering an initial dose of exogenous lactate and locally maintaining an abundant concentration of this compound for a prolonged period (i.e., around 10-14 days) through sustained release. The aim of this study is to develop a scaffold based on poly(lactic acid) (PLA) for achieving a sustained daily release of lactate from the first day to the end of the recommended period. First, a five-layered electroresponsive scaffold has been engineered using three PLA layers (first, third, and fifth), each composed of electrospun microfibers (MFs), separated by spin coated lactate (second) and poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) (fourth) intermediate layers. The hydrophobicity of the outer PLA layers (first and fifth) has been used to maintain the release of lactate from the intermediate second layer over 3 days, while the conducting fourth PEDOT:PSS layer has ensured a complete lactate release by electrostimulation. After that, in a second step, the same scaffold has been re-engineered to maintain the sustained release not only for a short period (3 days) but also for a prolonged period (>10 days). For this purpose, the PLA MFs of the intermediate third layer have been substituted by plasma-treated proteinase K-containing PLA MFs, obtained by electrospinning a PLA:enzyme mixture. The activity of the enzyme, which decomposes the ester bonds of PLA, combined with the effect of the plasma on the PLA structure, results in a prolonged sustained release that, in addition, can be modulated.
JTD Keywords: 4-ethylenedioxythiophene), Cardiac tissue regeneratio, Conducting polymer, Drug-release, Electroresponsivescaffolds, Electrospinning, Energy, Enzymatic degradation, Hydrogel, Nanofibers, Poly(3, Poly(lactic acid), Raman-spectroscopy
Keridou, I, Franco, L, del Valle, LJ, Martínez, JC, Funk, L, Turon, P, Puiggalí, J, (2021). Hydrolytic and enzymatic degradation of biobased poly(4-hydroxybutyrate) films. Selective etching of spherulites Polymer Degradation And Stability 183, 109451
© 2020 Hydrolytic degradation of poly(4-hydroxybutyrate) (P4HB) films has been studied considering media of different pH values (i.e., 3, 7 and 10) and temperatures (i.e., 37 and 55 °C). Enzymatic degradation has also been evaluated at physiological conditions using two different lipases: Pseudomonas cepacia and Rhizopus oryzae. Different bulk and surface erosion mechanisms with random chain scissions and successive removal of monomer units have been supported through weight loss measurements, molecular weight determinations by GPC and NMR spectroscopy and changes on thermal properties by DSC. Thermal annealing during exposure to different media and even degradation influenced on the melting temperature and crystallinity of samples, as well as on the lamellar geometrical parameters as evaluated by SAXS. Enzymatic degradation was ideal to selectively eliminate the amorphous regions and highlight the spherulitic morphology. Presence of ringed textures were therefore evident in bright field optical micrographs in addition to SEM images, namely observations under polarized light was not necessary to distinguish the presence of banded spherulites. Rhizopus oryzae was revealed to be the most suitable enzyme to crop out the P4HB spherulites that form part of the initial smooth surfaces of solvent casting films. After determining the appropriate activity and exposure time, the presence of rings constituted by cooperative C-shaped edge-on lamellae and flat-on lamellae was highlighted.
JTD Keywords: biodegradable polymers, enzymatic degradation, films, hydrolytic degradation, microstructure, thermal properties, Biodegradable polymers, Enzymatic degradation, Films, Hydrolytic degradation, Microstructure, Poly(4-hydroxybutyrate), Thermal properties