@misc{tarazona_relation_between_2020, 
author={Tarazona, N.,Machatschek, R.,Lendlein, A.},
title={Relation between Surface Area and Surface Potential Change during (co)Polyesters Degradation as Langmuir Monolayer},
year={2020},
howpublished = {journal article},
doi = {https://doi.org/10.1557/adv.2019.458},
abstract = {Polyhydroxyalkanoates (PHAs) are degradable (co)polyesters synthesized by microorganisms with a variety of side-chains and co-monomer ratios. PHAs can be efficiently hydrolyzed under alkaline conditions and by PHA depolymerase enzymes, altering their physicochemical properties. Using 2D Langmuir monolayers as model system to study the degradation behavior of macromolecules, we aim to describe the the interdependency between the degradation of two PHAs and the surface potential, which influences material-proteins interaction and cell response. We hypothesize that the mechanism of hydrolysis of the labile ester bonds in (co)polyesters defines the evolution of the surface potential, owing to the rate of accumulation of charged insoluble degradation products. The alkaline hydrolysis and the enzymatically catalyzed hydrolysis of PHAs were previously defined as chain-end scission and random-scission mechanisms, respectively. In this study, these two distinct scenarios are used to validate our model. The surface potential change during the chain-end scission of poly(3-R-hydroxybutyrate) (PHB) under alkaline conditions was compared to that of the enzymatically catalyzed hydrolysis (random-scission) of poly[(3-R-hydroxyoctanoate)-co-(3-R-hydroxyhexanoate)] (PHOHHx), using the Langmuir monolayer technique. In the random-scission mechanism the dissolution of degradation products, measured as a decrease in the area per molecule, was preceded by a substantial change of the surface potential, provoked by the negative charge of the broken ester bonds accumulated in the air-water interface. In contrast, when chains degraded via the chain-ends, the surface potential changed in line with the dissolution of the material, presenting a kinetic dependent on the surface area of the monolayers. These results provide a basis for understanding PHAs degradation mechanism. Future research on (co)polymers with different main-chain lengths might extend the elucidation of the surface potential development of (co)polyesters as Langmuir monolayer.},
note = {Online available at: \url{https://doi.org/10.1557/adv.2019.458} (DOI). Tarazona, N.; Machatschek, R.; Lendlein, A.: Relation between Surface Area and Surface Potential Change during (co)Polyesters Degradation as Langmuir Monolayer. MRS Advances. 2020. vol. 5, no. 11 -12, 667-677. DOI: 10.1557/adv.2019.458}}