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Tuning the Degradation Profiles of Poly(l-lactide)-Based Materials through Miscibility

[Image: see text] The effective use of biodegradable polymers relies on the ability to control the onset of and time needed for degradation. Preferably, the material properties should be retained throughout the intended time frame, and the material should degrade in a rapid and controlled manner aft...

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Autores principales: Arias, Veluska, Höglund, Anders, Odelius, Karin, Albertsson, Ann-Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892759/
https://www.ncbi.nlm.nih.gov/pubmed/24279455
http://dx.doi.org/10.1021/bm401667b
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author Arias, Veluska
Höglund, Anders
Odelius, Karin
Albertsson, Ann-Christine
author_facet Arias, Veluska
Höglund, Anders
Odelius, Karin
Albertsson, Ann-Christine
author_sort Arias, Veluska
collection PubMed
description [Image: see text] The effective use of biodegradable polymers relies on the ability to control the onset of and time needed for degradation. Preferably, the material properties should be retained throughout the intended time frame, and the material should degrade in a rapid and controlled manner afterward. The degradation profiles of polyester materials were controlled through their miscibility. Systems composed of PLLA blended with poly[(R,S)-3-hydroxybutyrate] (a-PHB) and polypropylene adipate (PPA) with various molar masses were prepared through extrusion. Three different systems were used: miscible (PLLA/a-PHB5 and PLLA/a-PHB20), partially miscible (PLLA/PPA5/comp and PLLA/PPA20/comp), and immiscible (PLLA/PPA5 and PLLA/PPA20) blends. These blends and their respective homopolymers were hydrolytically degraded in water at 37 °C for up to 1 year. The blends exhibited entirely different degradation profiles but showed no diversity between the total degradation times of the materials. PLLA presented a two-stage degradation profile with a rapid decrease in molar mass during the early stages of degradation, similar to the profile of PLLA/a-PHB5. PLLA/a-PHB20 presented a single, constant linear degradation profile. PLLA/PPA5 and PLLA/PPA20 showed completely opposing degradation profiles relative to PLLA, exhibiting a slow initial phase and a rapid decrease after a prolonged degradation time. PLLA/PPA5/comp and PLLA/PPA20/comp had degradation profiles between those of the miscible and the immiscible blends. The molar masses of the materials were approximately the same after 1 year of degradation despite their different profiles. The blend composition and topographical images captured at the last degradation time point demonstrate that the blending component was not leached out during the period of study. The hydrolytic stability of degradable polyester materials can be tailored to obtain different and predetermined degradation profiles for future applications.
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spelling pubmed-38927592014-01-16 Tuning the Degradation Profiles of Poly(l-lactide)-Based Materials through Miscibility Arias, Veluska Höglund, Anders Odelius, Karin Albertsson, Ann-Christine Biomacromolecules [Image: see text] The effective use of biodegradable polymers relies on the ability to control the onset of and time needed for degradation. Preferably, the material properties should be retained throughout the intended time frame, and the material should degrade in a rapid and controlled manner afterward. The degradation profiles of polyester materials were controlled through their miscibility. Systems composed of PLLA blended with poly[(R,S)-3-hydroxybutyrate] (a-PHB) and polypropylene adipate (PPA) with various molar masses were prepared through extrusion. Three different systems were used: miscible (PLLA/a-PHB5 and PLLA/a-PHB20), partially miscible (PLLA/PPA5/comp and PLLA/PPA20/comp), and immiscible (PLLA/PPA5 and PLLA/PPA20) blends. These blends and their respective homopolymers were hydrolytically degraded in water at 37 °C for up to 1 year. The blends exhibited entirely different degradation profiles but showed no diversity between the total degradation times of the materials. PLLA presented a two-stage degradation profile with a rapid decrease in molar mass during the early stages of degradation, similar to the profile of PLLA/a-PHB5. PLLA/a-PHB20 presented a single, constant linear degradation profile. PLLA/PPA5 and PLLA/PPA20 showed completely opposing degradation profiles relative to PLLA, exhibiting a slow initial phase and a rapid decrease after a prolonged degradation time. PLLA/PPA5/comp and PLLA/PPA20/comp had degradation profiles between those of the miscible and the immiscible blends. The molar masses of the materials were approximately the same after 1 year of degradation despite their different profiles. The blend composition and topographical images captured at the last degradation time point demonstrate that the blending component was not leached out during the period of study. The hydrolytic stability of degradable polyester materials can be tailored to obtain different and predetermined degradation profiles for future applications. American Chemical Society 2013-11-26 2014-01-13 /pmc/articles/PMC3892759/ /pubmed/24279455 http://dx.doi.org/10.1021/bm401667b Text en Copyright © 2013 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html)
spellingShingle Arias, Veluska
Höglund, Anders
Odelius, Karin
Albertsson, Ann-Christine
Tuning the Degradation Profiles of Poly(l-lactide)-Based Materials through Miscibility
title Tuning the Degradation Profiles of Poly(l-lactide)-Based Materials through Miscibility
title_full Tuning the Degradation Profiles of Poly(l-lactide)-Based Materials through Miscibility
title_fullStr Tuning the Degradation Profiles of Poly(l-lactide)-Based Materials through Miscibility
title_full_unstemmed Tuning the Degradation Profiles of Poly(l-lactide)-Based Materials through Miscibility
title_short Tuning the Degradation Profiles of Poly(l-lactide)-Based Materials through Miscibility
title_sort tuning the degradation profiles of poly(l-lactide)-based materials through miscibility
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3892759/
https://www.ncbi.nlm.nih.gov/pubmed/24279455
http://dx.doi.org/10.1021/bm401667b
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