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Preparation of an Antioxidant Assembly Based on a Copolymacrolactone Structure and Erythritol following an Eco-Friendly Strategy

The study presents the achievement of a new assembly with antioxidant behaviour based on a copolymacrolactone structure that encapsulates erythritol (Eryt). Poly(ethylene brassylate-co-squaric acid) (PEBSA) was synthesised in environmentally friendly conditions, respectively, through a process in su...

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Autores principales: Chiriac, Aurica P., Ghilan, Alina, Serban, Alexandru-Mihail, Macsim, Ana-Maria, Bargan, Alexandra, Doroftei, Florica, Chiriac, Vlad Mihai, Nita, Loredana Elena, Rusu, Alina Gabriela, Sandu, Andreea-Isabela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9774145/
https://www.ncbi.nlm.nih.gov/pubmed/36552679
http://dx.doi.org/10.3390/antiox11122471
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author Chiriac, Aurica P.
Ghilan, Alina
Serban, Alexandru-Mihail
Macsim, Ana-Maria
Bargan, Alexandra
Doroftei, Florica
Chiriac, Vlad Mihai
Nita, Loredana Elena
Rusu, Alina Gabriela
Sandu, Andreea-Isabela
author_facet Chiriac, Aurica P.
Ghilan, Alina
Serban, Alexandru-Mihail
Macsim, Ana-Maria
Bargan, Alexandra
Doroftei, Florica
Chiriac, Vlad Mihai
Nita, Loredana Elena
Rusu, Alina Gabriela
Sandu, Andreea-Isabela
author_sort Chiriac, Aurica P.
collection PubMed
description The study presents the achievement of a new assembly with antioxidant behaviour based on a copolymacrolactone structure that encapsulates erythritol (Eryt). Poly(ethylene brassylate-co-squaric acid) (PEBSA) was synthesised in environmentally friendly conditions, respectively, through a process in suspension in water by opening the cycle of ethylene brassylate macrolactone, followed by condensation with squaric acid. The compound synthesised in suspension was characterised by comparison with the polymer obtained by polymerisation in solution. The investigations revealed that, with the exception of the molecular masses, the compounds generated by the two synthetic procedures present similar properties, including good thermal stability, with a T(peak) of 456 °C, and the capacity for network formation. In addition, the investigation by dynamic light scattering techniques evidenced a mean diameter for PEBSA particles of around 596 nm and a zeta potential of −25 mV, which attests to their stability. The bio-based copolymacrolactone was used as a matrix for erythritol encapsulation. The new PEBSA–Eryt compound presented an increased sorption/desorption process, compared with the PEBSA matrix, and a crystalline morphology confirmed by X-ray diffraction analysis. The bioactive compound was also characterised in terms of its biocompatibility and antioxidant behaviour.
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spelling pubmed-97741452022-12-23 Preparation of an Antioxidant Assembly Based on a Copolymacrolactone Structure and Erythritol following an Eco-Friendly Strategy Chiriac, Aurica P. Ghilan, Alina Serban, Alexandru-Mihail Macsim, Ana-Maria Bargan, Alexandra Doroftei, Florica Chiriac, Vlad Mihai Nita, Loredana Elena Rusu, Alina Gabriela Sandu, Andreea-Isabela Antioxidants (Basel) Article The study presents the achievement of a new assembly with antioxidant behaviour based on a copolymacrolactone structure that encapsulates erythritol (Eryt). Poly(ethylene brassylate-co-squaric acid) (PEBSA) was synthesised in environmentally friendly conditions, respectively, through a process in suspension in water by opening the cycle of ethylene brassylate macrolactone, followed by condensation with squaric acid. The compound synthesised in suspension was characterised by comparison with the polymer obtained by polymerisation in solution. The investigations revealed that, with the exception of the molecular masses, the compounds generated by the two synthetic procedures present similar properties, including good thermal stability, with a T(peak) of 456 °C, and the capacity for network formation. In addition, the investigation by dynamic light scattering techniques evidenced a mean diameter for PEBSA particles of around 596 nm and a zeta potential of −25 mV, which attests to their stability. The bio-based copolymacrolactone was used as a matrix for erythritol encapsulation. The new PEBSA–Eryt compound presented an increased sorption/desorption process, compared with the PEBSA matrix, and a crystalline morphology confirmed by X-ray diffraction analysis. The bioactive compound was also characterised in terms of its biocompatibility and antioxidant behaviour. MDPI 2022-12-15 /pmc/articles/PMC9774145/ /pubmed/36552679 http://dx.doi.org/10.3390/antiox11122471 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chiriac, Aurica P.
Ghilan, Alina
Serban, Alexandru-Mihail
Macsim, Ana-Maria
Bargan, Alexandra
Doroftei, Florica
Chiriac, Vlad Mihai
Nita, Loredana Elena
Rusu, Alina Gabriela
Sandu, Andreea-Isabela
Preparation of an Antioxidant Assembly Based on a Copolymacrolactone Structure and Erythritol following an Eco-Friendly Strategy
title Preparation of an Antioxidant Assembly Based on a Copolymacrolactone Structure and Erythritol following an Eco-Friendly Strategy
title_full Preparation of an Antioxidant Assembly Based on a Copolymacrolactone Structure and Erythritol following an Eco-Friendly Strategy
title_fullStr Preparation of an Antioxidant Assembly Based on a Copolymacrolactone Structure and Erythritol following an Eco-Friendly Strategy
title_full_unstemmed Preparation of an Antioxidant Assembly Based on a Copolymacrolactone Structure and Erythritol following an Eco-Friendly Strategy
title_short Preparation of an Antioxidant Assembly Based on a Copolymacrolactone Structure and Erythritol following an Eco-Friendly Strategy
title_sort preparation of an antioxidant assembly based on a copolymacrolactone structure and erythritol following an eco-friendly strategy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9774145/
https://www.ncbi.nlm.nih.gov/pubmed/36552679
http://dx.doi.org/10.3390/antiox11122471
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