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Screening the Degradation of Polymer Microparticles on a Chip
[Image: see text] Enzymatic degradation of polymers has advantages over standard degradation methods, such as soil burial and weathering, which are time-consuming and cannot provide time-resolved observations. We have developed a microfluidic device to study the degradation of single microparticles....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835179/ https://www.ncbi.nlm.nih.gov/pubmed/36643556 http://dx.doi.org/10.1021/acsomega.2c07704 |
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author | Davachi, Seyed Mohammad Mokhtare, Amir Torabi, Hooman Enayati, Mojtaba Deisenroth, Ted Van Pho, Toan Qu, Liangliang Tücking, Katrin-Stephanie Abbaspourrad, Alireza |
author_facet | Davachi, Seyed Mohammad Mokhtare, Amir Torabi, Hooman Enayati, Mojtaba Deisenroth, Ted Van Pho, Toan Qu, Liangliang Tücking, Katrin-Stephanie Abbaspourrad, Alireza |
author_sort | Davachi, Seyed Mohammad |
collection | PubMed |
description | [Image: see text] Enzymatic degradation of polymers has advantages over standard degradation methods, such as soil burial and weathering, which are time-consuming and cannot provide time-resolved observations. We have developed a microfluidic device to study the degradation of single microparticles. The enzymatic degradation of poly (1,4-butylene adipate-co-terephthalate) (PBAT) microparticles was studied using Novozym 51032 cutinase. PBAT microparticles were prepared via an oil-in-water emulsion solvent removal method, and their morphology and chemical composition were characterized. Then, microparticles with varying diameters of 30–60 μm were loaded into the microfluidic chip. Enzyme solutions at different concentrations were introduced to the device, and changes in the size and transparency of PBAT microparticles were observed over time. The physicochemical properties of degraded products were analyzed by FT-IR, NMR, mass spectrometry, and differential scanning calorimetry. The degradation process was also performed in bulk, and the results were compared to those of the microfluidic method. Our analysis confirms that the degradation process in both bulk and microfluidic methods was similar. In both cases, degradation takes place on aliphatic and soft segments of PBAT. Our findings serve as a proof of concept for a microfluidic method for easy and time-resolved degradation analysis, with degradation results comparable to those of conventional bulk methods. |
format | Online Article Text |
id | pubmed-9835179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98351792023-01-13 Screening the Degradation of Polymer Microparticles on a Chip Davachi, Seyed Mohammad Mokhtare, Amir Torabi, Hooman Enayati, Mojtaba Deisenroth, Ted Van Pho, Toan Qu, Liangliang Tücking, Katrin-Stephanie Abbaspourrad, Alireza ACS Omega [Image: see text] Enzymatic degradation of polymers has advantages over standard degradation methods, such as soil burial and weathering, which are time-consuming and cannot provide time-resolved observations. We have developed a microfluidic device to study the degradation of single microparticles. The enzymatic degradation of poly (1,4-butylene adipate-co-terephthalate) (PBAT) microparticles was studied using Novozym 51032 cutinase. PBAT microparticles were prepared via an oil-in-water emulsion solvent removal method, and their morphology and chemical composition were characterized. Then, microparticles with varying diameters of 30–60 μm were loaded into the microfluidic chip. Enzyme solutions at different concentrations were introduced to the device, and changes in the size and transparency of PBAT microparticles were observed over time. The physicochemical properties of degraded products were analyzed by FT-IR, NMR, mass spectrometry, and differential scanning calorimetry. The degradation process was also performed in bulk, and the results were compared to those of the microfluidic method. Our analysis confirms that the degradation process in both bulk and microfluidic methods was similar. In both cases, degradation takes place on aliphatic and soft segments of PBAT. Our findings serve as a proof of concept for a microfluidic method for easy and time-resolved degradation analysis, with degradation results comparable to those of conventional bulk methods. American Chemical Society 2022-12-23 /pmc/articles/PMC9835179/ /pubmed/36643556 http://dx.doi.org/10.1021/acsomega.2c07704 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Davachi, Seyed Mohammad Mokhtare, Amir Torabi, Hooman Enayati, Mojtaba Deisenroth, Ted Van Pho, Toan Qu, Liangliang Tücking, Katrin-Stephanie Abbaspourrad, Alireza Screening the Degradation of Polymer Microparticles on a Chip |
title | Screening the Degradation
of Polymer Microparticles
on a Chip |
title_full | Screening the Degradation
of Polymer Microparticles
on a Chip |
title_fullStr | Screening the Degradation
of Polymer Microparticles
on a Chip |
title_full_unstemmed | Screening the Degradation
of Polymer Microparticles
on a Chip |
title_short | Screening the Degradation
of Polymer Microparticles
on a Chip |
title_sort | screening the degradation
of polymer microparticles
on a chip |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835179/ https://www.ncbi.nlm.nih.gov/pubmed/36643556 http://dx.doi.org/10.1021/acsomega.2c07704 |
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