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Biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering

OBJECTIVE: We aimed to evaluate cytocompatibility of hyaluronic acid (HA) and gelatin (Gela) conjugation with phenolic groups (Phs) via enzyme-mediated crosslinking. Phenolic moieties were substituted on the backbone of HA (HA-Ph) and Gela (Gela-Ph) and subsequently were subjected for horseradish pe...

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Autores principales: Khanmohammadi, Mehdi, Jalessi, Maryam, Asghari, Alimohamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9103298/
https://www.ncbi.nlm.nih.gov/pubmed/35562776
http://dx.doi.org/10.1186/s13104-022-06060-w
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author Khanmohammadi, Mehdi
Jalessi, Maryam
Asghari, Alimohamad
author_facet Khanmohammadi, Mehdi
Jalessi, Maryam
Asghari, Alimohamad
author_sort Khanmohammadi, Mehdi
collection PubMed
description OBJECTIVE: We aimed to evaluate cytocompatibility of hyaluronic acid (HA) and gelatin (Gela) conjugation with phenolic groups (Phs) via enzyme-mediated crosslinking. Phenolic moieties were substituted on the backbone of HA (HA-Ph) and Gela (Gela-Ph) and subsequently were subjected for horseradish peroxidase crosslinking in the presence of H(2)O(2) as an electron donor to create a stable hybrid microenvironment for cellular behavior and cartilage tissue engineering. RESULTS: Successful synthesis of biopolymers confirmed by NRM and UV–Vis spectrophotometry. The physical characteristic of hydrogels including mechanical properties and water contact angle of hydrogels enhanced with addition of Gela-Ph in HA-based hydrogel. The Gela-Ph showed longest gelation time and highest degradation rate. The cellular studies showed cells did not attach to HA-Ph hydrogel. While, proper cell attachment and proliferation observed on blend hydrogel surface compared with the neat hydrogels which interpret by the existence of cell-adhesive motifs of utilized Gela-Ph in this hydrogel. The encapsulated cells in HA-Ph hydrogel were spheroid and just maintained their viability. Hydrogels containing Gela-Ph, the cells were spindle shape with high degrees of cytoplasmic extension. Overall, the results suggest that hybrid biomimetic hydrogel can provide a superior biological microenvironment for chondrocytes in 3D cartilage tissue engineering.
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spelling pubmed-91032982022-05-14 Biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering Khanmohammadi, Mehdi Jalessi, Maryam Asghari, Alimohamad BMC Res Notes Research Note OBJECTIVE: We aimed to evaluate cytocompatibility of hyaluronic acid (HA) and gelatin (Gela) conjugation with phenolic groups (Phs) via enzyme-mediated crosslinking. Phenolic moieties were substituted on the backbone of HA (HA-Ph) and Gela (Gela-Ph) and subsequently were subjected for horseradish peroxidase crosslinking in the presence of H(2)O(2) as an electron donor to create a stable hybrid microenvironment for cellular behavior and cartilage tissue engineering. RESULTS: Successful synthesis of biopolymers confirmed by NRM and UV–Vis spectrophotometry. The physical characteristic of hydrogels including mechanical properties and water contact angle of hydrogels enhanced with addition of Gela-Ph in HA-based hydrogel. The Gela-Ph showed longest gelation time and highest degradation rate. The cellular studies showed cells did not attach to HA-Ph hydrogel. While, proper cell attachment and proliferation observed on blend hydrogel surface compared with the neat hydrogels which interpret by the existence of cell-adhesive motifs of utilized Gela-Ph in this hydrogel. The encapsulated cells in HA-Ph hydrogel were spheroid and just maintained their viability. Hydrogels containing Gela-Ph, the cells were spindle shape with high degrees of cytoplasmic extension. Overall, the results suggest that hybrid biomimetic hydrogel can provide a superior biological microenvironment for chondrocytes in 3D cartilage tissue engineering. BioMed Central 2022-05-13 /pmc/articles/PMC9103298/ /pubmed/35562776 http://dx.doi.org/10.1186/s13104-022-06060-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Note
Khanmohammadi, Mehdi
Jalessi, Maryam
Asghari, Alimohamad
Biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering
title Biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering
title_full Biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering
title_fullStr Biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering
title_full_unstemmed Biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering
title_short Biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering
title_sort biomimetic hydrogel scaffolds via enzymatic reaction for cartilage tissue engineering
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9103298/
https://www.ncbi.nlm.nih.gov/pubmed/35562776
http://dx.doi.org/10.1186/s13104-022-06060-w
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