<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(25)</volume><submitter>Abdollahi Baghban S</submitter><pubmed_abstract>This study deals with the development of an LED-curable methacrylated gelatin (GelMA) synthesis &lt;i>via&lt;/i> microwave (MW) irradiation with a reaction and purification time-, energy-, and methacrylation reagent-saving approach. To investigate the efficiency of MW irradiation in GelMA synthesis, characteristics of the GelMAs prepared by using glycidyl methacrylate (GMA) or methacrylic anhydride (MA) &lt;i>via&lt;/i> the MW-assisted (MWA) method were compared comprehensively with those synthesized &lt;i>via&lt;/i> the conventional heating method. Moreover, MWA reaction conditions were optimized in terms of methacrylation reagent concentrations (&lt;i>C&lt;/i>), reaction time (&lt;i>t&lt;/i>), and MW power (&lt;i>P&lt;/i>). Characterization and assessment of the GelMAs were conducted with &lt;sup>1&lt;/sup>H NMR, FT-IR, and Raman spectroscopy along with physical-mechanical, thermal, and hydrophilicity analysis. The results demonstrated that the MWA synthesized GMA-GelMA hydrogels were possessed of increased methacrylation degree (MD), gel fraction (GF), tensile strength (TS), elongation at break (EB), glass transition temperature (&lt;i>T&lt;/i> &lt;sub>g&lt;/sub>), and water contact angle (WCA) as well as decreased swelling degree (SD) values in comparison to those of MA-GelMA and GMA-GelMA hydrogels prepared &lt;i>via&lt;/i> the MWA and conventional method, respectively. Enhanced properties of the MWA synthesized GMA-hydrogels suggested an effective methacryloyl conjugation leading to a greater amount of covalent crosslinking density justified by the dipolar moment calculations. Optimal GMA &lt;i>C&lt;/i>, &lt;i>t&lt;/i>, &lt;i>P&lt;/i>, and purification time for a highly crosslinked GelMA hydrogel (MD: 96.1%, GF: 98.3%, SD: 10.11%, TS: 6.7 MPa, EB: 175.2%, &lt;i>T&lt;/i> &lt;sub>g&lt;/sub>: 75.34 °C, and WCA: 72.22°) were found to be a 5 times molar excess over the primary amine groups of gelatin, 5 min, 500 W, and 24 h, respectively. Thus, the optimized MW conditions offer a promising green method to prepare GelMAs for bio applications.</pubmed_abstract><journal>RSC advances</journal><pagination>14996-15009</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8697925</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A highly efficient microwave-assisted synthesis of an LED-curable methacrylated gelatin for bio applications.</pubmed_title><pmcid>PMC8697925</pmcid><pubmed_authors>Ebrahimi M</pubmed_authors><pubmed_authors>Bagheri-Khoulenjani S</pubmed_authors><pubmed_authors>Khorasani M</pubmed_authors><pubmed_authors>Abdollahi Baghban S</pubmed_authors></additional><is_claimable>false</is_claimable><name>A highly efficient microwave-assisted synthesis of an LED-curable methacrylated gelatin for bio applications.</name><description>This study deals with the development of an LED-curable methacrylated gelatin (GelMA) synthesis &lt;i>via&lt;/i> microwave (MW) irradiation with a reaction and purification time-, energy-, and methacrylation reagent-saving approach. To investigate the efficiency of MW irradiation in GelMA synthesis, characteristics of the GelMAs prepared by using glycidyl methacrylate (GMA) or methacrylic anhydride (MA) &lt;i>via&lt;/i> the MW-assisted (MWA) method were compared comprehensively with those synthesized &lt;i>via&lt;/i> the conventional heating method. Moreover, MWA reaction conditions were optimized in terms of methacrylation reagent concentrations (&lt;i>C&lt;/i>), reaction time (&lt;i>t&lt;/i>), and MW power (&lt;i>P&lt;/i>). Characterization and assessment of the GelMAs were conducted with &lt;sup>1&lt;/sup>H NMR, FT-IR, and Raman spectroscopy along with physical-mechanical, thermal, and hydrophilicity analysis. The results demonstrated that the MWA synthesized GMA-GelMA hydrogels were possessed of increased methacrylation degree (MD), gel fraction (GF), tensile strength (TS), elongation at break (EB), glass transition temperature (&lt;i>T&lt;/i> &lt;sub>g&lt;/sub>), and water contact angle (WCA) as well as decreased swelling degree (SD) values in comparison to those of MA-GelMA and GMA-GelMA hydrogels prepared &lt;i>via&lt;/i> the MWA and conventional method, respectively. Enhanced properties of the MWA synthesized GMA-hydrogels suggested an effective methacryloyl conjugation leading to a greater amount of covalent crosslinking density justified by the dipolar moment calculations. Optimal GMA &lt;i>C&lt;/i>, &lt;i>t&lt;/i>, &lt;i>P&lt;/i>, and purification time for a highly crosslinked GelMA hydrogel (MD: 96.1%, GF: 98.3%, SD: 10.11%, TS: 6.7 MPa, EB: 175.2%, &lt;i>T&lt;/i> &lt;sub>g&lt;/sub>: 75.34 °C, and WCA: 72.22°) were found to be a 5 times molar excess over the primary amine groups of gelatin, 5 min, 500 W, and 24 h, respectively. Thus, the optimized MW conditions offer a promising green method to prepare GelMAs for bio applications.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2024-11-12T06:23:59.418Z</modification><creation>2024-11-12T06:23:59.418Z</creation></dates><accession>S-EPMC8697925</accession><cross_references><pubmed>35424032</pubmed><doi>10.1039/d1ra01269j</doi></cross_references></HashMap>