Development of enzymatically crosslinked natural deep eutectogels: versatile gels for enhanced drug delivery
Injectable hydrogels have been extensively studied due to their minimally invasive properties, ease of application, and void-filling properties. In this work, we tested the possibility to prepare a new type of gels, so called eutectogels, where water is replaced by a natural deep eutectic system (NA...
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creator | Meneses, Liane Bagaki, Dimitra Antonia Roda, Ana Paiva, Alexandre Duarte, Ana Rita C |
description | Injectable hydrogels have been extensively studied due to their minimally invasive properties, ease of application, and void-filling properties. In this work, we tested the possibility to prepare a new type of gels, so called eutectogels, where water is replaced by a natural deep eutectic system (NADES), conferring it longer stability. Eutectogels based on betaine : glycerol 1 : 2, were prepared by enzymatic mediated crosslinking, using horseradish peroxidase (HRP) as catalyst and gelatine-phenol conjugated polymer. In comparison to hydrogels, that required higher enzyme concentration (15 U mL
−1
) to have gelation time under 2 minutes, the eutectogels were obtained using 10 and 5 U mL
−1
of HRP, with gelation times of 30 and 50 seconds, respectively. Finally, ketoprofen was loaded into the polymeric matrix, and release studies were conducted. The presence of NADES was essential for the formulation of the drug loaded gel, which was able to release up to 70% of the drug within 10 days, therefore, it was possible to conclude that these eutectogels work as matrix for the controlled delivery of ketoprofen in aqueous medium. The
in vitro
biological evaluation of the individual components of the eutectogel support no cytotoxic effect, an early indication of potential biocompatibility.
We propose a new injectable eutectogel prepared by enzymatic crosslinking, using NADES, betaine : glycerol (2 : 1), as solvent. The potential of using this material with improved rheological properties as drug delivery system, has also been evaluated. |
doi_str_mv | 10.1039/d4tb01672f |
format | Article |
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−1
) to have gelation time under 2 minutes, the eutectogels were obtained using 10 and 5 U mL
−1
of HRP, with gelation times of 30 and 50 seconds, respectively. Finally, ketoprofen was loaded into the polymeric matrix, and release studies were conducted. The presence of NADES was essential for the formulation of the drug loaded gel, which was able to release up to 70% of the drug within 10 days, therefore, it was possible to conclude that these eutectogels work as matrix for the controlled delivery of ketoprofen in aqueous medium. The
in vitro
biological evaluation of the individual components of the eutectogel support no cytotoxic effect, an early indication of potential biocompatibility.
We propose a new injectable eutectogel prepared by enzymatic crosslinking, using NADES, betaine : glycerol (2 : 1), as solvent. The potential of using this material with improved rheological properties as drug delivery system, has also been evaluated.</description><identifier>ISSN: 2050-750X</identifier><identifier>ISSN: 2050-7518</identifier><identifier>EISSN: 2050-7518</identifier><identifier>DOI: 10.1039/d4tb01672f</identifier><identifier>PMID: 39503597</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Animals ; Anti-Inflammatory Agents, Non-Steroidal - chemistry ; Anti-Inflammatory Agents, Non-Steroidal - pharmacology ; Aqueous solutions ; Betaine - analogs & derivatives ; Betaine - chemistry ; Biocompatibility ; Biological effects ; Cross-Linking Reagents - chemistry ; Crosslinking ; Cytotoxicity ; Drug Carriers - chemistry ; Drug delivery ; Drug Delivery Systems ; Drug Liberation ; Gelatin - chemistry ; Gelation ; Gels - chemistry ; Glycerol - chemistry ; Horseradish peroxidase ; Horseradish Peroxidase - chemistry ; Horseradish Peroxidase - metabolism ; Humans ; Hydrogels ; Hydrogels - chemical synthesis ; Hydrogels - chemistry ; Ketoprofen ; Ketoprofen - chemistry ; Ketoprofen - pharmacology ; Peroxidase ; Phenols ; Polymers</subject><ispartof>Journal of materials chemistry. B, Materials for biology and medicine, 2024-12, Vol.12 (48), p.12567-12576</ispartof><rights>Copyright Royal Society of Chemistry 2024</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c226t-a5b47f98346a7ae3f57225b43a5de38e03ec58c6cc99ef0e1904895f17db58f43</cites><orcidid>0000-0001-6478-245X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39503597$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meneses, Liane</creatorcontrib><creatorcontrib>Bagaki, Dimitra Antonia</creatorcontrib><creatorcontrib>Roda, Ana</creatorcontrib><creatorcontrib>Paiva, Alexandre</creatorcontrib><creatorcontrib>Duarte, Ana Rita C</creatorcontrib><title>Development of enzymatically crosslinked natural deep eutectogels: versatile gels for enhanced drug delivery</title><title>Journal of materials chemistry. B, Materials for biology and medicine</title><addtitle>J Mater Chem B</addtitle><description>Injectable hydrogels have been extensively studied due to their minimally invasive properties, ease of application, and void-filling properties. In this work, we tested the possibility to prepare a new type of gels, so called eutectogels, where water is replaced by a natural deep eutectic system (NADES), conferring it longer stability. Eutectogels based on betaine : glycerol 1 : 2, were prepared by enzymatic mediated crosslinking, using horseradish peroxidase (HRP) as catalyst and gelatine-phenol conjugated polymer. In comparison to hydrogels, that required higher enzyme concentration (15 U mL
−1
) to have gelation time under 2 minutes, the eutectogels were obtained using 10 and 5 U mL
−1
of HRP, with gelation times of 30 and 50 seconds, respectively. Finally, ketoprofen was loaded into the polymeric matrix, and release studies were conducted. The presence of NADES was essential for the formulation of the drug loaded gel, which was able to release up to 70% of the drug within 10 days, therefore, it was possible to conclude that these eutectogels work as matrix for the controlled delivery of ketoprofen in aqueous medium. The
in vitro
biological evaluation of the individual components of the eutectogel support no cytotoxic effect, an early indication of potential biocompatibility.
We propose a new injectable eutectogel prepared by enzymatic crosslinking, using NADES, betaine : glycerol (2 : 1), as solvent. The potential of using this material with improved rheological properties as drug delivery system, has also been evaluated.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</subject><subject>Aqueous solutions</subject><subject>Betaine - analogs & derivatives</subject><subject>Betaine - chemistry</subject><subject>Biocompatibility</subject><subject>Biological effects</subject><subject>Cross-Linking Reagents - chemistry</subject><subject>Crosslinking</subject><subject>Cytotoxicity</subject><subject>Drug Carriers - chemistry</subject><subject>Drug delivery</subject><subject>Drug Delivery Systems</subject><subject>Drug Liberation</subject><subject>Gelatin - chemistry</subject><subject>Gelation</subject><subject>Gels - chemistry</subject><subject>Glycerol - chemistry</subject><subject>Horseradish peroxidase</subject><subject>Horseradish Peroxidase - chemistry</subject><subject>Horseradish Peroxidase - metabolism</subject><subject>Humans</subject><subject>Hydrogels</subject><subject>Hydrogels - chemical synthesis</subject><subject>Hydrogels - chemistry</subject><subject>Ketoprofen</subject><subject>Ketoprofen - chemistry</subject><subject>Ketoprofen - pharmacology</subject><subject>Peroxidase</subject><subject>Phenols</subject><subject>Polymers</subject><issn>2050-750X</issn><issn>2050-7518</issn><issn>2050-7518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1LxDAQxYMoKqsX70rAiwir-WjaxJu6rgoLXlbwVtJ0otX0w6QV1r_erKsrmMskmd97DPMQOqDkjBKuzsukLwhNM2Y30C4jgowzQeXm-k6edtB-CK8kHklTyZNttMOVIFyobBe5CXyAa7samh63FkPzuah1Xxnt3AIb34bgquYNStzofvDa4RKgwzD0YPr2GVy4wB_gQ5Q4wMs3tq2PNi-6MVFV-uE5SlwVocUe2rLaBdj_qSP0OL2ZX9-NZw-399eXs7FhLO3HWhRJZlUcNdWZBm5Fxlj841qUwCUQDkZIkxqjFFgCVJFEKmFpVhZC2oSP0MnKt_Pt-wChz-sqGHBON9AOIeeUJalimeARPf6HvraDb-J0kUqYIlJKFqnTFfW9EA8273xVa7_IKcmXMeSTZH71HcM0wkc_lkNRQ7lGf5cegcMV4INZd_9y5F8EBo2Z</recordid><startdate>20241211</startdate><enddate>20241211</enddate><creator>Meneses, Liane</creator><creator>Bagaki, Dimitra Antonia</creator><creator>Roda, Ana</creator><creator>Paiva, Alexandre</creator><creator>Duarte, Ana Rita C</creator><general>Royal Society of Chemistry</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6478-245X</orcidid></search><sort><creationdate>20241211</creationdate><title>Development of enzymatically crosslinked natural deep eutectogels: versatile gels for enhanced drug delivery</title><author>Meneses, Liane ; 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B, Materials for biology and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meneses, Liane</au><au>Bagaki, Dimitra Antonia</au><au>Roda, Ana</au><au>Paiva, Alexandre</au><au>Duarte, Ana Rita C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of enzymatically crosslinked natural deep eutectogels: versatile gels for enhanced drug delivery</atitle><jtitle>Journal of materials chemistry. B, Materials for biology and medicine</jtitle><addtitle>J Mater Chem B</addtitle><date>2024-12-11</date><risdate>2024</risdate><volume>12</volume><issue>48</issue><spage>12567</spage><epage>12576</epage><pages>12567-12576</pages><issn>2050-750X</issn><issn>2050-7518</issn><eissn>2050-7518</eissn><abstract>Injectable hydrogels have been extensively studied due to their minimally invasive properties, ease of application, and void-filling properties. In this work, we tested the possibility to prepare a new type of gels, so called eutectogels, where water is replaced by a natural deep eutectic system (NADES), conferring it longer stability. Eutectogels based on betaine : glycerol 1 : 2, were prepared by enzymatic mediated crosslinking, using horseradish peroxidase (HRP) as catalyst and gelatine-phenol conjugated polymer. In comparison to hydrogels, that required higher enzyme concentration (15 U mL
−1
) to have gelation time under 2 minutes, the eutectogels were obtained using 10 and 5 U mL
−1
of HRP, with gelation times of 30 and 50 seconds, respectively. Finally, ketoprofen was loaded into the polymeric matrix, and release studies were conducted. The presence of NADES was essential for the formulation of the drug loaded gel, which was able to release up to 70% of the drug within 10 days, therefore, it was possible to conclude that these eutectogels work as matrix for the controlled delivery of ketoprofen in aqueous medium. The
in vitro
biological evaluation of the individual components of the eutectogel support no cytotoxic effect, an early indication of potential biocompatibility.
We propose a new injectable eutectogel prepared by enzymatic crosslinking, using NADES, betaine : glycerol (2 : 1), as solvent. The potential of using this material with improved rheological properties as drug delivery system, has also been evaluated.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>39503597</pmid><doi>10.1039/d4tb01672f</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-6478-245X</orcidid></addata></record> |
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source | MEDLINE; Royal Society Of Chemistry Journals |
subjects | Animals Anti-Inflammatory Agents, Non-Steroidal - chemistry Anti-Inflammatory Agents, Non-Steroidal - pharmacology Aqueous solutions Betaine - analogs & derivatives Betaine - chemistry Biocompatibility Biological effects Cross-Linking Reagents - chemistry Crosslinking Cytotoxicity Drug Carriers - chemistry Drug delivery Drug Delivery Systems Drug Liberation Gelatin - chemistry Gelation Gels - chemistry Glycerol - chemistry Horseradish peroxidase Horseradish Peroxidase - chemistry Horseradish Peroxidase - metabolism Humans Hydrogels Hydrogels - chemical synthesis Hydrogels - chemistry Ketoprofen Ketoprofen - chemistry Ketoprofen - pharmacology Peroxidase Phenols Polymers |
title | Development of enzymatically crosslinked natural deep eutectogels: versatile gels for enhanced drug delivery |
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