Development of enzymatically crosslinked natural deep eutectogels: versatile gels for enhanced drug delivery.

Liane Meneses, Dimitra Antonia Bagaki, Ana Roda, Alexandre Paiva, Ana Rita C Duarte
{"title":"Development of enzymatically crosslinked natural deep eutectogels: versatile gels for enhanced drug delivery.","authors":"Liane Meneses, Dimitra Antonia Bagaki, Ana Roda, Alexandre Paiva, Ana Rita C Duarte","doi":"10.1039/d4tb01672f","DOIUrl":null,"url":null,"abstract":"<p><p>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<sup>-1</sup>) to have gelation time under 2 minutes, the eutectogels were obtained using 10 and 5 U mL<sup>-1</sup> 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 <i>in vitro</i> biological evaluation of the individual components of the eutectogel support no cytotoxic effect, an early indication of potential biocompatibility.</p>","PeriodicalId":94089,"journal":{"name":"Journal of materials chemistry. B","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of materials chemistry. B","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/d4tb01672f","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

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.

开发酶交联天然深层共晶凝胶:增强药物输送的多功能凝胶。
可注射水凝胶具有微创、易于应用和空隙填充等特性,因此已被广泛研究。在这项工作中,我们测试了制备新型凝胶(即共晶凝胶)的可能性,在这种凝胶中,水被天然深共晶体系(NADES)取代,从而使其具有更长的稳定性。我们使用辣根过氧化物酶(HRP)作为催化剂和明胶-苯酚共轭聚合物,通过酶介导交联法制备了甜菜碱-甘油 1:2 共晶凝胶。与需要较高酶浓度(15 U mL-1)才能在 2 分钟内凝胶的水凝胶相比,使用 10 U mL-1 和 5 U mL-1 的 HRP 可分别获得 30 秒和 50 秒的凝胶时间。最后,在聚合物基质中加入酮洛芬,并进行了释放研究。NADES 的存在对药物负载凝胶的配制至关重要,这种凝胶能在 10 天内释放高达 70% 的药物,因此可以得出结论,这些共晶凝胶可作为基质在水介质中控制酮洛芬的给药。对优特凝胶各成分进行的体外生物评估表明,它们没有细胞毒性作用,这表明它们具有潜在的生物相容性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of materials chemistry. B
Journal of materials chemistry. B 化学科学, 工程与材料, 生命科学, 分析化学, 高分子组装与超分子结构, 高分子科学, 免疫生物学, 免疫学, 生化分析及生物传感, 组织工程学, 生物力学与组织工程学, 资源循环科学, 冶金与矿业, 生物医用高分子材料, 有机高分子材料, 金属材料的制备科学与跨学科应用基础, 金属材料, 样品前处理方法与技术, 有机分子功能材料化学, 有机化学
CiteScore
12.00
自引率
0.00%
发文量
0
审稿时长
1 months
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信