Characterization by FTIR and Ampicillin Release in Collagen-Polyurethane Hydrogels Coupled with Metal-Organic Frameworks

Nadia J. Amaya-Chantaca
{"title":"Characterization by FTIR and Ampicillin Release in Collagen-Polyurethane Hydrogels Coupled with Metal-Organic Frameworks","authors":"Nadia J. Amaya-Chantaca","doi":"10.38177/ajast.2020.4214","DOIUrl":null,"url":null,"abstract":"In this work, the capacity of encapsulation and subsequent release of the drug ampicillin was evaluated, for this, two different hydrogels were made by the microemulsion method, having different crosslinking agent based on polyurethane: P(IPDI) and P(HDI), the metal-organic framework (MOF) that was used inside the two composite hydrogels was MIL-53, which is a derivative of the hydrothermal synthesis of terephthalic acid and Al (III) ions. Characterization tests were carried out on the hydrogels, the FTIR sprectra were obtained to evaluate the encapsulation of the drug and the quantification by UV-Vis spectrophotometry to monitor the mass of ampicillin released in the two systems studied. Hydrogels based on C-P(HDI)-MIL53 show higher intermolecular interactions with encapsulated ampicillin, observed by the variation in the intensities of the FTIR signals related to the -NH, -OH, amide I and II bonds that make up the systems; in addition this type of hydrogel also exhibits a higher release of ampicillin than C-P(IPDI)-MIL53 hydrogel. These hydrogels can be studied as 3D culture systems or materials for wound healing, thus avoiding the formation of bacterial infections.","PeriodicalId":119595,"journal":{"name":"Nanomaterials eJournal","volume":"29 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanomaterials eJournal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.38177/ajast.2020.4214","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

In this work, the capacity of encapsulation and subsequent release of the drug ampicillin was evaluated, for this, two different hydrogels were made by the microemulsion method, having different crosslinking agent based on polyurethane: P(IPDI) and P(HDI), the metal-organic framework (MOF) that was used inside the two composite hydrogels was MIL-53, which is a derivative of the hydrothermal synthesis of terephthalic acid and Al (III) ions. Characterization tests were carried out on the hydrogels, the FTIR sprectra were obtained to evaluate the encapsulation of the drug and the quantification by UV-Vis spectrophotometry to monitor the mass of ampicillin released in the two systems studied. Hydrogels based on C-P(HDI)-MIL53 show higher intermolecular interactions with encapsulated ampicillin, observed by the variation in the intensities of the FTIR signals related to the -NH, -OH, amide I and II bonds that make up the systems; in addition this type of hydrogel also exhibits a higher release of ampicillin than C-P(IPDI)-MIL53 hydrogel. These hydrogels can be studied as 3D culture systems or materials for wound healing, thus avoiding the formation of bacterial infections.
FTIR表征及氨苄西林在金属有机骨架偶联的胶原-聚氨酯水凝胶中的释放
为了评价氨苄西林的包封能力和后续释放能力,本文采用微乳液法制备了两种不同的水凝胶,采用不同的聚氨酯交联剂:P(IPDI)和P(HDI),两种复合水凝胶内部使用的金属有机骨架(MOF)为MIL-53,它是水热合成对苯二甲酸和Al (III)离子的衍生物。对水凝胶进行表征试验,获得FTIR谱图评价药物的包封性,紫外可见分光光度法定量监测两种体系中氨苄西林的释放量。基于C-P(HDI)-MIL53的水凝胶与包封的氨苄西林表现出更高的分子间相互作用,这是通过与组成系统的- nhh, -OH,酰胺I和II键相关的FTIR信号的强度变化观察到的;此外,这种类型的水凝胶还表现出比C-P(IPDI)-MIL53水凝胶更高的氨苄西林释放量。这些水凝胶可以作为三维培养系统或伤口愈合材料进行研究,从而避免细菌感染的形成。
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
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信