Adsorption and release profile analysis of oxytetracycline drug on functionalized graphene oxide nanoparticles

Wesam R. Kadhum , Marianna Budai , Lívia Budai , Ehsan kianfar
{"title":"Adsorption and release profile analysis of oxytetracycline drug on functionalized graphene oxide nanoparticles","authors":"Wesam R. Kadhum ,&nbsp;Marianna Budai ,&nbsp;Lívia Budai ,&nbsp;Ehsan kianfar","doi":"10.1016/j.rinma.2025.100711","DOIUrl":null,"url":null,"abstract":"<div><div>In this study graphite particles were converted to graphene oxide (GO) via Hummer's method. Synthesized graphene oxide was used for studying adsorption and release of oxytetracycline in dog's simulated gastric. This material the synthesized GO was functionalized with epichlorohydrin and Cibacron blue. Due to the relatively high-water solubility of oxytetracycline, it can be easily dissolved in body fluids without sufficient absorption and storage time. Drugs which are soluble in water, easily dissolve in body fluids and won't store in body well enough according to their ease of solubility in water. Therefore, the drug is likely to be eliminated via kidney and urinary system without adequate adsorption and satisfactory therapeutic effect. won't have convenient effect. In order to overcome the rapid elimination of oxytetracycline prolonged drug release was considered. Oxytetracycline is an antibiotic. antibiotics are generally linked with bacterial ribosomal unit and thus inhibit protein synthesis in bacteria. In this study optimum pH for drug was investigated firstly and according to results obtain acidic environment has the best adsorption for the studied drug. First, the optimal pH value for the drug was investigated. Based on the results obtained the acidic environment provided the best adsorption conditions for oxytetracycline. According to studies dog's digestive system is acidic and drugs and food remains in it for approximately 8 h. Experiments demonstrated that oxytetracycline GO nanoparticles show the highest drug release in the first 2 h making the investigation of drug release in the intestines unnecessary. Finally, the accuracy of synthesis, adsorption and release were investigated by UV–Vis experiments. The obtained adsorption isotherm fits Langmuir and Temkin models well, and the theoretical maximum of adsorption capacity calculated by Langmuir model is 495 mg/g.The adsorption capacities of tetracycline oxytetracycline on GO decreased with increasing pH. The adsorption isotherms of oxytetracycline on graphene oxide were discussed and compared. The aim of this study is to make and modify graphene oxide in order to make a pharmaceutical adsorbent for the slow adsorption and release of the drug oxytetracycline in the simulated environment of the dog's body and the release of oxytetracycline was modified and enhanced by epichlorohydrin and Cibacron Blue and was investigated.</div></div>","PeriodicalId":101087,"journal":{"name":"Results in Materials","volume":"26 ","pages":"Article 100711"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Results in Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590048X25000561","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 study graphite particles were converted to graphene oxide (GO) via Hummer's method. Synthesized graphene oxide was used for studying adsorption and release of oxytetracycline in dog's simulated gastric. This material the synthesized GO was functionalized with epichlorohydrin and Cibacron blue. Due to the relatively high-water solubility of oxytetracycline, it can be easily dissolved in body fluids without sufficient absorption and storage time. Drugs which are soluble in water, easily dissolve in body fluids and won't store in body well enough according to their ease of solubility in water. Therefore, the drug is likely to be eliminated via kidney and urinary system without adequate adsorption and satisfactory therapeutic effect. won't have convenient effect. In order to overcome the rapid elimination of oxytetracycline prolonged drug release was considered. Oxytetracycline is an antibiotic. antibiotics are generally linked with bacterial ribosomal unit and thus inhibit protein synthesis in bacteria. In this study optimum pH for drug was investigated firstly and according to results obtain acidic environment has the best adsorption for the studied drug. First, the optimal pH value for the drug was investigated. Based on the results obtained the acidic environment provided the best adsorption conditions for oxytetracycline. According to studies dog's digestive system is acidic and drugs and food remains in it for approximately 8 h. Experiments demonstrated that oxytetracycline GO nanoparticles show the highest drug release in the first 2 h making the investigation of drug release in the intestines unnecessary. Finally, the accuracy of synthesis, adsorption and release were investigated by UV–Vis experiments. The obtained adsorption isotherm fits Langmuir and Temkin models well, and the theoretical maximum of adsorption capacity calculated by Langmuir model is 495 mg/g.The adsorption capacities of tetracycline oxytetracycline on GO decreased with increasing pH. The adsorption isotherms of oxytetracycline on graphene oxide were discussed and compared. The aim of this study is to make and modify graphene oxide in order to make a pharmaceutical adsorbent for the slow adsorption and release of the drug oxytetracycline in the simulated environment of the dog's body and the release of oxytetracycline was modified and enhanced by epichlorohydrin and Cibacron Blue and was investigated.
功能化氧化石墨烯纳米颗粒对土霉素的吸附与释放分析
在这项研究中,石墨颗粒通过Hummer的方法转化为氧化石墨烯(GO)。采用合成的氧化石墨烯研究了土霉素在狗模拟胃中的吸附和释放。将合成的氧化石墨烯用环氧氯丙烷和奇巴龙蓝进行了功能化。由于土霉素的水溶性比较高,很容易溶解在体液中,没有足够的吸收和储存时间。易溶于水的药物,由于易溶于水,易溶于体液,不能很好地贮存在体内。因此,药物很可能经肾脏和泌尿系统排出,没有充分的吸附和满意的治疗效果。不会有方便的效果。为了克服土霉素快速消除的问题,考虑延长药物释放时间。土霉素是一种抗生素。抗生素通常与细菌核糖体单位结合,从而抑制细菌的蛋白质合成。本研究首先对药物的最佳pH进行了研究,根据研究结果得出酸性环境对所研究药物的吸附效果最好。首先,对药物的最佳pH值进行了研究。结果表明,酸性环境为土霉素的吸附提供了最佳条件。根据研究,狗的消化系统是酸性的,药物和食物在其中停留约8小时。实验表明,土霉素氧化石墨烯纳米颗粒在前2小时的药物释放量最高,因此无需研究药物在肠道中的释放。最后通过UV-Vis实验考察了其合成、吸附和释放的准确性。所得吸附等温线与Langmuir和Temkin模型拟合较好,Langmuir模型计算的吸附容量理论最大值为495 mg/g。四环素、土霉素在氧化石墨烯上的吸附量随着ph的增加而下降。本研究的目的是制备和修饰氧化石墨烯,制备一种药物吸附剂,用于在模拟犬体环境中缓慢吸附和释放药物土霉素,并研究了环氧氯丙烷和Cibacron Blue对土霉素释放的修饰和增强作用。
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
CiteScore
5.30
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