用于治疗牙周炎的盐酸莫西沙星醋酸纤维素丁酯原位成形凝胶

IF 3.4 4区 医学 Q2 PHARMACOLOGY & PHARMACY AAPS PharmSciTech Pub Date : 2024-10-14 DOI:10.1208/s12249-024-02960-1
Warakon Thammasut, Catleya Rojviriya, Pornsit Chaiya, Thawatchai Phaechamud, Sucharat Limsitthichaikoon
{"title":"用于治疗牙周炎的盐酸莫西沙星醋酸纤维素丁酯原位成形凝胶","authors":"Warakon Thammasut,&nbsp;Catleya Rojviriya,&nbsp;Pornsit Chaiya,&nbsp;Thawatchai Phaechamud,&nbsp;Sucharat Limsitthichaikoon","doi":"10.1208/s12249-024-02960-1","DOIUrl":null,"url":null,"abstract":"<p>Periodontitis presents significant treatment challenges due to its complexity and potential complications. In response, an <i>in situ</i> forming gel (ISG) loaded with moxifloxacin HCl (Mx) and cellulose acetate butyrate (CAB) was developed for targeted periodontitis therapy. Mx-loaded 10–45% CAB-based ISGs were developed, and their physicochemical properties such as rheology, viscosity, contact angle, gel morphology and gel formation, interface interaction were investigated. Moreover, the formulation performance studies including drug release and kinetics, <i>in vitro</i> degradation, and antimicrobial activities were also evaluated. The Mx-loaded ISGs containing 25–45% CAB demonstrated rapid matrix formation in both macroscopic and microscopic examinations and presented plastic deformation matrix. Tracking with sodium fluorescein and Nile red fluorescence probes indicated delayed solvent movement owing to CAB matrix formation. Adequate CAB content sustained Mx release for one week, following Peppas-Sahlin model and indicating a predominantly Fickian diffusion mechanism. Higher CAB content likely contributed to a denser matrix structure, leading to a slower <i>in vitro</i> degradation rate. Synchrotron radiation X-ray tomographic and SEM imaging provided insights into the CAB matrix structure and porous network formation. These ISG formulations effectively inhibited <i>Staphylococcus aureus, Escherichia coli, Candida albicans,</i> and <i>Porphyromonas gingivalis</i>. The Mx-loaded 40% CAB-based ISG shows promise as a dosage form for treating periodontitis. Further clinical trials are necessary to ensure the safety of this new ISG formulation, despite existing safety data for other medicinal uses of CAB.</p>","PeriodicalId":6925,"journal":{"name":"AAPS PharmSciTech","volume":"25 7","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Moxifloxacin HCl -loaded Cellulose Acetate Butylate In Situ Forming Gel for Periodontitis Treatment\",\"authors\":\"Warakon Thammasut,&nbsp;Catleya Rojviriya,&nbsp;Pornsit Chaiya,&nbsp;Thawatchai Phaechamud,&nbsp;Sucharat Limsitthichaikoon\",\"doi\":\"10.1208/s12249-024-02960-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Periodontitis presents significant treatment challenges due to its complexity and potential complications. In response, an <i>in situ</i> forming gel (ISG) loaded with moxifloxacin HCl (Mx) and cellulose acetate butyrate (CAB) was developed for targeted periodontitis therapy. Mx-loaded 10–45% CAB-based ISGs were developed, and their physicochemical properties such as rheology, viscosity, contact angle, gel morphology and gel formation, interface interaction were investigated. Moreover, the formulation performance studies including drug release and kinetics, <i>in vitro</i> degradation, and antimicrobial activities were also evaluated. The Mx-loaded ISGs containing 25–45% CAB demonstrated rapid matrix formation in both macroscopic and microscopic examinations and presented plastic deformation matrix. Tracking with sodium fluorescein and Nile red fluorescence probes indicated delayed solvent movement owing to CAB matrix formation. Adequate CAB content sustained Mx release for one week, following Peppas-Sahlin model and indicating a predominantly Fickian diffusion mechanism. Higher CAB content likely contributed to a denser matrix structure, leading to a slower <i>in vitro</i> degradation rate. Synchrotron radiation X-ray tomographic and SEM imaging provided insights into the CAB matrix structure and porous network formation. These ISG formulations effectively inhibited <i>Staphylococcus aureus, Escherichia coli, Candida albicans,</i> and <i>Porphyromonas gingivalis</i>. The Mx-loaded 40% CAB-based ISG shows promise as a dosage form for treating periodontitis. Further clinical trials are necessary to ensure the safety of this new ISG formulation, despite existing safety data for other medicinal uses of CAB.</p>\",\"PeriodicalId\":6925,\"journal\":{\"name\":\"AAPS PharmSciTech\",\"volume\":\"25 7\",\"pages\":\"\"},\"PeriodicalIF\":3.4000,\"publicationDate\":\"2024-10-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"AAPS PharmSciTech\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://link.springer.com/article/10.1208/s12249-024-02960-1\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"AAPS PharmSciTech","FirstCategoryId":"3","ListUrlMain":"https://link.springer.com/article/10.1208/s12249-024-02960-1","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

牙周炎因其复杂性和潜在并发症给治疗带来了巨大挑战。为此,我们开发了一种负载盐酸莫西沙星(Mx)和醋酸丁酸纤维素(CAB)的原位成型凝胶(ISG),用于牙周炎的靶向治疗。研究人员开发了含盐酸莫西沙星(Mx)和醋酸纤维素丁酸酯(CAB)的 ISG,并对其流变学、粘度、接触角、凝胶形态和凝胶形成、界面相互作用等理化性质进行了研究。此外,还评估了药物释放和动力学、体外降解和抗菌活性等制剂性能研究。含有 25-45% CAB 的 Mx 负载 ISGs 在宏观和微观检查中都显示出基质的快速形成,并呈现出塑性变形基质。荧光素钠和尼罗河红荧光探针的跟踪显示,CAB基质的形成延迟了溶剂的移动。根据 Peppas-Sahlin 模型,充足的 CAB 含量可使 Mx 的释放持续一周,这表明主要是一种 Fickian 扩散机制。CAB 含量越高,基质结构越致密,体外降解速度越慢。同步辐射 X 射线断层扫描和扫描电子显微镜成像深入揭示了 CAB 的基质结构和多孔网络的形成。这些 ISG 配方能有效抑制金黄色葡萄球菌、大肠杆菌、白色念珠菌和牙龈卟啉单胞菌。以 Mx 为载体、40% CAB 为基质的 ISG 作为治疗牙周炎的剂型前景广阔。尽管已有 CAB 其他药用用途的安全数据,但仍有必要进行进一步的临床试验,以确保这种新型 ISG 制剂的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Moxifloxacin HCl -loaded Cellulose Acetate Butylate In Situ Forming Gel for Periodontitis Treatment

Periodontitis presents significant treatment challenges due to its complexity and potential complications. In response, an in situ forming gel (ISG) loaded with moxifloxacin HCl (Mx) and cellulose acetate butyrate (CAB) was developed for targeted periodontitis therapy. Mx-loaded 10–45% CAB-based ISGs were developed, and their physicochemical properties such as rheology, viscosity, contact angle, gel morphology and gel formation, interface interaction were investigated. Moreover, the formulation performance studies including drug release and kinetics, in vitro degradation, and antimicrobial activities were also evaluated. The Mx-loaded ISGs containing 25–45% CAB demonstrated rapid matrix formation in both macroscopic and microscopic examinations and presented plastic deformation matrix. Tracking with sodium fluorescein and Nile red fluorescence probes indicated delayed solvent movement owing to CAB matrix formation. Adequate CAB content sustained Mx release for one week, following Peppas-Sahlin model and indicating a predominantly Fickian diffusion mechanism. Higher CAB content likely contributed to a denser matrix structure, leading to a slower in vitro degradation rate. Synchrotron radiation X-ray tomographic and SEM imaging provided insights into the CAB matrix structure and porous network formation. These ISG formulations effectively inhibited Staphylococcus aureus, Escherichia coli, Candida albicans, and Porphyromonas gingivalis. The Mx-loaded 40% CAB-based ISG shows promise as a dosage form for treating periodontitis. Further clinical trials are necessary to ensure the safety of this new ISG formulation, despite existing safety data for other medicinal uses of CAB.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
AAPS PharmSciTech
AAPS PharmSciTech 医学-药学
CiteScore
6.80
自引率
3.00%
发文量
264
审稿时长
2.4 months
期刊介绍: AAPS PharmSciTech is a peer-reviewed, online-only journal committed to serving those pharmaceutical scientists and engineers interested in the research, development, and evaluation of pharmaceutical dosage forms and delivery systems, including drugs derived from biotechnology and the manufacturing science pertaining to the commercialization of such dosage forms. Because of its electronic nature, AAPS PharmSciTech aspires to utilize evolving electronic technology to enable faster and diverse mechanisms of information delivery to its readership. Submission of uninvited expert reviews and research articles are welcomed.
期刊最新文献
The Role of Phase Separation and Local Mobility in the Stabilization of a Lyophilized IgG2 Formulation Predicting the Thermodynamic Solubility and Stability of Co-crystals and Eutectics of Febuxostat by using a Thermodynamic Model involving Flory Huggins Interaction Parameter The Role of Amphiphilic Compounds in Nasal Nanoparticles Correction: Croscarmellose Sodium as Pelletization Aid in Extrusion-Spheronization Chitosan-Based Nanoformulations: Preclinical Investigations, Theranostic Advancements, and Clinical Trial Prospects for Targeting Diverse Pathologies
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1