含有粘土的pla -淀粉微粒聚焦控释利福平

L. M. Brito, M. Tavares
{"title":"含有粘土的pla -淀粉微粒聚焦控释利福平","authors":"L. M. Brito, M. Tavares","doi":"10.4236/msa.2022.137026","DOIUrl":null,"url":null,"abstract":"Polymer nanocomposites have been successfully used as excipients in pharmaceutical technology because of the convenient features that make them suitable for many applications, especially in controlled drug delivery therapies. The objective of this work was to prepare and characterize PLA and starch microparticles containing Viscogel B8 organophilic clay as a matrix for controlled release of rifampicin, one of the most spread drugs for tuberculosis treatment. The systems obtained by the spray drying technique were charac-terized by DRX, FTIR, SEM and low-field NMR. In addition, dissolution tests were performed on simulated gastric fluid. The micrographs indicate that the presence of the drug caused a small change in the shape and size of the particles. In the presence of the drug, the particles were spherical and presented wider size distribution. The XRD assays didn’t show crystalline peaks of rifampicin in the microparticles, which suggests that rifampicin exists in an amorphous solid solution inside the starch-PLA particles. The mathematical model of Baker-Lonsdale was chosen for the treatment of the dissolution data, describing the controlled release of the drug from the matrix by a spherical diffusion process. The results suggest that the proposed release system may be used for the delivery of orally administered drugs, such as rifampicin. treatment, reducing the required doses and systemic side effects.","PeriodicalId":68376,"journal":{"name":"材料科学与应用期刊(英文)","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PLA-Starch Microparticles Containing Clays Focusing Controlled Release of Rifampicin\",\"authors\":\"L. M. Brito, M. Tavares\",\"doi\":\"10.4236/msa.2022.137026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Polymer nanocomposites have been successfully used as excipients in pharmaceutical technology because of the convenient features that make them suitable for many applications, especially in controlled drug delivery therapies. The objective of this work was to prepare and characterize PLA and starch microparticles containing Viscogel B8 organophilic clay as a matrix for controlled release of rifampicin, one of the most spread drugs for tuberculosis treatment. The systems obtained by the spray drying technique were charac-terized by DRX, FTIR, SEM and low-field NMR. In addition, dissolution tests were performed on simulated gastric fluid. The micrographs indicate that the presence of the drug caused a small change in the shape and size of the particles. In the presence of the drug, the particles were spherical and presented wider size distribution. The XRD assays didn’t show crystalline peaks of rifampicin in the microparticles, which suggests that rifampicin exists in an amorphous solid solution inside the starch-PLA particles. The mathematical model of Baker-Lonsdale was chosen for the treatment of the dissolution data, describing the controlled release of the drug from the matrix by a spherical diffusion process. The results suggest that the proposed release system may be used for the delivery of orally administered drugs, such as rifampicin. treatment, reducing the required doses and systemic side effects.\",\"PeriodicalId\":68376,\"journal\":{\"name\":\"材料科学与应用期刊(英文)\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"材料科学与应用期刊(英文)\",\"FirstCategoryId\":\"91\",\"ListUrlMain\":\"https://doi.org/10.4236/msa.2022.137026\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"材料科学与应用期刊(英文)","FirstCategoryId":"91","ListUrlMain":"https://doi.org/10.4236/msa.2022.137026","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

聚合物纳米复合材料已成功地用作赋形剂在制药技术,因为方便的特点,使其适合于许多应用,特别是在控制药物输送治疗。本研究的目的是制备含有粘胶B8亲有机粘土的聚乳酸和淀粉微颗粒,并对其进行表征,以作为控释利福平的基质。利福平是最广泛的结核病治疗药物之一。用DRX、FTIR、SEM和低场NMR对喷雾干燥得到的体系进行了表征。此外,还对模拟胃液进行了溶出试验。显微照片显示,药物的存在引起了颗粒形状和大小的微小变化。药物存在时,颗粒呈球形,粒径分布较宽。XRD分析显示,微颗粒中没有利福平的结晶峰,说明利福平存在于淀粉-聚乳酸颗粒内部的无定形固溶体中。采用Baker-Lonsdale数学模型处理溶出度数据,描述药物通过球形扩散过程从基质中控制释放。结果表明,该释放系统可用于口服药物的释放,如利福平。治疗,减少所需剂量和全身副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PLA-Starch Microparticles Containing Clays Focusing Controlled Release of Rifampicin
Polymer nanocomposites have been successfully used as excipients in pharmaceutical technology because of the convenient features that make them suitable for many applications, especially in controlled drug delivery therapies. The objective of this work was to prepare and characterize PLA and starch microparticles containing Viscogel B8 organophilic clay as a matrix for controlled release of rifampicin, one of the most spread drugs for tuberculosis treatment. The systems obtained by the spray drying technique were charac-terized by DRX, FTIR, SEM and low-field NMR. In addition, dissolution tests were performed on simulated gastric fluid. The micrographs indicate that the presence of the drug caused a small change in the shape and size of the particles. In the presence of the drug, the particles were spherical and presented wider size distribution. The XRD assays didn’t show crystalline peaks of rifampicin in the microparticles, which suggests that rifampicin exists in an amorphous solid solution inside the starch-PLA particles. The mathematical model of Baker-Lonsdale was chosen for the treatment of the dissolution data, describing the controlled release of the drug from the matrix by a spherical diffusion process. The results suggest that the proposed release system may be used for the delivery of orally administered drugs, such as rifampicin. treatment, reducing the required doses and systemic side effects.
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
自引率
0.00%
发文量
1046
×
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