• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

药物从可生物侵蚀的球形胶囊中的扩散和释放。

Drug diffusion and release from a bioerodible spherical capsule.

机构信息

Mechanical and Aerospace Engineering Department, University of Texas at Arlington, Arlington, TX, USA.

Division of Biomedical Engineering, University of Glasgow, UK; Glasgow Computational Engineering Centre, University of Glasgow, Glasgow, UK.

出版信息

Int J Pharm. 2022 Mar 25;616:121442. doi: 10.1016/j.ijpharm.2021.121442. Epub 2022 Jan 4.

DOI:10.1016/j.ijpharm.2021.121442
PMID:34990743
Abstract

Controlled release of a drug contained in a spherical polymer capsule is of significant interest in many fields of medicine. There is growing interest in tailoring the erosion properties of the drug to help control and optimize the drug release process. Theoretical understanding of the nature of drug release from a bioerodible capsule is, therefore, important for designing effective drug delivery systems. While drug release from a fixed-radius capsule is relatively easier to model, the shrinking nature of a bioerodible capsule due to surface erosion presents several difficulties in theoretical modeling. This work presents a closed-form solution for the drug concentration distribution and drug delivery characteristics from a spherical capsule undergoing linear surface erosion. This problem is solved by a transformation that converts the moving boundary problem into a fixed boundary problem. For uniform initial drug distribution, the solution is shown to depend on a single non-dimensional parameter. The theoretical model is used to develop an understanding of the impact of varying the drug diffusion coefficient and rate of erosion on drug delivery characteristics. It is found that, in general, the nature of drug release in a bioerodible sphere is determined by a delicate balance between two simultaneously occurring processes - erosion and diffusion. This work improves the theoretical understanding of diffusion in drug delivery systems by accounting for the practical erosion phenomena, and may contribute towards the design and optimization of drug delivery systems.

摘要

球形聚合物胶囊中药物的控制释放在许多医学领域都具有重要意义。人们越来越感兴趣的是调整药物的侵蚀特性,以帮助控制和优化药物释放过程。因此,从理论上理解生物可蚀胶囊中药物释放的性质对于设计有效的药物输送系统非常重要。虽然从固定半径胶囊中释放药物的模型相对简单,但由于表面侵蚀导致生物可蚀胶囊的收缩性质在理论建模方面存在一些困难。本工作提出了一种用于线性表面侵蚀球形胶囊中药物浓度分布和药物输送特性的封闭解。通过一种将移动边界问题转化为固定边界问题的变换来解决这个问题。对于均匀的初始药物分布,该解仅取决于一个无量纲参数。该理论模型用于了解改变药物扩散系数和侵蚀速率对药物输送特性的影响。结果表明,一般来说,生物可蚀球体中药物释放的性质取决于两个同时发生的过程——侵蚀和扩散之间的微妙平衡。本工作通过考虑实际的侵蚀现象,提高了药物输送系统中扩散的理论理解,并可能有助于药物输送系统的设计和优化。

相似文献

1
Drug diffusion and release from a bioerodible spherical capsule.药物从可生物侵蚀的球形胶囊中的扩散和释放。
Int J Pharm. 2022 Mar 25;616:121442. doi: 10.1016/j.ijpharm.2021.121442. Epub 2022 Jan 4.
2
Mathematical modeling of bioerodible, polymeric drug delivery systems.生物可蚀解性聚合物药物递送系统的数学建模
Adv Drug Deliv Rev. 2001 Jun 11;48(2-3):229-47. doi: 10.1016/s0169-409x(01)00116-8.
3
Biodegradable polymers in controlled drug delivery.用于控释给药的可生物降解聚合物。
Crit Rev Ther Drug Carrier Syst. 1984;1(1):39-90.
4
Simulation of drug release from biodegradable polymeric microspheres with bulk and surface erosions.具有整体和表面侵蚀的可生物降解聚合物微球药物释放模拟。
J Pharm Sci. 2003 Oct;92(10):2040-56. doi: 10.1002/jps.10463.
5
Modeling of drug release from bioerodible polymer matrices.可生物降解聚合物基质中药物释放的建模
Drug Deliv. 2005 Sep-Oct;12(5):251-9. doi: 10.1080/10717540500176043.
6
Controlled diffusional release of dispersed solute drugs from biodegradable implants of various geometries.各种几何形状的可生物降解植入物中分散溶质药物的可控扩散释放。
Biomed Sci Instrum. 1997;33:137-42.
7
Mathematical modeling of polymer erosion: consequences for drug delivery.聚合物侵蚀的数学建模:对药物输送的影响。
Int J Pharm. 2011 Oct 10;418(1):104-14. doi: 10.1016/j.ijpharm.2010.11.048. Epub 2010 Dec 3.
8
Mathematical modeling of drug release from bioerodible microparticles: effect of gamma-irradiation.可生物降解微粒药物释放的数学模型:γ 辐射的影响
Eur J Pharm Biopharm. 2003 Sep;56(2):271-9. doi: 10.1016/s0939-6411(03)00104-8.
9
Controlling release from encapsulated drug-loaded devices: insights from modeling the dissolution front propagation.控制包载药物的设备中的药物释放:从溶解前沿推进建模中获得的认识。
J Control Release. 2023 Aug;360:225-235. doi: 10.1016/j.jconrel.2023.06.019. Epub 2023 Jun 26.
10
Investigation of the Size Distribution for Diffusion-Controlled Drug Release From Drug Delivery Systems of Various Geometries.研究不同几何形状给药系统中扩散控制药物释放的粒径分布。
J Pharm Sci. 2019 Aug;108(8):2690-2697. doi: 10.1016/j.xphs.2019.03.036. Epub 2019 Apr 11.

引用本文的文献

1
A review on selenium and gold nanoparticles combined photodynamic and photothermal prostate cancer tumors ablation.硒与金纳米颗粒联合光动力和光热消融前列腺癌肿瘤的综述。
Discov Nano. 2023 Dec 7;18(1):150. doi: 10.1186/s11671-023-03936-z.
2
Hydrophobic Drug Carrier from Polycaprolactone--Poly(Ethylene Glycol) Star-Shaped Polymers Hydrogel Blend as Potential for Wound Healing Application.聚己内酯-聚(乙二醇)星形聚合物水凝胶共混物制成的疏水性药物载体在伤口愈合应用中的潜力
Polymers (Basel). 2023 Apr 27;15(9):2072. doi: 10.3390/polym15092072.
3
Optimization of Initial Drug Distribution in Spherical Capsules for Personalized Release.
优化用于个性化释放的球形胶囊中的初始药物分布。
Pharm Res. 2022 Oct;39(10):2607-2620. doi: 10.1007/s11095-022-03359-y. Epub 2022 Sep 7.