• 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-聚合物复合片剂扩散的统一数学模型

A unified mathematical model for diffusion from drug-polymer composite tablets.

作者信息

Fu J C, Hagemeir C, Moyer D L

出版信息

J Biomed Mater Res. 1976 Sep;10(5):743-58. doi: 10.1002/jbm.820100507.

DOI:10.1002/jbm.820100507
PMID:977604
Abstract

The derivation and experimental verification of a unified mathematical model for the estimation of drug release rate from drug-polymer composite tablets are presented. Cylindrical coordinates are utilized in the solution of the diffusion equation for a three-dimensional system. The model is applicable to tablets that range from the shape of a flat disk (radius greater than thickness) to that of a cylindrical rod (radius less than thickness). The general solution for the fraction of drug released at a time t is (see article). This approach to a three-dimensional system, utilizing cylindrical coordinates, presents a comprehensive method for the estimation of drug release rates from sustained release tablets with drug distributed homogeneously throughout a polymer matrix. The calculated and experimental drug diffusion rate of pyrimethamine from pyrimethamine-silicone rubber composite tablets that range in shape from that of a disk to a cylinder, and of hydrocortisone from EVA, polycaprolactone, and PVA terpolymer, are compared.

摘要

本文介绍了一种用于估算药物-聚合物复合片剂药物释放速率的统一数学模型的推导及实验验证。在求解三维系统的扩散方程时采用了圆柱坐标系。该模型适用于从扁平圆盘形状(半径大于厚度)到圆柱形棒状(半径小于厚度)的片剂。在时间t时药物释放分数的通解见文章。这种利用圆柱坐标系处理三维系统的方法,为估算药物均匀分布于聚合物基质中的缓释片剂的药物释放速率提供了一种全面的方法。比较了从圆盘到圆柱形状的乙胺嘧啶-硅橡胶复合片剂中乙胺嘧啶以及从乙烯-醋酸乙烯共聚物、聚己内酯和聚乙烯醇三元共聚物中氢化可的松的计算和实验药物扩散速率。

相似文献

1
A unified mathematical model for diffusion from drug-polymer composite tablets.药物-聚合物复合片剂扩散的统一数学模型
J Biomed Mater Res. 1976 Sep;10(5):743-58. doi: 10.1002/jbm.820100507.
2
Mathematical models for the release of drugs from matrix tablets.骨架片药物释放的数学模型。
J Biomed Mater Res. 1978 Sep;12(5):627-34. doi: 10.1002/jbm.820120505.
3
Effect of comonomer ratio on hydrocortisone diffusion from sustained-release composite capsules.共聚单体比例对氢化可的松从缓释复合胶囊中扩散的影响。
J Biomed Mater Res. 1978 May;12(3):249-54. doi: 10.1002/jbm.820120302.
4
A model for the drug release from a polymer matrix tablet--effects of swelling and dissolution.聚合物基质片剂药物释放模型——溶胀与溶解的影响
J Control Release. 2006 Jul 20;113(3):216-25. doi: 10.1016/j.jconrel.2006.05.004. Epub 2006 May 12.
5
Extended release of a large amount of highly water-soluble diltiazem hydrochloride by utilizing counter polymer in polyethylene oxides (PEO)/polyethylene glycol (PEG) matrix tablets.通过在聚环氧乙烷(PEO)/聚乙二醇(PEG)基质片剂中利用反聚合物实现大量高水溶性盐酸地尔硫䓬的缓释。
Eur J Pharm Biopharm. 2008 Oct;70(2):556-62. doi: 10.1016/j.ejpb.2008.05.032. Epub 2008 Jun 19.
6
Mathematical modeling and in vitro study of controlled drug release via a highly swellable and dissoluble polymer matrix: polyethylene oxide with high molecular weights.通过高膨胀性和溶解性聚合物基质实现药物控释的数学建模与体外研究:高分子量聚环氧乙烷
J Control Release. 2005 Feb 16;102(3):569-81. doi: 10.1016/j.jconrel.2004.11.002.
7
[Two sorts of problems on drug controlled release from swellable polymer].[关于可膨胀聚合物药物控释的两类问题]
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2003 Mar;20(1):17-21.
8
Mechanisms of chlorpheniramine maleate release from hydrophilic swellable polymer systems.马来酸氯苯那敏从亲水性可溶胀聚合物体系中的释放机制。
P R Health Sci J. 1997 Sep;16(3):259-63.
9
Modeling of dispersed-drug release from two-dimensional matrix tablets.二维矩阵片剂中分散药物释放的建模。
Biomaterials. 2005 Mar;26(8):945-52. doi: 10.1016/j.biomaterials.2004.03.034.
10
Two galactomannans and scleroglucan as matrices for drug delivery: preparation and release studies.两种半乳甘露聚糖和硬葡聚糖作为药物递送载体:制备与释放研究
Eur J Pharm Biopharm. 2007 May;66(2):200-9. doi: 10.1016/j.ejpb.2006.10.024. Epub 2006 Dec 6.

引用本文的文献

1
From Microscale to Macroscale: Nine Orders of Magnitude for a Comprehensive Modeling of Hydrogels for Controlled Drug Delivery.从微观尺度到宏观尺度:用于药物控释的水凝胶综合建模的九个数量级
Gels. 2019 May 15;5(2):28. doi: 10.3390/gels5020028.
2
Novel bioerodable eluting-spacers for radiotherapy applications with dose painting.用于剂量描绘放射治疗应用的新型生物可蚀性洗脱间隔物。
Br J Radiol. 2019 Jun;92(1098):20180745. doi: 10.1259/bjr.20180745. Epub 2019 May 14.
3
Prediction of the partition coefficients using QSPR modeling and simulation of paclitaxel release from the diffusion-controlled drug delivery devices.
应用 QSPR 模型预测分配系数并模拟扩散控制型药物释放装置中紫杉醇的释放。
Drug Deliv Transl Res. 2018 Oct;8(5):1300-1312. doi: 10.1007/s13346-018-0530-8.
4
Addition of perfluorocarbons to alginate hydrogels significantly impacts molecular transport and fracture stress.向藻酸盐水凝胶中添加全氟碳化合物会显著影响分子传递和断裂应力。
J Biomed Mater Res A. 2013 Feb;101(2):438-46. doi: 10.1002/jbm.a.34344. Epub 2012 Aug 3.
5
Transport of biological molecules in surfactant-alginate composite hydrogels.表面活性剂-海藻酸盐复合水凝胶中生物分子的传输。
Acta Biomater. 2011 Nov;7(11):3988-98. doi: 10.1016/j.actbio.2011.07.009. Epub 2011 Jul 14.
6
A reappraisal of drug release laws using Monte Carlo simulations: the prevalence of the Weibull function.使用蒙特卡洛模拟对药物释放规律的重新评估:威布尔函数的普遍性
Pharm Res. 2003 Jul;20(7):988-95. doi: 10.1023/a:1024497920145.
7
Controlled release of plasmid DNA from a genetically engineered silk-elastinlike hydrogel.从基因工程化的丝-弹性蛋白样水凝胶中控制释放质粒DNA。
Pharm Res. 2002 Jul;19(7):954-9. doi: 10.1023/a:1016406120288.