Understanding release kinetics of biopolymer drug delivery microcapsules for biomedical applications

被引:30
作者
Desai, Salil [1 ,2 ,3 ]
Perkins, Jessica [1 ,2 ]
Harrison, Benjamin S. [3 ]
Sankar, Jag [2 ]
机构
[1] N Carolina Agr & Tech State Univ, Dept Ind & Syst Engn, Greensboro, NC 27411 USA
[2] N Carolina Agr & Tech State Univ, Ctr Adv Mat & Smart Struct, Greensboro, NC 27411 USA
[3] Wake Forest Univ, Inst Regenerat Med, Winston Salem, NC 27157 USA
来源
MATERIALS SCIENCE AND ENGINEERING B-ADVANCED FUNCTIONAL SOLID-STATE MATERIALS | 2010年 / 168卷 / 1-3期
基金
美国国家科学基金会;
关键词
Drug delivery; Release kinetics; Direct-write inkjet; Bio-polymers; Calcium alginate microcapsules; ALGINATE; MICROPARTICLES; EXCHANGE; BEADS; MICROSPHERES; MICROBEADS;
D O I
10.1016/j.mseb.2009.11.006
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Drug delivery and dosage concentrations are considered as major focal points in conventional as well as battlefield emergency medicine. The concept of localizing drug delivery via microcapsules is an evolving field to confine the adverse side effects of high concentration drug doses. This paper focuses on understanding release kinetics through biopolymer microcapsules for time-dependent drug release. Calcium alginate microcapsules were manufactured using a direct-write inkjet technique. Rhodamine 6G was used as the release agent to observe the release kinetics from calcium alginate beads in distilled water. A design of experiments was constructed to compare the effect of the microcapsule diameter and different concentrations of calcium chloride (M) and sodium alginate (%, w/v) solutions on the release kinetics profiles of the microcapsules. This research gives insight to identify favorable sizes of microcapsules and concentrations of sodium alginate and calcium chloride solutions for controlled release behavior of drug delivery microcapsules. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:127 / 131
页数:5
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