Configurational biomimesis in drug delivery: molecular imprinting of biologically significant molecules

被引:190
作者
Hilt, JZ
Byrne, ME [1 ]
机构
[1] Auburn Univ, Biomimet & Biohybrid Mat Lab, Auburn, AL 36849 USA
[2] Auburn Univ, Biomed Devices Lab, Auburn, AL 36849 USA
[3] Auburn Univ, Drug Dev Lab, Dept Chem Engn, Auburn, AL 36849 USA
[4] Univ Kentucky, Dept Chem & Mat Engn, Lexington, KY 40506 USA
关键词
configurational biomimesis; biomimetic; imprinting; molecular imprinting; drug delivery; controlled release; modulated release; intelligent gels; analyte sensitive gels; biosensors;
D O I
10.1016/j.addr.2004.04.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This review focuses on trends in the macromolecular recognition of biologically significant molecules (e.g., drugs, amino acids, steroids, nucleotide bases, carbohydrates, etc.) via molecular imprinting methods. An extensive list of prior art including type of functional monomers and crosslinkers for each biomolecule imprinted polymer is presented. Representative samples of receptor-ligand dissociation constants and polymer capacities are presented as well as typical values that occur in classes of biological recognition systems. Imprinting technology has direct impact in enhanced drug loading of control led-release carriers for the sustained release of therapeutic agents as well as robust biosensors for novel therapeutic and diagnostic devices. This review also discusses the future of designed recognition, configurational biomimesis within polymeric gels, and highlights recent efforts toward integrating imprinted polymers in controlled drug delivery systems and sensing devices. In particular, the application of imprinted polymers for sustained release, enhanced loading capacity, and enantioselective loading or release are discussed. This article also highlights the most important problems to be solved in the design of synthetic recognition-based networks for biological molecules. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:1599 / 1620
页数:22
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