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阴离子共聚物凝胶的溶胀/消溶胀

Swelling/deswelling of anionic copolymer gels.

作者信息

Khare A R, Peppas N A

机构信息

School of Chemical Engineering, Purdue University, West Lafayette, IN 47907-1283, USA.

出版信息

Biomaterials. 1995 May;16(7):559-67. doi: 10.1016/0142-9612(95)91130-q.

Abstract

Studies of dynamic and equilibrium swelling of ionic gels are important in understanding the diffusion of physiologically important fluids in materials for site-specific controlled drug delivery applications. The dynamic and equilibrium swelling properties of dry glassy poly(2-hydroxyethyl methacrylate-co-methacrylic acid) and poly(2-hydroxyethyl methacrylate-co-acrylic acid) polymeric networks were studied as a function of pH, ionic strength, nature of the counterion and buffer composition. The mechanism of water diffusion in these gels became more anomalous as the pH of the swelling medium increased and as the ionic strength decreased at a constant pH > or = pKa,gel. The mechanism of water diffusion was Fickian in all unbuffered swelling media at pH 4.0, which is lower than the pKa,gel. The pKa,gel of these gels was between 5.5 and 6. At pH 4.0, the diffusion mechanism was independent of ionic strength. This swelling behaviour is explained in terms of the concept of ion osmotic swelling pressure and ion exchange kinetics.

摘要

离子凝胶的动态和平衡溶胀研究对于理解生理重要流体在用于特定部位控制药物递送应用的材料中的扩散至关重要。研究了干燥玻璃态聚(甲基丙烯酸2-羟乙酯-共-甲基丙烯酸)和聚(甲基丙烯酸2-羟乙酯-共-丙烯酸)聚合物网络的动态和平衡溶胀性质,作为pH值、离子强度、抗衡离子性质和缓冲液组成的函数。在恒定pH≥pKa,凝胶时,随着溶胀介质pH值的增加和离子强度的降低,这些凝胶中水扩散的机制变得更加反常。在pH 4.0(低于pKa,凝胶)的所有无缓冲溶胀介质中,水扩散机制是菲克扩散。这些凝胶的pKa,凝胶在5.5至6之间。在pH 4.0时,扩散机制与离子强度无关。这种溶胀行为根据离子渗透溶胀压力和离子交换动力学的概念进行了解释。

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