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离子交换纤维与药物:一项瞬态研究。

Ion-exchange fibers and drugs: a transient study.

作者信息

Vuorio M, Manzanares J A, Murtomäki L, Hirvonen J, Kankkunen T, Kontturi K

机构信息

Laboratory of Physical Chemistry and Electrochemistry, Helsinki University of Technology, P.O. Box 6100, FIN-02015 HUT, Finland.

出版信息

J Control Release. 2003 Sep 4;91(3):439-48. doi: 10.1016/s0168-3659(03)00270-0.

Abstract

The objective of this study was to theoretically model and experimentally measure the kinetics and extent of drug release from different ion-exchange materials using an in-house-designed flow-cell. Ion-exchange fibers (staple fibers and fiber cloth) were compared with commercially available ion-exchange materials (resins and gels). The functional ion-exchange groups in all the materials were weak -COOH or strong -SO3H groups. The rate and extent of drug release from the fibers (staple fiber>fiber cloth) was much higher than that from the resin or the gel. An increase in the hydrophilicity of the model drugs resulted in markedly higher rates of drug release from the fibers (nadolol>metoprolol>propranolol>tacrine). Theoretical modelling of the kinetics of ion exchange provided satisfactory explanations for the experimental observations: firstly, a change in the equilibrium constant of the ion-exchange reaction depending on the drug and the ion-exchange material and, secondly, a decrease in the Peclet number (Pe) with decreasing flow-rate of the drug-releasing salt solution.

摘要

本研究的目的是使用自行设计的流通池,从理论上对不同离子交换材料的药物释放动力学和释放程度进行建模,并通过实验进行测量。将离子交换纤维(短纤维和纤维布)与市售离子交换材料(树脂和凝胶)进行比较。所有材料中的功能性离子交换基团均为弱-COOH或强-SO3H基团。纤维(短纤维>纤维布)的药物释放速率和程度远高于树脂或凝胶。模型药物亲水性的增加导致纤维的药物释放速率显著提高(纳多洛尔>美托洛尔>普萘洛尔>他克林)。离子交换动力学的理论建模为实验观察结果提供了令人满意的解释:首先,离子交换反应的平衡常数会根据药物和离子交换材料而变化;其次,随着药物释放盐溶液流速的降低,佩克莱数(Pe)会减小。

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