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首页> 外文期刊>European journal of pharmaceutics and biopharmaceutics: official journal of Arbeitsgemeinschaft fuer Pharmazeutische Verfahrenstechnik e.V >The influence of multivalent phosphate structure on the properties of ionically cross-linked chitosan films for controlled drug release.
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The influence of multivalent phosphate structure on the properties of ionically cross-linked chitosan films for controlled drug release.

机译:多价磷酸盐结构对离子交联壳聚糖膜控制药物释放性能的影响。

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摘要

The aim of this paper was to investigate the electrostatic interactions between multivalent phosphates (phosphate (Phos), pyrophosphate (Pyro) and tripolyphosphate (TPP)) and chitosan, as well as the influence of electrostatic interactions on the properties of chitosan films ionically cross-linked by the above mentioned phosphates. The charge number of Phos was too low to interact with chitosan, while Pyro and TPP with more negative charges showed a significant ability to ionically cross-link chitosan. Solution pH played an important role on the charge numbers carried by Pyro, TPP and chitosan, especially for Pyro/chitosan. For instance, at pH less than 2.0 the interaction between Pyro and chitosan disappeared, while for TPP/chitosan even in solutions at pH less than 0.5 it still existed. Media pH and ionic strength also had a significant influence on the properties of cross-linked chitosan film with multivalent phosphates. Usually these films swelled and drug was released quickly in acidic conditions (such as in simulated gastric fluid) while under neutral conditions (such as in simulated intestinal fluid) they remained in a shrinkage state and drug was released slowly. Compared to TPP/chitosan films, Pyro/chitosan films exhibited much better pH-sensitive swelling and controlled release properties due to their relatively weak electrostatic interaction. The same reasoning was used to explain the significant acceleration of Pyro/chitosan film swelling and model drug release observed on adding sodium chloride. These films may be promising for site-specific drug delivery in the stomach.
机译:本文的目的是研究多价磷酸盐(磷酸盐(Phos),焦磷酸盐(Pyro)和三聚磷酸盐(TPP))与壳聚糖之间的静电相互作用,以及静电相互作用对壳聚糖膜离子交联性能的影响。由上述磷酸盐连接。 Phos的电荷数太低,无法与壳聚糖相互作用,而带有更多负电荷的Pyro和TPP显示出显着的使壳聚糖离子交联的能力。溶液的pH值对Pyro,TPP和壳聚糖所带电荷的数量起着重要作用,尤其是对于Pyro /壳聚糖而言。例如,在pH值小于2.0时,吡咯和壳聚糖之间的相互作用消失了,而对于TPP /壳聚糖,即使在pH值小于0.5的溶液中仍然存在。介质的pH值和离子强度也对具有多价磷酸盐的交联壳聚糖膜的性能产生重大影响。通常,这些薄膜在酸性条件下(例如在模拟的胃液中)会溶胀并快速释放药物,而在中性条件下(例如在模拟的肠液中)它们会保持收缩状态,药物释放缓慢。与TPP /壳聚糖薄膜相比,由于其相对弱的静电相互作用,Pyro /壳聚糖薄膜表现出更好的pH敏感溶胀和控释特性。使用相同的推理可以解释加入氯化钠后观察到的Pyro /壳聚糖膜溶胀明显加速和模型药物释放。这些薄膜可能有望在胃中进行特定部位的药物递送。

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