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Interfacial interaction between transmembrane ocular mucins and adhesive polymers and dendrimers analyzed by surface plasmon resonance

机译:通过表面等离振子共振分析跨膜眼粘蛋白与黏附聚合物和树枝状聚合物之间的界面相互作用

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摘要

Purpose Development of the first in vitro method based on biosensor chip technology designed for probing the interfacial interaction phenomena between transmembrane ocular mucins and adhesive polymers and dendrimers intended for ophthalmic administration. Methods The surface plasmon resonance (SPR) technique was used. A transmembrane ocular mucin surface was prepared on the chip surface and characterized by QCM-D (Quartz Crystal Microbalance with Dissipation) and XPS (X-ray photoelectron spectroscopy). The mucoadhesive molecules tested were: hyaluronic acid (HA), carboxymethyl cellulose (CMC), hydroxypropylmethyl cellulose (HPMC), chitosan (Ch) and polyamidoamine dendrimers (PAMAM). Results While Ch originated interfacial interaction with ocular transmembrane mucins, for HA, CMC and HPMC, chain interdiffusion seemed to be mandatory for bioadherence at the concentrations used in ophthalmic clinical practise. Interestingly, PAMAM dendrimers developed permanent interfacial interactions with transmembrane ocular mucins whatever their surface chemical groups, showing a relevant importance of co-operative effect of these multivalent systems. Polymers developed interfacial interactions with ocular membrane-associated mucins in the following order: Ch(1 %) > G4PAMAM-NH2(2 %) 0 G4PAMAM-OH(2 %) > G3.5PAMAMCOOH( 2 %)CMC(0.5 %) 0 HA(0.2 %) 0 HPMC(0.3 %). Conclusions The method proposed is useful to discern between the mucin-polymer chemical interactions at molecular scale. Results reinforce the usefulness of chitosan and dendrimers as polymers able to increase the retention time of drugs on the ocular surface and hence their bioavailability.
机译:目的开发第一种基于生物传感器芯片技术的体外方法,该方法旨在探测跨膜眼粘蛋白与打算用于眼科给药的粘合性聚合物和树状聚合物之间的界面相互作用现象。方法采用表面等离子体共振(SPR)技术。在芯片表面上制备跨膜眼粘蛋白表面,并通过QCM-D(带耗散的石英晶体微天平)和XPS(X射线光电子能谱)进行表征。测试的粘膜粘附分子为:透明质酸(HA),羧甲基纤维素(CMC),羟丙基甲基纤维素(HPMC),壳聚糖(Ch)和聚酰胺型胺树枝状聚合物(PAMAM)。结果虽然Ch起源于眼跨膜粘蛋白的界面相互作用,但对于HA,CMC和HPMC,在眼科临床实践中所用的浓度下,链间扩散似乎是生物粘附所必需的。有趣的是,无论其表面化学基团如何,PAMAM树状大分子都与跨膜眼粘蛋白形成了永久性的界面相互作用,显示出这些多价系统协同作用的重要性。聚合物按以下顺序与眼膜相关黏蛋白发展了界面相互作用:Ch(1%)> G4PAMAM-NH2(2%)0 G4PAMAM-OH(2%)> G3.5PAMAMCOOH(2%)CMC(0.5%)0 HA(0.2%)0 HPMC(0.3%)。结论所提出的方法对于在分子尺度上区分粘蛋白-聚合物化学相互作用是有用的。结果加强了壳聚糖和树状聚合物作为能够增加药物在眼表上的保留时间并因此增加其生物利用度的聚合物的有用性。

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