首页> 外文会议>International Conference on Polymer-Solvent Complexes and Intercalates; 20020722-20020725; Prague; CZ >A Novel pH Sensitive Porous Membrane Carrier for Various Biomedical Applications Based on pHEMA/chitosan: Preparation and Its Drug Release Characteristics
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A Novel pH Sensitive Porous Membrane Carrier for Various Biomedical Applications Based on pHEMA/chitosan: Preparation and Its Drug Release Characteristics

机译:基于pHEMA /壳聚糖的多种生物医学应用的新型pH敏感多孔膜载体:制备及其释药特性

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The synthetic hydrogels based on pHEMA have been widely studied and used in biomedical fields. Numerous techniques exist for entrapment of drugs or proteins in the hydrogels. The suitable biomaterials for biomedical applications include poly(hydroxyethyl methacrylate), (pHEMA), and chitosan. In this work, a novel pH sensitive interpenetrating polymer networks (IPNs) were prepared in the membrane form by using 2-hydroxyethyl-methacrylate monomer (HEMA) and chitosan via UV initiated photo-polymerization in the presence of an initiator (i.e., α-α'-azo-isobutyronitrile; AIBN). UV-free-radical polymerization techniques are often used to synthesize hydrogels for controlled release applications. A series of HEMA and chitosan IPNs hydrogels were prepared and the equilibrium swelling studies were conducted to investigate swelling behaviors of the membrane according to the pH of the swelling medium. The swelling properties of the membrane were changed with the medium pH. The equilibrium water uptake is reached in about 60 min. The pHEMA/chitosan membrane thickness and density was measured to be 600 μm and 1.26 g cm~(-3), respectively. Antibiotic release experiments were also performed with amoxicillin loaded pHEMA/chitosan membrane in physiological saline solution. The IPNs membrane loaded with 100 mg antibiotic (i.e., amoxicillin) g hydrogel released around 80 % of the amoxicillin in 10 h at pH 7.4. The presented well-characterized novel pHEMA/chitosan membrane is a potential candidate for transdermal antibiotic carrier or a support in bioseparation.
机译:基于pHEMA的合成水凝胶已被广泛研究并用于生物医学领域。存在用于将药物或蛋白质截留在水凝胶中的多种技术。用于生物医学应用的合适生物材料包括聚(甲基丙烯酸羟乙酯),(pHEMA)和壳聚糖。在这项工作中,通过使用甲基丙烯酸2-羟乙酯(HEMA)和脱乙酰壳多糖在引发剂(即α-烯烃)存在下通过UV引发的光聚合反应,以膜形式制备了一种新型的pH敏感的互穿聚合物网络(IPN)。 α'-偶氮异丁腈; AIBN)。 UV-自由基聚合技术通常用于合成水凝胶以用于控释应用。制备了一系列HEMA和壳聚糖IPNs水凝胶,并根据溶胀介质的pH值进行了平衡溶胀研究,以研究膜的溶胀行为。膜的溶胀性质随介质pH值而变化。在约60分钟内达到平衡的吸水量。测量的pHEMA /壳聚糖膜厚度和密度分别为600μm和1.26 g cm〜(-3)。还用载有阿莫西林的pHEMA /壳聚糖膜在生理盐水溶液中进行了抗生素释放实验。装有100 mg抗生素(即阿莫西林)g水凝胶的IPNs膜在pH 7.4的10小时内释放了约80%的阿莫西林。呈现的特征良好的新型pHEMA /壳聚糖膜是透皮抗生素载体或生物分离支持物的潜在候选者。

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