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柔软水凝胶互穿硅酮——一种用于药物释放医疗设备的聚合物网络

Soft hydrogels interpenetrating silicone--A polymer network for drug-releasing medical devices.

作者信息

Steffensen Søren L, Vestergaard Merete H, Møller Eva H, Groenning Minna, Alm Martin, Franzyk Henrik, Nielsen Hanne M

机构信息

Department of Pharmacy, Faculty of Health and Medical Sciences, University of Copenhagen, DK-2100, Copenhagen, Denmark.

BioModics ApS, DK-2800, Lyngby, Denmark.

出版信息

J Biomed Mater Res B Appl Biomater. 2016 Feb;104(2):402-10. doi: 10.1002/jbm.b.33371. Epub 2015 Apr 17.

Abstract

Materials for the next generation of medical devices will require not only the mechanical stability of current devices, but must also possess other properties such as sustained release of drugs in a controlled manner over a prolonged period of time. This work focuses on creating such a sophisticated material by forming an interpenetrating polymer network (IPN) material through modification of silicone elastomers with a poly(2-hydroxyethyl methacrylate) (PHEMA)-based hydrogel. IPN materials with a PHEMA content in the range of 13%-38% (w/w) were synthesized by using carbon dioxide-based solvent mixtures under high pressure. These IPNs were characterized with regard to microstructure as well as ability of the hydrogel to form a surface-connected hydrophilic carrier network inside the silicone. A critical limit for hydrogel connectivity was found both via simulation and by visualization of water uptake in approximately 25% (w/w) PHEMA, indicating that entrapment of gel occurs at low gel concentrations. The optimized IPN material was loaded with the antibiotic ciprofloxacin, and the resulting drug release was shown to inhibit bacterial growth when placed on agar, thus demonstrating the potential of this IPN material for future applications in drug-releasing medical devices.

摘要

下一代医疗设备所需的材料不仅要具备当前设备的机械稳定性,还必须拥有其他特性,比如能够在较长时间内以可控方式持续释放药物。这项工作聚焦于通过用基于聚甲基丙烯酸2-羟乙酯(PHEMA)的水凝胶对硅橡胶进行改性,形成互穿聚合物网络(IPN)材料,从而制造出这种复杂的材料。通过在高压下使用基于二氧化碳的溶剂混合物,合成了PHEMA含量在13%-38%(w/w)范围内的IPN材料。对这些IPN材料的微观结构以及水凝胶在硅橡胶内部形成表面连接的亲水性载体网络的能力进行了表征。通过模拟以及对约25%(w/w)PHEMA中水吸收情况的可视化观察,发现了水凝胶连通性的一个关键限度,这表明在低凝胶浓度下会发生凝胶截留。将优化后的IPN材料负载抗生素环丙沙星,结果表明,当置于琼脂上时,释放的药物能够抑制细菌生长,从而证明了这种IPN材料在未来药物释放医疗设备应用中的潜力。

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