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首页> 外文期刊>Biomacromolecules >In Situ Cross-Linkable Novel Alginate-Dextran Methacrylate IPN Hydrogels for Biomedical Applications: Mechanical Characterization and Drug Delivery Properties
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In Situ Cross-Linkable Novel Alginate-Dextran Methacrylate IPN Hydrogels for Biomedical Applications: Mechanical Characterization and Drug Delivery Properties

机译:用于生物医学的原位可交联新型藻酸盐-右旋甲基丙烯酸甲酯IPN水凝胶:机械表征和药物传递性质

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摘要

In situ polymerizable hydrogels are extensively investigated to implement new biomedical and pharmaceutical approaches. In the present paper a novel polysaccharide matrix based on calcium alginate (Ca(II)-Alg) hydrogel and dextran methacrylate derivative (Dex-MA), showing potential applicability in the field of pharmaceutics is described. The semi-interpenetrating polymer system (semi-IPN) obtained by a dispersion of Dex-MA chains into a Ca(II) hydrogel leads to a hydrogel with Theological properties quite different from those of Ca(H)-Alg, allowing to inject the semi-IPN easily through an hypodermic needle. The UV curing of the semi-IPN, by cross-linking of the methacrylate moieties, leads to an IPN strong hydrogel that can be used for a modulated delivery of bioactive molecules. In the present paper, rheological and mechanical behaviors of the semi-IPN and of the IPN are discussed. The release of model molecules, including a protein, are also presented to show the suitability of the novel system as a drug delivery system.
机译:对可聚合水凝胶进行了广泛的研究,以实施新的生物医学和药学方法。在本文中,描述了一种基于藻酸钙(Ca(II)-Alg)水凝胶和右旋糖酐甲基丙烯酸酯衍生物(Dex-MA)的新型多糖基质,显示了在制药领域的潜在适用性。通过将Dex-MA链分散到Ca(II)水凝胶中而获得的半互穿聚合物系统(semi-IPN)导致其流变学性质与Ca(H)-Alg完全不同的水凝胶,从而可以注入半IPN易于通过皮下注射针头进行。通过甲基丙烯酸酯部分的交联,半IPN的UV固化可形成IPN强的水凝胶,可用于调节生物活性分子的递送。在本文中,讨论了半IPN和IPN的流变和力学行为。还提出了包括蛋白质在内的模型分子的释放,以显示该新型系统作为药物输送系统的适用性。

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