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Covalent and injectable chitosan-chondroitin sulfate hydrogels embedded with chitosan microspheres for drug delivery and tissue engineering

机译:共价和可注射的壳聚糖 - 软骨素硫酸盐水凝胶嵌入壳聚糖微球,用于药物递送和组织工程

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摘要

Injectable hydrogels and microspheres derived from natural polysaccharides have been extensively investigated as drug delivery systems and cell scaffolds. In this study, we report a preparation of covalent hydrogels basing polysaccharides via the Schiff base reaction. Water soluble carboxymethyl chitosan (CMC) and oxidized chondroitin sulfate (OCS) were prepared for cross-linking of hydrogels. The mechanism of cross-linking is attributed to the Schiff base reaction between amino and aldehyde groups of polysaccharides. Furthermore, bovine serum albumin (BSA) loaded chitosan-based microspheres (CMs) with a diameter of 3.8-61.6 mu m were fabricated by an emulsion cross-linking method, followed by embedding into CMC-OCS hydrogels to produce a composite CMs/gel scaffold. In the current work, gelation rate, morphology, mechanical properties, swelling ratio, in vitro degradation and BSA release of the CMs/gel scaffolds were examined. The results show that mechanical and bioactive properties of gel scaffolds can be significantly improved by embedding CMs. The solid CMs can serve as a filler to toughen the soft CMC-OCS hydrogels. Compressive modulus of composite gel scaffolds containing 20 mg/ml of microspheres was 13 KPa, which was higher than the control hydrogel without CMs. Cumulative release of BSA during 2 weeks from CMs embedded hydrogel was 30%, which was significantly lower than those of CMs and hydrogels. Moreover, the composite CMs/gel scaffolds exhibited lower swelling ratio and slower degradation rate than the control hydrogel without CMs. The potential of the composite hydrogel as an injectable scaffold was demonstrated by encapsulation of bovine articular chondrocytes in vitro. These results demonstrate the potential of CMs embedded CMC-OCS hydrogels as an injectable drug and cell delivery system in cartilage tissue engineering. (C) 2016 Elsevier B.V. All rights reserved.
机译:从天然多糖衍生自天然多糖的可注射水凝胶和微球被广泛地研究了药物递送系统和细胞支架。在这项研究中,我们通过Schiff基础反应报告了碱基碱基化水凝胶的制备。制备水溶性羧甲基壳聚糖(CMC)和氧化软骨素硫酸盐(OCS),用于交联水凝胶。交联机理归因于多糖的氨基和醛基之间的席夫基础反应。此外,通过乳液交联方法制造直径为3.8-61.6μm的牛血清白蛋白(BSA)的壳聚糖基微球(CMS),然后将其嵌入CMC-OCS水凝胶中以产生复合CMS /凝胶脚手架。在当前的工作中,研究了CMS /凝胶支架的凝胶化速率,形态,机械性能,溶胀比,体外降解和BSA释放。结果表明,通过嵌入CMS,可以显着改善凝胶支架的机械和生物活性性能。固体CMS可以用作加强软质CMC-OCS水凝胶的填料。含有20mg / ml微球的复合凝胶支架的压缩模量为13kPa,其没有CMS的对照水凝胶。 CMS嵌入水凝胶2周内BSA的累积释放为30%,显着低于CMS和水凝胶。另外,复合CMS /凝胶支架表现出低于对照水凝胶的溶胀比和较慢的降解速率而没有CMS。通过在体外包封牛关节软骨细胞来证明复合水凝胶作为可注射支架的潜力。这些结果证明了CMS嵌入式CMC-OCS水凝胶的潜力作为软骨组织工程中的可注射药物和细胞输送系统。 (c)2016年Elsevier B.v.保留所有权利。

著录项

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  • 作者单位

    Nanjing Univ Sci &

    Technol Sch Mat Sci &

    Engn Nanjing 210094 Jiangsu Peoples R China;

    Nanjing Univ Sci &

    Technol Sch Mat Sci &

    Engn Nanjing 210094 Jiangsu Peoples R China;

    Nanjing Univ Sci &

    Technol Sch Mat Sci &

    Engn Nanjing 210094 Jiangsu Peoples R China;

    Nanjing Univ Sci &

    Technol Sch Mat Sci &

    Engn Nanjing 210094 Jiangsu Peoples R China;

    Nanjing Univ Sci &

    Technol Sch Mat Sci &

    Engn Nanjing 210094 Jiangsu Peoples R China;

    Nanjing Univ Sci &

    Technol Sch Mat Sci &

    Engn Nanjing 210094 Jiangsu Peoples R China;

    Nanjing Univ Sci &

    Technol Sch Mat Sci &

    Engn Nanjing 210094 Jiangsu Peoples R China;

    Nanjing Univ Sci &

    Technol Sch Mat Sci &

    Engn Nanjing 210094 Jiangsu Peoples R China;

    Jinling Hosp Dept Orthopaed Nanjing 210002 Jiangsu Peoples R China;

    Jinling Hosp Dept Orthopaed Nanjing 210002 Jiangsu Peoples R China;

    Jinling Inst Technol Sch Mat Engn Nanjing 211169 Jiangsu Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 工程材料学;
  • 关键词

    Hydrogel; Microsphere; Drug delivery; Tissue engineering;

    机译:水凝胶;微球;药物递送;组织工程;

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