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Development of braided drug-loaded nanofiber sutures

机译:编织载药纳米纤维缝合线的研制

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The objectives of this work are twofold. Firstly, while most work on electrospinning is limited to the development of only functional materials, a structural application of electrospun nanofibers is explored. Secondly, a drug-loaded tissue suture is fabricated and its various properties are characterized. Braided drug-loaded nanofiber sutures are obtained by combining an electrospinning process with a braiding technique followed by a coating procedure. Two different electrospinning techniques, i.e. blend and coaxial electrospinning, to incorporate a model drug cefotaxime sodium (CFX-Na) into poly(L-lactic acid) (PLLA) nanofibers have been applied and compared with each other. Properties of the braided drug-loaded sutures are characterized through a variety of methods including SEM, TEM and tensile testing. The results show that the nanofibers had a preferable micromorphology. The drug was incorporated into the polymer nanofibers homogeneously, with no cross-linking. The nanofibers maintained their fibrous structures. An in vitro release study indicates that the drug-loaded nanofibers fabricated by blend electrospinning and coaxial electrospinning had a different drug release behavior. An inhibition zone experiment shows that both sutures obtained from the nanofibers of the different electrospinning techniques had favorable antibacterial properties. The drug-loaded sutures had preferable histological compatibility performance compared with commercial silk sutures in an in vivo comparative study.
机译:这项工作的目标是双重的。首先,虽然大多数静电纺丝工作仅限于仅开发功能材料,但仍在探索静电纺丝纳米纤维的结构应用。其次,制造载药组织缝合线并表征其各种性质。通过将电纺丝工艺与编织技术相结合,然后进行涂覆程序,可以得到载有药物的编织纳米纤维缝合线。已经应用了两种不同的静电纺丝技术,即共混和同轴静电纺丝,将模型药物头孢噻肟钠(CFX-Na)掺入聚(L-乳酸)(PLLA)纳米纤维中,并进行了比较。通过多种方法(包括SEM,TEM和拉伸测试)来表征编织的载药缝合线的特性。结果表明,纳米纤维具有较好的微观形态。药物被均匀地掺入聚合物纳米纤维中,没有交联。纳米纤维保持其纤维结构。体外释放研究表明,通过混合电纺丝和同轴电纺丝制备的载有药物的纳米纤维具有不同的药物释放行为。抑制区实验表明,从不同电纺丝技术的纳米纤维获得的两种缝合线均具有良好的抗菌性能。在体内的比较研究中,与商用丝线缝合相比,载药线具有更好的组织相容性。

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