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Preparation and characterization of electrospun, biodegradable membranes

机译:静电纺丝,可生物降解膜的制备和表征

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Nonwoven, biodegradable membranes fabricated by electrospinning have recently attracted a great deal of attention for biomedical applications. In this study, microporous, nonwoven membranes Of poly(L-lactide) and its copolymers and blends were fabricated through electrospinning. The structures and morphologies of the electrospun membranes were investigated with scanning electron microscopy, differential scanning calorimetry, and X-ray diffraction. Different polymer membranes, incorporated with carmofur, were fabricated, and their drug release profiles were investigated. Scanning electron microscopy images showed that the fiber diameters were down to the nanometer range. The diameters and morphologies of the nanofibers depended on processing parameters such as the solution properties (concentration and polymer molecular weight), applied electric voltage, solution feeding rate, and needle diameter. Differential scanning calorimetry showed that the crystallinity of the electrospun membranes was lower than that of the cast film. For all the membranes incorporated with the drug, there was a burst release in the first 10 h of incubation in phosphate-buffered saline at 37 degrees C. Poly(glycolide-co-lactide) membranes showed faster and more complete drug release than poly(L-lactide), and this could be attributed to its faster degradation. The incorporation of polylactide-poly(ethylene glycol) could shorten the drug release time. A combination of suitable degradable biomaterials with an appropriate electrospinning process could be useful in the fabrication of a new kind of membrane suitable for different biomedical applications such as tissue engineering and drug delivery. (C) 2008 Wiley Periodicals, Inc.
机译:通过电纺丝制造的非织造的,可生物降解的膜最近在生物医学应用中引起了极大的关注。在这项研究中,聚(L-丙交酯)的微孔非织造膜及其共聚物和共混物是通过静电纺丝制造的。用扫描电子显微镜,差示扫描量热法和X射线衍射研究了电纺膜的结构和形态。制备了与呋喃呋喃结合的不同聚合物膜,并研究了它们的药物释放曲线。扫描电子显微镜图像显示纤维直径降低至纳米范围。纳米纤维的直径和形态取决于加工参数,例如溶液性质(浓度和聚合物分子量),施加的电压,溶液进料速率和针头直径。差示扫描量热法显示,电纺膜的结晶度低于流延膜的结晶度。对于所有与药物结合的膜,在磷酸盐缓冲液中于37°C孵育的前10小时都有爆发释放。聚(乙交酯-丙交酯)膜比聚(乙交酯)膜释放更快,更完全L-丙交酯),这可以归因于其降解速度更快。聚丙交酯-聚乙二醇的掺入可以缩短药物释放时间。合适的可降解生物材料与合适的静电纺丝工艺的结合可用于制造适用于不同生物医学应用(例如组织工程和药物输送)的新型膜。 (C)2008 Wiley期刊公司

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