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Electrospinning of collagen with nanocapsules of PLGA for delivery of paclitaxel in drug -eluting stents

机译:PLGA纳米胶囊对胶原蛋白的静电纺丝,用于在药物洗脱支架中递送紫杉醇

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This work develops a new delivery system trying to understand better, the factors that influences the drug release. This system use nanofiber produced by electrospinning technic and bioabsorbable polymeric nanocapsules produced by the nanoprecipitation processes in a recirculated system develop in the research group. For this work, we used an electrospinning equipment built at the university, in which you can control the process parameters such as voltage, deposition rate, collector distance, speed and direction of rotation of the collector, to control the morphology and diameter of the nanofibers. The final electrospinning condition to obtain nanofiber of collagen (Sigma-Aldrich) with 99 ± 26 nm was 18 V, collector distance of 14cm, flow rate of 0.1mL/h and polymer concentration was 25% W/V in acetic acid and distilled water 9:1. On the other hand, we encapsulated Paclitaxel in bioabsorbible polymeric nanocapsules of PLGA (Resomer 752 H, Evonik) produced in a recirculated system design in the university. The conditions used to encapsulate the paclitaxel was 4mg/mL of polymer concertation, 20% of drug respect to dry polymer, 162 mL/min of flow rate in the recirculating system, 0.25% of Pluronic F-127 (Sigma-Aldrich) as surfactant in the aqueous phase and 2:1 ratio between aqueous phase and organic phase.
机译:这项工作开发了一个尝试了解更好的新送货系统,这是影响药物释放的因素。该系统使用通过在研究组的再循环系统中的纳米沉淀方法产生的耐电纺技术和生物可吸收聚合物纳米胶囊生产的纳米纤维。对于这项工作,我们使用了大学内置的静电纺纱设备,您可以在其中控制电压,沉积速率,收集器距离,收集器的速度和旋转方向等过程参数,以控制纳米纤维的形态和直径。获得99±26nm的胶原型纳米纤维的最终静电纺丝条件为18V,收集器距离为14cm,流速为0.1ml / h,聚合物浓度为乙酸和蒸馏水25%w / v 9:1。另一方面,我们将在大学的再循环系统设计中生产的PLGA(Remer 752h,Evonik)的Bioablylabible聚合物纳米胶囊中封装了紫杉醇。用于包封紫杉醇的条件是4mg / ml的聚合物吻合,20%的药物对干燥聚合物,162mL / min在再循环系统中的流速,0.25%的Pluronic F-127(Sigma-Aldrich)作为表面活性剂在水相和2:1之间的水相和有机相之间的比例。

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