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

机译:胶原蛋白与PLGA纳米胶囊的静电纺丝,用于在药物的紫杉醇中递送紫杉醇

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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:这项工作开发新的传输系统试图更好地理解,是影响药物释放的因素。该系统使用纳米纤维产生通过电纺丝通过纳米沉淀过程中再循环系统中产生TECHNIC和生物可吸收聚合物纳米胶囊的研究小组开发。对于这项工作中,我们使用在大学建立了一个静电设备,在其中可以控制工艺参数,如电压,沉积速率,收集器距离,速度和方向的集电体的旋转,来控制纳米纤维的形态和直径。最终电纺丝条件与得到的胶原蛋白纳米纤维(Sigma-Aldrich公司)99±26纳米为18 V,14厘米的收集器的距离,流速为0.1mL / h,并且聚合物浓度的率为25%w / v在乙酸和蒸馏水9:1。在另一方面,我们在PLGA的在再循环系统设计在大学产生bioabsorbible聚合物纳米胶囊(RESOMER 752 H,赢创)包封的紫杉醇。用于封装紫杉醇的条件是为4mg / mL的聚合物concertation的,药物对于干聚合物的20%,162毫升的再循环系统的流量的/分钟,尼克F-127(Sigma-Aldrich公司)的0.25%作为表面活性剂在水相中和2:水相和有机相之间1倍的比例。

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