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Electrospun PVP-indomethacin constituents for transdermal dressings and drug delivery devices

机译:用于经皮敷料和药物输送装置的电纺PVP-吲哚美辛成分

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摘要

A method in layering dressings with a superficial active layer of sub-micrometer scaled fibrous structures is demonstrated. For this, polyvinylpyrolidone (PVP)-indomethacin (INDO) fibres (5% w/v PVP, 5% w/w indomethacin, using a 50:50 ethanol-methanol solvent system) were produced at different flow rates (50 ?min and 100 ?min) via a modified electrospinning device head (applied voltage varied between 15 ? kV). We further assessed these structures for their morphological, physical and chemical properties using SEM, AFM, DSC, XRD, FTIR and HPLC-UV. The average diameter of the resulting 3D (ca. 500 nm in height) PVP-INDO fibres produced at 50 ?min flow rate was 2.58 ?.30 ? while an almost two-fold increase in the diameter was observed (5.22 ?.83 ? when the flow rate was doubled. However, both of these diameters were appreciably smaller than the existing dressing fibres (ca. 30 ?, which were visible even when layered with the active spun fibres. Indomethacin was incorporated in the amorphous state. The encapsulation efficiency was 75% w/w, with complete drug release in 45 min. The advantages are the ease of fabrication and deposition onto any existing normal or functionalised dressing (retaining the original fabric functionality), elimination of topical product issues (application, storage and transport), rapid release of active and controlled loading of drug content (fibre layer).
机译:演示了一种使用亚微米级纤维结构表面活性层将敷料分层的方法。为此,在不同的流速(50?min和50?min和50?min的压力下)下生产了聚乙烯吡咯烷酮(PVP)-吲哚美辛(INDO)纤维(5%w / v PVP,5%w / w吲哚美辛)。通过改进的静电纺丝机头(施加电压在15 kV之间变化)达到100Ωmin。我们使用SEM,AFM,DSC,XRD,FTIR和HPLC-UV对这些结构的形态,物理和化学性质进行了进一步评估。以50?min的流速生产的所得3D(高度约500 nm)PVP-INDO纤维的平均直径为2.58?.30?当流量增加一倍时,直径几乎增加了两倍(5.22?.83?)。但是,这两个直径都比现有的敷料纤维小得多(大约30?,即使当吲哚美辛以无定形状态掺入,包封效率为75%w / w,在45分钟内完全释放药物,其优点是易于制造和沉积在任何现有的常规或功能化敷料上(保留原始的织物功能),消除局部产品问题(应用,存储和运输),快速释放有效且受控的药物含量(纤维层)。

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