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Electrosprayed core–shell solid dispersions of acyclovir fabricated using an epoxy-coated concentric spray head

机译:电喷涂阿昔洛韦的核-壳固体分散体使用环氧涂层同心喷头制造

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摘要

A novel structural solid dispersion (SD) taking the form of core–shell microparticles for poorly water-soluble drugs is reported for the first time. Using polyvinylpyrrolidone (PVP) as a hydrophilic polymer matrix, the SDs were fabricated using coaxial electrospraying (characterized by an epoxy-coated concentric spray head), although the core fluids were unprocessable using one-fluid electrospraying. Through manipulating the flow rates of the core drug-loaded solutions, two types of core–shell microparticles with tunable drug contents were prepared. They had average diameters of 1.36±0.67 and 1.74±0.58 μm, and were essentially a combination of nanocomposites with the active ingredient acyclovir (ACY) distributed in the inner core, and the sweeter sucralose and transmembrane enhancer sodium dodecyl sulfate localized in the outer shell. Differential scanning calorimetry and X-ray diffraction results demonstrated that ACY, sodium dodecyl sulfate, and sucralose were well distributed in the PVP matrix in an amorphous state because of favorable second-order interactions. In vitro dissolution and permeation studies showed that the core–shell microparticle SDs rapidly freed ACY within 1 minute and promoted nearly eightfold increases in permeation rate across the sublingual mucosa compared with raw ACY powders.
机译:首次报道了一种新型的结构固体分散体(SD),其形式为核壳微粒,用于水溶性差的药物。使用聚乙烯吡咯烷酮(PVP)作为亲水性聚合物基质,尽管使用单流体电喷雾无法处理核心流体,但SD是使用同轴电喷雾(以环氧涂层同心喷雾头为特征)制造的。通过控制载药核心溶液的流速,制备了两种类型的具有可调药物含量的核壳微粒。它们的平均直径为1.36±0.67和1.74±0.58μm,本质上是纳米复合物,其活性成分无环鸟苷(ACY)分布在内核中,甜味的三氯蔗糖和跨膜增强剂十二烷基硫酸钠位于外壳中。差示扫描量热法和X射线衍射结果表明,由于有利的二阶相互作用,ACY,十二烷基硫酸钠和三氯蔗糖以无定形状态良好地分布在PVP基质中。体外溶出度和渗透性研究表明,与原始ACY粉末相比,核-壳微粒SD可以在1分钟内迅速释放ACY,并促进整个舌下粘膜的渗透率增加近八倍。

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