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首页> 外文期刊>Advanced Powder Technology: The internation Journal of the Society of Powder Technology, Japan >Development and tableting of directly compressible powder from electrospun nanofibrous amorphous solid dispersion
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Development and tableting of directly compressible powder from electrospun nanofibrous amorphous solid dispersion

机译:静电纺丝纳米纤维状无定形固体分散体可直接压缩粉末的开发与压片

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This work was carried out to explore the unknown area of converting non-woven fibres, prepared by high speed electrospinning, into a directly compressible blend by mixing with excipients. An experimental design, with independent variables of compression force and fillers fraction, was realized to investigate tabletability of electrospun material (EM) and to produce hard tablets with appropriate disintegration time. The models proved to be adequate; fitted to the results and predicted values well for the optimal tablet, which was found to be at 76.25 fillers fraction and 6 kN compression force. Besides standard characterizations, distribution of EM was investigated by Raman mapping and scanning electron microscopy revealing the propensity of EM to cover the surface of microcrystalline cellulose and not of mannitol. These analytical tools were also found to be useful at investigating the possible formation of the socalled gelling polymer network in tablets. Scanning electron microscopic pictures of tablets confirmed the maintenance of fibrous structure after compression. The moisture absorption of EM under increasing humidity was studied by dynamic vapour sorption measurement, which suggested good physical stability at 25 degrees C and 60 relative humidity (corroborated by modulated DSC). These results demonstrate the feasibility of a pharmaceutically acceptable downstream processing for EMs. (C) 2017 The Society of Powder Technology Japan. Published by Elsevier B.V. and The Society of Powder Technology Japan. All rights reserved.
机译:这项工作旨在探索通过高速静电纺丝制备的无纺布纤维通过与赋形剂混合转化为直接可压缩混合物的未知领域。通过实验设计,利用压缩力和填料分数等自变量,研究静电纺丝材料(EM)的压片性,并生产具有适当崩解时间的硬片。事实证明,这些模型是足够的;最佳片剂的结果和预测值拟合良好,发现最佳片剂的填充分数为 76.25%,压缩力为 6 kN。除了标准表征外,还通过拉曼成像和扫描电子显微镜研究了EM的分布,揭示了EM覆盖微晶纤维素表面而不是甘露醇表面的倾向。这些分析工具还被发现可用于研究片剂中所谓的胶凝聚合物网络的可能形成。片剂的扫描电子显微镜图像证实了压缩后纤维结构的维持。通过动态蒸汽吸附测量研究了EM在湿度增加下的吸湿性,表明在25°C和60%相对湿度下具有良好的物理稳定性(由调制DSC证实)。这些结果证明了对EM进行药学上可接受的下游处理的可行性。(C) 2017年日本粉末技术学会。由以下开发商制作:Elsevier B.V.和日本粉末技术协会。保留所有权利。

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