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首页> 外文期刊>International Journal of Pharmaceutics >Aerodynamic properties and in silico deposition of meloxicam potassium incorporated in a carrier-free DPI pulmonary system
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Aerodynamic properties and in silico deposition of meloxicam potassium incorporated in a carrier-free DPI pulmonary system

机译:空气动力学性质和硅氧胞菌磷酸盐的硅沉积在无载体的DPI肺系统中

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摘要

Dry powder inhalers (DPIs) have been among the fastest developing inhaler forms in the past decades. Researches are focusing on the formulation of carrier-free powders to obtain a higher deep-lung deposition and hereby to increase the effectiveness of the medicine. The aim of our study was to prepare a carrier-free dry powder formulation of meloxicam potassium (MP), a novel salt form of meloxicam, using a one-step co-spray drying technology. Different types of excipients were used to modify the crystal structure and to increase aerosolization efficacy. Micrometric properties and the crystal structure were characterized. Aerodynamic properties were tested in vitro using an Andersen Cascade Impactor. A new in silico Stochastic Lung Model was also applied to quantify the amount of particles deposited at the target area. The results have shown that formulated DPI samples are fulfilling the requirements of effective pulmonary drug delivery: they include spherical particles with low density and 1-5 mu m size distribution. The in silica deposition results correspond with the in vitro measurements and demonstrate that the engineered microcomposites reach a high lung deposition. MP offers a novel opportunity for a well controlled DPI formulation prepared by a solution-based co-spray drying method. (C) 2017 Elsevier B.V. All rights reserved.
机译:干粉吸入器(DPI)是过去几十年中最快的开发吸入器形式之一。研究专注于制剂的无载体粉末,以获得更高的深肺沉积,从而提高药物的有效性。我们研究的目的是制备美洛昔康钾(MP)的无载体干粉配方,新型盐形式的美洛昔康,使用一步的共吸入干燥技术。使用不同类型的赋形剂来改变晶体结构并增加雾化功效。表征微米特性和晶体结构。使用Andersen Cascade撞击器在体外测试空气动力学性质。还应用了一种新的硅随机肺模型,以量化沉积在靶区域的颗粒量。结果表明,配制的DPI样品正在满足有效肺药递送的要求:它们包括具有低密度和1-5μm尺寸分布的球形颗粒。在二氧化硅沉积结果中对应于体外测量,并证明了工程化的微孔复合材料达到高肺部沉积。 MP为通过基于溶液的共喷干燥方法制备的良好控制的DPI制剂提供了一种新的机会。 (c)2017年Elsevier B.V.保留所有权利。

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