首页> 外文期刊>International Journal of Pharmaceutics >Design and evaluation of a dry coated drug delivery system with an impermeable cup, swellable top layer and pulsatile release.
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Design and evaluation of a dry coated drug delivery system with an impermeable cup, swellable top layer and pulsatile release.

机译:具有不透水杯,可溶胀顶层和脉冲释放的干式涂层药物递送系统的设计和评估。

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摘要

In this investigation a novel oral pulsatile drug delivery system based on a core-in-cup dry coated tablet, where the core tablet surrounded on the bottom and circumference wall with inactive material, is proposed. The system consists of three different parts, a core tablet, containing the active ingredient, an impermeable outer shell and a top cover layer-barrier of a soluble polymer. The core contained either diclofenac sodium or ketoprofen as model drugs. The impermeable coating cup consisted of cellulose acetate propionate and the top cover layer of hydrophilic swellable materials, such as polyethylene oxide, sodium alginate or sodium carboxymethyl cellulose. The effect of the core, the polymer characteristics and quantity at the top cover layer, on the lag time and drug release was investigated. The results show that the system release of the drug after a certain lag time generally due to the erosion of the top cover layer. The quantity of the material, its characteristics (viscosity, swelling, gel layer thickness) and the drug solubility was found to modify lag time and drug release. The lag time increased when the quantity of top layer increased, whereas drug release decreased. The use of sodium carboxymethyl cellulose resulted in the greatest swelling, gel thickness and lag time, but the lowest drug release from the system. Polyethylene oxide showed an intermediate behaviour while, the sodium alginate exhibited the smallest swelling, gel thickness and the shortest lag time, but the fastest release. These findings suggest that drug delivery can be controlled by manipulation of these formulations.
机译:在这项研究中,提出了一种新型的基于杯中核心干包衣片剂的口服脉动药物输送系统,其中该核心片剂在底壁和圆周壁上被惰性物质包围。该系统由三个不同部分组成:包含活性成分的核心片剂,不可渗透的外壳和可溶性聚合物的顶层覆盖层。核心包含双氯芬酸钠或酮洛芬作为模型药物。不可渗透的涂层杯由乙酸丙酸纤维素和亲水性可溶胀材料(例如聚环氧乙烷,藻酸钠或羧甲基纤维素钠)的顶层组成。研究了核,顶盖层的聚合物特性和数量对滞后时间和药物释放的影响。结果表明,在一定的滞后时间之后,系统释放的药物通常是由于顶盖层的腐蚀所致。发现材料的数量,其特性(粘度,溶胀,凝胶层厚度)和药物溶解度可改变滞后时间和药物释放。当顶层数量增加时滞后时间增加,而药物释放减少。羧甲基纤维素钠的使用导致最大的溶胀,凝胶厚度和滞后时间,但从系统中释放的药物最少。聚环氧乙烷显示出中间行为,而藻酸钠显示出最小的溶胀,凝胶厚度和最短的滞后时间,但释放最快。这些发现表明,可以通过操纵这些制剂来控制药物递送。

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