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热处理作为一种工具,用于生产基于尤特奇RS PO和RL PO的塑料颗粒,用于压片。

Thermal treating as a tool to produce plastic pellets based on Eudragit RS PO and RL PO aimed for tableting.

作者信息

Abbaspour M R, Sadeghi F, Afrasiabi Garekani H

机构信息

School of Pharmacy, Ahvaz Jundishapur University of Medical Science, Ahvaz, Iran.

出版信息

Eur J Pharm Biopharm. 2007 Aug;67(1):260-7. doi: 10.1016/j.ejpb.2007.01.018. Epub 2007 Feb 1.

Abstract

A 3(2) full-factorial design was used for preparation of pellets using extrusion-spheronization technique. Independent variables were %ibuprofen (40, 60, 80) and %Eudragit RS PO/RL PO (0, 50, 100). In all formulations 3% w/w PVP K30 and 10% Avicel PH101 were also used. The pellets were cured in oven at 60 degrees C for 24h. The evaluated responses were crushing strength or yield point, elastic modulus and mean dissolution time (MDT) of pellets. The cured pellets were also compressed at 15kN compaction force and then observed under scanning electron microscope. It was shown that the cured pellets containing 40% or 60% drug exhibited a plastic deformation without any fracture under mechanical tests. The curing process resulted in significant decrease in the elastic modulus of the pellets. The SEM of the compressed pellets were also confirmed the plastic behavior of these pellets. The transition of pellet behavior from brittle to plastic upon curing was due to shift of Eudragit structure from glassy to rubbery state which was supported by DSC studies. However pellets with 80% drug showed brittle properties even after curing due to presence of less amount of Eudragit in their structure. Increasing the ratio of Eudragit RS in the pellets decreased the yield point and elastic modulus of cured pellets containing 40% or 60% drug, indicating more plastic behavior of these pellets. This was attributed to lower Tg of Eudragit RS than Eudragit RL. The curing process also retarded drug release from pellets and increased MDT. Increasing the ratio of Eudragit RS in the pellets increased MDT in cured pellets containing 40% or 60% drug but had no effect in pellets with 80% drug. Overall the results of this study revealed that thermal treating is a proper tool to produce plastic ibuprofen pellets based on Eudragit RS PO and Eudragit RL PO.

摘要

采用3(2)全因子设计,运用挤出滚圆法制备微丸。自变量为布洛芬的含量(40%、60%、80%)以及丙烯酸树脂RS PO/RL PO的含量(0%、50%、100%)。在所有配方中,还使用了3%(w/w)的聚乙烯吡咯烷酮K30和10%的微晶纤维素PH101。微丸在60℃的烘箱中固化24小时。评估的响应指标为微丸的抗压强度或屈服点、弹性模量和平均溶出时间(MDT)。固化后的微丸还在15kN的压制力下进行压制,然后在扫描电子显微镜下观察。结果表明,含40%或60%药物的固化微丸在力学测试中表现出塑性变形,无任何断裂。固化过程导致微丸的弹性模量显著降低。压制后微丸的扫描电子显微镜结果也证实了这些微丸的塑性行为。固化后微丸行为从脆性转变为塑性是由于丙烯酸树脂结构从玻璃态转变为橡胶态,差示扫描量热法研究支持了这一点。然而,含80%药物的微丸即使在固化后仍表现出脆性,这是因为其结构中丙烯酸树脂的含量较少。增加微丸中丙烯酸树脂RS的比例会降低含40%或60%药物的固化微丸的屈服点和弹性模量,表明这些微丸具有更多的塑性行为。这归因于丙烯酸树脂RS的玻璃化转变温度低于丙烯酸树脂RL。固化过程还延缓了药物从微丸中的释放并增加了平均溶出时间。增加微丸中丙烯酸树脂RS的比例会增加含40%或60%药物的固化微丸的平均溶出时间,但对含80%药物的微丸没有影响。总体而言,本研究结果表明,热处理是基于丙烯酸树脂RS PO和丙烯酸树脂RL PO制备塑性布洛芬微丸的合适方法。

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