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一种具有各种层配方和体外释放曲线的新型三层缓释片剂。

A novel three-layered tablet for extended release with various layer formulations and in vitro release profiles.

机构信息

GL PharmTech Corp., Seongnam, Gyeonggi, South Korea.

出版信息

Drug Dev Ind Pharm. 2011 Jun;37(6):664-72. doi: 10.3109/03639045.2010.535211. Epub 2011 Mar 30.

Abstract

A novel three-layered tablet consisting of a water-soluble mid-layer and two barrier layers with swellable polymers was investigated to develop a preferable once-a-day formulation containing terazosin HCl as a hydrophilic model drug. When the tablet was exposed to a release medium, the medium quickly permeated to the mid-layer and the two barrier layers swelled surrounding the mid-layer rapidly. It facilitated the tablet to absorb a lot of water compared with monolithic matrix. Moreover, formation of a lot of pores in the tablet during dissolution could be observed, suggesting significant water absorption in the inner matrix and swollen polymers of the tablet. Barrier layers influenced drug release profiles significantly, potentially due to differences in viscosity after swelling that produce different diffusion coefficients and mechanical strength. The drug in the mid-layer showed the sigmoid type of release pattern because a period of time might be needed to release the drug from the mid-layer through the barrier layers, but the drug in barrier layers showed the typical release pattern of monolithic matrix. As the amount of water-soluble excipient in the mid-layer increased, the degree of swelling also increased, suggesting that its amount in the layer may affect the overall swelling properties of the tablet. It was also shown that more hydrophilic mid-layer caused faster erosion rate, which was related to the results of swelling property. The three-layered tablets showed more consistent release kinetics than the matrix tablets. These results can give good information for the development of sustained drug delivery systems, especially once-a-day administration.

摘要

研究了一种由水溶性中间层和两层具有溶胀性聚合物的阻挡层组成的新型三层片剂,以开发含有盐酸特拉唑嗪作为亲水性模型药物的更优的每日一次制剂。当片剂暴露于释放介质中时,介质迅速渗透到中间层,并且两层阻挡层迅速围绕中间层溶胀。与整体基质相比,它使片剂能够吸收更多的水。此外,在溶解过程中可以观察到片剂中形成了许多孔,表明片剂的内基质和溶胀聚合物大量吸收了水分。阻挡层显著影响药物释放曲线,可能是由于溶胀后的粘度差异导致扩散系数和机械强度不同。中间层中的药物呈现出 S 型释放模式,因为可能需要一段时间才能将药物从中间层通过阻挡层释放出来,但阻挡层中的药物呈现出整体基质的典型释放模式。随着中间层中水溶性赋形剂的增加,溶胀程度也增加,表明该层中的量可能会影响片剂的整体溶胀性能。还表明,更亲水的中间层导致更快的侵蚀速率,这与溶胀性能的结果有关。三层片剂的释放动力学比基质片剂更一致。这些结果可以为持续药物输送系统的开发提供良好的信息,特别是每日一次的给药。

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