Maghsoodi Maryam
Drug applied Research Center and Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Adv Pharm Bull. 2012;2(2):253-7. doi: 10.5681/apb.2012.039. Epub 2012 Aug 15.
Direct tableting has been renewed as a preferable process by simply mixing and compressing powder to save time and cost in comparison with granule tableting. Direct compression tableting as a technique has been successfully applied to numerous drugs on the industrial scale, although the success of any procedure, and resulting mechanical properties of tablets, is strongly affected by the quality of the crystals used. Good flowability, packability and compactability are prerequisite for drug to be prepared by direct tableting. When the mechanical properties of the drug particles are inadequate a primary granulation is necessary. The use of spherical crystallization as a technique appears to be an efficient alternative for obtaining suitable particles for direct tableting. Spherical crystallization is a particle design technique, by which crystallization and agglomeration can be carried out simultaneously in one step and which has been successfully utilized for improvement the micromeritic properties of crystalline drugs. In this review, we will discuss how the micromeritic properties of the particles such as flowability, packability and compactability can be improved by spherical crystallization technique.
与制粒压片相比,直接压片通过简单地混合和压缩粉末来节省时间和成本,从而再次成为一种更可取的工艺。直接压片技术已在工业规模上成功应用于多种药物,尽管任何工艺的成功以及由此产生的片剂机械性能都受到所用晶体质量的强烈影响。良好的流动性、可压性和压缩性是药物直接压片制备的先决条件。当药物颗粒的机械性能不足时,需要进行一次制粒。使用球形结晶技术似乎是获得适合直接压片的颗粒的有效替代方法。球形结晶是一种颗粒设计技术,通过该技术可以在一步中同时进行结晶和团聚,并且已成功用于改善结晶药物的微粉特性。在本综述中,我们将讨论如何通过球形结晶技术改善颗粒的微粉特性,如流动性、可压性和压缩性。