Ozeki Yuichi, Watanabe Yukinao, Inoue Susumu, Danjo Kazumi
Pharmaceutical Research & Technology Laboratory, Sanwa Kagaku Kenkyusho Co. Ltd., 855-1 Mitabora, Gifu City, 502-0004, Japan.
Int J Pharm. 2003 Nov 28;267(1-2):69-78. doi: 10.1016/j.ijpharm.2003.07.011.
This study was conducted in order to clarify the compression characteristics, and to confirm the superiority of the physical properties, of the newly invented One-Step DRy-Coated tablets (OSDRC). We compared both the compression characteristics and the physical properties of OSDRC with those of physical-mixture tablets (PM) that were prepared with the same ingredients, quantity, and compression pressures. We selected potassium chloride (KCl) and acetaminophen (AAP) as the model drugs, since the former is known for its appropriate compression characteristics and the latter for its brittleness. The advantage of OSDRC is that they are capable of maintaining any kind of drug in their core, because the core is tightly surrounded by the outer layer, even when the drugs in the core have poor compression characteristics, which causes difficulties in forming a solid core tablet using conventional dry-coated tablet methods. The radial tensile strength of OSDRC was the same as, or superior to, that of PM containing of AAP. The results were in accordance with the compression process analysis performed according to Kawakita's equation. The friability of OSDRC was also superior to that of PM. These preferable characteristics were attributable to the high intensity of the OSDRC outer layer surface in comparison to that of PM. It was difficult to clarify the difference between OSDRC and PM in their physical properties when KCl was applied, since the tabletability of the whole tablet was high due to KCl's physical properties. The OSDRC containing AAP in their cores showed a controlled release pattern, though no other materials that have been known to influence drug release was present. It was considered that this controlled release pattern was caused by a reduced AAP particle surface area due to compression. It was confirmed with these experiments that the compression characteristics and the physical properties of AAP-OSDRC were superior to those of PM. These results indicated that it is possible to produce tablets that have materials with poor compression characteristics in the core portion, and high tabletability materials for the outer layers. In other words, it is possible to produce capsule-like tablets using the OSDRC compression method.
本研究旨在阐明新发明的一步干包衣片(OSDRC)的压缩特性,并确认其物理性能的优越性。我们将OSDRC的压缩特性和物理性能与用相同成分、数量和压缩压力制备的物理混合物片(PM)进行了比较。我们选择氯化钾(KCl)和对乙酰氨基酚(AAP)作为模型药物,因为前者以其合适的压缩特性而闻名,后者则以其脆性而闻名。OSDRC的优点在于,即使核心中的药物压缩特性较差,使用传统干包衣片方法难以制成实心核心片剂,但由于核心被外层紧密包围,它们能够在核心中保持任何种类的药物。含AAP的OSDRC的径向拉伸强度与含AAP的PM相同或更高。结果与根据河合公式进行的压缩过程分析一致。OSDRC的脆碎度也优于PM。这些优良特性归因于与PM相比,OSDRC外层表面的高强度。当使用KCl时,由于KCl的物理性质,整个片剂的可压性较高,因此难以阐明OSDRC和PM在物理性质上的差异。核心中含有AAP的OSDRC呈现出控释模式,尽管不存在其他已知会影响药物释放的材料。据认为,这种控释模式是由于压缩导致AAP颗粒表面积减小所致。通过这些实验证实,AAP-OSDRC的压缩特性和物理性能优于PM。这些结果表明,有可能生产出核心部分含有压缩特性较差的材料,而外层具有高可压性材料的片剂。换句话说,使用OSDRC压缩方法有可能生产出胶囊状片剂。