...
首页> 外文期刊>International Journal of Pharmaceutics >Development and evaluation of a novel dry-coated tablet technology for pellets as a substitute for the conventional encapsulation technology.
【24h】

Development and evaluation of a novel dry-coated tablet technology for pellets as a substitute for the conventional encapsulation technology.

机译:开发和评估一种新型的干丸片剂技术,以替代传统的包囊技术。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Pellet formulations as represented by multiparticulate systems are often contained in hard capsules. We examined the use of a different approach to the making of compressed tablets containing pellets, OSDRC-technology. OSDRC-technology employs a double-structure punch (center punch and outer punch) allowing for dry-coated tablets to be assembled in a single run. We examined the effects of the thickness of the outer punch, formability of pellets, and diameter of tablets on pellet filling. The results revealed that thinner outer punches are not always better for filling small tablets with large amounts of pellets. We considered that this was because the core pellets spread in a cone shape within the formulating tablets at filling, requiring a thickness of the outer punch and a particle density of the diluents at which pellets would not exude from the formulating tablets. It was suggested that the formability of core pellets affects the maximum number of layers of pellets, and higher formability would yield better results. However, we found that pellets with poor formability (tensile strength of < or =2 kPa) could be used in tablets. For the tablets, the larger the diameter, the greater the maximum number of layers. We considered this to be due to the friction between the pellets and punch wall. We concluded that OSDRC-technology could be applied to capsule-like forms containing pellets > or =50 wt% through an unconventional approach.
机译:以多颗粒系统为代表的颗粒制剂通常包含在硬胶囊中。我们研究了OSDRC技术使用另一种方法制备含有小球的压缩片剂的方法。 OSDRC技术采用双重结构的打孔器(中心打孔器和外部打孔器),使干片片剂可以单次组装。我们检查了外部冲头的厚度,粒料的可成型性和片剂直径对粒料填充的影响。结果表明,较薄的外部冲头并非总是能为大量片剂填充小药片提供更好的效果。我们认为这是因为核心药丸在填充时在配方片剂内呈圆锥形散布,需要外冲头的厚度和稀释剂的颗粒密度,在该浓度下药丸不会从配方片剂中散出。有人提出,芯粒料的可成形性影响粒料的最大层数,而较高的可成形性将产生更好的结果。但是,我们发现可成型性差(抗张强度<或= 2 kPa)的颗粒可用于片剂。对于片剂,直径越大,最大层数越大。我们认为这是由于颗粒和冲头壁之间的摩擦引起的。我们得出的结论是,OSDRC技术可以通过非常规方法应用于包含大于或等于50 wt%的颗粒的胶囊状形式。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号