• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

由二水磷酸氢钙和微晶纤维素按4比1的混合物制备的丸剂在压缩过程中出现破碎情况。

Occurrence of fragmentation during compression of pellets prepared from a 4 to 1 mixture of dicalcium phosphate dihydrate and microcrystalline cellulose.

作者信息

Nicklasson F, Johansson B, Alderborn G

机构信息

Department of Pharmacy, Uppsala University, Box 580, S-751 23 Uppsala, Sweden.

出版信息

Eur J Pharm Sci. 1999 Feb;7(3):221-31. doi: 10.1016/s0928-0987(98)00020-7.

DOI:10.1016/s0928-0987(98)00020-7
PMID:9845809
Abstract

The occurrence of pellet fragmentation during the compression of pellets prepared mainly from a hard pharmaceutical filler material was investigated. The pellets consisted of 4 parts dicalcium phosphate dihydrate (generally considered as a hard material) to 1 part microcrystalline cellulose (used as a pellet forming material). Pellets of two porosities, 36% and 55%, were prepared. Compacts formed at 100 MPa applied pressure were fractured and the fracture surfaces were then visually examined. Lubricated pellets were also compacted in order to obtain tablets which could be easily deaggregated. Pellets retrieved from deaggregated tablets were compared with uncompacted pellets with respect to size and fracture resistance. The results showed that many pellets exposed in the tablet fracture surface were fractured, especially those with higher porosity. However, the lubricated pellets retrieved from deaggregated tablets were similar in size to the uncompacted pellets, i.e. fragmentation of these pellets was minimal. Furthermore, these retrieved pellets were more resistant to fracture than the original uncompacted pellets, indicating that the formation of cracks or flaws in the pellets during compaction was also minimal. It was thus concluded that deformation and probably densification, and not fragmentation, was the dominant compression mechanisms of this pellet formulation.

摘要

研究了主要由硬质药用填充材料制备的微丸在压制过程中微丸破碎的情况。微丸由4份二水磷酸氢钙(通常被认为是一种硬质材料)和1份微晶纤维素(用作微丸成型材料)组成。制备了孔隙率分别为36%和55%的两种微丸。在100MPa的施加压力下形成的压片被破碎,然后对破碎表面进行目视检查。还对润滑后的微丸进行压制以获得易于崩解的片剂。将从崩解片剂中回收的微丸与未压制的微丸在尺寸和抗破碎性方面进行比较。结果表明,许多暴露在片剂破碎表面的微丸发生了破碎,尤其是那些孔隙率较高的微丸。然而,从崩解片剂中回收的润滑微丸在尺寸上与未压制的微丸相似,即这些微丸的破碎程度最小。此外,这些回收的微丸比原始未压制的微丸更抗破碎,这表明在压制过程中微丸中裂纹或缺陷的形成也最小。因此得出结论,变形以及可能的致密化而非破碎是这种微丸制剂的主要压制机制。

相似文献

1
Occurrence of fragmentation during compression of pellets prepared from a 4 to 1 mixture of dicalcium phosphate dihydrate and microcrystalline cellulose.由二水磷酸氢钙和微晶纤维素按4比1的混合物制备的丸剂在压缩过程中出现破碎情况。
Eur J Pharm Sci. 1999 Feb;7(3):221-31. doi: 10.1016/s0928-0987(98)00020-7.
2
Tabletting behaviour of pellets of a series of porosities--a comparisonbetween pellets of two different compositions.一系列孔隙率的微丸的压片行为——两种不同成分微丸之间的比较
Eur J Pharm Sci. 1999 Apr;8(1):11-7. doi: 10.1016/s0928-0987(98)00056-6.
3
Modulation of the tabletting behaviour of microcrystalline cellulose pellets by the incorporation of polyethylene glycol.通过加入聚乙二醇对微晶纤维素微丸压片行为的调节
Eur J Pharm Sci. 1999 Oct;9(1):57-65. doi: 10.1016/s0928-0987(99)00042-1.
4
Compression behaviour of kappa-carrageenan pellets.角叉菜胶球的压缩行为。
Int J Pharm. 2010 May 10;390(2):117-27. doi: 10.1016/j.ijpharm.2009.12.062. Epub 2010 Jan 25.
5
The degree of compression of spherical granular solids controls the evolution of microstructure and bond probability during compaction.球形颗粒固体的压缩程度控制着压实过程中微观结构和键合概率的演变。
Int J Pharm. 2013 Feb 14;442(1-2):3-12. doi: 10.1016/j.ijpharm.2012.08.011. Epub 2012 Aug 17.
6
Effect of intragranular porosity on compression behaviour of and drug release from reservoir pellets.颗粒内孔隙率对储库型微丸压缩行为及药物释放的影响。
Eur J Pharm Sci. 2003 Aug;19(5):333-44. doi: 10.1016/s0928-0987(03)00106-4.
7
A mechanistic understanding of compression damage to the dissolubility of coated pellets in tablets.一种对片剂中包衣丸剂溶出度压缩损伤的机械理解。
Eur J Pharm Biopharm. 2020 Jan;146:93-100. doi: 10.1016/j.ejpb.2019.11.006. Epub 2019 Nov 28.
8
[Evaluation with compression equations of compression behavior of pellets with different intragranular pore volumes].[使用压缩方程评估具有不同颗粒内孔隙体积的颗粒的压缩行为]
Yao Xue Xue Bao. 2009 Apr;44(4):412-6.
9
Cushioning pellets based on microcrystalline cellulose - Crospovidone blends for MUPS tableting.基于微晶纤维素-共聚维酮混合物的 MUPS 片剂缓冲颗粒。
Int J Pharm. 2020 Aug 30;586:119573. doi: 10.1016/j.ijpharm.2020.119573. Epub 2020 Jun 26.
10
Incidence of drying on microstructure and drug release profiles from tablets of MCC-lactose-Carbopol and MCC-dicalcium phosphate-Carbopol pellets.微晶纤维素-乳糖-卡波姆片剂及微晶纤维素-磷酸二钙-卡波姆微丸的干燥对其微观结构和药物释放曲线的影响
Eur J Pharm Biopharm. 2008 Jun;69(2):675-85. doi: 10.1016/j.ejpb.2007.11.016. Epub 2007 Dec 5.

引用本文的文献

1
Key formulation variables in tableting of coated pellets.包衣微丸压片的关键处方变量。
Indian J Pharm Sci. 2008 Sep;70(5):555-64. doi: 10.4103/0250-474X.45391.
2
Effect of surface energy on powder compactibility.表面能对粉末可压性的影响。
Pharm Res. 2008 Dec;25(12):2750-9. doi: 10.1007/s11095-008-9639-7. Epub 2008 Jun 12.