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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.

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。

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