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干法制粒对大环内酯类抗生素制剂可压性和裂片倾向的影响。

Influence of dry granulation on compactibility and capping tendency of macrolide antibiotic formulation.

作者信息

Bozic Damjana Zupancic, Dreu Rok, Vrecer Franc

机构信息

Krka d.d., Novo mesto, Smarjeska cesta 6, 8501 Novo mesto, Slovenia.

出版信息

Int J Pharm. 2008 Jun 5;357(1-2):44-54. doi: 10.1016/j.ijpharm.2008.01.023. Epub 2008 Jan 20.

DOI:10.1016/j.ijpharm.2008.01.023
PMID:18308490
Abstract

The effect of dry granulation (roller compaction and slugging) on compactibility and tablet capping tendency in a formulation with macrolide antibiotic and microcrystalline cellulose (MCC) was investigated. Direct tableting of this formulation revealed a pronounced capping tendency. Both dry granulated systems exhibit better compactibility and significant reductions in capping tendency compared to direct tableting. The capping tendency was also reduced through the use of precompression during direct tableting. The main volume reduction mechanism for macrolide antibiotic is fragmentation; this was confirmed by Heckel analysis, the lubricant sensitivity test, and SEM images. The yield pressure (Py) of the direct tableting system is lower than the Py of dry granulated systems, which indicates the lower plasticity of dry granulated systems. These findings do not explain the lower capping tendency of dry granulated systems compared to direct tableting. The main differentiating bonding mechanism is attributed to long distance intermolecular bonds due to the intense amorphization of macrolide antibiotic that occurs during dry granulation. Amorphization leads to a significant increase in surface free energy and consequently stronger long distance bonding between particles, which can withstand elastic relaxation and therefore reduce the capping problem. Solid bridges probably do not make a notable contribution to the mechanical strength of tablets, due to the brittle nature of the particles and the complex molecular structure of macrolide antibiotic.

摘要

研究了干法制粒(滚压和制粒)对含大环内酯类抗生素和微晶纤维素(MCC)制剂的可压性和片剂裂片倾向的影响。该制剂直接压片显示出明显的裂片倾向。与直接压片相比,两种干法制粒体系均表现出更好的可压性,且裂片倾向显著降低。直接压片过程中通过预压也降低了裂片倾向。大环内酯类抗生素的主要体积减小机制是破碎;这通过赫克尔分析、润滑剂敏感性试验和扫描电子显微镜图像得到了证实。直接压片体系的屈服压力(Py)低于干法制粒体系的Py,这表明干法制粒体系的可塑性较低。这些发现无法解释干法制粒体系与直接压片相比裂片倾向较低的原因。主要的区别结合机制归因于干法制粒过程中发生的大环内酯类抗生素强烈非晶化导致的长距离分子间键。非晶化导致表面自由能显著增加,从而使颗粒间的长距离键更强,能够承受弹性松弛,因此减少了裂片问题。由于颗粒的脆性和大环内酯类抗生素复杂的分子结构,固体桥可能对片剂的机械强度贡献不大。

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