Incompatibility of croscarmellose sodium with alkaline excipients in a tablet formulation

被引:11
作者
Bindra, Dilbir S. [1 ]
Stein, Daniel [1 ]
Pandey, Preetanshu [1 ]
Barbour, Nancy [1 ]
机构
[1] Bristol Myers Squibb Co, Drug Prod Sci & Technol, New Brunswick, NJ 08903 USA
关键词
Alkalinity; croscarmellose sodium; dissolution slowdown; gel formation; hydrolysis; slurry pH; wet granulation; WET GRANULATED TABLETS; DISSOLUTION; SUPERDISINTEGRANTS; AGENTS; DRUGS;
D O I
10.3109/10837450.2013.778869
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The objective of the current work was to study an observed incompatibility between croscarmellose sodium and basic excipients in a tablet formulation. Significant dissolution slowdown was observed for alkaline tablet compositions of an acid-labile drug containing croscarmellose sodium (CCS) as a disintegrant. The severity of the dissolution slowdown was directly proportional to both the degree of alkalinity and the level of CCS in the tablet formulation. It is postulated that the ester cross-links in CCS were partially or fully hydrolyzed under basic conditions (pH values49) forming by-products of increased water solubility. This increase in the level of water-soluble polymer can lead to the formation of a viscous barrier in the tablet upon moisture uptake, thus slowing down its dissolution. The dissolution slowdown was not observed for a similar alkaline tablet preparation containing crospovidone as a disintegrant.
引用
收藏
页码:285 / 289
页数:5
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