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破坏力对人体多单元控释剂型药物释放的影响。

Effect of destruction force on drug release from multiple unit controlled release dosage forms in humans.

作者信息

Katori N, Ma W S, Aoyagi N, Kojima S

机构信息

Division of Drugs, National Institute of Health Sciences, Tokyo, Japan.

出版信息

Pharm Res. 1996 Oct;13(10):1541-6. doi: 10.1023/a:1016087814824.

Abstract

PURPOSE

This study examined the effects of mechanical destructive forces on drug release from controlled release (CR) multiple unit dosage forms in vitro and in vivo and their colonic release, using two CR granules of acetaminophen, AG and BG, which differed in hardness (AG was hard and BG was soft), but which did not depend on agitation speed or pH for their release.

METHODS

In vitro release rates were determined using several official methods and the rotating dialysis cell method. Granules were administered to healthy volunteers under fasting and fed conditions.

RESULTS

Both granules showed similar release rates under mild destructive conditions in official dissolution tests, but BG showed a faster release rate in the rotating dialysis cell method. In the fasting state, the drug absorption-time profiles of AG and BG were almost equal. In the fed state, the drug release rate of BG increases whereas that of AG is almost equal to the fasted state. The food effect on BG could be caused by an increase in the mechanical stress of the GI tract due to food intake judging from the findings in vitro and in dogs. The colonic release from multiple unit CR products was larger than that from single unit ones.

CONCLUSIONS

In vivo release of drug from a multiple unit CR product that is structurally weak is affected by mechanical stresses, which differ among human subjects but are increased by food ingestion. Colonic release from multiple unit CR products is larger than that from single unit products.

摘要

目的

本研究使用两种对乙酰氨基酚控释(CR)多单元剂型AG和BG,考察机械破坏力对其体外、体内药物释放及结肠释放的影响。AG和BG硬度不同(AG硬,BG软),但释放不依赖搅拌速度或pH值。

方法

采用几种法定方法和旋转透析池法测定体外释放率。在禁食和进食条件下将颗粒剂给予健康志愿者。

结果

在法定溶出度试验的温和破坏条件下,两种颗粒剂显示出相似的释放率,但在旋转透析池法中BG显示出更快的释放率。在禁食状态下,AG和BG的药物吸收-时间曲线几乎相同。在进食状态下,BG的药物释放速率增加,而AG的释放速率几乎与禁食状态相同。根据体外和犬体内研究结果判断,进食对BG的影响可能是由于食物摄入导致胃肠道机械应力增加所致。多单元CR产品的结肠释放量大于单单元产品。

结论

结构较弱的多单元CR产品在体内的药物释放受机械应力影响,不同个体的机械应力不同,但食物摄入会使其增加。多单元CR产品的结肠释放量大于单单元产品。

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