Miyazaki S, Yamaguchi H, Yokouchi C, Takada M, Hou W M
Faculty of Pharmaceutical Sciences, Higashi-Nippon-Gakuen University, Hokkaido, Japan.
J Pharm Pharmacol. 1988 Sep;40(9):642-3. doi: 10.1111/j.2042-7158.1988.tb05325.x.
The potential of chitosan granules as an oral sustained-release dosage form of indomethacin has been compared with conventional capsules in beagle dogs. When a commercial capsule was administered orally, the plasma concentrations reached the maximum level in 30 min. The granules did not give a sharp peak to the plasma concentration, but produced a sustained plateau of the drug. This may be due to the slow rate of release and a longer residence time in the stomach. Thus, in terms of reducing the peak in plasma concentration and maintenance of drug concentration in plasma, the chitosan granules were superior to conventional capsules.
在比格犬中,已将壳聚糖颗粒作为吲哚美辛口服缓释剂型的潜力与传统胶囊进行了比较。口服市售胶囊时,血浆浓度在30分钟内达到最高水平。颗粒剂并未使血浆浓度出现尖峰,而是产生了药物的持续平稳状态。这可能是由于释放速率缓慢以及在胃中的停留时间较长。因此,在降低血浆浓度峰值和维持血浆中药物浓度方面,壳聚糖颗粒优于传统胶囊。