Podczeck Fridrun, Jones Brian E
School of Pharmacy, University of London, 29/39 Brunswick Square, London WC1N 1AX, UK.
Drug Dev Ind Pharm. 2002 Oct;28(9):1163-9. doi: 10.1081/ddc-120014583.
The in vitro dissolution of theophylline from two-piece hard shell capsules has been investigated using different types of capsule shells (gelatin, gelatin/polyethylene glycol, hydroxypropyl methylcellulose), different formulations, different capsule fill weights, and different tamping forces. Analysis of variance confirmed that the formulation and the capsule shell materials were the most important factors influencing drug dissolution. The maximum extent of drug dissolution was significantly increased when hydroxypropyl methylcellulose (HPMC) capsules were used. The mean dissolution time (MDT) was significantly reduced, indicating a faster dissolution rate of the drug from HPMC capsules. The addition of microfine cellulose to the formulations as filler reduced the MDT in all cases, whereas the addition of lactose monohydrate did not enhance drug dissolution. The study confirmed that a change from gelatin hard shell capsules to gelatin/PEG or HPMC hard shell capsules should not pose problems with respect to drug absorption or bioavailability.
使用不同类型的胶囊壳(明胶、明胶/聚乙二醇、羟丙基甲基纤维素)、不同配方、不同胶囊填充重量和不同夯实力,对茶碱从双片硬壳胶囊中的体外溶出度进行了研究。方差分析证实,配方和胶囊壳材料是影响药物溶出的最重要因素。使用羟丙基甲基纤维素(HPMC)胶囊时,药物溶出的最大程度显著增加。平均溶出时间(MDT)显著缩短,表明药物从HPMC胶囊中的溶出速率更快。在配方中添加微晶纤维素作为填充剂在所有情况下均降低了MDT,而添加一水乳糖并未提高药物溶出度。该研究证实,从明胶硬壳胶囊改为明胶/聚乙二醇或HPMC硬壳胶囊在药物吸收或生物利用度方面不应存在问题。