龙晓英, 曾新文, 卢如斌, 徐世平. 双氯灭痛控释小丸的制备及健康自愿者多剂量给药后体内评价J. 药学学报, 1996, 31(3): 209-213.
引用本文: 龙晓英, 曾新文, 卢如斌, 徐世平. 双氯灭痛控释小丸的制备及健康自愿者多剂量给药后体内评价J. 药学学报, 1996, 31(3): 209-213.
XY Long, XW Zeng, RB Lu , SP Xu, . PREPARATION OF DICLOFENAC SODIUM CONTROLLED RELEASE PELLETS AND MULTIPLE-DOSE EVALUATION IN HEALTHY VOLUNTEERSJ. Acta Pharmaceutica Sinica, 1996, 31(3): 209-213.
Citation: XY Long, XW Zeng, RB Lu , SP Xu, . PREPARATION OF DICLOFENAC SODIUM CONTROLLED RELEASE PELLETS AND MULTIPLE-DOSE EVALUATION IN HEALTHY VOLUNTEERSJ. Acta Pharmaceutica Sinica, 1996, 31(3): 209-213.

双氯灭痛控释小丸的制备及健康自愿者多剂量给药后体内评价

PREPARATION OF DICLOFENAC SODIUM CONTROLLED RELEASE PELLETS AND MULTIPLE-DOSE EVALUATION IN HEALTHY VOLUNTEERS

  • 摘要: 双氯灭痛(DC-Na)控释小丸的制备,成丸百分率受种粒中乳糖/淀粉比例、粘合剂溶液粘度及种粒在包衣锅中滚动时间的影响;小丸的园整度与粘合剂溶液的表面张力显著相关;包衣液组成及浓度,小丸大小分布范围对包衣中粘连影响较大。6名健康自愿者多剂量口服DC-Na控释小丸(CRP)及普通片(CT),比较最低血浆浓度,说明d3已达稳态。稳态时两者之间血浆药物浓度波动指数(FI)存在显著差异(P<0.05),而稳态时一个给药间隔内血浆药物浓度—时间曲线下的面积(AUC)无显著差异(P>0.05),相对生物利用度为86%。

     

    Abstract: The yield of pellets obtained in preparing diclofenac sodium(DC-Na)controlled release pellets was affected by the lactose/starch ratio of the feed granules,viscosity of the binding solution and residence time in the rolling pot.The pellet shape was found to be correlatde with surface tension of the binding solution.The concentration and composition of the coating solution and pellet size distribution were responsible for the agglutination in coating.The controlled release pellets(CRP) and commercial tablets (CT) of DC-Na were administrated orally to healthy volunteers by multiple-dose.The steady-state condition,based on trough plasma concentration on day 3~5 ,was achieved on day 3.A great difference in plasma drug concentration fluctuation index (FI) between CRP (0.476±0.0484) and CT (0.935±0.092) was observed (P<0.05) during steady-state.The area under the plasma drug concentration-time curve for a 0~12 h interval (AUC) on day 5 of CRP (6.493±0.4169 μg·h · ml-1) and CT (7.551± 0.4745μg·h·ml-1) was shown to be not significantly different (P>0.05).The relative bioavailability in the human was about 86%.

     

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