...
首页> 外文期刊>Indian journal of pharmaceutical sciences. >Optimization of Fast Dissolving Etoricoxib Tablets Prepared by Sublimation Technique
【24h】

Optimization of Fast Dissolving Etoricoxib Tablets Prepared by Sublimation Technique

机译:升华技术制备速溶依托昔布片的工艺优化

获取原文
获取原文并翻译 | 示例

摘要

The purpose of this investigation was to develop fast dissolving tablets of etoricoxib. Granules containing etoricoxib, menthol, crospovidone, aspartame and mannitol were prepared by wet granulation technique. Menthol was sublimed from the granules by exposing the granules to vacuum. The porous granules were then compressed in to tablets. Alternatively, tablets were first prepared and later exposed to vacuum. The tablets were evaluated for percentage friability and disintegration time. A 32 full factorial design was applied to investigate the combined effect of 2 formulation variables: amount of menthol and crospovidone. The results of multiple regression analysis indicated that for obtaining fast dissolving tablets; optimum amount of menthol and higher percentage of crospovidone should be used. A surface response plots are also presented to graphically represent the effect of the independent variables on the percentage friability and disintegration time. The validity of a generated mathematical model was tested by preparing a checkpoint batch. Sublimation of menthol from tablets resulted in rapid disintegration as compared with the tablets prepared from granules that were exposed to vacuum. The optimized tablet formulation was compared with conventional marketed tablets for percentage drug dissolved in 30 min (Q_(30)) and dissolution efficiency after 30 min (DE_(30)). From the results, it was concluded that fast dissolving tablets with improved etoricoxib dissolution could be prepared by sublimation of tablets containing suitable subliming agent.
机译:该研究的目的是开发快速溶解的依托昔布片。通过湿法制粒技术制备了含依托昔布,薄荷醇,交聚维酮,阿斯巴甜和甘露醇的颗粒。通过将颗粒暴露于真空中将薄荷醇升华。然后将多孔颗粒压制成片剂。或者,首先制备片剂,然后将其暴露于真空中。评价片剂的易碎百分比和崩解时间。应用32个全因子设计来研究2个配方变量(薄荷醇和交聚维酮的量)的综合作用。多元回归分析的结果表明,该方法可制得速溶片剂;应该使用最适量的薄荷醇和更高比例的交聚维酮。还显示了表面响应图,以图形方式表示自变量对脆性百分比和崩解时间的影响。通过准备检查点批次来测试生成的数学模型的有效性。与由暴露于真空的颗粒制备的片剂相比,由片剂升华的薄荷醇导致快速崩解。将优化的片剂配方与常规市售片剂进行比较,了解药物在30分钟内的溶解百分比(Q_(30))和30分钟后的溶解效率(DE_(30))。从结果得出结论,可以通过升华含有合适升华剂的片剂来制备具有改善的依托昔布溶解性的快速溶解的片剂。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号