首页> 外文OA文献 >Design and evaluation of effervescent floating tablets based on hydroxyethyl cellulose and sodium alginate using pentoxifylline as a model drug
【2h】

Design and evaluation of effervescent floating tablets based on hydroxyethyl cellulose and sodium alginate using pentoxifylline as a model drug

机译:基于羟乙基纤维素的泡腾浮动片剂的设计与评价,羟乙基纤维素与藻酸钠用Pentoximiflline作为模范药物

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The aim of this work was to design and evaluate effervescent floating gastro-retentiveuddrug delivery matrix tablets with sustained-release behavior using a binary mixture ofudhydroxyethyl cellulose and sodium alginate. Pentoxifylline was used as a highly water-soluble,udshort half-life model drug with a high density. The floating capacity, swelling, and drug releaseudbehaviors of drug-loaded matrix tablets were evaluated in 0.1 N HCl (pH 1.2) at 37°C±0.5°C.udRelease data were analyzed by fitting the power law model of Korsmeyer–Peppas. The effectudof different formulation variables was investigated, such as wet granulation, sodium bicarbonateudgas-forming agent level, and tablet hardness properties. Statistical analysis was appliedudby paired sample t-test and one-way analysis of variance depending on the type of data touddetermine significant effect of different parameters. All prepared tablets through wet granulationudshowed acceptable physicochemical properties and their drug release profiles followedudnon-Fickian diffusion. They could float on the surface of dissolution medium and sustain drugudrelease over 24 hours. Tablets prepared with 20% w/w sodium bicarbonate at 50–54 N hardnessudwere promising with respect to their floating lag time, floating duration, swelling ability, andudsustained drug release profile.udKeywords: floating tablets, sodium alginate, pentoxifylline, dissolution, swelling,udeffervescent
机译:这项工作的目的是使用 udhydroxyethyl纤维素和藻酸钠的二元混合物设计和评估具有持续释放行为的泡腾漂浮性胃滞留性 uddrug给药基质片剂。己酮可可碱被用作具有高密度的高度水溶性,超短半衰期模型药物。在37°C±0.5°C的0.1 N HCl(pH 1.2)中评估了载药基质片剂的漂浮能力,溶胀和药物释放行为。 ud通过拟合Korsmeyer的幂定律模型分析了释放数据– Peppas。研究了不同配方变量的影响,如湿法制粒,碳酸氢钠,成气剂含量和片剂硬度特性。根据数据类型应用统计分析配对样本t检验和单向方差分析确定不同参数的显着影响。通过湿法制粒制备的所有片剂均显示可接受的理化性质,并且其药物释放曲线遵循udnon-Fickian扩散。它们可能漂浮在溶出介质的表面,并在24小时内持续释放药物。用20%w / w碳酸氢钠在50-54 N硬度下制备的片剂,其漂浮滞后时间,漂浮持续时间,溶胀能力和持续的药物释放特性令人鼓舞。 ud关键字:漂浮片剂,海藻酸钠,己酮可可碱,溶解,肿胀,去泡

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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