首页> 外文会议>International Symposium on Current Progress in Mathematics and Sciences >Effectivenes of K_2CO_3 and KHCO_3 as pore forming agents on floating drug delivery system hydrogel chitosan poly(N-vinyl pyrrolidone) semi-IPN: In vitro
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Effectivenes of K_2CO_3 and KHCO_3 as pore forming agents on floating drug delivery system hydrogel chitosan poly(N-vinyl pyrrolidone) semi-IPN: In vitro

机译:K_2CO_3和CaCO3作为浮孔壳聚糖聚糖聚合物(N-乙烯基吡咯烷酮)半IPN的孔形成剂:体外

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This research was related to the preparation of Floating Drug Delivery System, consisted of hydrogel chitosan-poly(N-vinyl pyrrolidone) with chitosan compositions: PVP monomer 70:30 and formaldehyde 2% used as crosslinking agent. Two kinds of pore-forming agent were used in this research, which were potassium carbonate (K_2CO_3) and potassium bicarbonate (KHCO_3) with variation of concentrations 0%, 1%, 2.5%, 5%, and 7.5% to the total mass of the initial reagents. The success of this research depends on the fast floating lag time and long floating time, as much as the percentage of the drug (amoxycillin) loading in the hydrogel and controlled drug release. FTIR characterization was used to analyze the changes of functional groups. Microscope Stereo Optical was used to identify the morphology of hydrogel and microcapsules. The best result showed that KHCO_3 7.5% produced hydrogel which have the floating lag time of 14 minutes 2 seconds, floating time > 3 hours, 86% of encapsulation efficiency of amoxycillin trihydrate and dissolution capability up to 100%.
机译:该研究与浮动药物输送系统的制备有关,由壳聚糖组合物的水凝胶壳聚糖 - 聚(N-乙烯基吡咯烷酮)组成:PVP单体70:30和甲醛2%用作交联剂。本研究使用两种孔隙成型剂,其碳酸钾(K_2CO_3)和碳酸氢钾(KHCO_3)的变化,浓度为0%,1%,2.5%,5%和7.5%至总质量初始试剂。该研究的成功取决于快速浮动滞后时间和长浮动时间,以及水凝胶和受控药物释放中的药物(阿莫西霉素)的百分比。 FTIR表征用于分析官能团的变化。显微镜立体声光学用于识别水凝胶和微胶囊的形态。最佳结果表明,KHCO_3 7.5%产生的水凝胶具有14分钟的浮动滞后时间为14分2秒,漂浮时间> 3小时,86%的阿莫西霉素Trihydrate的封装效率和溶解能力高达100%。

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