首页> 外文期刊>Drug development and industrial pharmacy >Investigations on factors affecting chitosan for dissolution enhancement of oxcarbazepine by spray dried microcrystal formulation with an experimental design approach.
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Investigations on factors affecting chitosan for dissolution enhancement of oxcarbazepine by spray dried microcrystal formulation with an experimental design approach.

机译:用实验设计方法研究壳聚糖通过喷雾干燥微晶制剂增强奥卡西平溶出度的影响因素。

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摘要

In the present work effect of chitosan on microcrystal formulation for dissolution enhancement of oxcarbazepine using controlled crystallization technique coupled with spray drying was explored. The work was extended for exploration of simplified approach for stable particle size reduction. The study was performed with an experimental design approach i. e. a fractional factorial design of resolution 5 (with all 2 factor interaction) for the screening of predefined independent variables drug concentration, chitosan concentration, feed rate, inlet temperature and percent aspiration for spray drying. Whereas percent drug dissolved, wettability time, flowability in terms of angle of repose and particle size were designated as response variables. Resultant models were analyzed using multiple linear regression analysis, which generated equation to plot response surface curves along with desirability function. Results showed that chitosan concentration had significant effect on dissolution enhancement of oxcarbazepine at a level of 2% w/v. Increase in drug concentration showed decreased dissolution rate however on particle size it did not show statistically significant effect. Topographical characterization was carried out by SEM which showed that feed rate, percent aspiration and inlet temperature had significant effect on particle morphology. For deriving optimized formulation results were analyzed using desirability function for the maximum percent drug dissolved and least drug polymer matrix particle size. DSC studies showed that drug was molecularly associated with chitosan matrix or particles.
机译:在本工作中,探索了壳聚糖对微晶制剂的影响,该微晶制剂采用控制结晶技术与喷雾干燥相结合来增强奥卡西平的溶出度。这项工作已扩展到探索简化方法以稳定地减小粒径的工作。该研究是通过实验设计方法进行的。 e。分辨率5的分数阶乘设计(具有所有2因子相互作用),用于筛选预定义的独立变量,药物浓度,壳聚糖浓度,进料速度,入口温度和喷雾干燥的抽吸百分比。而将药物溶解百分比,润湿时间,在休止角和粒度方面的流动性指定为响应变量。使用多重线性回归分析对生成的模型进行分析,该模型生成方程以绘制响应表面曲线以及所需函数。结果表明,壳聚糖浓度对奥卡西平的溶出度提高有显着影响,浓度为2%w / v。药物浓度的增加显示出溶出度降低,但是对粒径却没有统计学上的显着影响。用SEM进行形貌表征,结果表明进料速度,抽吸百分比和入口温度对颗粒形态有显着影响。为了获得优化的制剂,使用期望函数分析了最大的药物溶解百分比和最小的药物聚合物基质粒径。 DSC研究表明,药物与壳聚糖基质或颗粒分子相关。

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