表面活性剂共磨法改善尼美舒利的溶出度

M. Gohel, L. Patel
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引用次数: 14

摘要

采用共磨法制备了水溶性较差的非甾体抗炎药尼美舒利的溶出度。研究了尼美舒利的溶解度,确定了不同浓度的吐温80在不同pH值下的增溶过程。在10%的Tween 80浓度下,当缓冲液的pH大于尼美舒利的pKa时,大部分(约90%)药物被胶束包裹。采用32因子设计,以吐温80浓度和十二烷基硫酸钠为自变量。先与表面活性剂水溶液混合,再与乳糖、微晶纤维素等佐剂混合,药物溶出度提高。与t80相比,十二烷基硫酸钠对提高药物溶出度更有效。使用Tween 80和十二烷基硫酸钠的混合物是合理的,因为45和120分钟内药物释放百分比的相互作用项(Tween 80 x十二烷基硫酸钠)不显著。在30min、45min和120min得到了药物的休止角和药物释放率的等高线图。当表面活性剂在高水平使用时,颗粒流动受到不利影响,并且没有进一步改善药物溶出度。由于表面活性剂或亲水性佐剂的存在,药物溶解性的改善可归因于润湿性和胶束化的改善。所选批次的药物溶出度提高了两倍以上。
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Improvement of Nimesulide Dissolution by a Co‐grinding Method Using Surfactants
A co-grinding method was used to improve the dissolution characteristics of nimesulide, a poorly water-soluble non-steroidal anti-inflammatory drug. Nimesulide solubility was studied to determine the solubilization process using different concentrations of Tween 80 at different pH values. At a 10% Tween 80 concentration, a large proportion (> 90%) of drug was entrapped in micelles when the pH of buffer solution was greater than pKa of nimesulide. A 32 factorial design was adopted using the concentration of Tween 80 and sodium lauryl sulphate as independent variables. Improved drug dissolution was obtained when the drug was mixed first with aqueous surfactant solution and later blended with adjuvant such as lactose and microcrystalline cellulose. Sodium lauryl sulphate was more effective in increasing the drug dissolution compared with Tween 80. The use of a blend of Tween 80 and sodium lauryl sulphate is justified since the interaction term (Tween 80 x sodium lauryl sulphate) for percentage drug release in 45 and 120 min was not significant. Contour plots were obtained for the angle of repose and percentage drug release in 30, 45 and 120 min. The study revealed that optimum level of surfactants should be used. The granule flow was adversely affected and no further improvement of drug dissolution was observed when the surfactants were used at high levels. The improved drug dissolution may be attributed to improved wetting and micellization due to presence of surfactants or hydrophilic adjuvant. More than two-fold increase in the drug dissolution was obtained by the selected batches.
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