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The influence of swelling capacity of superdisintegrants in different pH media on the dissolution of hydrochlorothiazide from directly compressed tablets

机译:超崩解剂在不同pH介质中的溶胀能力对氢氯噻嗪从直接压片中溶出的影响

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摘要

The purpose of this study was to investigate the efficiency of superdisintegrants in promoting tablet disintegration and drug dissolution under varied media pH. Significant reductions in the rate and extent of water uptake and swelling were observed for both sodium starch glycolate (Primojel) and croscarmellose sodium (Ac-Di-Sol) in an acidic medium (0.1 N HCl) but not for crospovidone NF (Polyplasdone XL10), a nonionic polymer. When Primojel and Ac-Di-Sol were incorporated in model formulations, a significant increase in tablet disintegration time was observed for slowly disintegrating tablets (lactose-based tablets) but not for the rapidly disintegrating tablets (dicalcium phosphate-based tablets). The dissolution rate of the model drug, hydrochlorothiazide, was found highly dependent on both tablet disintegration efficiency and the solubility of base material(s) in the testing medium. A laser diffraction particle size analyzer proved to be an effective tool for determining the intrinsic swelling of disintegrant particles in different media. Water uptake and swelling were confirmed as 2 important functions of superdisintegrants. The reduced water uptake and swelling capacity of disintegrants containing ionizable substituents in an acidic medium can potentially jeopardize their efficiency in promoting tablet disintegration and the drug dissolution rate.
机译:这项研究的目的是研究在不同的培养基pH值下超级崩解剂在促进片剂崩解和药物溶解中的效率。在酸性介质(0.1 N HCl)中,羟乙酸淀粉钠(Primojel)和交联羧甲基纤维素钠(Ac-Di-Sol)的吸水率和溶胀率均显着降低,而交聚维酮NF(Polyplasdone XL10)则没有,一种非离子聚合物。当将Primojel和Ac-Di-Sol掺入模型制剂中时,对于缓慢崩解的片剂(基于乳糖的片剂),观察到片剂崩解时间的显着增加,而对于快速崩解的片剂(基于磷酸二钙的片剂)则观察不到。发现模型药物氢氯噻嗪的溶解速率高度依赖于片剂崩解效率和基材在测试介质中的溶解度。事实证明,激光衍射粒度分析仪是确定崩解剂颗粒在不同介质中固有溶胀的有效工具。水分吸收和溶胀被确认为超级崩解剂的两个重要功能。酸性介质中含有可电离取代基的崩解剂的吸水率和溶胀能力降低,可能会危害其促进片剂崩解和药物溶解速率的效率。

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