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利用顺丁烯二酸单十八酯作为酒石酸氢可待因口腔崩解片中掩味剂的质量源于设计方法的应用。

Application of a quality-by-design approach for utilizing sodium stearyl fumarate as a taste-masking agent in dextromethorphan hydrobromide orally disintegrating tablets.

机构信息

a Department of Pharmaceutics , College of Pharmacy, King Saud University , Riyadh , Kingdom of Saudi Arabia.

b Department of Pharmaceutics and Industrial Pharmacy , College of Pharmacy, Al Azhar University , Assiut , Egypt.

出版信息

Pharm Dev Technol. 2019 Jul;24(6):711-719. doi: 10.1080/10837450.2019.1579228. Epub 2019 Mar 6.

Abstract

Orally dissolving tablets (ODTs) represent one of the recent advances in drug delivery. The foremost objective of this study was to optimize the utilization of lubricant sodium stearyl fumarate in the preparation of dextromethorphan hydrobromide ODTs with enhanced taste-masking properties. The simple blending of sodium stearyl fumarate with the powder bed would result in taste-masking through physical adsorption of the lubricant particles on the drug particles. A randomized 3 full factorial experimental design was used to characterize the relationship between lubricant ratio (X1), mixing time (X2), and the tablet properties. The tablets were assessed for friability, hardness, disintegration time, and in-vitro dissolution. All tablets showed hardness within the range of 3.0-3.7 kp, and the % loss in friability test was less than 1.1%. The in-vitro disintegration time ranged between 9 and 25 s. An in-vitro drug release study of the prepared ODTs showed that more than 90% of the drug was released within 30 min. A palatability test of the optimized formula conducted in human volunteers showed acceptable taste and mouthfeel with in-vivo disintegration time of 17 s. Thus, results obtained convincingly showed successful fast disintegration of the prepared tablets and acceptable palatability when using sodium stearyl fumarate as a taste masking agent.

摘要

口溶片(ODT)是药物传递领域的最新进展之一。本研究的首要目标是优化润滑剂富马酸硬脂酸钠在制备具有增强掩味性能的氢溴酸右美沙芬 ODT 中的应用。富马酸硬脂酸钠与粉末床的简单混合将通过润滑剂颗粒在药物颗粒上的物理吸附来实现掩味。采用完全 3 因子随机实验设计来描述润滑剂比例(X1)、混合时间(X2)和片剂性质之间的关系。对片剂的脆碎度、硬度、崩解时间和体外溶出度进行了评估。所有片剂的硬度均在 3.0-3.7 kp 范围内,脆碎度测试中的%损失小于 1.1%。体外崩解时间在 9 到 25 秒之间。对制备的 ODT 的体外药物释放研究表明,超过 90%的药物在 30 分钟内释放。在人体志愿者中进行的优化配方的适口性测试显示,口感和口感可接受,体内崩解时间为 17 秒。因此,结果令人信服地表明,使用富马酸硬脂酸钠作为掩味剂可以成功地快速崩解制备的片剂,并具有可接受的口感。

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