Formulation and In Vitro Evaluation of Taste- Masked Prednisolone Orodispersible Tablets

Hiba mohammed Suza ali, Eman B. H. Al-Khedairy
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Abstract

Background: prednisolone is a corticosteroid with a very bitter taste acts as anti- anti-inflammatory and immune suppressant drug and it is used at any age. Objective: To improve patient compliance by masking the bitter taste of the drug to be delivered as an orodispersible tablet. Methods: External ionic gelation using sodium alginate (0.5%w/v) and calcium chloride (1% w/v) in presence of 0.5% w/v carbopol 940 was used to prepare taste masked beads loaded with prednisolone to be compressed as orodispersible tablets. Results: The bitter taste of was masked by preparing beads composed of 1:1:1 (sodium alginate: Carbopol 940: prednisolone) which released only 0.77 % of the drug in pH 6.8 (pH of oral cavity). The ODT prepared by direct compression using taste masked beads equivalent to 5 mg PRD, 3% crospovidone, 2% PVP, 1% talc, 1% magnesium stearate and combination of Avcil® PH 102 and mannitol at (1:1) ratio was the optimum formula (T6) with hardness of 3.9± 0.32 kg, , friability 0.45%, thickness 2.5 ± 0.05 mm, % drug content 98.2% ± 1.8, wetting time 18.7 ± 1.3 sec, water absorption 41 ± 2.1%, disintegration time 15.3 ± 0.5 sec. and released only 0.75% ± 0.01 of PRD in an oral pH of 6.8 within one minute (indicating good taste masking). Its release in the stomach (pH 0.1N HCl) and intestine (pH 6.8) was continued for up to two hours. Conclusion: it can be concluded that the external ionic gelation method successfully masked the bitter taste of prednisolone and can also be formulated as taste-masked orodispersible tablets by the direct compression method. Received: Jan. 2023 Accepted: May 2023 Published: Oct.2023
隐味强的松龙口腔分散片的制备及体外评价
背景:强的松龙是一种极苦的皮质类固醇,具有抗炎和免疫抑制作用,适用于任何年龄。目的:通过掩盖口服分散片剂给药时的苦味,提高患者服药依从性。方法:采用海藻酸钠(0.5%w/v)和氯化钙(1% w/v)在0.5%w/v卡波醇940的存在下进行外离子凝胶法制备强尼松龙味掩珠压缩成分散片。结果:制备的海藻酸钠:卡波波尔940:强的松龙比例为1:1:1的微丸,在pH 6.8(口腔pH)下仅释放0.77%的药物。以相当于5 mg PRD、3%聚氯维酮、2% PVP、1%滑石粉、1%硬脂酸镁、Avcil®PH 102和甘露醇(1:1)的比例直接压缩制备的ODT为最佳配方(T6),硬度为3.9±0.32 kg,脆度0.45%,厚度2.5±0.05 mm,含药率98.2%±1.8,润湿时间18.7±1.3秒,吸水率41±2.1%,崩解时间为15.3±0.5秒,在口腔pH为6.8的条件下,1分钟内仅释放0.75%±0.01的PRD(口感掩蔽良好)。它在胃(pH 0.1N HCl)和肠(pH 6.8)中的释放持续了两个小时。结论:外离子凝胶法制备强的松龙可成功掩盖其苦味,也可采用直接压片法制备掩味片或分散片。收稿日期:2023年1月录用日期:2023年5月发表日期:2023年10月
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
24 weeks
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