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雷尼替丁口腔崩解片的处方设计与掩味

Formulation and Taste Masking of Ranitidine Orally Disintegrating Tablet.

作者信息

Hesari Zahra, Shafiee Akram, Hooshfar Shirin, Mobarra Naser, Mortazavi Seyed Alireza

机构信息

Department of Pharmaceutics, School of Pharmacy, Guilan University of Medical Sciences, Rasht, Iran.

Deptartment of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran 1417614411, Iran.

出版信息

Iran J Pharm Res. 2016 Fall;15(4):677-686.

Abstract

Orally Disintegrating Tablets (ODT) have the advantages of both solid dosage form specially the stability and ease of handling and liquid dosage forms including ease of swallowing and pre-gastric absorption. We focused on taste masking and formulation of ranitidine ODT which disintegrates rapidly in the mouth within 60 sec using super-disintegrants, special polymers, water soluble and even insoluble excipients, sweeteners and essence. Various formulations were designed and made in four series. The amount of ranitidine in each formulation was 150 mg, and the final weight of tablets was around 500 mg. Prepared formulations were evaluated in terms of several physicochemical tests including powder/granule flowability, appearance, thickness, uniformity of weight, hardness, friability and disintegration time. Several taste masking techniques were investigated in each series of formulation, in order to cover the bitter taste of wranitidine. These included the addition of sweetener, granulation, solid dispersion with soluble and insoluble agents and complex formation with cellulose derivatives. The best formulation(s) in each group was/were chosen for taste evaluations with the help of 10 volunteers. Finally, formulation F14 was selected as the ultimate formulation, based on its better taste and shorter disintegration time (around 5 seconds). Formulation F14 contained Na CMC, avicel, Na starch glycolate, xylitol, saccharin, Na benzoate and menthol. The chosen formulation successfully passed the complementary evaluations such as assay of active ingredient and dissolution time. Na CMC was found to be acceptable in terms of decreasing disintegration time and enhanced taste masking potential and can be used in further ODT formulations.

摘要

口腔崩解片(ODT)兼具固体剂型(特别是稳定性和易于处理)和液体剂型(包括易于吞咽和胃前吸收)的优点。我们专注于雷尼替丁口腔崩解片的掩味和制剂研发,该制剂使用超级崩解剂、特殊聚合物、水溶性甚至不溶性辅料、甜味剂和香精,能在60秒内在口腔中迅速崩解。设计并制作了四个系列的各种制剂。每个制剂中雷尼替丁的含量为150毫克,片剂的最终重量约为500毫克。对制备的制剂进行了多项物理化学测试评估,包括粉末/颗粒流动性、外观、厚度、重量均匀性、硬度、脆碎度和崩解时间。在每个制剂系列中研究了几种掩味技术,以掩盖雷尼替丁的苦味。这些技术包括添加甜味剂、制粒、与可溶性和不溶性试剂进行固体分散以及与纤维素衍生物形成复合物。在10名志愿者的帮助下,选择每组中最佳的制剂进行口感评估。最后,基于其较好的口感和较短的崩解时间(约5秒),制剂F14被选为最终制剂。制剂F14含有羧甲基纤维素钠、微晶纤维素、羟丙基淀粉钠、木糖醇、糖精、苯甲酸钠和薄荷醇。所选制剂成功通过了活性成分含量测定和溶出时间等补充评估。发现羧甲基纤维素钠在缩短崩解时间和增强掩味潜力方面是可接受的,可用于进一步的口腔崩解片制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/447d/5316246/d67a47719aa3/ijpr-15-677-g001.jpg

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