首页> 外文期刊>Saudi Pharmaceutical Journal >Taste-masking assessment of orally disintegrating tablets and lyophilisates with cetirizine dihydrochloride microparticles
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Taste-masking assessment of orally disintegrating tablets and lyophilisates with cetirizine dihydrochloride microparticles

机译:西替利嗪二盐酸盐微粒对口腔崩解片和冻干品的掩味评估

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Orally disintegrating tablets and oral lyophilisates are novel attractive dosage forms that disintegrate or dissolve in the buccal cavity within seconds without necessity of drinking. The major limitation in designing of these dosage forms is unpleasant taste of the drug substance. Cetirizine dihydrochloride is a H1-antihistamine substance indicated for the treatment of allergy. It is characterized by extremely bitter taste, therefore in order to deliver cetirizine dihydrochloride using orodispersible formulations, effective taste-masking is required. The aim of this study was to investigate whether microparticles containing cetirizine dihydrochloride could be successfully used to formulate orally disintegrating tablets by direct compression method and oral lyophilisates by freeze-drying process. Taste masking of cetirizine dihydrochloride was achieved by the spray-drying technique using Eudragit? E PO as the drug agent carrier. Based on the preliminary studies, optimal compositions of microparticles, tablets and lyophilisates were chosen. Obtained dosage forms were characterized for drug content, disintegration time and mechanical properties. In order to determine whether the microparticles subjected to direct compression and freeze-drying process effectively mask the bitter taste of cetirizine dihydrochloride, the in vivo and in vitro evaluation was performed. The results showed that designed formulates with microparticles containing cetirizine dihydrochloride were characterized by appropriate mechanical properties, uniformity of weight and thickness, short disintegration time, and the uniform content of the drug substance. Taste-masking assessment performed by three independent methods (e-tongue evaluation, human test panel and the in vitro drug release) revealed that microparticles with Eudragit? E PO are effective taste – masking carriers of cetirizine dihydrochloride and might be used to formulate orally disintegrating tablets and oral lyophilisates.
机译:口服崩解片剂和口服冻干物是新颖的有吸引力的剂型,其在几秒钟内崩解或溶解在颊腔中而无需饮用。这些剂型设计的主要限制是原料药的味道不佳。西替利嗪二盐酸盐是一种用于治疗过敏的H1-抗组胺物质。它的特征是极苦的味道,因此,为了使用口分散性制剂递送盐酸西替利嗪,需要有效的掩盖味道。这项研究的目的是研究含有西替利嗪二盐酸盐的微粒是否可以成功地通过直接压片法成功地制成口腔崩解片,并通过冷冻干燥法成功地制成口服冻干物。通过使用Eudragit?的喷雾干燥技术掩盖了盐酸西替利嗪的味道。 E PO作为药物的载体。在初步研究的基础上,选择了微粒,片剂和冻干物的最佳组成。对获得的剂型进行药物含量,崩解时间和机械性能的表征。为了确定经受直接压缩和冷冻干燥过程的微粒是否有效掩盖了西替利嗪二盐酸盐的苦味,进行了体内和体外评估。结果表明,所设计的含西替利嗪二盐酸盐微粒的配方具有适当的机械性能,重量和厚度均匀性,短的崩解时间和均匀的药物含量。通过三种独立的方法(电子舌评估,人体测试小组和体外药物释放)进行掩味评估,结果表明含有Eudragit®的微粒具有抗微生物作用。 E PO是有效的味道–掩盖西替利嗪二盐酸盐的载体,可用于配制口腔崩解片和口服冻干物。

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