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Preparation and Evaluation of Taste Masked Famotidine Formulation Using Drug/β-cyclodextrin/Polymer Ternary Complexation Approach

机译:药物/β-环糊精/聚合物三元络合方法制备和掩味法莫替丁制剂

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摘要

The main aim of the present study was to evaluate potential of ternary complexation (comprising of drug, cyclodextrin and polymer) as an approach for taste masking. For this purpose famotidine with property of bitter taste was selected as a model drug. Improvement in taste masking capability of cyclodextrin towards famotidine was evaluated by formulating a ternary complex including hydrophilic polymer hydroxyl propyl methyl cellulose (HPMC 5 cps) as the third component. Phase solubility analysis at 25 °C was carried out for both the binary systems (viz. drug–cyclodextrin and drug–polymer) and the ternary system (drug–cyclodextrin–polymer). Ternary complex was prepared using solution method and was further characterized using XRD, DSC, FT-IR and microscopic studies. In vitro dissolution study was carried out to see the effect of ternary complexation on drug release. Taste perception study was carried out on human volunteers to evaluate the taste masking ability of ternary complexation. Results obtained from phase solubility analysis showed that the combined use of polymer and cyclodextrin effectively increased the stability constant of the complex [from 538 M−1 for binary system to 15,096 M−1 for ternary system]. Ternary system showed effective taste masking as compared to binary complex and at the same time showed no limiting effect on the drug release (D.E15min = 90%). The effective taste masking was attributed to the enhanced complexation of famotidine in ternary system compared to binary system and the same was confirmed from the characterization studies. In conclusion, the study confirmed that ternary complexation can be utilized as an alternative approach for effective taste masking.
机译:本研究的主要目的是评估三元复合(包括药物,环糊精和聚合物)作为掩味方法的潜力。为此目的,选择具有苦味特性的法莫替丁作为模型药物。通过配制包含亲水聚合物羟丙基甲基甲基纤维素(HPMC 5 cps)作为第三组分的三元复合物,评估环糊精对法莫替丁的掩味能力的改善。在25°C下对二元系统(即药物-环糊精和药物-聚合物)和三元系统(药物-环糊精-聚合物)进行了相溶解度分析。使用溶液法制备三元配合物,并使用XRD,DSC,FT-IR和显微镜研究对其进行进一步表征。进行了体外溶出研究,以观察三元络合对药物释放的影响。对人类志愿者进行了味觉研究,以评估三元络合物的掩味能力。从相溶解度分析获得的结果表明,聚合物和环糊精的联合使用有效地提高了配合物的稳定性常数[从二元体系的538M-1增至三元体系的15,096M-1]。与二元复合物相比,三元系统显示出有效的掩味作用,同时对药物释放没有限制作用(D.E15min == 90%)。与二元体系相比,有效的掩味归因于法莫替丁在三元体系中增强的络合,并且从表征研究中也证实了这一点。总之,该研究证实三元络合物可以用作有效掩味的替代方法。

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