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抗组胺和解痰药物的口感掩蔽口腔崩解微丸:制剂、表征及人体体内研究

Taste Masked Orally Disintegrating Pellets of Antihistaminic and Mucolytic Drug: Formulation, Characterization, and In Vivo Studies in Human.

作者信息

Taj Yasmeen, Pai Roopa S, Kusum Devi V, Singh Gurinder

机构信息

Department of Pharmaceutics, Faculty of Pharmacy, Al-Ameen College of Pharmacy, Lal Bagh Main gate, Hosur Road, Bangalore, Karnataka 560027, India.

出版信息

Int Sch Res Notices. 2014 Oct 28;2014:504536. doi: 10.1155/2014/504536. eCollection 2014.

DOI:10.1155/2014/504536
PMID:27379290
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4897477/
Abstract

The main aim of the present study was to evaluate the potential of orally disintegrating pellets (ODPs) as an approach for taste masking of bitter drugs, namely, Ambroxol hydrochloride (A-HCl) and Cetirizine dihydrochloride (C-DHCl). Pellets were prepared by extrusion/spheronization with Eudragit EPO, kyron T-134, Kyron T-314, mannitol, sorbitol, MCC (Avicel PH-101), sucralose, chocolate flavor, and 5% xanthum gum. The prepared pellets were characterized for percentage yield, drug content, particle size, in vitro drug release, and in vivo evaluation on humans for taste, mouth feel, and in vivo disintegration time. The results revealed that the average size of pellets was influenced greatly by the percentage of binder and extrusion speed. The optimized ODPs disintegrated in less than 20 s and showed more than 98% of drugs in ODPs dissolved within 15 min. Taste perception study was carried out on human volunteers to evaluate the taste masking ability of ODPs for taste, mouth feel, and in vivo disintegration time. Crystalline state evaluation of drugs in the optimized ODPs was conducted for X-ray powder diffraction. In conclusion, the study confirmed that ODPs can be utilized as an alternative approach for effective taste masking and rapid disintegration in the oral cavity.

摘要

本研究的主要目的是评估口腔崩解微丸(ODPs)作为掩盖苦味药物(即盐酸氨溴索(A-HCl)和盐酸西替利嗪(C-DHCl))味道的一种方法的潜力。采用挤出滚圆法,使用聚丙烯酸树脂EPO、凯松T-134、凯松T-314、甘露醇、山梨醇、微晶纤维素(微晶纤维素PH-101)、三氯蔗糖、巧克力香料和5%黄原胶制备微丸。对制备的微丸进行了收率、药物含量、粒径、体外药物释放以及人体口感、口腔感觉和体内崩解时间的体内评价。结果表明,微丸的平均粒径受粘合剂百分比和挤出速度的影响很大。优化后的ODPs在20秒内崩解,15分钟内ODPs中98%以上的药物溶解。对人类志愿者进行了味觉感知研究,以评估ODPs在味道、口腔感觉和体内崩解时间方面的掩味能力。对优化后的ODPs中的药物进行了X射线粉末衍射的晶态评价。总之,该研究证实ODPs可作为一种有效的掩味和口腔快速崩解的替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/072502c6ae0f/ISRN2014-504536.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/f820cd13566a/ISRN2014-504536.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/a3eeca341a42/ISRN2014-504536.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/ee0ae3f7965b/ISRN2014-504536.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/6c9cfa27b21d/ISRN2014-504536.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/072502c6ae0f/ISRN2014-504536.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/f820cd13566a/ISRN2014-504536.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/a3eeca341a42/ISRN2014-504536.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/ee0ae3f7965b/ISRN2014-504536.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/6c9cfa27b21d/ISRN2014-504536.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ed7/4897477/072502c6ae0f/ISRN2014-504536.005.jpg

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