Taste-masking mechanism of brivaracetam oral solution using cyclodextrin and sodium carboxymethyl cellulose

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY International Journal of Pharmaceutics Pub Date : 2025-03-03 DOI:10.1016/j.ijpharm.2025.125368
Conghui Li , Junlin Yuan , Hui Zhang , Nan Liu , Zengming Wang , Aiping Zheng , Xiaochen Bo
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Abstract

Brivaracetam is a novel antiepileptic medication that can be indicated for the management of epilepsy in pediatric patients over one month old. To facilitate its administration to children, an oral solution is the most suitable option. However, the inherently bitter taste of brivaracetam poses a challenge in terms of palatability, necessitating the development of a taste masking strategy for the solution. In this study, a palatable brivaracetam oral solution was prepared by meticulously screening various taste masking techniques. Then the interaction relationship between brivaracetam and pivotal excipients (sodium carboxymethyl cellulose (CMC-Na) and 2-Hydroxypropyl-β-cyclodextrin (HP-β-CD)) within the optimized formulation was investigated by molecular dynamics simulations. It turned out that brivaracetam did not encapsulate within HP-β-CD, but instead forms a robust association through hydrogen bonding and π-stacking interactions, facilitated by the presence of CMC-Na. Further exploration through molecular docking elucidated that the optimized formulation effectively masks the bitter taste by diminishing the binding affinity of brivaracetam to bitter taste receptors. In summary, this study achieved taste masking of brivaracetam under solution conditions by investigated the interactions of brivaracetam and key excipient interactions as well as the mechanisms of taste masking of optimized formulations, providing valuable insights for similar pharmaceutical applications.

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用环糊精和羧甲基纤维素钠制备布瓦西坦口服液的掩味机理。
布瓦西坦是一种新型抗癫痫药物,可用于一个月以上儿童癫痫患者的治疗。为了方便儿童服用,口服溶液是最合适的选择。然而,布瓦西坦固有的苦味在适口性方面提出了挑战,需要为解决方案开发味道掩盖策略。在本研究中,精心筛选各种掩味技术,制备了美味的布瓦西坦口服液。然后通过分子动力学模拟研究了优化配方中布瓦西坦与关键辅料(羧甲基纤维素钠(CMC-Na)和2-羟丙基-β-环糊精(HP-β-CD))的相互作用关系。结果表明,布伐西坦并没有在HP-β-CD内包封,而是在CMC-Na的作用下,通过氢键和π堆积相互作用形成了牢固的结合。通过分子对接进一步探索发现,优化后的配方通过降低布伐西坦对苦味受体的结合亲和力,有效地掩盖了苦味。综上所述,本研究通过研究布瓦西坦与关键赋形剂的相互作用以及优化配方的味觉掩蔽机制,实现了布瓦西坦在溶液条件下的味觉掩蔽,为类似的药物应用提供了有价值的洞见。
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来源期刊
CiteScore
10.70
自引率
8.60%
发文量
951
审稿时长
72 days
期刊介绍: The International Journal of Pharmaceutics is the third most cited journal in the "Pharmacy & Pharmacology" category out of 366 journals, being the true home for pharmaceutical scientists concerned with the physical, chemical and biological properties of devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture and evaluation. This includes evaluation of the properties of drugs, excipients such as surfactants and polymers and novel materials. The journal has special sections on pharmaceutical nanotechnology and personalized medicines, and publishes research papers, reviews, commentaries and letters to the editor as well as special issues.
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