Zhao Fang, Dave Vivek S, Mar Mazin Z, Perri Jonathan R
Wegmans School of Pharmacy, St. John Fisher College, Rochester, New York.
Int J Pharm Compd. 2018 Sep-Oct;22(5):433-439.
Eslicarbazepine acetate is an anticonvulsant drug with a recent U.S. Food and Drug Administration approval for expanded use in children and adolescents. Currently, eslicarbazepine acetate is only available in the U.S. as 200-mg to 800-mg strength tablets (Aptiom), which are not easy to administer for pediatric patients. This study was initiated to develop an oral suspension formulation for extemporaneous compounding by pharmacists and to generate stability data for storage recommendations. Nine suspension formulations of eslicarbazepine acetate were prepared from Aptiom tablets and commercially available liquid vehicles using the standard mortar/pestle method. The vehicles varied mainly in their solvents, viscosities, and sweeteners. The formulations were evaluated for ease of preparation, physical properties, and initial potency. Two lead formulations were selected for a two-month stability study at room temperature or under refrigeration (2°C to 8°C). The stability samples were withdrawn at pre-determined time points and analyzed by visual inspection, pH measurement, and a stability-indicating high-performance liquid chromatographic assay. The majority of the 9 formulations were found to be easy to prepare and administer at a concentration of 40-mg/mL eslicarbazepine acetate. Particle settling was observed in several formulations over time, but they were re-suspended satisfactorily upon shaking. Two suspensions in 50:50 v/v mixtures of Ora-Sweet or Ora-Sweet SF with Ora-Plus were selected as the lead formulations for the two-month stability study. At the initiation of the study, all samples appeared as white and smooth suspensions with pH ranging from 4.39 to 4.46. The high-performance liquid chromatographic results confirmed that the initial samples contained 100.4% to 102.2% of the label claim strength. Over two months of storage at room temperature or refrigeration, there were no significant changes in visual appearance, re-suspendability, pH, or potency for any samples. No new degradation peaks were observed in any highperformance liquid chromatograms. Based on the study results, two eslicarbazepine acetate suspensions are recommended for extemporaneous compounding from Aptiom tablets. The formulations consist of 40 mg/mL eslicarbazepine acetate in 50:50 v/v Ora-Sweet:Ora-Plus or Ora-Sweet SF:Ora-Plus. Once prepared, these suspensions can be stored at room temperature or under refrigeration for up to two months.
醋酸艾司利卡西平是一种抗惊厥药物,最近获得美国食品药品监督管理局批准可扩大用于儿童和青少年。目前,醋酸艾司利卡西平在美国仅以200毫克至800毫克规格的片剂(Aptiom)形式提供,这对于儿科患者来说不易给药。开展本研究是为了开发一种可供药剂师临时调配的口服混悬液制剂,并生成储存建议的稳定性数据。使用标准研钵/杵棒法,由Aptiom片剂和市售液体赋形剂制备了九种醋酸艾司利卡西平混悬液制剂。赋形剂主要在溶剂、粘度和甜味剂方面有所不同。对这些制剂的制备简易程度、物理性质和初始效价进行了评估。选择两种主要制剂在室温或冷藏(2°C至8°C)条件下进行为期两个月的稳定性研究。在预定时间点取出稳定性样品,通过目视检查、pH测量和一种稳定性指示高效液相色谱法进行分析。发现9种制剂中的大多数在醋酸艾司利卡西平浓度为40毫克/毫升时易于制备和给药。随着时间推移,在几种制剂中观察到颗粒沉降,但摇晃后它们能令人满意地重新悬浮。选择两种由Ora - Sweet或Ora - Sweet SF与Ora - Plus按50:50 v/v混合而成的混悬液作为为期两个月稳定性研究的主要制剂。在研究开始时,所有样品均呈现白色且均匀的混悬液,pH值范围为4.39至4.46。高效液相色谱结果证实初始样品中含有标示量效价的100.4%至102.2%。在室温或冷藏条件下储存两个月期间,任何样品的外观、再悬浮性、pH值或效价均无显著变化。在任何高效液相色谱图中均未观察到新的降解峰。基于研究结果,推荐两种由Aptiom片剂临时调配的醋酸艾司利卡西平混悬液。制剂由醋酸艾司利卡西平40毫克/毫升与Ora - Sweet:Ora - Plus或Ora - Sweet SF:Ora - Plus按50:50 v/v混合而成。一旦制备完成,这些混悬液可在室温或冷藏条件下储存长达两个月。