Department of Pharmaceutics and Bioavailability and Bioequivalence Research Facility, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, 75270, Pakistan.
Department of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, 75270, Pakistan.
Sci Rep. 2020 Sep 10;10(1):14765. doi: 10.1038/s41598-020-71751-y.
This study is based on the QbD development of extended-release (ER) extruded-spheronized pellets of Meclizine HCl and its comparative pharmacokinetic evaluation with immediate-release (IR) pellets. HPLC-fluorescence method was developed and validated for plasma drug analysis. IR drug cores were prepared from lactose, MCC, and PVP using water as granulating fluid. Three-level, three-factor CCRD was applied for modeling and optimization to study the influence of Eudragit (RL100-RS100), TEC, and talc on drug release and sphericity of coated pellets. HPLC-fluorescence method was sensitive with LLOQ 1 ng/ml and linearity between 10 and 200 ng/ml with R > 0.999. Pharmacokinetic parameters were obtained by non-compartmental analysis and results were statistically compared using logarithmically transformed data, where p > 0.05 was considered as non-significant with a 90% CI limit of 0.8-1.25. The AUC and AUC of ER pellets were not significantly different with geometric mean ratio 1.0096 and 1.0093, respectively. The C of IR pellets (98.051 ng/ml) was higher than the ER pellets (84.052 ng/ml) and the T of ER pellets (5.116 h) was higher than the IR pellets (3.029 h). No significant food effect was observed on key pharmacokinetic parameters of ER pellets. Eudragit RL100 (6%) coated Meclizine HCl pellets have a potential therapeutic effect for an extended time period.
本研究基于 QbD 开发了盐酸美克洛嗪的缓释(ER)挤出球形化微丸,并对其与速释(IR)微丸的比较药代动力学进行了评估。建立并验证了 HPLC-荧光法用于血浆药物分析。IR 药物核采用乳糖、MCC 和 PVP 制备,以水为制粒液。采用三水平三因素 CCRD 进行建模和优化,研究了 Eudragit(RL100-RS100)、TEC 和滑石粉对包衣微丸药物释放和球形度的影响。HPLC-荧光法具有灵敏度,LLOQ 为 1ng/ml,线性范围为 10-200ng/ml,R>0.999。药代动力学参数采用非房室分析获得,并对数转换后的数据进行统计比较,p>0.05 认为无显著性差异,90%CI 限为 0.8-1.25。ER 微丸的 AUC 和 AUC 无显著差异,几何均数比值分别为 1.0096 和 1.0093。IR 微丸的 C(98.051ng/ml)高于 ER 微丸(84.052ng/ml),ER 微丸的 T(5.116h)高于 IR 微丸(3.029h)。ER 微丸的关键药代动力学参数无明显食物效应。包衣 6%Eudragit RL100 的盐酸美克洛嗪微丸具有延长治疗时间的潜在疗效。