盐酸奈拉曲坦快溶膜的制备及优化。

Q3 Pharmacology, Toxicology and Pharmaceutics
K. Krishna, Sidhdhapara T Pradip, S. Navin
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引用次数: 2

摘要

背景纳曲普坦是第二代曲普坦类抗迁移药物,可选择性地与5-HT(1B/1D)受体结合。与其他曲坦相比,它具有更好的耐受性和更低的复发率,因此被广泛用于治疗偏头痛发作。尽管具有适用性,但纳曲普坦也有一些缺点,如起效缓慢和拳头代谢降低了其疗效。为了提高那曲普坦的药效,制备了快速溶解膜。方法采用溶剂浇铸法制备盐酸那曲普坦的快速溶解膜。在专利调查(US 7648712 B2,WO 2012053006 A2,US 20090047330 A1,EP 2821066 A4,WO 2008108940 A1,WO 2010151020 A3)的基础上,筛选赋形剂,找出聚合物和增塑剂的合适组合,并选择羟丙基甲基纤维素(HPMC E6)和甘油作为成膜剂聚合物和增塑剂。为了研究自变量对因变量的影响,采用32全因子设计,以HPMC E6浓度和甘油浓度为自变量,崩解时间、耐折性、拉伸强度和2分钟累积药物释放%为因变量或反应变量。采用包含交互项和多项式项的统计模型来评估响应。结果与结论:从统计评价结果中,F3批次被选为最佳批次,其崩解时间较短(22秒),具有令人满意的机械性能(拉伸强度652.17gm/mm2)。药物从F3制剂中的溶解是快速的,在120秒内药物释放约91%。使用Franz扩散池对优化的批次进行了进一步的体外渗透研究评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation and Optimization of Fast Dissolving Film of Naratr iptan Hydrochloride.
BACKGROUND Naratriptan is second-generation triptan class of antimigraine drug which selectively bind with 5-HT(1B/1D) receptor. It is widely used to treat the migraine attack due to its better tolerability and lower recurrence rate as compared to other triptans. Despite of the applicability, Naratriptan also have several drawback like slow onset of action and fist pass metabolism which reduce its efficacy. In order to increase the efficacy of naratriptan fast dissolving film is prepared. METHOD Fast dissolving film of Naratriptan hydrochloride was prepared by solvent casting method Based on the patent survey (US 7648712 B2, WO 2012053006 A2, US 20090047330 A1, EP 2821066 A4, WO 2008108940 A1, WO 2010151020 A3) excipients were screened to find out suitable combination of polymer and plasticizer and Hydroxypropylmethyl Cellulose (HPMC E6) and glycerol were selected as film forming polymer and plasticizer respectively. To study the effect of independent variables on dependent variables 32 full factorial design was applied using Concentration of HPMC E6 and Concentration of Glycerol as independent variables and disintegration time, folding endurance, tensile strength and cumulative % drug release at 2 min as dependent or response variables. A statistical model incorporating interactive and polynomial terms was utilized to evaluate the responses. Result & Conclusion: From the results of statistical evaluation batch F3 was selected as the optimized batch which exhibited shorter disintegration time (22sec) with satisfactory mechanical properties (tensile strength 652.17 gm/mm2). Dissolution of drug from F3 formulation was rapid with around 91% drug release in 120sec. Optimized batch was further evaluated for in vitro permeation study using Franz diffusion cell.
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来源期刊
Recent Patents on Drug Delivery and Formulation
Recent Patents on Drug Delivery and Formulation Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
2.30
自引率
0.00%
发文量
0
期刊介绍: Recent Patents on Drug Delivery & Formulation publishes review and research articles, drug clinical trial studies and guest edited thematic issues on recent patents on drug delivery and formulation. A selection of important and recent patents on drug delivery and formulation is also included in the journal. The journal is essential reading for all researchers involved in the fields of drug delivery and formulation. The journal also covers recent research (where patents have been registered) in fast emerging therapeutic areas/targets & therapeutic agents related to drug delivery and formulations.
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