Oral Gastroretentive Film of Lacidipine for the Treatment of Gastroparesis.

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Mrunali Navin Kantak, Lalit Kumar, Prashant Jivaji Bhide, Rupesh Kalidas Shirodkar
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引用次数: 0

Abstract

The research work was aimed to formulate and evaluate gastroretentive mucoadhesive film of calcium channel blocker, Lacidipine for treatment of gastroparesis. Box-Behnken design was used for preparation of optimized formulation using solvent casting method. In this design, different concentrations of mucoadhesive polymers HPMC E15, Eudragit RL100, and Eudragit RS100 were considered as independent variables and its effect on responses like percent drug release, swelling index at 12 h, and folding endurance of the film were examined. Drug and polymer compatibility studies were performed using Fourier transform infrared spectroscopy and differential scanning calorimetry. Optimized formulation was evaluated for organoleptic properties, weight variation, thickness, swelling index, folding endurance, drug content, tensile strength, percent elongation, drug release, and percent moisture loss. The results revealed that the film possessed considerable flexibility and smoothness, and in vitro drug release was found to be 95.22% ± 0.93% at the end of 12 h. Scanning electron microscopy imaging of film displayed smooth, uniform, and porous surface texture. The dissolution followed Higuchi's model and Hixson Crowell model displayed non-Fickian drug release mechanism. Furthermore, the film was incorporated in capsule and the presence of capsule showed no effect on the drug release profile. In addition, no change was observed in the appearance, drug content, swelling index, folding endurance, and drug release upon storage at 25°C ± 2°C and 60% ± 5% relative humidity for 3 months. Collectively, the study revealed that gastroretentive mucoadhesive film of Lacidipine could serve as an effective and alternate site-specific targeted delivery in the management of gastroparesis.

口服拉西地平胃保留膜治疗胃轻瘫。
本研究旨在研制并评价钙通道阻滞剂拉西地平胃保留黏附膜治疗胃轻瘫的疗效。采用Box-Behnken设计,采用溶剂铸造法制备最佳配方。本设计以不同浓度的黏附聚合物HPMC E15、el100、RL100为自变量,考察其对药物释放率、12 h溶胀指数、膜折叠耐久性等反应的影响。采用傅里叶变换红外光谱和差示扫描量热法进行了药物和聚合物的相容性研究。对优化后的配方进行感官性能、重量变化、厚度、膨胀指数、折叠耐力、药物含量、拉伸强度、伸长率、药物释放率和水分损失率的评价。结果表明,该膜具有相当的柔韧性和光滑度,12 h时体外释药率为95.22%±0.93%。扫描电镜成像显示薄膜表面光滑、均匀、多孔。溶出符合Higuchi模型,Hixson Crowell模型显示非fickian释药机制。此外,该膜被掺入胶囊中,胶囊的存在对药物释放谱没有影响。在25°C±2°C、60%±5%相对湿度条件下存放3个月,外观、药物含量、肿胀指数、折叠耐力、药物释放量均无变化。总的来说,该研究表明拉西地平的胃保留黏附膜可以作为一种有效的替代部位特异性靶向递送治疗胃轻瘫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Assay and drug development technologies
Assay and drug development technologies 医学-生化研究方法
CiteScore
3.60
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: ASSAY and Drug Development Technologies provides access to novel techniques and robust tools that enable critical advances in early-stage screening. This research published in the Journal leads to important therapeutics and platforms for drug discovery and development. This reputable peer-reviewed journal features original papers application-oriented technology reviews, topical issues on novel and burgeoning areas of research, and reports in methodology and technology application. ASSAY and Drug Development Technologies coverage includes: -Assay design, target development, and high-throughput technologies- Hit to Lead optimization and medicinal chemistry through preclinical candidate selection- Lab automation, sample management, bioinformatics, data mining, virtual screening, and data analysis- Approaches to assays configured for gene families, inherited, and infectious diseases- Assays and strategies for adapting model organisms to drug discovery- The use of stem cells as models of disease- Translation of phenotypic outputs to target identification- Exploration and mechanistic studies of the technical basis for assay and screening artifacts
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