Kantak Mrunali Navin, Kumar Lalit, Bhide Prashant Jivaji, Shirodkar Rupesh Kalidas
Department of Pharmaceutics, Goa College of Pharmacy, Panaji, Goa, India.
Department of Pharmaceutics, Manipal College of Pharmaceutical Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, India.
Assay Drug Dev Technol. 2023 Apr;21(3):97-109. doi: 10.1089/adt.2022.091. Epub 2023 Mar 28.
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.
该研究工作旨在制备并评估用于治疗胃轻瘫的钙通道阻滞剂拉西地平胃滞留型粘膜粘附膜。采用Box-Behnken设计,通过溶剂浇铸法制备优化配方。在该设计中,将不同浓度的粘膜粘附聚合物羟丙甲纤维素E15、丙烯酸树脂RL100和丙烯酸树脂RS100视为自变量,并考察其对药物释放百分比、12小时溶胀指数和膜的耐折性等响应的影响。使用傅里叶变换红外光谱和差示扫描量热法进行药物与聚合物的相容性研究。对优化配方进行了感官特性、重量差异、厚度、溶胀指数、耐折性、药物含量、拉伸强度、伸长百分比、药物释放和水分损失百分比的评估。结果表明,该膜具有相当的柔韧性和平滑度,12小时结束时体外药物释放率为95.22%±0.93%。膜的扫描电子显微镜成像显示表面质地光滑、均匀且多孔。溶出符合Higuchi模型,Hixson Crowell模型显示为非Fickian药物释放机制。此外,该膜被装入胶囊,胶囊的存在对药物释放曲线没有影响。另外,在25°C±2°C和60%±5%相对湿度下储存3个月后,外观、药物含量、溶胀指数、耐折性和药物释放均未观察到变化。总体而言,该研究表明拉西地平胃滞留型粘膜粘附膜可作为胃轻瘫管理中一种有效且替代的位点特异性靶向给药制剂。