Department of Pharmaceutical Technology, Faculty of Pharmacy, Tanta University, Tanta, Egypt.
Department of Pharmaceutics, Faculty of Pharmacy, Delta University for Science & Technology, Belkas, Egypt.
Pharm Dev Technol. 2023 Sep;28(7):650-659. doi: 10.1080/10837450.2023.2231076. Epub 2023 Jul 5.
Developing mucoadhesive buccal films loaded with metoclopramide for the treatment of migraine-associated vomiting.
Buccal films were prepared using the solvent casting method. Several tests were conducted, including measurement of film weight, thickness, drug content, moisture uptake, swelling index, and DSC analysis. The bioadhesion properties were also assessed. Furthermore, in vitro release profiles and in human bioavailability were studied.
The developed films were transparent, homogeneous, and easy to remove. Film weight and thickness increased with higher drug content. The drug entrapment exceeded 90%. Film weight increased with moisture uptake, and DSC analysis indicated the absence of drug crystallinity. Bioadhesion properties and swelling index decreased with increasing drug content. In vitro release demonstrated that drug release depended on the drug-polymer ratio. The in vivo study showed significant improvements in T (from 1.21 ± 0.33 to 0.50 ± 0.0) and C (from 45.29 ± 14.66 to 63.27 ± 24.85) compared to conventional tablets.
The prepared mucoadhesive buccal films exhibited the desired characteristics and demonstrated enhanced drug absorption, evidenced by the significantly reduced T and increased C compared to conventional tablets. The results indicate the successful achievement of the study objectives in selecting and designing an effective pharmaceutical dosage form. as cm.
开发载有多潘立酮的黏膜黏附型颊膜,用于治疗偏头痛相关呕吐。
采用溶剂浇铸法制备颊膜。进行了多项测试,包括测量膜重、厚度、药物含量、吸湿性、溶胀指数和 DSC 分析。还评估了生物黏附性能。此外,研究了体外释放曲线和人体生物利用度。
所开发的薄膜为透明、均匀且易于去除。随着药物含量的增加,膜重和厚度增加。药物包封率超过 90%。膜重随吸湿性增加而增加,DSC 分析表明无药物结晶性。生物黏附性能和溶胀指数随药物含量的增加而降低。体外释放表明药物释放取决于药物-聚合物比例。体内研究表明,与普通片剂相比,T(从 1.21 ± 0.33 降至 0.50 ± 0.0)和 C(从 45.29 ± 14.66 降至 63.27 ± 24.85)有显著改善。
所制备的黏膜黏附型颊膜表现出所需的特性,并表现出增强的药物吸收,与普通片剂相比,T 和 C 的显著降低表明这一点。结果表明,在选择和设计有效的药物剂型方面成功实现了研究目标。