Ammar Hussein O, Ghorab Mahmoud M, Mahmoud Azza A, Shahin Hend I
Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences and Pharmaceutical Industries, Future University in Egypt, Cairo, Egypt.
Department of Pharmaceutical Technology, National Research Center, Dokki, Cairo, Egypt.
AAPS PharmSciTech. 2017 Jan 1;18(1):93-103. doi: 10.1208/s12249-016-0496-0. Epub 2016 Feb 16.
Fluticasone propionate is a synthetic corticosteroid drug distinguished by its potent anti-inflammatory action with low systemic side effects in comparison to other corticosteroids making it a potential drug for local buccal delivery. The aim of the present study was to design mucoadhesive buccal film containing fluticasone that is aesthetically acceptable and could maintain local drug release for a sustained period to manage the sign and symptoms of severe erosive mouth lesions. Solvent casting technique was used in film preparation. Different polymeric blends were used either alone or in combination with mucoadhesive polymers, sodium carboxymethyl cellulose (SCMC), or Carbopol 971P at different concentrations. The physicochemical properties, in vitro mucoadhesion time as well as the drug release properties for all prepared formulations were determined. Selected formulations with adequate properties were further examined by differential scanning calorimetry (DSC) and X-ray diffraction (XRD) and subjected to in vivo evaluation. Films containing hydroxypropyl methylcellulose (HPMC)/ethyl cellulose (EC) showed acceptable physicochemical properties, homogenous drug distribution, convenient mucoadhesion time, moderate swelling as well as sustained drug release up to 12 h. The biological performance of these formulations was assessed on healthy human volunteers and compared with a prepared mouthwash which showed enhanced pharmacokinetic parameters for the selected films in comparison to the mouthwash. The results revealed that the optimized formulation containing HPMC/EC and 10% SCMC could successfully achieve sustained drug release for 10 h which is considered promising for local treatment of severe mouth lesions.
丙酸氟替卡松是一种合成皮质类固醇药物,与其他皮质类固醇相比,它具有强大的抗炎作用且全身副作用较低,这使其成为局部口腔给药的潜在药物。本研究的目的是设计一种含丙酸氟替卡松的黏膜黏附口腔膜,该膜在美学上是可接受的,并且能够持续维持局部药物释放,以控制严重糜烂性口腔病变的体征和症状。采用溶剂浇铸技术制备薄膜。单独或与不同浓度的黏膜黏附聚合物、羧甲基纤维素钠(SCMC)或卡波姆971P组合使用不同的聚合物共混物。测定了所有制备制剂的理化性质、体外黏膜黏附时间以及药物释放性质。通过差示扫描量热法(DSC)和X射线衍射(XRD)对具有适当性质的选定制剂进行进一步检查,并进行体内评价。含有羟丙基甲基纤维素(HPMC)/乙基纤维素(EC)的薄膜表现出可接受的理化性质、均匀的药物分布、适宜的黏膜黏附时间、适度的溶胀以及长达12小时的持续药物释放。在健康人类志愿者身上评估了这些制剂的生物学性能,并与制备的漱口水进行了比较,结果显示与漱口水相比,选定薄膜的药代动力学参数有所提高。结果表明,含有HPMC/EC和10% SCMC的优化制剂能够成功实现10小时的持续药物释放,这对于严重口腔病变的局部治疗具有前景。