Department of Pharmaceutics, Institute of Pharmacy, Nirma University, Ahmedabad, 382481, India.
Department of Pharmaceutical Sciences, College of Pharmacy, Gulf Medical University, 4184, Ajman, United Arab Emirates.
AAPS PharmSciTech. 2024 Aug 21;25(7):194. doi: 10.1208/s12249-024-02905-8.
The oral bioavailability of sildenafil citrate is approximately 43%, primarily limited by the low aqueous solubility and first-pass effect. Considering the drug properties and biopharmaceutical considerations, this study aimed to develop an immediate release, taste masked orodispersible film (ODF) of sildenafil citrate for the efficient management of pulmonary arterial hypertension (PAH). The optimization was done by applying 3 full-factorial design. The drug-loaded film was prepared and evaluated for the physical and mechanical parameters like; thickness, disintegration time, tensile strength, elongation, swelling index, content uniformity, disintegration and in vitro drug release in pH 6.2 stimulated salivary fluid. The FTIR and DSC data proved excellent compatibility between the drug and polymers used. The time taken for disintegration by the optimized film was about 62.66 s, while the drug release was observed ~ 96% in 10 min. Pharmacokinetic studies exhibited better sildenafil plasma level (p < 0.05) and C (p < 0.001) of orally disintegrating film which is significantly higher than the oral drug solution. The AUC (24874.425 ± 1234.45 ng. h/mL) in the oromucosal application was 1.2-fold more (p < 0.0001) than the control. The presence of sweetening and flavoring agents in the formulation masked the drug bitterness, resulting in a higher intake of the formulation in rats compared to the unmasked drug solution, as observed with in vivo taste masking studies. The importance of ODF as a feasible, effective, and optimal approach for delivering sildenafil citrate via oromucosal administration for the treatment of PAH was successfully highlighted by these results.
枸橼酸西地那非的口服生物利用度约为 43%,主要受低水溶性和首过效应限制。考虑到药物性质和生物药剂学因素,本研究旨在开发枸橼酸西地那非的即释、掩味口腔分散片(ODF),以有效治疗肺动脉高压(PAH)。通过应用 3 因素完全设计进行优化。制备载药薄膜并评估其物理和机械参数,如厚度、崩解时间、拉伸强度、伸长率、溶胀指数、含量均匀性、在 pH 6.2 刺激唾液中的崩解和体外药物释放。FTIR 和 DSC 数据证明药物与所用聚合物之间具有极好的相容性。优化薄膜的崩解时间约为 62.66s,而在 10 分钟内观察到药物释放约 96%。药代动力学研究表明,口腔分散片的西地那非血浆水平(p<0.05)和 C(p<0.001)更好,明显高于口服溶液。口腔黏膜给药的 AUC(24874.425±1234.45ng.h/mL)是对照组的 1.2 倍(p<0.0001)。配方中甜味剂和调味剂的存在掩盖了药物的苦味,与未掩味药物溶液相比,这导致大鼠对配方的摄入量更高,这与体内味觉掩蔽研究一致。这些结果成功地强调了 ODF 作为一种可行、有效和优化的方法,通过口腔黏膜给药来治疗 PAH 时递送枸橼酸西地那非的重要性。