Department of Pharmaceutics, National Organization for Drug Control and Research, Cairo, Egypt.
Acta Pharm. 2012 Nov;62(3):411-32. doi: 10.2478/v10007-012-0027-9.
Sildenafilcitrate (SILD) orodispersable sublingual tablets (ODSTs) have been developed using two comparative techniques for improving their oral disintegration, dissolution and bioavailability in order to manage acute attacks of pulmonary arterial hypertension (PAH). The techniques employed were direct compression of SILD-poloxamer 188 solid dispersions (SDs) and freeze drying using various excipients. The physicochemical and solid-state properties, as well as the dissolution behavior of the tablets were evaluated. Moreover, SILD bioavailability in human volunteers from the prepared ODSTs was compared to that of the conventional oral tablet. Incorporation of SD of poloxamer188 in sublingual tablets together with Pharmaburst using the direct compression technique enhanced the extent and dissolution rate of SILD with 100% of drug being dissolved after 7 minutes. However, the lyophilization process was superior in enhancing dissolution and 100% of SILD was dissolved after only one minute. Moreover, the in vivo study showed that the AUC₀₋₁₂ of lyophilized tablets was significantly higher than that of directly compressed tablets, with bioavailability values of 159.81 and 140.85%, respectively, compared to the commercial oral product.
西地那非枸橼酸盐(SILD)口崩片(ODST)采用两种比较技术开发,旨在改善其口腔崩解、溶解和生物利用度,以治疗肺动脉高压(PAH)急性发作。所采用的技术是直接压缩 SILD-泊洛沙姆 188 固体分散体(SD)和使用各种赋形剂进行冷冻干燥。评估了片剂的物理化学和固态特性以及溶解行为。此外,将制备的 ODST 中的 SILD 生物利用度与人志愿者进行了比较。将 SILD-泊洛沙姆 188 的 SD 与 Pharmaburst 一起直接压片技术,可提高 SILD 的程度和溶解速率,在 7 分钟后,药物的 100%溶解。然而,冻干过程在提高溶解度方面更具优势,仅一分钟后,SILD 的 100%溶解。此外,体内研究表明,冻干片剂的 AUC₀₋₁₂明显高于直接压缩片剂,与商业口服产品相比,冻干片剂的生物利用度值分别为 159.81%和 140.85%。