Pharmaceutics, Prince Sattam Bin Abdulaziz University, Alkharj, Saudi Arabia.
Department of Pharmacology and Toxicology, College of Pharmacy, Prince Sattam Bin Abdulaziz University, Alkharj, Saudi Arabia.
PeerJ. 2022 May 26;10:e13482. doi: 10.7717/peerj.13482. eCollection 2022.
The objective of the present study was to improve the dissolution rate and aphrodisiac activity of tadalafil by using hydrophilic polymers. Solid dispersions were prepared by solvent evaporation-Rota evaporator using Koliphore 188, Kollidon VA64, and Kollidon 30 polymers in a 1:1 ratio. Prepared tadalafil-solid dispersions (SDs) evaluated for yield, drug content, micromeritics properties, physicochemical characterizations, and aphrodisiac activity assessment. The optimized SDs TK188 showed size (2.175 ± 0.24 µm), percentage of content (98.89 ± 1.23%), yield (87.27 ± 3.13%), bulk density (0.496 ± 0.005 g/cm3), true density (0.646 ± 0.003 g/cm3), Carr's index (23.25 ± 0.81), Hausner ratio (1.303 ± 0.003) and angle of repose (<25°). FTIR spectrums revealed tadalafil doesn't chemically interact with used polymers. XRD and DSC analysis represents TK188 SDs were in the amorphous state. Drug release was 97.17 ± 2.43% for TK188, whereas it was 32.76 ± 2.65% for pure drug at the end of 2 h with 2.96-fold increase in dissolution and followed release kinetics of Korsmeyer Peppa's model. MDT and DE were noted to be 17.48 minutes and 84.53%, respectively. Furthermore, TK188 SDs showed relative improvement in the sexual behavior of the male rats. Thus the developed SDs TK188 could be potential tadalafil carriers for the treatment of erectile dysfunction.
本研究的目的是通过使用亲水性聚合物来提高他达拉非的溶出速率和壮阳活性。采用溶剂蒸发-旋转蒸发器法,以Koliphore 188、Kollidon VA64 和 Kollidon 30 聚合物以 1:1 的比例制备固体分散体。对制备的他达拉非-固体分散体(SD)进行产率、药物含量、微粉学性质、理化特性和壮阳活性评估。优化的 SDs TK188 显示粒径(2.175±0.24μm)、含量百分比(98.89±1.23%)、产率(87.27±3.13%)、堆密度(0.496±0.005g/cm3)、真密度(0.646±0.003g/cm3)、卡尔指数(23.25±0.81)、哈斯纳比(1.303±0.003)和休止角(<25°)。傅里叶变换红外光谱显示他达拉非与所用聚合物未发生化学相互作用。XRD 和 DSC 分析表明 TK188 SDs 处于无定形状态。TK188 的药物释放率在 2 小时末达到 97.17±2.43%,而纯药物仅为 32.76±2.65%,溶出度提高了 2.96 倍,随后符合 Korsmeyer Peppa 的模型释放动力学。MDT 和 DE 分别为 17.48 分钟和 84.53%。此外,TK188 SDs 显示雄性大鼠性行为得到了相对改善。因此,所开发的 SDs TK188 可能是治疗勃起功能障碍的潜在他达拉非载体。