Birer Mehmet, Acartürk Füsun
Department of Pharmaceutical Technology, Faculty of Pharmacy, Gazi University, Ankara, Turkey.
Pharm Dev Technol. 2021 Jul;26(6):661-672. doi: 10.1080/10837450.2021.1916031. Epub 2021 Apr 28.
Telmisartan (TEL) is an antihypertensive BCS class II drug with low solubility at physiological pH. However, the solubility of TEL increases with the presence of an alkalizer. Electrospinning is one of the most recent techniques for the solubility enhancement studies. In this study, an electrospun orally disintegrating film (ODF) formulation of TEL was developed with L-arginine and polyvinylpyrrolidone K90 (PVP), and its characterization studies were performed. Preformulation studies were performed to investigate possible incompatibilities in the components of formulation with differential scanning calorimetry (DSC) and Fourier transform infrared spectrometer (FT-IR) analyses. ODFs were characterized in terms of drug content and uniformity, mechanical properties, fiber shape and diameter and dissolution profile. Smooth nanofibers without any beads were obtained. The dissolution rate of the TEL significantly increased. The chosen formulation had acceptable mechanical properties with much faster dissolution compared to the commercially available product. Developed ODF and marketed product were compared with a dissolution study in phosphate-buffered solution (pH 7.4). ODF and marketed product both reached 100% release in the 45th minute, and ODF results showed that ODF had much faster release than marketed product. In this study, TEL ODF formulation was successfully produced and characterized.
替米沙坦(TEL)是一种抗高血压的BCS II类药物,在生理pH值下溶解度较低。然而,在有碱化剂存在的情况下,替米沙坦的溶解度会增加。静电纺丝是最近用于溶解度增强研究的技术之一。在本研究中,开发了一种含有L-精氨酸和聚乙烯吡咯烷酮K90(PVP)的替米沙坦口服崩解膜(ODF)制剂,并进行了表征研究。通过差示扫描量热法(DSC)和傅里叶变换红外光谱仪(FT-IR)分析进行了处方前研究,以调查制剂成分中可能存在的不相容性。对ODF进行了药物含量与均匀度、机械性能、纤维形状与直径以及溶出曲线等方面的表征。获得了没有任何珠粒的光滑纳米纤维。替米沙坦的溶出速率显著提高。所选制剂具有可接受的机械性能,与市售产品相比溶出速度快得多。在磷酸盐缓冲溶液(pH 7.4)中进行溶出度研究,对所开发的ODF和市售产品进行了比较。ODF和市售产品在第45分钟时均达到100%释放,且ODF的结果表明其释放速度比市售产品快得多。在本研究中,成功制备并表征了替米沙坦ODF制剂。