Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Assiut University, Assiut, 71526, Egypt.
J Pharm Biomed Anal. 2018 Jul 15;156:358-365. doi: 10.1016/j.jpba.2018.04.049. Epub 2018 May 1.
Sofosbuvir (SOF) and daclatasvir (DCS) are newly discovered anti-hepatitis C drugs that have direct antiviral activity. A novel and simple high-performance thin-layer chromatography (HPTLC) method was designed for simultaneous determination of SOF and DCS in miscellaneous matrices. The method adopts coupling HPTLC with dual wavelength spectrodensitometry. Consequently, this enabled sensitive, specific and cost-effective determination of the SOF-DCS mixture. The developed HPTLC procedure is based on a simple liquid-liquid extraction, enrichment of the analytes and subsequent chromatographic separation with UV detection. Separations were performed on HPTLC silica gel 60 F aluminum plates with a mobile phase consisting of ethyl acetate-isopropanol (85:15, v/v). Dual wavelength scanning was carried out in the absorbance mode at 265 and 311 nm for SOF and DCS, respectively. The linear ranges were 40-640 and 20-320 ng band for SOF and DCS, respectively with correlation coefficients of ≥0.9997. The detection limits were 11.3 and 6.5 ng band for SOF and DCS, respectively indicating high sensitivity of the proposed method. Consequently, this permits in vitro and in vivo application of the proposed method in human plasma with good percentage recovery (94.1-103.5%). Validation parameters were assessed according to ICH guidelines and US-FDA guidelines. Furthermore, the application was extended to analysis of SOF and DCS in their pharmaceutical formulations.
索非布韦(SOF)和达卡他韦(DCS)是新发现的具有直接抗病毒活性的抗丙型肝炎药物。设计了一种新颖且简单的高效薄层色谱(HPTLC)方法,用于同时测定各种基质中的 SOF 和 DCS。该方法采用 HPTLC 与双波长分光光度法相结合。因此,能够对 SOF-DCS 混合物进行灵敏、特异和具有成本效益的测定。所开发的 HPTLC 程序基于简单的液 - 液萃取、分析物的富集以及随后的色谱分离,并用 UV 检测。在 HPTLC 硅胶 60F 铝板上进行分离,流动相由乙酸乙酯-异丙醇(85:15,v/v)组成。SOF 和 DCS 分别在 265 和 311nm 处进行双波长扫描,在吸收模式下进行。SOF 和 DCS 的线性范围分别为 40-640 和 20-320ng 条带,相关系数均≥0.9997。SOF 和 DCS 的检测限分别为 11.3 和 6.5ng 条带,表明该方法具有高灵敏度。因此,允许在人类血浆中进行体内和体外应用,并具有良好的百分回收率(94.1-103.5%)。验证参数根据 ICH 指南和美国 FDA 指南进行评估。此外,该应用扩展到 SOF 和 DCS 在其药物制剂中的分析。