Department of Analytical Chemistry, Faculty of Pharmacy, Anadolu University, 26470, Eskisehir, Turkey.; Doping and Narcotic Compounds Analysis Laboratory (DOPNA-LAB), Faculty of Pharmacy, Anadolu University, 26470, Eskisehir, Turkey..
Doping and Narcotic Compounds Analysis Laboratory (DOPNA-LAB), Faculty of Pharmacy, Anadolu University, 26470, Eskisehir, Turkey.; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Anadolu University, 26470, Eskisehir, Turkey..
J Pharm Biomed Anal. 2020 Nov 30;191:113490. doi: 10.1016/j.jpba.2020.113490. Epub 2020 Jul 30.
Novel stability-indicating HPLC methods have been presented for the analysis of Tasimelteon (TSM) besides its main degradation products in bulk and pseudo tablet formulations in this study. For the LC-DAD method; quantitation of TSM and its separation with other degradation products were achieved on an Ascentis Express pentafluorophenylpropyl (F)-bonded fused-core silica particle column (2.7 μm particle size 100 × 4.6 mm, Supelco) using the mobile phase consisted of acetonitrile: acetate buffer (0.025 M, pH 4.5): water (40:10:50, v/v/v); the elution was performed at 0.8 mL min flow rate, detecting the compounds at 281 nm. In addition to regular in- house validation studies, the developed method was tested on another UPLC instrument to assess its ruggedness for possible method transfer demands. For the LC-MS/MS method, analyte quantitation was achieved on a second-generation monolithic silica column (Chromolith™ High-Resolution RP-18e, 100 × 4.6 mm from Merck KGaA, Germany); the mobile phase was a mixture with 0.1 % (v/v) formic acid in water and 0.1 % (v/v) formic acid in acetonitrile (60: 40 (v/v), pH = 2.5). The instrumental and analytical performances of all three instrumental systems were compared with each other in terms of the working range, LOD, and LOQ. In addition to the above, a new degradation product was identified using LCMS-IT-TOF system. It can be concluded that among the similar ones in the literature, this study is the most comprehensive method optimization and validation study to date about TSM, in which a novel degradation product was also reported.
本研究提出了一种新的 HPLC 法,可用于分析 Tasimelteon(TSM)及其在原料药和伪片剂制剂中的主要降解产物。对于 LC-DAD 方法,TSM 的定量及其与其他降解产物的分离是在 Ascentis Express 五氟苯基丙基(F)键合的熔融核硅胶颗粒柱(2.7μm 粒径 100×4.6mm,Supelco)上实现的,使用的流动相由乙腈:醋酸缓冲液(0.025M,pH4.5):水(40:10:50,v/v/v)组成,洗脱流速为 0.8mL min,在 281nm 处检测化合物。除了常规的内部验证研究外,还在另一台 UPLC 仪器上测试了所开发的方法,以评估其在可能的方法转移需求方面的稳健性。对于 LC-MS/MS 方法,在第二代整体式硅胶柱(Chromolith™高分辨率 RP-18e,100×4.6mm,Merck KGaA,德国)上实现了分析物的定量,流动相为水和乙腈中的 0.1%(v/v)甲酸的混合物(60:40(v/v),pH=2.5)。在工作范围、LOD 和 LOQ 方面,比较了所有三种仪器系统的仪器和分析性能。此外,还使用 LCMS-IT-TOF 系统鉴定了一种新的降解产物。可以得出结论,与文献中的类似方法相比,本研究是迄今为止关于 TSM 的最全面的方法优化和验证研究,其中还报道了一种新的降解产物。