College of Pharmacy, Kangwon National University, Chuncheon, 24341, South Korea.
College of Pharmacy, Chungnam National University, Daejeon, 34134, South Korea.
Arch Pharm Res. 2017 Aug;40(8):962-971. doi: 10.1007/s12272-017-0936-8. Epub 2017 Aug 1.
Capillary zone electrophoresis was successfully applied to the enantiomeric purity determination of dexlansoprazole using sulfobutyl ether-β-cyclodextrin and methyl-β-cyclodextrin as chiral selectors. Separations were carried out in a 50 μm, 64/56 cm fused-silica capillary. The optimized conditions included 90 mM phosphate buffer, pH 6.0, containing 30 mM sulfobutyl ether-β-cyclodextrin, 20 mM methyl-β-cyclodextrin as background electrolyte, an applied voltage of 25 kV and a temperature of 16 °C, detection was at 280 nm. The assay was validated for the S-(-)-lansoprazole in the range of 0.2-1.0%. The limit of detection was 0.07%, the limit of quantitation was 0.20%, relative to a total concentration of 4.0 mg mL. Intra-day precision varied between 1.72 and 2.07%. Relative standard deviations of inter-day precision ranged between 1.62 and 1.96% for peak area ratio. The assay was applied for the determination of the chiral purity of dexlansoprazole capsules. Recovery in capsules was ranged between 101.7 and 103.1%.
毛细管区带电泳成功应用于使用磺丁基醚-β-环糊精和甲基-β-环糊精作为手性选择剂对右旋兰索拉唑对映体纯度的测定。在 50 µm、64/56 cm 熔融硅毛细管中进行分离。优化条件包括 90 mM 磷酸盐缓冲液,pH 值为 6.0,含 30 mM 磺丁基醚-β-环糊精,20 mM 甲基-β-环糊精作为背景电解质,施加电压为 25 kV,温度为 16°C,检测波长为 280nm。该测定法在 0.2-1.0%范围内验证了 S-(-)-兰索拉唑的含量。检测限为 0.07%,定量限为 0.20%,相对于总浓度为 4.0 mg mL。日内精密度在 1.72%和 2.07%之间变化。峰面积比的日间精密度的相对标准偏差在 1.62%和 1.96%之间。该测定法用于测定右旋兰索拉唑胶囊的手性纯度。胶囊中的回收率在 101.7%和 103.1%之间。