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毛细管区带电泳法测定右旋兰索拉唑制剂中的 S-(-)-兰索拉唑。

Determination of S-(-)-lansoprazole in dexlansoprazole preparation by capillary zone electrophoresis.

机构信息

College of Pharmacy, Kangwon National University, Chuncheon, 24341, South Korea.

College of Pharmacy, Chungnam National University, Daejeon, 34134, South Korea.

出版信息

Arch Pharm Res. 2017 Aug;40(8):962-971. doi: 10.1007/s12272-017-0936-8. Epub 2017 Aug 1.

Abstract

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%.

摘要

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。

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