Hu Liandong, Liu Yang, Cheng Shan
College of Pharmacy, Hebei University, No.180, WuSi Road, Baoding, 071002, China.
J Chromatogr Sci. 2011 Feb;49(2):124-8. doi: 10.1093/chrsci/49.2.124.
A methodology for the simultaneous determination of six control analytes, including carbamazepine, desipramine, guanabenz, methotrexate, propranolol, and warfarin, was developed and validated utilizing reversed-phase high-performance liquid chromatography with ultraviolet detection for high throughput analysis for permeability assessment. The analytes were separated on Agilent Zorbax SB-C18 (50 × 4.6 mm I.D., 5 μm) with a gradient mobile phase consisting of water (containing 1% isopropyl alcohol and 0.01% heptafluorobutyric acid) and acetonitrile (containing 1% isopropyl alcohol and 0.01% heptafluorobutyric acid). The flow rate was 2.0 mL/min and the eluent was monitored at 280 nm. A linear response was found for all six analytes over a broad concentration range (1.00-200 μM). The correlation coefficient for each analyte was greater than 0.999. The limit of detection and limit of quantitation were 0.03 and 0.10 μM, 0.10 and 0.30 μM, 0.05 and 0.15 μM, 0.03 and 0.10 μM, 0.05 and 0.15 μM, 0.10 and 0.30 μM for carbamazepine, desipramine, guanabenz, methotrexate, propranolol, and warfarin, respectively. The optimized method was further successfully applied to high throughput analysis for parallel artificial permeability assay.
开发并验证了一种同时测定六种对照分析物(包括卡马西平、地昔帕明、胍那苄、甲氨蝶呤、普萘洛尔和华法林)的方法,该方法采用反相高效液相色谱法并结合紫外检测,用于高通量渗透性评估分析。分析物在安捷伦Zorbax SB-C18(内径50×4.6 mm,粒径5μm)色谱柱上进行分离,流动相为梯度洗脱,由水(含1%异丙醇和0.01%七氟丁酸)和乙腈(含1%异丙醇和0.01%七氟丁酸)组成。流速为2.0 mL/min,在280 nm波长处监测洗脱液。在较宽的浓度范围(1.00 - 200μM)内,六种分析物均呈现线性响应。每种分析物的相关系数均大于0.999。卡马西平、地昔帕明、胍那苄、甲氨蝶呤、普萘洛尔和华法林的检测限和定量限分别为0.03和0.10μM、0.10和0.30μM、0.05和0.15μM、0.03和0.10μM、0.05和0.15μM、0.10和0.30μM。该优化方法进一步成功应用于平行人工渗透性试验的高通量分析。