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高效液相色谱法测定胎盘灌流液中格列苯脲的浓度

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目的 建立测定胎盘灌流液中格列苯脲浓度的高效液相色谱(HPLC)检测方法。方法 采用的色谱柱为Symmetry Shield RP C18( 150mm×4。6 mm,5μm),柱温40℃,流动相为NaH2PO4缓冲盐(25mmol/L,pH值5。2)∶乙腈=1∶1;内标为格列齐特,流速1。0mL/min,检测波长228 nm,采用液-液萃取预处理方法测定胎盘灌流液中格列苯脲的浓度。结果 格列苯脲浓度线性范围为2。0~25。0μg/mL,线性方程为:y=0。226x+0。002,r=0。9999(n=6),日内相对标准偏差(RSD)<3。1%,日间RSD<9。5%,方法学回收率为95。32%~103。35%。结论 HPLC检测方法灵敏、简便,可用于胎盘灌流液中格列苯脲浓度的检测。
Determination of Glibenclamide Concentration in Placental Perfusion Medium by High Performance Liquid Chromatography
Objective To establish a high performance liquid chromatography (HPLC) method for determining the concentration of glibenclamide in placental perfusion medium. Methods The liquid chromatography column was Symmetry Shield RP C18 (150 mm×4.6 mm, 5 μm) at 40 ℃ . The mobile phase consisted of a mixture of NaH2PO4 (25 mmol/L, pH 5.2)-acetonitrile (1 : 1, V/V). The flow rate was 1.0 mL/min. UV detection wavelength was set at 228 nm. A liquid-liquid extraction pretreatment method was used to detect the concentration of glibenclamide placental perfusion medium. Results A linearity was obtained from 2.0 to 25.0 μg/mL for glibenclamide. The calibration equation of glibenclamide was y=0.226x+0.002, r=0.999 9 (n=6). The relative standard deviations within day and between days were less than 3.1% and less than 9.5% for glibenclamide. The mean recoveries of glibenclamide were 95.32% to 103.35%. Conclusion This method can be used for determining glibenclamide concentration in placental perfusion medium.

GlibenclamideHigh performance liquid chromatographyPlacental perfusion mediumDetectionFoundation item: Applied Basic Research on Projects in Yunnan Province (2008ZC128M)

闫晨、姚勤、黄桦、张峻

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昆明医学院第一附属医院临床药学中心,昆明,650032

格列苯脲 高效液相色谱法 胎盘灌流液 检测

云南省应用基础研究面上项目

2008ZC128M

2012

华西医学
四川大学华西医院

华西医学

CSTPCD
影响因子:0.744
ISSN:1002-0179
年,卷(期):2012.27(6)
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