基于非手性离子液体对手性配体交换的促进作用，建立了一种测定去氧肾上腺素手性异构体的毛细管电泳分离分析方法。在系统优化了电泳条件后，采用20 kV的分离电压、25℃的毛细管柱温、254 nm的检测波长以及5 s的压力（3447 Pa）进样时间，在添加4.0 mmol／L Cu（Ⅱ）、8.0 mmol／L L-脯氨酸（L-Pro）和15 mmol／L 氯化-1-丁基-3-甲基咪唑（[BMIM]Cl）的20 mmol／L Tris-H3PO4缓冲溶液（pH 5.4）中，R-去氧肾上腺素和 S-去氧肾上腺素的分离度为1.42，峰面积与质量浓度分别在12.5~150.0 mg／L 和15.0~150.0 mg／L 范围内有线性关系。将该方法用于加标血液和尿液样品中 R和 S型去氧肾上腺素的测定，尿液中的加标回收率为93.7％~108.2％，相对标准偏差在3.18％（ n=3）以内；血液中的加标回收率为91.4％~113.1％，相对标准偏差在4.82％（ n=3）以内。
A method for the separation and determination of optical isomers of phenylephrine was developed based on the promoting effect of non-chiral ionic liquid on chiral ligand-exchange capillary electrophoresis after the electrophoretic parameters were optimized system-atically. R-phenylephrine and S-phenylephrine can be separated and determined effectively in 20 mmol/L Tris-H3PO4 buffer solution(pH 5. 4)composed of 4. 0 mmol/L Cu(Ⅱ),8. 0 mmol/L L-proline(L-Pro)and 15 mmol/L 1-butyl-3-methylimidazolium chloride([BMIM]Cl)with the applied voltage of 20 kV,capillary temperature of 25 ℃,detection wavelength of 254 nm,and injection of 5 s at 3 447 Pa. The resolution of R- and S-phenylephrines was 1. 42. The linear ran-ges for the determination of R-phenylephrine and S-phenylephrine were 12. 5-150 mg/L and 15. 0-150 mg/L,respectively. The method has been satisfactorily used for the determination of R-phenylephrine and S-phenylephrine in the spiked blood and urine samples. The spiked recov-eries in the urine sample were in the range of 93. 7%-108. 2% with the RSDs lower than 3. 18%( n=3),and the spiked recoveries in the blood sample were in the range of 91. 4% and 113. 1%with the RSDs lower than 4. 82%( n=3).
参考文献
- 下载量()
- 访问量()
- 您的评分：
-
10%
-
20%
-
30%
-
40%
-
50%