Validated assay for the determination of celiprolol in plasma using high-performance liquid chromatography and a silanol deactivated reversed-phase support
被引:12
作者:
Chiu, FCK
论文数: 0引用数: 0
h-index: 0
机构:
CHINESE UNIV HONG KONG,FAC MED,DEPT PHARM,SHATIN,NT,HONG KONGCHINESE UNIV HONG KONG,FAC MED,DEPT PHARM,SHATIN,NT,HONG KONG
Chiu, FCK
[1
]
Raymond, K
论文数: 0引用数: 0
h-index: 0
机构:
CHINESE UNIV HONG KONG,FAC MED,DEPT PHARM,SHATIN,NT,HONG KONGCHINESE UNIV HONG KONG,FAC MED,DEPT PHARM,SHATIN,NT,HONG KONG
Raymond, K
[1
]
机构:
[1] CHINESE UNIV HONG KONG,FAC MED,DEPT PHARM,SHATIN,NT,HONG KONG
来源:
JOURNAL OF CHROMATOGRAPHY B
|
1996年
/
687卷
/
02期
关键词:
celiprolol;
D O I:
10.1016/S0378-4347(96)00246-0
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Previously reported methods for the determination of celiprolol in plasma could not be satisfactorily employed due to interference from plasma components. Thus, an improved, convenient and efficient method for the determination of the plasma concentration of celiprolol was developed using a simple solvent extraction step followed by high-performance liquid chromatography on a silanol deactivated C-18 column with fluorescence detection. The plasma interference was resolved from celiprolol and the typical trailing of basic compounds on reversed-phase HPLC was eliminated. The peak-area ratio versus plasma concentration was linear over the range of 5-1000 ng/ml and the detection limit was 5 ng/ml.