OBJECTIVE To establish a reversed phase high performance liquid chromatographic method for the determination of captopril in human plasma and to investigate the pharmacokinetics of captopril in Chinese healthy volunteers.METHODS The drug was extracted from human plasma with ethyl acetate-benzene(1∶1).The plasma concentrations of captopril were separated on a HYPERSIL C18 column(4.6 mm×250 mm,5 μm)by Waters 510 HPLC.The mobile phase was a mixture of acetonitrile-1%acetic acid(45∶55).The detection wavelength was 257 nm.RESULTS A good linearity was obtained over the range of 6.25 to 800 μg·L-1 in human plasma.The limit of detection was 6.25 μg·L-1.The recoverys of method were from 101.00% to 108.88%.The precisions of intra-day and inter-day were in the rangs of 4.40%~7.88% and 2.87%~9.34%,respectively.CONCLUSION The method is sensitive,accurate,reliable,and can be used in clinical research of captopril.
WNG Mo-yi;DONG Y-lin;YOU Hi-sheng;DONG Wei-hu;ZHENG Xin.
Determination of Captopril in Human Plasma by RP-HPLC [J]. Chinese Pharmaceutical Journal, 2007, 42(07): 528-530
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
[1]ZHANG B K,LI H D, DENG H, et al.Detection of captopril in human plasma by pre-column derivation HPLC with solid phase extraction [J].Chin J Pharm Anal(药物分析杂志),2002,22(1):27-29.
[2]LI K,TAN L,YAN W L. Determination of captopril concentration in human plasma by reversed- phase high performance liquid chromatography [J].Chin Pharm J(中国药学杂志),1995,30(12):740-742.
[3]MANOOCHEHR B,AZARM K,CAMELLIA,et al.Determination of captopril in human serum by high performance liquid chromatography using solid-phase extraction[J].J Pharm Biomed Anal,1997,15:1181-1186.