DETERMINATION OF A NEW CALCIUM-ANTAGONIST IN HUMAN PLASMA BY LIQUID EXTRACTION ENRICHMENT AND HPLC WITH UV DETECTION
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FLAMINIO, L
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SYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALYSYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALY
FLAMINIO, L
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]
MALAVASI, B
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SYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALYSYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALY
MALAVASI, B
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]
RIPAMONTI, M
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SYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALYSYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALY
RIPAMONTI, M
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ASCALONE, V
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SYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALYSYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALY
ASCALONE, V
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[1] SYNTHELABO RECH,CLIN RES UNIT,PHARMACOKINET SECT,VIA N RIVOLTANA 35,I-20090 LIMITO,ITALY
An HPLC method has been developed for the determination of SL 85.1016, a new calcium antagonist arylbenzylamide methylthioether derivative. SL 85.1016 and the internal standard, SL 87.0210, are extracted from alkaline human plasma with n-hexane and back extracted into 0.05 M phosphate buffer (pH 2.5; 0.2 ml). Acetonitrile (50 mul) is added to the final aqueous extract in order to prevent absorption of the compounds of interest onto the walls of the glass tube; this solution then is partially processed by HPLC on a C18 column with UV detection (254 nm). The determination limit of the method is 2 ng.ml-1 of SL 85.1016 in human plasma; the response to the drug is linear in the range 2-200 ng.mg-1.