Study design The study design was a sequential, openlabel, two period trial conducted at the Drug Clinical Research Organization (-)-MK 801 of Yijishan Hospital. About the morning of day 1, following fasting overnight, a single dose of 15 mg midazolam was administered orally. The volunteers had been offered a light standard meal at 4 h and 10 h following medication intake. At 10 and
min, next 5A : 95B to 70A : 30B and for 6 min. The ow price was 0. 2 ml min1. Separation by HPLC on a C18 column was followed by mass spectrometric detection. This assay had a reduced limit of quantitation of 1. 0 ng ml1, with (-)-MK 801 a calibration curve range from 1. 0 to 500. 0 ng ml1. Intra and interday CV of midazolam and 1 hydroxymidazolam had been beneath 15%. The liquid chromatographCmass spectrometer consisted of an HPLC program plus a Finnigan TSQ Quantum Discovery max program equipped with an ESI probe. Lipophilic analytes had been extracted from 0. 5 ml plasma, diluted with 10 l of diazepam answer, with 4 ml ethyl acetate. The samples had been centrifuged, evaporated and reconstituted within the mobile phase. Separation by HPLC on a C18 column was followed by tandem mass
included geometric means, arithmetic means and standard deviation. 90% condence intervals were constructed for the ratios of with to without danshen treatment using the log transformed data for the geometric least squares means of Cmax, AUC, t1/2 and CL/F. The resulting condence limits had been transformed by exponentiation and reported on the original measurement scale. The statistical limits had been set at 0. 80C1. 25. tmax was analyzed working with Wilcoxons signed rank test. The DAS statistical analysis program was used. NSCLC Ratios of geometric LS
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