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We described the first results of a quantitative ultra performance liquid chromatographytandem mass spectrometry method for a novel antimicrobial peptide (phylloseptin,PSN-1).Chromatographic separation was accomplished on a Waters bridged ethyl hybrid (BEH) C 18 (50 mm 2.1 mm,1.7 mm) column with acetonitrile-water (25:75,v/v) as isocratic mobile phase.Mass spectrometry detection was performed in the positive electrospray ionization mode and by monitoring of the transitions at m/z 679.6/120,509.6/120 (PSN-1) and m/z 340.7/165 (Thymopentin,IS).Protein precipitation was investigated and the recovery was satisfactory (above 82%).The method was shown to be reproducible and reliable with intra-day precision below 5.3%,inter-day precision below 14.2%,and linear range from 0.02 to 2 mg/mL with r40.994.The method was successfully applied to a pharmacokinetic study of PSN-1 in rats after intravenous administration.
We described the first results of a quantitative ultra performance liquid chromatography tandem mass spectrometry method for a novel antimicrobial peptide (phylloseptin, PSN-1). Chromatographic separation was accomplished on a Waters bridged ethyl hybrid (BEH) C 18 (50 mm 2.1 mm, 1.7 (25:75, v / v) as isocratic mobile phase. Mass spectrometry detection was performed in the positive electrospray ionization mode and by monitoring of the transitions at m / z 679.6 / 120, 509.6 / 120 (PSN- 1) and m / z 340.7 / 165 (Thymopentin, IS) .Protein precipitation was investigated and the recovery was satisfactory (above 82%). The method was shown to be reproducible and reliable with intra-day precision below 5.3% day precision below 14.2%, and linear range from 0.02 to 2 mg / mL with r40.994. The method was successfully applied to a pharmacokinetic study of PSN-1 in rats after intravenous administration.