6533b7dcfe1ef96bd1272bd2
RESEARCH PRODUCT
Analysis of neuropeptide Y and its metabolites by high-performance liquid chromatography-electrospray ionization mass spectrometry and integrated sample clean-up with a novel restricted-access sulphonic acid cation exchanger.
E.s.m LutzKarl-siegfried BoosK.k. UngerK RačaitytDieter Lubdasubject
ChromatographyFormic acidElectrospray ionizationOrganic ChemistryMolecular Sequence DataGeneral MedicineReversed-phase chromatographyMass spectrometryBiochemistryHigh-performance liquid chromatographyMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundchemistryTrifluoroacetic acidAnimalsSample preparationNeuropeptide YSolid phase extractionAmino Acid SequenceCation Exchange ResinsSulfonic AcidsChromatography High Pressure Liquiddescription
A novel restricted access cation exchanger with sulphonic acid groups at the internal surface was proven to be highly suitable in the sample clean up of peptides on-line coupled to HPLC-electrospray ionization (ESI)-MS. Neuropeptide Y (NPY) and several of its fragments in plasma were subjected to the sample clean-up procedure. The peptides were eluted by a step gradient from the restricted access column, applying 10 mM phosphate buffer pH 3.5 from 5 to 20% (v/v) of acetonitrile with 1 M NaCl and transferred to a Micra ODS II column (33x4.6 mm). The separation of the peptides and their fragments was performed by a linear gradient from 20 to 60% (v/v) acetonitrile in water with 0.1% formic acid and 0.01% trifluoroacetic acid in 4 min at a flow-rate of 0.75 ml/min. An integrated and completely automated system composed of sample clean up-HPLC-ESI-MS was used to analyze real life samples. The sample volumes ranged between 20 and 100 microl. Peaks due to the fragments NPY 1-36, 3-36 and 13-36 in porcine plasma were identified by ESI-MS. The limit of detection was in the 5 nmol/ml range. The total analysis required 21 min and allowed the direct injection of plasma.
year | journal | country | edition | language |
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2000-09-08 | Journal of chromatography. A |