LC-MS/MS analysis of lipidized analogs of prolactin-releasing peptide utilizing a monolithic column and simple sample preparation
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
28901165
DOI
10.4155/bio-2017-0125
Knihovny.cz E-zdroje
- Klíčová slova
- LC–MS, lipopeptides, monolithic column, prolactin-releasing peptide, stability,
- MeSH
- biochemická analýza krve metody MeSH
- chromatografie kapalinová metody MeSH
- hormon uvolňující prolaktin krev chemie MeSH
- kalibrace MeSH
- krysa rodu Rattus MeSH
- lipidy chemie MeSH
- metody pro přípravu analytických vzorků * MeSH
- sekvence aminokyselin MeSH
- tandemová hmotnostní spektrometrie metody MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- hormon uvolňující prolaktin MeSH
- lipidy MeSH
AIM: Novel compounds for obesity treatment are currently being studied employing lipidized analogs of anorexigenic neuropeptides. Various analogs of prolactin-releasing peptide have demonstrated their ability to decrease food intake. Adequate analytical tools are required to support corresponding research. Methodology & results: An analytical method was developed that includes simple dilution of plasma samples prior to liquid chromatography-mass spectrometry and employs a monolithic column for the determination of lipidized analogs of prolactin-releasing peptide in complex biological samples. A multiple reaction monitoring approach was applied that included matrix calibration and an internal standard and produced a linear calibration range 20-200 ng ml-1 in rat and macaque plasma samples. CONCLUSION: A straightforward, simple and reliable analytical method was developed satisfying major validation criteria.
Citace poskytuje Crossref.org
Lipidization as a tool toward peptide therapeutics