LC-MS/MS analysis of lipidized analogs of prolactin-releasing peptide utilizing a monolithic column and simple sample preparation
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
28901165
DOI
10.4155/bio-2017-0125
Knihovny.cz E-resources
- Keywords
- LC–MS, lipopeptides, monolithic column, prolactin-releasing peptide, stability,
- MeSH
- Blood Chemical Analysis methods MeSH
- Chromatography, Liquid methods MeSH
- Prolactin-Releasing Hormone blood chemistry MeSH
- Calibration MeSH
- Rats MeSH
- Lipids chemistry MeSH
- Analytic Sample Preparation Methods * MeSH
- Amino Acid Sequence MeSH
- Tandem Mass Spectrometry methods MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Prolactin-Releasing Hormone MeSH
- Lipids 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.
References provided by Crossref.org
Lipidization as a tool toward peptide therapeutics