Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

GHRP-2

Pralmorelin, Growth Hormone Releasing Peptide-2, KP-102

Quick Stats
Studies 230
Trials 1
Score 2
2010 pubmed 52 citations

Determination of growth hormone secretagogue pralmorelin (GHRP-2) and its metabolite in human urine by liquid chromatography/electrospray ionization tandem mass spectrometry.

Okano. Masato M; Sato. Mitsuhiko M; Ikekita. Ayako A; Kageyama. Shinji S

Key Findings

  • A liquid‑chromatography/tandem‑mass‑spectrometry method can detect GHRP‑2 and its metabolite AA‑3 in urine between 0.5 and 10 ng/mL.
  • The assay is precise (1.6‑4.3% variation) and recovers 84‑101% of the peptide from samples.
  • After a single IV dose in ten men, unchanged GHRP‑2 and its specific metabolite AA‑3 were consistently found in urine.

Practical Outcomes

  • For self‑experimenters, this means anti‑doping labs can reliably detect GHRP‑2 use even at low concentrations, so using the peptide carries a clear risk of a positive test. The study does not give dosing or safety advice, but it highlights that the peptide is quickly excreted and detectable.

Summary

Scientists created a lab test that can spot the peptide GHRP‑2 (also called pralmorelin) and its breakdown product in urine at very low levels. They showed the test works well and that after an IV dose, both the original peptide and its metabolite show up in the urine of all volunteers.

Abstract

GHRP-2 (pralmorelin, D-Ala-D-(beta-naphthyl)-Ala-Ala-Trp-D-Phe-Lys-NH(2)), which belongs to a class of growth hormone secretagogue (GHS), is intravenously used to diagnose growth hormone (GH) deficiency. Because it may be misused in expectation of a growth-promoting effect by athletes, the illicit use of GHS by athletes has been prohibited by the World Anti-Doping Agency (WADA). Therefore, the mass spectrometric identification of urinary GHRP-2 and its metabolite D-Ala-D-(beta-naphthyl)-Ala-Ala-OH (AA-3) was studied using liquid chromatography/electrospray ionization tandem mass spectrometry for doping control purposes. The method consists of solid-phase extraction using stable-isotope-labeled GHRP-2 as an internal standard and subsequent ultra-performance liquid chromatography/tandem mass spectrometry, and the two target peptides were determined at urinary concentrations of 0.5-10 ng/mL. The recoveries ranged from 84 to 101%, and the assay precisions were calculated as 1.6-3.8% (intra-day) and 1.9-4.3% (inter-day). Intravenous administration of GHRP-2 in ten male volunteers was studied to demonstrate the applicability of the method. In all ten cases, unchanged GHRP-2 and its specific metabolite AA-3 were detected in urine.

Study Information

Provider

pubmed

Year

2010

Date

2010-07-30T00:00:00.000Z

DOI

10.1002/rcm.4619

Citations

52

References

28