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GHRP-6

Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2

Quick Stats
Studies 702
Trials 0
Score 1
2011 pubmed 29 citations

Development and validation of a bioanalytical LC-MS method for the quantification of GHRP-6 in human plasma.

Gil. Jeovanis J; Cabrales. Ania A; Reyes. Osvaldo O; Morera. Vivian V; Betancourt. Lázaro L; Sánchez. Aniel A; García. Gerardo G; Moya. Galina G; Padrón. Gabriel G; Besada. Vladimir V; González. Luis Javier LJ

Key Findings

  • A quantitative LC‑MS method using a carbon‑13 labeled internal standard was created for GHRP-6 detection in plasma.
  • The assay is sensitive (lower limit of quantification = 5 ng/mL) and linear from 5 to 50 ng/mL with R² > 0.988.
  • The method was fully validated for accuracy, precision, and stability, and successfully measured GHRP-6 in plasma from nine healthy volunteers in a phase I trial.

Practical Outcomes

  • This validated assay lets researchers reliably track GHRP-6 levels in blood, which could help study dosing, metabolism, and safety. However, it requires specialized LC‑MS equipment, so it isn’t directly usable for most DIY biohackers without access to a professional lab.

Summary

The paper describes a new lab test that can accurately measure the amount of GHRP-6 peptide in human blood plasma, working down to very low levels (5 ng/mL) and proving reliable across multiple runs.

Abstract

Growth hormone-releasing peptide 6 (GHRP-6, His-(DTrp)-Ala-Trp-(DPhe)-Lys-NH₂, MW=872.44 Da) is a potent growth hormone secretagogue that exhibits a cytoprotective effect, maintaining tissue viability during acute ischemia/reperfusion episodes in different organs like small bowel, liver and kidneys. In the present work a quantitative method to analyze GHRP-6 in human plasma was developed and fully validated following FDA guidelines. The method uses an internal standard (IS) of GHRP-6 with ¹³C-labeled Alanine for quantification. Sample processing includes a precipitation step with cold acetone to remove the most abundant plasma proteins, recovering the GHRP-6 peptide with a high yield. Quantification was achieved by LC-MS in positive full scan mode in a Q-Tof mass spectrometer. The sensitivity of the method was evaluated, establishing the lower limit of quantification at 5 ng/mL and a range for the calibration curve from 5 ng/mL to 50 ng/mL. A dilution integrity test was performed to analyze samples at higher concentration of GHRP-6. The validation process involved five calibration curves and the analysis of quality control samples to determine accuracy and precision. The calibration curves showed R² higher than 0.988. The stability of the analyte and its internal standard (IS) was demonstrated in all conditions the samples would experience in a real time analyses. This method was applied to the quantification of GHRP-6 in plasma from nine healthy volunteers participating in a phase I clinical trial.

Study Information

Provider

pubmed

Year

2011

Date

2011-11-15T00:00:00.000Z

DOI

10.1016/j.jpba.2011.11.007

Citations

29

References

29