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Mod GRF 1-29

Sermorelin, Growth Hormone Releasing Hormone (1-29), hGRF(1-29)NH2

Quick Stats
Studies 227
Trials 47
Score 2
2018 pubmed 2 citations

An immuno polymerase chain reaction screen for the detection of CJC-1295 and other growth-hormone-releasing hormone analogs in equine plasma.

Timms. Mark M; Ganio. Katherine K; Forbes. Grace G; Bailey. Simon S; Steel. Rohan R

Key Findings

  • CJC‑1295 covalently attaches to plasma proteins, extending its circulation time.
  • Standard mass‑spectrometry often misses CJC‑1295 because it becomes part of a larger protein complex.
  • An immuno‑PCR test can detect the CJC‑1295‑protein conjugate down to 0.8 pg/mL, with a practical screening cutoff of 50 pg/mL in equine plasma.

Practical Outcomes

  • For self‑experimenters, this study mainly signals that CJC‑1295 is hard to detect with typical screening tools, but specialized tests exist. It underscores the peptide’s long‑lasting presence in the body, which may affect dosing intervals and detection risk if used in competitive settings.

Summary

The paper describes a super‑sensitive test that can spot the performance‑enhancing peptide CJC‑1295 in horse blood, even though the drug sticks to plasma proteins and hides from usual mass‑spec methods. It shows the peptide stays in the bloodstream much longer because of this binding, and the new assay can detect it at very low levels.

Abstract

CJC-1295 is a 30 amino acid peptide-based drug that stimulates the release of growth hormone (GH) from the pituitary gland. It is unique among performance-enhancing peptides due to the presence of a reactive maleimidopropionic acid group that covalently links the peptide to free thiols on the surface of plasma proteins. Once conjugated, CJC-1295 remains active in the bloodstream for significantly longer than non-conjugated peptide-based drugs that are rapidly excreted. Conjugation of CJC-1295 to plasma proteins prevents its detection by top-down mass-spectrometry-based peptide screening protocols as it effectively becomes a macromolecular protein with an undefined molecular weight. Using a pair of monoclonal antibodies raised against the CJC-1295 peptide, we present an immuno-polymerase chain reaction (I-PCR) assay that is capable of detecting the CJC-1295-protein conjugate at concentrations down to 0.8 pg/mL. Detection of endogenous equine GHRH necessitated a screening threshold for CJC-1295 in equine plasma of 50 pg/mL. The effectiveness of the assay for controlling the illicit use of CJC-1295 was confirmed in equine blood samples after administration in thoroughbred race horses.

Study Information

Provider

pubmed

Year

2018

Date

2018-12-25T00:00:00.000Z

DOI

10.1002/dta.2554

Citations

2

References

29