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Sermorelin

GHRH (1-29), GRF 1-29 NH2, Sermorelin acetate

Quick Stats
Studies 223
Trials 41
Score 1
2023 pubmed 9 citations

Online large volume sample staking preconcentration and separation of enantiomeric GHRH analogs by capillary electrophoresis.

Otin. Joanie J; Tran. N Thuy NT; Benoit. Aurélie A; Buisson. Corinne C; Taverna. Myriam M

Key Findings

  • Dimethyl‑β‑cyclodextrin enabled separation of very similar GHRH peptides, including sermorelin, by capillary electrophoresis.
  • Large‑volume sample stacking with polarity switching (PS‑LVSS) boosted signal strength up to 640‑fold compared to standard runs.
  • Detection limits for the four GHRH analogs were achieved between 75 and 200 ng/mL after a simple urine desalting step.

Practical Outcomes

  • For biohackers, the study shows that highly sensitive urine testing for sermorelin is possible, but only with advanced lab tools. It doesn’t provide new dosing advice or performance benefits, just a way to verify if the peptide is present in a sample.

Summary

Scientists developed a lab test that can spot tiny amounts of growth‑hormone‑releasing peptides like sermorelin in urine. By using a special chemical and a technique that concentrates a large sample before analysis, they can detect levels as low as about 0.1 µg/mL. The method works, but it needs specialized equipment and chemicals.

Abstract

A capillary electrophoresis method is proposed to analyze the four most well-known growth hormone-releasing hormone (GHRH) analogs that are misused by athletes. Dimethyl-β-cyclodextrin used as a chiral selector allowed, for the first time, the separation of those basic peptide analogs, including enantiopeptides (sermorelin and CJC-1293) that differ by the chirality of only one amino acid. To increase the method sensitivity, electrokinetic preconcentration methods have been investigated. The large volume sample stacking with polarity switching (PS-LVSS) method with an injected sample volume corresponding to 80% of the capillary one was found superior to the sweeping in terms of signal enhancement factor (SEF). Acid and organic solvent addition to the sample (0.1 mM phosphoric acid with 30% methanol) led to a twofold signal improvement, when compared to water as a matrix. We increased capillary dimensions to provide a signal enhancement through the injection of a larger sample volume. Finally, using a combination of the optimized PS-LVSS preconcentration with the chiral capillary zone electrophoresis (CZE), the GHRH analogs were separated and limits of detection between 75 and 200 ng/mL were reached. This method was successfully applied to urine after a desalting step. An optimized C18 SPE was used for that purpose in order to provide low sample conductivity (<130 µS/cm) and preserve the efficiency of LVSS preconcentration. SEF of 640 was obtained with desalted urine spiked with sermorelin by comparison to the CZE (without preconcentration) method.

Study Information

Provider

pubmed

Year

2023

Date

2023-02-27T00:00:00.000Z

DOI

10.1002/elps.202200278

Citations

9

References

58