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GHK-Cu

Copper Tripeptide-1, Glycyl-L-Histidyl-L-Lysine Copper, Prezatide Copper

Quick Stats
Studies 149
Trials 1
Score 2
1997 pubmed

Simultaneous determination of glycyl-L-histidyl-L-lysine and its metabolite, L-histidyl-L-lysine, in rat plasma by high-performance liquid chromatography with post-column derivatization.

Endo. T T; Miyagi. M M; Ujiie. A A

Key Findings

  • A sensitive HPLC method can reliably detect GHK and HK in tiny plasma samples.
  • After an IV injection, GHK is rapidly metabolized to HK in rats.
  • Both GHK and its metabolite are cleared from the blood quickly, indicating a short half‑life.

Practical Outcomes

  • For biohackers, the main takeaway is that GHK does not stay in the bloodstream for long after a single injection, so frequent dosing or alternative delivery methods (e.g., sustained‑release formulations) may be needed to maintain its levels. The study is in rats and uses IV administration, so human relevance and oral dosing remain uncertain.

Summary

Researchers created a lab test to measure the peptide GHK and its breakdown product HK in rat blood. They gave rats a single IV dose of GHK and found that it quickly turns into HK, and both disappear from the bloodstream fast.

Abstract

A selective and sensitive high-performance liquid chromatographic (HPLC) method was developed for the determination of glycyl-L-histidyl-L-lysine (GHK), a liver-cell growth factor isolated from human plasma, and its metabolite, L-histidyl-L-lysine (HK), in rat plasma. Both high selectivity and sensitivity were achieved by the use of solid-phase extraction with a Bond-Elut Certify cartridge, ion-pair chromatography with 1-pentanesulfonate on a 5-microm Capcell Pak C18 UG120 column (250x4.6 mm I.D.) with a guard column, and by post-column derivatization with o-phthalaldehyde (OPA). GHK and HK were extracted from 0.1 ml of rat plasma after addition of o-phenanthroline to protect against degradation. The limit of detection for GHK and HK were 50 and 15 ng/ml, respectively, and the calibration curves were linear in the range 0.1-5.0 microg/ml. The developed method was applied to the pharmacokinetic study of GHK after a single dose was administered intravenously to rats. GHK was rapidly degraded to HK, which was eliminated rapidly.

Study Information

Provider

pubmed

Year

1997

Date

1997-04-25T00:00:00.000Z

DOI

10.1016/s0378-4347(96)00460-4