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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 2
2012 pubmed 9 citations

Interaction between PEO-PPO-PEO copolymers and a hexapeptide in aqueous solutions.

Jia. Lianwei L; Guo. Chen C; Xiang. Junfeng J; Wang. Ning N; Yang. Liangrong L; Tang. Yalin Y; Liu. Huizhou H

Key Findings

  • PEO‑PPO‑PEO copolymers interact with specific parts of GHRP‑6 (Ala, Trp, Phe, Lys).
  • The peptide and polymer form a stable 1:1 complex; binding strength increases with higher EO/PO content.
  • NMR and ITC measurements both confirm the binding and its thermodynamic profile.

Practical Outcomes

  • For DIY peptide users, the study hints that formulating GHRP‑6 with certain block‑copolymers might improve its stability and absorption, but no ready‑to‑use recipe or dosage guidance is provided. Until a safe, tested delivery system is available, the findings are mainly of scientific interest rather than a direct protocol to adopt.

Summary

Scientists studied how a special block‑copolymer (PEO‑PPO‑PEO) sticks to the peptide GHRP‑6 in water. They found the polymer and peptide bind together in a 1:1 ratio, and that polymers with more ethylene oxide (EO) and propylene oxide (PO) units bind stronger. This suggests these polymers could be used to carry GHRP‑6 into the body more effectively.

Abstract

Interaction between PEO-PPO-PEO copolymers and a hexapeptide, growth hormone releasing peptide-6 (GHRP-6), was investigated by NMR to study the potential use of the copolymers in peptide drug delivery. (1)H NMR and nuclear Overhauser effect spectroscopy (NOESY) measurements determined that PO methyl protons interacted with methyl protons of the Ala moiety, aromatic protons of the Trp moiety, and some of the Phe aromatic protons. The Lys moiety and part of the Phe moiety entered the hydrophilic EO environment via hydrogen bonding. PEO-PPO-PEO copolymers and the peptide formed a complex in 1:1 stoichiometry. Binding constants between copolymers and GHRP-6 were determined, and it was indicated that the copolymers containing more EO and PO units will lead to greater affinity with the peptide. Isothermal titration calorimetry (ITC) measurements confirmed the results of NMR experiments. This study indicates that PEO-PPO-PEO copolymers have great potential in delivering peptide drugs.

Study Information

Provider

pubmed

Year

2012

Date

2012-01-09T00:00:00.000Z

DOI

10.1021/la203693c

Citations

9

References

52