Development of a Novel Covalently Bonded Conjugate of Caprylic Acid Tripeptide (Isoleucine-Leucine-Aspartic Acid) for Wound-Compatible and Injectable Hydrogel to Accelerate Healing

Biomolecules. 2024 Jan 11;14(1):94. doi: 10.3390/biom14010094.

Abstract

Third-degree burn injuries pose a significant health threat. Safer, easier-to-use, and more effective techniques are urgently needed for their treatment. We hypothesized that covalently bonded conjugates of fatty acids and tripeptides can form wound-compatible hydrogels that can accelerate healing. We first designed conjugated structures as fatty acid-aminoacid1-amonoacid2-aspartate amphiphiles (Cn acid-AA1-AA2-D), which were potentially capable of self-assembling into hydrogels according to the structure and properties of each moiety. We then generated 14 novel conjugates based on this design by using two Fmoc/tBu solid-phase peptide synthesis techniques; we verified their structures and purities through liquid chromatography with tandem mass spectrometry and nuclear magnetic resonance spectroscopy. Of them, 13 conjugates formed hydrogels at low concentrations (≥0.25% w/v), but C8 acid-ILD-NH2 showed the best hydrogelation and was investigated further. Scanning electron microscopy revealed that C8 acid-ILD-NH2 formed fibrous network structures and rapidly formed hydrogels that were stable in phosphate-buffered saline (pH 2-8, 37 °C), a typical pathophysiological condition. Injection and rheological studies revealed that the hydrogels manifested important wound treatment properties, including injectability, shear thinning, rapid re-gelation, and wound-compatible mechanics (e.g., moduli G″ and G', ~0.5-15 kPa). The C8 acid-ILD-NH2(2) hydrogel markedly accelerated the healing of third-degree burn wounds on C57BL/6J mice. Taken together, our findings demonstrated the potential of the Cn fatty acid-AA1-AA2-D molecular template to form hydrogels capable of promoting the wound healing of third-degree burns.

Keywords: amphiphile; caprylic acid; covalently bonded conjugate; flow point; fmoc/tBu solid-phase peptide synthesis; gel state; hydrogel; hydrogelability; hydrogelable; injectable; loss modulus; modulus; molecular template; rational design; re-epithelialization; re-gelation; rheology; sheer thinning; skin third-degree burn; sol state; storage modulus; thixotropy; tripeptide; ultrashort peptide; viscoelasticity; wound closure; wound healing.

MeSH terms

  • Animals
  • Aspartic Acid*
  • Caprylates*
  • Fatty Acids
  • Hydrogels / pharmacology
  • Isoleucine
  • Leucine
  • Mice
  • Mice, Inbred C57BL
  • Wound Healing

Substances

  • octanoic acid
  • Caprylates
  • Aspartic Acid
  • Isoleucine
  • Leucine
  • Hydrogels
  • Fatty Acids