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Insulin Degludec Multi-Hexamer Chains

Self-assembly of insulin degludec into soluble multi-hexamer chains in subcutaneous tissue for ultra-long basal release.

By Encyclopeptide Editorial | 1 min read
insulin degludec hexamer self-assembly pharmacokinetics

Overview

Insulin degludec forms soluble multi-hexamer chains upon subcutaneous injection, creating a depot that slowly releases insulin monomers over more than 42 hours.

Self-Assembly Mechanism

  1. Formulation: Clear solution with phenol and zinc
  2. Injection: Phenol diluted by tissue fluid
  3. Hexamer formation: Zinc-mediated hexamer assembly
  4. Chain formation: Hexamers link via zinc bridges
  5. Gradual dissolution: Multi-hexamer chains dissociate slowly
  6. Monomer release: Active monomers enter circulation

Structural Features

  • Fatty acid linker: Hexadecanedioic acid at LysB29
  • Glutamic acid spacer: Connects fatty acid to peptide
  • Zinc coordination: Bridges between hexamers
  • Soluble depot: No precipitation (unlike glargine)

Chemical Identity

PropertyValue
NameInsulin Degludec Multi-Hexamer Chains
CategoryInsulin Family

References

  1. Encyclopeptide Database. “Insulin Degludec Multi-Hexamer Chains” monograph. encyclopeptide.com.

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