Specialized Research

Aviptadil

Also known as: RLF-100, VIP sintético, Peptídeo Intestinal Vasoativo sintético

Molecular Identifiers

Molecular Formula

C147H237N43O43S

CAS Number

40077-57-4

PubChem CID

16132300

Molecular Weight

3326.8 Da

Overview

Synthetic analog of vasoactive intestinal peptide (VIP), composed of 28 amino acids. Originally developed for respiratory and vascular conditions, it acts as a potent pulmonary vasodilator and anti-inflammatory agent. Extensively researched for lung protection and surfactant function regulation.

Aviptadil is a synthetic analog of vasoactive intestinal peptide (VIP), and its clinical interest is concentrated in the lungs: VPAC1/VPAC2 receptor agonism produces pulmonary vasodilation, anti-inflammatory modulation of the alveoli, stimulation of surfactant production by type II pneumocytes, and protection of the respiratory epithelium against apoptosis. It has been investigated in pulmonary arterial hypertension and in acute respiratory failure.

The peptide gained prominence during the COVID-19 pandemic, when it was tested (under the name RLF-100) as a treatment for severe ARDS; the program advanced through clinical trials but did not obtain drug approval. It currently remains an investigational compound, available in some countries through compassionate use. It has no registered indication with the FDA, EMA, or ANVISA. The very short half-life (1-2 minutes IV) explains the need for continuous infusion or multiple administrations, and intravenous use requires clinical supervision due to the risk of hypotension.

Sequence (1 letter): HSDAVFTDNYTRLRKQMAVKKYLNSILN
Extended notation: His-Ser-Asp-Ala-Val-Phe-Thr-Asp-Asn-Tyr-Thr-Arg-Leu-Arg-Lys-Gln-Met-Ala-Val-Lys-Lys-Tyr-Leu-Asn-Ser-Ile-Leu-Asn

Half-life

~1-2 minutes (IV)

Administration Route

Intravenous or subcutaneous

Category

Specialized Research

Mechanism of Action

  • Agonism of VIP VPAC1 and VPAC2 receptors
  • Pulmonary and systemic vasodilation via cAMP increase
  • Anti-inflammatory action in pulmonary alveoli with reduction of pro-inflammatory cytokines
  • Stimulation of surfactant production by type II pneumocytes
  • Inhibition of apoptosis in alveolar epithelial cells
  • Modulation of the innate immune response in the lungs

Dosage Protocol

Data compiled from the literature. This does not constitute medical advice.

Parameter Value
Dose 50-150 mcg per administration (IV or subcutaneous)
Frequency 1-3 times daily per protocol
Timing Per clinical guidance
Duration 4-8 weeks

Reported Side Effects

Adverse effects described in the literature. Severity and frequency vary between individuals.

  • Hypotension
  • Tachycardia
  • Nausea
  • Diarrhea
  • Facial flushing

Product Properties

Purity >98%
Appearance White lyophilized powder
Solubility Soluble in water, sterile saline, and bacteriostatic water
Source Solid-phase peptide synthesis (SPPS)
Storage Lyophilized: -20°C for up to 2 years, 2-8°C for up to 6 months. Reconstituted: 2-8°C, use within 24 hours. Protect from light and moisture. Short half-life — use reconstituted solution promptly.

Presentations & Preparation

Vials of Aviptadil found in the research market:

5 mg10 mg

Reconstitution

  • Diluent: Bacteriostatic water or sterile saline solution
  • Volume: 1-2 ml per vial
  • Inject the diluent slowly against the vial wall
  • Gently swirl until fully dissolved — never shake
  • For IV use, dilute in saline solution per protocol

Storage

  • Lyophilized: Refrigerated 2-8°C
  • Reconstituted: Refrigerated 2-8°C (up to 24 hours)
  • Protect from direct light
  • Do not freeze after reconstitution
  • Use reconstituted solution as soon as possible
Reconstitution Calculator

Scientific Studies

Published studies on Aviptadil.

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