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Specimen Atlas of Research Peptides81 plates · MIT
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81Plate 81Reviewed 2026-04-27

VIP

Neuropeptide

also known as Vasoactive Intestinal Peptide, Aviptadil, RLF-100

28-amino-acid endogenous neuropeptide and VPAC1/VPAC2 GPCR agonist. Mediates vasodilation, smooth muscle relaxation, and potent anti-inflammatory effects in pulmonary tissue. Aviptadil (synthetic VIP analogue) received Emergency Use Authorization for COVID-19 ARDS and is under investigation for congenital diaphragmatic hernia, transfusion-related acute lung injury, and post-COVID pulmonary fibrosis.

§ I

At a glance

Primary route
Intravenous
Lead indication
ARDS
Development stage
Phase 3
Route

IV infusion · Inhaled (investigational)

§ II

Mechanism

Edit ↗

Primary target — VPAC1 and VPAC2 G-protein-coupled receptors [udupa-2025].

Pathway — VIP → VPAC1/VPAC2 activation → cAMP elevation → Pulmonary vasodilation + epithelial protection.

Downstream effect — Anti-inflammatory cytokine modulation, alveolar-capillary membrane stabilization, pulmonary smooth muscle relaxation, reduced neutrophil infiltration.

Origin — Endogenous 28-amino-acid neuropeptide; synthetic analogue (aviptadil) identical to natural VIP.

Feedback intact — Yes — exogenous VIP acts as physiological agonist.

§ III

Dosage

Protocols described in the cited literature; not medical advice.

Edit ↗
ParameterValue
Intravenous (ARDS protocol)60–90 mcg/kg/day via continuous infusionTESICO trial protocol for COVID-19 ARDS.
Infusion duration12-hour continuous IV infusion daily [brown-2023]
Inhaled (investigational)Variable dosing under clinical trial protocols [boesing-2022]Delivered via nebulizer for direct pulmonary deposition.
Treatment duration3–14 days (acute ARDS)
Evidence basisPhase 3 RCT (TESICO) [brown-2023]816-patient randomized controlled trial in COVID-19 ARDS.
ReconstitutionLyophilized powder reconstituted with sterile diluent per protocol
Half-life~2 minutes (plasma)Rapid clearance necessitates continuous infusion.
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
mg
mL
mcg
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to VIP's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.100mL
10.0 units on a U-100 insulin syringe
Concentration
2500
mcg per mL
Doses per vial
20
at this dose
§ V

Adverse events

Severities follow the FDA / CTCAE convention.

Edit ↗
Hypotensionmoderate
Transient vasodilation-related blood pressure drop
Tachycardiamild
Reflex tachycardia secondary to vasodilation
Infusion site reactionsmild
Erythema, phlebitis (IV administration)
GI symptomsmild
Nausea, diarrhea (VIP is endogenous GI peptide)
Overall tolerabilitymild
Well-tolerated in Phase 3 trials; adverse event profile comparable to placebo
Absolute contraindications
  • Known hypersensitivity to aviptadil or formulation components
Relative contraindications
  • Severe hypotension or shock states (monitor blood pressure)
  • Pregnancy — insufficient safety data
§ VI

Administration

Edit ↗
  1. 01
    Preparation (IV)

    Reconstitute lyophilized aviptadil powder with sterile diluent per manufacturer protocol. Inspect solution for particulates — should be clear and colorless.

  2. 02
    IV infusion

    Administer as continuous 12-hour intravenous infusion via central or peripheral line. Use infusion pump for precise dosing (60–90 mcg/kg/day divided over infusion duration).

  3. 03
    Monitoring

    Monitor blood pressure, heart rate, and oxygenation continuously during first infusion. Assess for hypotension and adjust infusion rate if needed.

  4. 04
    Inhaled protocol (investigational)

    Deliver via jet or mesh nebulizer per clinical trial protocol. Patient seated upright, normal tidal breathing for 10–15 minutes.

  5. 05
    Storage

    Store lyophilized powder at 2–8 °C, light-protected. Reconstituted solution: use immediately or within 24 hours if refrigerated.

Appendix

Sources

21%

of 42 rendered claims carry a resolvable citation.

  1. [boesing-2022]
    Boesing 2022Inhaled aviptadil for the possible treatment of COVID-19 in patients at high risk for ARDS: study protocol for a randomized, placebo-controlled, and multicenter trial.
    journal, 2022
  2. [brown-2023]
    Brown 2023Intravenous aviptadil and remdesivir for treatment of COVID-19-associated hypoxaemic respiratory failure in the USA (TESICO): a randomised, placebo-controlled trial.
    journal, 2023
  3. [chen-2025]
    Chen 2025Investigation of vasoactive intestinal peptide expression and significance in a congenital diaphragmatic hernia animal model.
    journal, 2025
  4. [udupa-2025]
    Udupa 2025Aviptadil Therapy in Acute Respiratory Distress Syndrome Patients: A Systematic Review and Meta-analysis.
    journal, 2025
Plate composed 2026-04-27 · maturity human-reviewed · schema v1 · Contributors: peptidesdb-ai · 33 fields uncited — open contributions