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Cyclic lipopeptide antibiotic

Polymyxin B

Polymyxin B is a cyclic lipopeptide antibiotic from Paenibacillus polymyxa, produced as a mixture of closely related components.

By The Peptides Codex Editorial TeamIndividual review date not recorded

Page data last changed: . Chemistry registry snapshot: . Registry refreshes and identity assessments are separate from scientific content review.

Length
n/a
Class
Cyclic lipopeptide antibiotic
Function
Binds lipopolysaccharide and disrupts the Gram-negative outer membrane
Context
Approved antibiotic for serious Gram-negative infections; also in topical products

A last-line polycationic lipopeptide that targets lipid A of Gram-negative bacteria; on the WHO Essential Medicines List.

Also known as: PMB

Part of the Foundational & therapeutic peptides cluster

Overview

Polymyxin B is a cyclic lipopeptide antibiotic from Paenibacillus polymyxa, produced as a mixture of closely related components. Its cationic diaminobutyric acid residues bind the lipid A of lipopolysaccharide, permeabilizing the Gram-negative outer membrane. Approved since 1964 and on the WHO Essential Medicines List, it is used for serious Gram-negative infections and in topical combinations. This page is educational and not medical advice.

Source & context

Biological / chemical source: Soil bacterium Paenibacillus polymyxa (formerly Bacillus polymyxa)

Primary research or clinical context: Approved antibiotic for serious Gram-negative infections; also in topical products

Structure and mechanism

Polymyxin B is a cyclic heptapeptide with a tripeptide side chain bearing a fatty-acyl tail and several 2,4-diaminobutyric acid (Dab) residues. The positively charged Dab groups bind anionic lipid A, displacing stabilizing cations and dissolving into the membrane so that it leaks. It is inactive against Gram-positive bacteria.

Clinical role

Once limited by kidney and nerve toxicity, polymyxin B re-emerged as a treatment for multidrug-resistant Gram-negative infections such as those from Pseudomonas aeruginosa. It also appears in over-the-counter topical antibiotic ointments alongside bacitracin and neomycin. Systemic use requires clinical supervision.

Structure & chemistry

Molecular identity & reference confidence

Source-supported reference

Reference values are taken from the cited molecular record or curated profile. A database match is not independent laboratory verification; modifications, counter-ions, and formulations can change the measured mass.

Molecular form
Polymyxin B (source record; form not independently established)
Species
Not established by this molecular identity audit
Termini (N / C)
Not specified / Not specified

Average reference mass

Reference policy updated: 2026-10-05

Molecular formula
C56H98N16O13
Average reference mass
≈ 1,203.5
Status
Approved medicine in at least one jurisdiction (IUPHAR record)
Identifiers

Chemistry values: PubChem, IUPHAR/BPS Guide to Pharmacology · fetched 2026-09-06.

Clinical development snapshot

ClinicalTrials.gov lists 84 registered studies with “Polymyxin B” as an intervention (snapshot 2026-10-01). A registry footprint is not evidence of efficacy or approval.

Registered studies
84
Highest phase reached
Phase 4
Active in latest 100
17
Most recent update
2026-09-24
Most recently updated studies
NCTTitlePhaseStatusUpdated
NCT05157113Evaluating a Dropless Postoperative Regimen After Cataract Surgery in a Vulnerable, County-hospital PopulationPhase 4completed2026-09-24
NCT05331664Dropless Pars Plana Vitrectomy StudyPhase 4completed2026-09-18
NCT07826351Exploring the Combination of Intracalvariosseous and Intravenous Antibiotics for Moderate to Severe Bacterial Not applicablenot yet recruiting2026-09-17
NCT07788144EAA-Guided AN69-oXiris and PMX-HP Therapy in Septic PatientsNot applicableenrolling by invitation2026-08-26
NCT07759934ASK0912 Versus Polymyxin B for Injection in Adults With Hospital-Acquired or Ventilator-Associated Bacterial PPhase 2recruiting2026-08-12
NCT03920007Study of Subretinally Injected ATSN-101 Administered in Patients With Leber Congenital Amaurosis Caused by BiaPhase 2active not recruiting2026-08-03
See all on ClinicalTrials.gov →
Concentration math

Polymyxin B — reconstitution calculator

Enter how much peptide is in the vial and how much diluent (e.g. bacteriostatic water) is added. The tool returns the resulting solution concentration — and, for any amount you type, the volume it corresponds to. This is educational arithmetic, not a dosing recommendation.

Reference form: Polymyxin B (source record; form not independently established)Average reference mass: 1,203.5 Da

Syringe graduation
Solution concentration
5 mg/mL5,000 mcg/mL
mcg

Enter an amount to see the volume it corresponds to.

Educational concentration mathematics only. This tool does not recommend a dose, amount, or protocol, and nothing here is medical advice. Many peptides are not authorized by Health Canada for human use — see our reconstitution and bacteriostatic-water guides for context.

Open the Polymyxin B calculator on its own page →

Change log

Dated observations from the data pipeline (registry flags, trial footprints, identifiers) and editorial reviews of this profile.

  1. Trials1 registered study added on ClinicalTrials.gov (now 84).

FAQ about Polymyxin B

What is Polymyxin B?+

Polymyxin B is a cyclic lipopeptide antibiotic from Paenibacillus polymyxa, produced as a mixture of closely related components. Its cationic diaminobutyric acid residues bind the lipid A of lipopolysaccharide, permeabilizing the Gram-negative outer membrane. Approved since 1964 and on the WHO Essential Medicines List, it is used for serious Gram-negative infections and in topical combinations. This page is educational and not medical advice.

What Canadian product status is recorded for Polymyxin B?+

Canadian product status for Polymyxin B has not been verified in this profile. No verified record here does not mean no authorization exists. Status depends on the product, formulation and use; consult Health Canada's product records.

What is the typical length of Polymyxin B?+

Polymyxin B is not a classic amino-acid chain peptide in the same sense; see the profile for classification details.

Related peptides

References & further reading

  1. 1.Rigatto et al. (2019). Clinical Use of Polymyxin B. Adv Exp Med Biol
  2. 2.Mohapatra et al. (2021). Polymyxin B accelerates the α-synuclein aggregation. Biophys Chem
  3. 3.Cai et al. (2015). Polymyxin B versus colistin: an update. Expert Rev Anti Infect Ther
  4. 4.Sharma et al. (2024). Polymyxin B Hemoperfusion in Sepsis: A Possible Silver Lining to the Dark Clouds?. Indian J Crit Care Med
  5. 5.Antonelli et al. (2015). Polymyxin B hemoperfusion in sepsis: growing body of evidence and occasional conflicting results. Blood Purif
  6. 6.Ilia et al. (2017). Polymyxin B hemoperfusion in septic shock: nothing overmuch (Meden Agan)!. J Thorac Dis
  7. 7.Horton et al. (1982). Polymyxin B, colistin, and sodium colistimethate. Med Clin North Am
  8. 8.Avedissian et al. (2019). A Review of the Clinical Pharmacokinetics of Polymyxin B. Antibiotics (Basel)
  9. 9.PubChem — compound summary for Polymyxin B (CID 49800004)
  10. 10.Wikipedia — Polymyxin B
Disclaimer: Educational content only. Not medical advice. Not instructions for human use. Research peptides and unapproved products may be restricted or illegal to market for human consumption in your jurisdiction. Consult qualified professionals and applicable law.
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