DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/17878146
Sources: http://www.ncbi.nlm.nih.gov/pubmed/17878146
Polymyxin B is a lipopeptide antibiotic isolated from Bacillus polymyxa. Its basic structure consists of a polycationic peptide ring and a tripeptide side chain with a fatty acid tail. Polymyxin B is a mixture of at least four closely related components, polymyxin B1 to B4, with polymyxin B1 and B2 being the two major components. Polymyxin B acts on Gram-negative bacteria by interacting with lipopolysaccharide (LPS) of the outer membrane and destabilizing it. Polymyxin B is indicated for the treatment of many bacterial diseases such as meningeal infections, urinary tract infections and bacteremia.
CNS Activity
Sources: http://www.ncbi.nlm.nih.gov/pubmed/19202043
Curator's Comment: Polymyxin B penetrates BBB and cause neurotoxic effect.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: Q28824 Gene ID: 338037.0 Gene Symbol: MYLK Target Organism: Bos taurus (Bovine) Sources: https://www.ncbi.nlm.nih.gov/pubmed/1847132 |
70.0 µM [IC50] | ||
Target ID: Protein kinase C (Bos taurus) Sources: https://www.ncbi.nlm.nih.gov/pubmed/1847132 |
4.0 µM [IC50] | ||
Target ID: Na,K-ATPase (rat) Sources: https://www.ncbi.nlm.nih.gov/pubmed/1847132 |
800.0 µM [IC50] | ||
Target ID: GO:0043165 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Curative | POLYMYXIN B SULFATE Approved UseAcute infections caused by susceptible strains of Pseudomonas aeruginosa. Launch Date1964 |
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| Curative | POLYMYXIN B SULFATE Approved UseAcute infections caused by susceptible strains of Pseudomonas aeruginosa. Launch Date1964 |
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| Curative | POLYMYXIN B SULFATE Approved UseAcute infections caused by susceptible strains of Pseudomonas aeruginosa. Launch Date1964 |
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| Curative | POLYMYXIN B SULFATE Approved UseAcute infections caused by susceptible strains of Pseudomonas aeruginosa. Launch Date1964 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Polymyxin-B hemoperfusion in septic patients: analysis of a multicenter registry. | 2016-12 |
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| Successful treatments with polymyxin B hemoperfusion and recombinant human thrombomodulin for fulminant Clostridium difficile-associated colitis with septic shock and disseminated intravascular coagulation: a case report. | 2016-12 |
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| The effects of direct hemoperfusion using a polymyxin B-immobilized column in a pig model of severe Pseudomonas aeruginosa pneumonia. | 2016-12 |
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| A feed-forward loop between SroC and MgrR small RNAs modulates the expression of eptB and the susceptibility to polymyxin B in Salmonella Typhimurium. | 2016-11 |
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| Polymyxin B Nephrotoxicity: From Organ to Cell Damage. | 2016 |
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| Antimicrobial Activity and Toxicity of the Major Lipopeptide Components of Polymyxin B and Colistin: Last-line Antibiotics against Multidrug-Resistant Gram-negative Bacteria. | 2015-11-13 |
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| Pharmacokinetics of intravenous polymyxin B in critically ill patients. | 2008-11-15 |
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| Evolution and dynamics of regulatory architectures controlling polymyxin B resistance in enteric bacteria. | 2008-10 |
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| Evolution and dynamics of regulatory architectures controlling polymyxin B resistance in enteric bacteria. | 2008-10 |
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| COMPARISON OF THE ACTION OF STREPTOMYCIN, POLYMYXIN B, AUREOMYCIN AND CHLOROMYCETIN ON H. PERTUSSIS, H. PARAPERTUSSIS, H. INFLUENZAE AND FIVE ENTERIC STRAINS OF GRAM-NEGATIVE BACILLI. | 1949-09 |
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| LABORATORY AND CLINICAL STUDIES OF POLYMYXIN B AND E. | 1949-09 |
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| CHEMICAL STUDIES ON POLYMYXIN B. | 1949-09 |
Patents
Sample Use Guides
In Vivo Use Guide
Curator's Comment: 25,000 to 30,000 units/kg/day (Intramuscular injection), 50,000 units once daily intrathecally for 3 to 4 days, then 50,000 units once every other day for at least 2 weeks (Intrathecal injection).
15,000 to 25,000 units/kg body weight/day
Route of Administration:
Intravenous
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1195418/
Polymyxin B MICs were determined for different strains of P. aeruginosa in Ca-MHB using a broth macrodilution method. The MIC was defined as the lowest concentration of drug that resulted in no visible growth after 24 h of incubation at 35°C in ambient air. The polymyxin B MIC ranged from 0.5 to 1 mg/liter.
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Mixture
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21 CFR 333.120
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C78160
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