Related Experiment Video
Updated: Aug 7, 2026

Antimicrobial Synergy Testing by the Inkjet Printer-assisted Automated Checkerboard Array and the Manual Time-kill Method
Published on: April 18, 2019
Polymyxin B sulfate and colistin: old antibiotics for emerging multiresistant gram-negative bacteria
M E Evans1, D J Feola, R P Rapp
1Department of Internal Medicine, College of Medicine, University of Kentucky, Lexington 40536, USA. meevan1@pop.uky.edu
Background:
Polymyxin B sulfate and colistin, also known as colistimethate, have not been used for many years because less toxic antimicrobials are available. Gram-negative bacteria that are resistant to the aminoglycosides, beta-lactams, and fluoroquinolones are becoming more common. These bacteria are often susceptible to the polymyxins.
Objective:
To present a review of the chemistry, antibacterial spectrum, dosing, pharmacokinetics, toxicity, and indications for polymyxin B sulfate and colistin.
Data Source:
A MEDLINE search (1966-1998) of the English-language literature was performed to identify primary literature on the polymyxins. Older citations ( 1949-1965) were identified through the bibliographies of these articles.
Study Selection:
All available reports of in vitro antibacterial activity, animal and clinical trials, and case reports were reviewed.
Data Synthesis:
The polymyxins are amphipathic molecules that interact with lipopolysaccharide in the bacterial outer membrane. They have potent antiendotoxic properties and antibacterial activity against Pseudomonas aeruginosa and many of the Enterobacteriaceae. Polymyxin B and colistin are usually given at a dose of 1.5-2.5 and 5 mg/kg/d, respectively, in two divided doses. Dosing must be altered in renal failure since the kidney is the primary route of elimination. Distribution into pleural fluid, joints, and cerebrospinal fluid is poor. Toxic effects involve the kidney and central nervous system. The polymyxins are recommended for serious systemic infections caused by gram-negative bacteria that are resistant to other agents.
Conclusions:
Polymyxin B sulfate and colistin have a role in the therapy of multidrug-resistant gram-negative bacterial infections.
Insights
Polymyxin B sulfate and colistin are effective against multidrug-resistant gram-negative bacteria. These older antibiotics are recommended for serious infections when other treatments fail, despite potential kidney and nervous system toxicities.
Area of Science:
- Microbiology and Infectious Diseases
- Pharmacology and Therapeutics
Background:
- Polymyxin B sulfate and colistin (colistimethate) are older antibiotics previously sidelined due to toxicity.
- Increasing resistance to common antibiotics (aminoglycosides, beta-lactams, fluoroquinolones) has led to renewed interest in polymyxins.
- Gram-negative bacteria, including Pseudomonas aeruginosa and Enterobacteriaceae, are often susceptible to polymyxins.
Purpose of the Study:
- To provide a comprehensive review of polymyxin B sulfate and colistin.
- To cover their chemistry, antibacterial spectrum, dosing, pharmacokinetics, toxicity, and clinical indications.
Main Methods:
- A systematic literature search of MEDLINE (1966-1998) and older citations (1949-1965) was conducted.
- All available in vitro data, animal studies, clinical trials, and case reports were reviewed.
Main Results:
- Polymyxins are amphipathic molecules targeting the bacterial outer membrane's lipopolysaccharide.
- They exhibit potent antiendotoxic and antibacterial activity against key Gram-negative pathogens.
- Typical dosing is 1.5-2.5 mg/kg/d for polymyxin B and 5 mg/kg/d for colistin, adjusted for renal impairment.
- Poor distribution into certain body fluids and potential nephrotoxicity and neurotoxicity are noted.
Conclusions:
- Polymyxin B sulfate and colistin are valuable agents for treating serious infections caused by multidrug-resistant Gram-negative bacteria.
- Their role is established in situations where conventional therapies are ineffective.
Related Concept Videos
Development of Antibiotic Resistance
Mechanism of Antibiotic Resistance in MRSA
Inhibitors of Gram-positive Cell Wall Synthesis
Inhibitors of Bacterial Protein Synthesis
Inhibitors of Bacterial DNA Synthesis
Clinical Significance of Antibiotic Resistance

