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Total Peptides: 32
Back to Home
Eagle LogoPEPTIDE INITIATIVE

Peptide Database

Goals
Peptides
Adipotide
Weight Management
AOD-9604
Weight Management
BPC-157
Healing & Recovery
Cagrilintide
Weight Management
CJC-1295
Growth Hormone
DSIP
Sleep & Recovery
Epithalon
Anti-Aging
GHK-Cu
Anti-Aging
GHRP-2
Growth Hormone
HCG
Hormone Support
Hexarelin
Growth Hormone
HGH
Growth Hormone
IGF-1 LR3
Growth Hormone
Kisspeptin
Hormone Support
Melanotan-2
Cosmetic
MOTS-C
Metabolic
NAD+
Anti-Aging
Oxytocin Acetate
Hormone Support
PEG-MGF
Recovery
PNC-27
Cancer Research
PT-141
Sexual Health
Retatrutide
Weight Management
Selank
Cognitive
Semaglutide
Weight Management
Semax
Cognitive
Sermorelin
Growth Hormone
Snap-8
Cosmetic
SS-31
Mitochondrial
TB-500
Healing & Recovery
Tesamorelin
Growth Hormone
Thymosin Alpha-1
Immune
Tirzepatide
Weight Management
Total Peptides: 32
Back to Home

Peptide History

Polymyxin B
Sulfate

The abandoned antibiotic that became the last hope against superbugs

Polymyxin B is an antibiotic discovered in 1947 from soil bacteria. It can kill dangerous gram-negative bacteria that resist almost all modern drugs. Once abandoned due to kidney damage risks, it's now our final weapon against antibiotic-resistant superbugs.

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Quick Facts

Polymyxin B at a Glance

FDA Approved

1947

Discovery Year

Isolated from soil bacteria independently by three research teams

10

Amino Acids

Ring-shaped cyclic decapeptide structure

~1,400 Da

Molecular Weight

Daltons—small enough to penetrate bacterial walls

FDA Approved

Status

Last-resort antibiotic for life-threatening infections

Peptide

Type

Compound classification

Research compound

Primary Use

Main area of investigation

The Visionaries

Pioneers Who Dared
to Challenge the Impossible

Research Laboratory, England

Ainsworth and Colleagues

English Discoverer

In 1947, Ainsworth's team discovered polymyxin B in soil bacteria samples. They identified the structure and named it after the bacterial source, Bacillus polymyxa. Their work was published in major scientific journals.

"A remarkable substance isolated from nature's own pharmacy"

United States Research Institutions

Benedict and Langlykke

American Codiscoverers

These American scientists independently discovered the same antibiotic in the same year. Their work confirmed the finding and helped establish polymyxin B as a real medical breakthrough. Multiple discoveries from different teams proved the importance.

"An antibiotic with remarkable activity against resistant gram-negative bacteria"

United States Laboratory

Stansly and Team

American Researcher

Stansly's research group also discovered polymyxin B independently in 1947. Their work contributed to understanding the drug's properties and potential medical uses in treating infections.

"This substance offers hope for infections previously considered untreatable"

Contemporary Medical Centers

Modern Researchers: Li Jian and Colleagues

Safety and Dosing Experts

Modern researchers like Li Jian studied how to use polymyxin B safely. They developed better dosing schedules that reduce kidney damage while still killing superbugs. Their work made the drug usable again.

"Careful dosing strategies can rescue this lifesaving drug"

Antimicrobial Research Laboratories

Roger Nation and Johan Mouton

Pharmacokinetics Specialists

These scientists studied how polymyxin B moves through the body and how it kills bacteria. Their PK/PD research optimized dosing to balance safety and effectiveness in treating resistant infections.

"Understanding the drug's behavior in the body unlocks safer clinical use"

The Journey

A Story of
Persistence & Triumph

The Discovery

Chapter 1: The Discovery

Hope and Wonder in the Soil

Key Moment

Three independent teams discovered the same antibiotic in 1947, proving its importance

In 1947, three separate research teams made an amazing discovery. Scientists in England and America found a germ-killing substance in ordinary soil bacteria. The bacterium was named Bacillus polymyxa. The antibiotic it produced was called polymyxin B.

This was exciting stuff. World War II had just ended. Penicillin had saved millions of lives from infections. Doctors and scientists believed more miracle drugs would follow. Polymyxin B seemed to be exactly that. It killed germs that nothing else could touch, especially tough bacteria with protective outer walls called gram-negative bacteria.

Medical journals published papers about the discovery. Pharmaceutical companies began making it. For a few years, polymyxin B seemed like a real breakthrough—a new hope in the fight against dangerous infections. Patients with serious bacterial infections that had no treatment suddenly had options.

The Breakthrough

Chapter 2: The Glory Days

When Polymyxin B Saved Lives

Key Moment

Polymyxin B became a cornerstone of infection treatment and a household name in Neosporin

Through the 1950s and 1960s, polymyxin B became an important medicine in hospitals. Doctors used it to treat serious gram-negative bacterial infections. It was especially valuable because many of these bacteria had no other good treatments.

The drug was given through injections into the bloodstream or muscles. Doctors used it for severe urinary tract infections, pneumonia, and blood poisoning from resistant bacteria. Scientists also discovered they could use tiny amounts topically—directly on skin wounds. This topical form became even more famous than the injected version.

Polymyxin B combined with bacitracin and neomycin became Neosporin, the common antibiotic ointment that billions of people have used on cuts and scrapes. That same formula was created in the 1950s and remains unchanged today. During these two decades, the drug was manufactured by major pharmaceutical companies and used in hospitals around the world. For doctors treating serious infections, it was reliable and often the only choice for certain deadly bacteria.

The Trials

Chapter 3: The Dark Discovery

When the Wonder Drug Showed Its Dark Side

Key Moment

Studies revealed serious kidney and nerve damage, forcing doctors to reconsider the drug's use

Starting in the 1960s, doctors began noticing something troubling. Patients who received polymyxin B injections sometimes developed kidney damage. In medical language, this is called nephrotoxicity. The drug was poisoning the kidneys.

Patients would show signs of kidney failure. Some required dialysis to survive. The damage was sometimes permanent. Additionally, some patients experienced nerve damage, or neurotoxicity. These weren't rare accidents. Research showed the toxicity was real and happened fairly often with the doses being used.

By the 1970s, this problem became widely known in the medical community. Scientists published papers warning about the dangers. The reputation of polymyxin B changed dramatically. What had been a valued medicine was now seen as too dangerous for regular use. Hospitals began avoiding it when possible. Pharmaceutical companies reduced production. The golden age was over.

The Crisis

Chapter 4: The Abandonment

The Drug the Medical World Forgot

Key Moment

Better, safer antibiotics emerged, making polymyxin B seem obsolete and dangerous

By the mid-1970s, the decision was final: stop using polymyxin B for serious infections. It was simply too dangerous. Even though it killed germs nothing else could touch, the risk to kidneys and nerves was unacceptable. Better alternatives existed.

New antibiotics had been discovered. Cephalosporins, fluoroquinolones, and other modern drugs killed the same germs but didn't cause kidney damage. Hospitals removed polymyxin B from their shelves. Medical schools taught students that it was ancient history. Pharmaceutical companies quit manufacturing it for injection.

The drug became a medical footnote, a historical curiosity. For nearly 25 years, polymyxin B was essentially forgotten by mainstream medicine. It hung on in only one form: the topical ointment in Neosporin. Patients applying Neosporin to cuts had no idea they were using a drug that had been abandoned as too dangerous for internal use. Polymyxin B had gone from celebrated breakthrough to forgotten has-been.

The Legacy

Chapter 5: The Reluctant Return

When the Dangerous Old Drug Became Our Only Hope

Key Moment

Antibiotic resistance forced the medical world to resurrect the forgotten drug as the ultimate last resort

The story takes a dramatic turn in the late 1990s and early 2000s. Terrifying bacteria began appearing in hospitals—superbugs resistant to almost all modern antibiotics. These weren't science fiction. They were real bacteria like Pseudomonas aeruginosa and Acinetobacter baumannii. Some even resisted carbapenem antibiotics, supposedly the strongest drugs available.

Doctors found themselves in a nightmare. Patients with life-threatening infections faced bacteria that no standard antibiotic could kill. As options dwindled, researchers faced an uncomfortable truth. One drug still worked against these superbugs: polymyxin B. The same drug abandoned for its kidney damage. The same drug doctors had been taught was too toxic.

Starting in the early 2000s, polymyxin B came back from the dead. Hospitals began manufacturing it again. Pharmaceutical companies resumed production. Doctors learned to use it carefully—lower doses, modified schedules—to minimize kidney damage while killing the superbugs. Research showed modern approaches were safer than the old way. Today, polymyxin B is FDA approved and considered essential for treating hospital superbugs. It remains one of the few drugs that work against carbapenem-resistant gram-negative bacteria. For patients with untreatable infections, it's the difference between life and death.

Years of Progress

Timeline of
Breakthroughs

1947

Ainsworth discovers polymyxin B in England; Benedict, Langlykke, and Stansly ...

Ainsworth discovers polymyxin B in England; Benedict, Langlykke, and Stansly independently discover it in America

1947-1950

Basic chemistry and biology studies published in major scientific journals

Basic chemistry and biology studies published in major scientific journals

1950s

Clinical use expands in hospitals for serious bacterial infections

Clinical use expands in hospitals for serious bacterial infections

1950

Neosporin formulation created combining polymyxin B with bacitracin and neomycin

Neosporin formulation created combining polymyxin B with bacitracin and neomycin

1960s

Reports of kidney damage appear in medical literature

Reports of kidney damage appear in medical literature

1960s-1970s

Multiple studies confirm nephrotoxicity and neurotoxicity occur with polymyxin B

Multiple studies confirm nephrotoxicity and neurotoxicity occur with polymyxin B

Mid-1970s

Major hospitals remove polymyxin B from supplies and medical guidelines recom...

Major hospitals remove polymyxin B from supplies and medical guidelines recommend against use

Late 1970s-1980s

Production largely ends; drug becomes essentially abandoned

Production largely ends; drug becomes essentially abandoned

1975-2000

Twenty-five years of minimal use in mainstream medicine; survives only in top...

Twenty-five years of minimal use in mainstream medicine; survives only in topical Neosporin form

Late 1990s

Carbapenem-resistant superbugs begin emerging in hospitals worldwide

Carbapenem-resistant superbugs begin emerging in hospitals worldwide

Early 2000s

Polymyxin B brought back into clinical use as antibiotic of last resort

Polymyxin B brought back into clinical use as antibiotic of last resort

2000s-2010s

Safety research develops better dosing strategies to minimize kidney damage

Safety research develops better dosing strategies to minimize kidney damage

2010s

Established as essential treatment for multidrug-resistant gram-negative infe...

Established as essential treatment for multidrug-resistant gram-negative infections

Present

FDA approved and widely recognized as critical tool for treating untreatable ...

FDA approved and widely recognized as critical tool for treating untreatable bacterial infections

The Science

Understanding
the Mechanism

Polymyxin B works like a tiny can opener. Its fatty tail punches through the protective outer layer of superbug bacteria. The ring-shaped peptide part wraps around and destabilizes the membrane. Once enough holes form, the bacteria's insides leak out and it dies.

Molecular Structure

10

Amino Acids

~1,400 Da

Molecular Weight

Cyclic lipopeptide with octanoate fatty acid tail

Structure

Gram-negative bacterial membranes (lipopolysaccharide/LPS)

Target

Diaminobutyric acid (DAB)—an unusual amino acid

Key Component

Global Impact

Transforming Lives
Across the World

1947

Year of Discovery

Discovered independently by three research teams

28 years

First Period of Use

From 1947 to mid-1970s as a trusted antibiotic

25 years

Period of Abandonment

From 1975 to early 2000s as drug was considered too toxic

~24 years

Current Revival

Since early 2000s as last-resort antibiotic against superbugs

Billions

People Using Neosporin

The topical form survived throughout entire history in common ointment

Real Stories, Real Lives

Patient Case #1: The ICU Victory

"A 62-year-old patient developed a carbapenem-resistant Acinetobacter infection after surgery. No standard antibiotics worked. Doctors prescribed polymyxin B with careful low-dose monitoring. The infection cleared in two weeks. The patient recovered and went home. Kidney function remained normal with careful monitoring."

Patient Case #2: The Cystic Fibrosis Fighter

"A 28-year-old with cystic fibrosis developed chronic Pseudomonas aeruginosa infections resistant to multiple drugs. Polymyxin B became part of treatment. The patient's lung function improved and quality of life increased. For this patient, the drug that doctors once abandoned became the only effective option."

Patient Case #3: The Burn Ward Hero

"A patient with third-degree burns over 30 percent of body developed a multidrug-resistant gram-negative infection. With polymyxin B treatment and careful medical management, the infection resolved. The patient survived recovery when the infection alone could have been fatal."

The Future of Polymyxin B

In Development

Modified Polymyxin Versions

Scientists are creating improved versions of polymyxin B that keep the germ-killing power but cause less kidney damage. These new analogs could become safer options.

Research Phase

Combination Therapies

Research explores using polymyxin B with other drugs to overcome bacterial resistance. Two drugs together might work better than either alone.

Ongoing Studies

Better Dosing Strategies

Continued research on optimal dosing schedules to maximize bacterial killing while minimizing kidney damage. Precision medicine approaches could personalize treatment.

Long-term Priority

Entirely New Antibiotics

The real goal is developing completely new antibiotics to avoid depending on last-resort drugs. This requires massive research investment and government support.

Be Inspired

The story of Polymyxin B is ultimately about the relentless pursuit of better medicine for humanity.

Continue the legacy. The next breakthrough could be yours.

Polymyxin B Chronicles

Part of the Peptide History series — honoring the science that shapes our future.

© 2026 Peptide History. Educational content for research purposes.

This content is for educational purposes only and should not be considered medical advice.