# Reviving Old Antibiotics: New Indications and Therapeutic Perspectives—A Review

**Authors:** Paweł Radkowski, Julia Oszytko, Kamil Sobolewski, Florian Trachte, Maja Czerwińska-Rogowska, Dariusz Onichimowski, Marta Majewska

PMC · DOI: 10.3390/ph19020278 · Pharmaceuticals · 2026-02-06

## TL;DR

This review explores how older antibiotics can be revived and repurposed to combat modern antibiotic resistance through new uses and formulations.

## Contribution

The paper provides a clinically oriented comparative analysis of repurposed antibiotics with a focus on new formulations and combination therapies.

## Key findings

- Old antibiotics like fosfomycin and colistin show renewed clinical potential with optimized dosing and delivery.
- Combination therapies and alternative administration routes improve efficacy and reduce toxicity of legacy antibiotics.
- Strategic repurposing of these drugs offers a complementary approach to address antimicrobial resistance.

## Abstract

The rapid global spread of antimicrobial resistance (AMR) has significantly reduced the effectiveness of many modern antibiotics, creating an urgent need for alternative therapeutic strategies. One promising approach is the revival and repurposing of older antimicrobial agents whose clinical potential was previously limited by toxicity concerns, pharmacokinetic challenges, or the availability of newer drugs. Recent advances in drug delivery, dosing optimization, and antimicrobial stewardship have renewed interest in these compounds as viable options for the treatment of multidrug-resistant infections. The aim of this review is to provide a comparative, clinically oriented analysis of selected “old” antibiotics, fosfomycin, colistin, streptomycin, and vancomycin, with emphasis on their current therapeutic roles, pharmacokinetic/pharmacodynamic (PK/PD) targets, toxicity mitigation strategies, resistance mechanisms, and evidence supporting combination therapies and alternative routes of administration. This narrative review was conducted using a structured PubMed search and manual reference screening, focusing on clinical, PK/PD, and translational studies relevant to the contemporary use of legacy antibiotics. The review summarises current evidence on the re-emerging clinical applications of these agents, each discussed in the context of historical use, mechanism of action, resistance patterns, and newly identified indications. Attention is given to novel formulations, combination strategies, and alternative routes of administration that enhance efficacy while limiting toxicity, including applications in biofilm-associated infections. Overall, strategic repurposing of older antibiotics represents a valuable complementary approach in the fight against AMR and may extend the therapeutic lifespan of existing agents in an era of limited antibiotic innovation.

## Linked entities

- **Chemicals:** fosfomycin (PubChem CID 441029), colistin (PubChem CID 5311054), streptomycin (PubChem CID 5297), vancomycin (PubChem CID 14969)

## Full-text entities

- **Genes:** ESBL [NCBI Gene 13906541], FOSB (FosB proto-oncogene, AP-1 transcription factor subunit) [NCBI Gene 2354] {aka AP-1, G0S3, GOS3, GOSB}, Mucin [NCBI Gene 100508689]
- **Diseases:** bacteremia (MESH:D016470), ESBL infections (MESH:D007239), E. faecalis infection (MESH:D004927), ototoxicity (MESH:D006311), wound infections (MESH:D014946), cytotoxicity (MESH:D064420), urinary tract infection (MESH:D014552), metastasis (MESH:D009362), Pseudomonas aeruginosa infections (MESH:D011552), central nervous system (CNS) infections (MESH:D002494), tuberculous meningitis (MESH:D014390), septic shock (MESH:D012772), hepatocellular carcinoma (MESH:D006528), sepsis (MESH:D018805), brucellosis (MESH:D002006), ABP (MESH:D011472), MRSA (MESH:D013203), colon and breast cancer (MESH:D001943), endocarditis (MESH:D004696), coagulase-negative Staphylococci (MESH:D064726), bacterial infections (MESH:D001424), osteomyelitis (MESH:D010019), tuberculosis (MESH:D014376), associated (MESH:D018886), Klebsiella pneumoniae (MESH:D007710), CRE (MESH:D060467), cancer (MESH:D009369), neurotoxicity (MESH:D020258), Meningeal irritation (MESH:D008580), cystic fibrosis (MESH:D003550), PK (MESH:C564858), injury to (MESH:D014947), lung infections (MESH:D012141), inflammation (MESH:D007249), abscesses (MESH:D000038), multidrug-resistant infections (MESH:D018088), PD (MESH:D010300), bronchospasm (MESH:D001986), cystitis (MESH:D003556), ventilator (MESH:D053717), staphylococcal (MESH:D011023), obese (MESH:D009765), fatty liver disease (MESH:D005234), diarrhoea (MESH:D003967), pneumonia (MESH:D011014), oncogenes (MESH:D000074723)
- **Chemicals:** cephalosporin (MESH:D002511), tris-hydroxymethyl-aminomethane (MESH:D014325), linezolid (MESH:D000069349), rifampicin (MESH:D012293), amikacin (MESH:D000583), fluoroquinolones (MESH:D024841), quinolones (MESH:D015363), Aztreonam-avibactam (-), para-aminosalicylic acid (MESH:D010131), penicillin (MESH:D010406), tetracycline (MESH:D013752), FOS (MESH:D005578), triphosphate (MESH:C005692), Aztreonam (MESH:D001398), epoxide (MESH:D004852), beta-lactams (MESH:D047090), diphosphate (MESH:D011756), ROS (MESH:D017382), chloramphenicol (MESH:D002701), D-Ala-D-Ala (MESH:C002956), imipenem (MESH:D015378), ampicillin (MESH:D000667), daptomycin (MESH:D017576), diol (MESH:D011276), LPS (MESH:D008070), cysteine (MESH:D003545), lipid (MESH:D008055), minocycline (MESH:D008911), EDTA (MESH:D004492), tigecycline (MESH:D000078304), STR (MESH:D013307), lipoteichoic acid (MESH:C009900), ciprofloxacin (MESH:D002939), 4-amino-4-deoxy-L-arabinose (MESH:C040134), azithromycin (MESH:D017963), spectinomycin (MESH:D000198), methionine (MESH:D008715), teicoplanin (MESH:D017334), isoniazid (MESH:D007538), foscarnet (MESH:D017245), chitosan (MESH:D048271), aminoglycoside (MESH:D000617), phosphate (MESH:D010710), gentamicin (MESH:D005839), glutamic acid (MESH:D018698), glycine (MESH:D005998), N-acetylmuramic acid (MESH:C031651), aldehyde (MESH:D000447), PEtN (MESH:C005448), methicillin (MESH:D008712), lipid A (MESH:D008050), PEP (MESH:D010728), ertapenem (MESH:D000077727), water (MESH:D014867), phospholipid (MESH:D010743), pullulan (MESH:C009109), lipid II (MESH:C069249), meropenem (MESH:D000077731), TB (MESH:D013725), ceftazidime (MESH:D002442)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Mycobacterium tuberculosis (species) [taxon 1773], Brucella melitensis (species) [taxon 29459], Rattus norvegicus (brown rat, species) [taxon 10116], Vibrio cholerae (species) [taxon 666], Staphylococcus aureus (species) [taxon 1280], Enterobacter cloacae (species) [taxon 550], Proteus mirabilis (species) [taxon 584], Homo sapiens (human, species) [taxon 9606], Klebsiella oxytoca (species) [taxon 571], Streptomyces viridochromogenes (species) [taxon 1938], Klebsiella planticola (species) [taxon 575], Brucella abortus (species) [taxon 235], Morganella morganii (species) [taxon 582], Serratia marcescens (species) [taxon 615], Acinetobacter baumannii (species) [taxon 470], Mus musculus (house mouse, species) [taxon 10090], Pseudomonas aeruginosa (species) [taxon 287], Streptomyces griseus (species) [taxon 1911], Burkholderia mallei (species) [taxon 13373], Klebsiella pneumoniae (species) [taxon 573], Amycolatopsis orientalis (species) [taxon 31958], Mycobacterium tuberculosis subsp. tuberculosis (subspecies) [taxon 182785], Campylobacter (genus) [taxon 194], Escherichia coli (E. coli, species) [taxon 562], Streptomyces wedmorensis (species) [taxon 43759], Enterobacterales (order) [taxon 91347], Legionella (genus) [taxon 445], Streptomyces fradiae (species) [taxon 1906], Enterococcus faecalis (species) [taxon 1351], Burkholderia cepacia (species) [taxon 292]
- **Mutations:** cysteine to aspartate

## Full text

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## References

111 references — full list in the complete paper: https://tomesphere.com/paper/PMC12944691/full.md

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Source: https://tomesphere.com/paper/PMC12944691