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Related Concept Videos

Combined Effects of Drugs: Synergism01:27

Combined Effects of Drugs: Synergism

Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called supra-additive interactions. The drugs collectively enhance the final therapeutic effect by acting on different targets. Another advantage is that the low dose of each constituent drug is sufficient to achieve the desired effect. This helps reduce the duration of therapy and lower the adverse effects of these drugs.
Such synergistic combinations...
Inhibitors of Bacterial Protein Synthesis01:25

Inhibitors of Bacterial Protein Synthesis

Aminoglycosides constitute a highly potent class of bactericidal antibiotics that exert their antimicrobial effects by targeting the bacterial ribosome, specifically disrupting protein synthesis. These polycationic molecules consist of amino-modified sugars linked via glycosidic bonds to an aminocyclitol core such as 2-deoxystreptamine or streptamine. Their strong positive charges facilitate tight binding to the negatively charged phosphate backbone of ribosomal RNA (rRNA), primarily at the 16S...
Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
Antibiotic Selection00:57

Antibiotic Selection

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Antifungal Agents01:15

Antifungal Agents

Amphotericin B is a broad-spectrum antifungal agent that exploits structural differences between fungal and mammalian cell membranes. Its amphipathic structure—featuring a hydrophobic polyene-lactone ring and a hydrophilic region containing mycosamine and carboxylic acid groups—enables selective binding to ergosterol, a sterol predominantly found in fungal plasma membranes. This selective interaction underlies the drug’s antifungal activity, although weak binding to cholesterol contributes to...
Microbial Interactions: Cooperation01:26

Microbial Interactions: Cooperation

Microbial cooperation involves beneficial interactions in which different species work together for individual or mutual advantage. These interactions can profoundly influence ecological dynamics and evolutionary processes, and they are essential to many pathogenic and symbiotic relationships.Nematode–Bacteria CooperationA striking example is the relationship between the Gram-negative bacterium Xenorhabdus nematophila and the parasitic nematode Steinernema carpocapsae. Juvenile nematodes...

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Related Experiment Video

Updated: Jun 18, 2026

Assay Development for High-Throughput Drug Screening Against Mycobacteria
07:50

Assay Development for High-Throughput Drug Screening Against Mycobacteria

Published on: October 25, 2024

Fosfomycin: an old, new friend?

M Popovic1, D Steinort, S Pillai

  • 1Department of Cardiovascular and Interventional Radiology, Medical University of Vienna, Vienna, Austria.

European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology
|November 17, 2009
PubMed
Summary

Fosfomycin (FOM) is a versatile antibiotic with a broad global usage history. Its efficacy against resistant bacteria like MRSA and ESBL is being re-evaluated for modern therapeutic applications.

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Area of Science:

  • Pharmacology and Microbiology
  • Antimicrobial resistance
  • Infectious diseases

Background:

  • Fosfomycin (FOM) usage varies globally, with broader applications in Europe, Japan, South Africa, and Brazil compared to the US.
  • Initial skepticism regarding FOM's in vitro activity has been overcome by extensive research and improved microbiological understanding since the 1970s.
  • FOM has undergone 40 years of pre-clinical and clinical evaluation across diverse settings and applications.

Observation:

  • Intravenous FOM-disodium is widely accepted in Europe for treating soft tissue infections, sepsis, and deep-seated infections.
  • Emerging antibiotic-resistant bacteria, including MRSA, ESBL, and MSSA, necessitate the revival of established antimicrobial agents like FOM.
  • Comprehensive pharmacokinetic and pharmacodynamic data support FOM's efficacy in large-scale studies.

Findings:

  • FOM demonstrates proven efficacy in a wide range of clinical applications.
  • Intravenous FOM-disodium is a well-established treatment option in many European countries.
  • FOM's characteristics make it a candidate for combating modern resistant bacterial strains.

Implications:

  • Revisiting and expanding the use of Fosfomycin is crucial for addressing current challenges in antimicrobial resistance.
  • Further research into FOM's mode of action, resistance, and combination therapies can optimize its clinical utility.
  • FOM's established safety and efficacy profile supports its consideration for broader indications, including against resistant pathogens.