Liofilchem® Imipenem+Cloxacillin IMI+CL Antimicrobial Susceptibility Discs

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Termini e condizioni
Garanzia di rimborso di 30 giorni
Spedizione: 2-3 giorni lavorativi

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    Specifications:
    Application Clinical microbiology
    Storage Temperature -20°C
    Product Type Antibiotic Disc
    Product Brand Liofilchem
    Product Grade Microbiology grade

    The Liofilchem® Imipenem+Cloxacillin IMI+CL Antimicrobial Susceptibility Discs are specialized tools designed for the detection of AmpC β-lactamase overproduction and carbapenem resistance in Gram-negative bacteria. The synergy between Imipenem (IMI) and Cloxacillin (CL) helps differentiate resistance mechanisms, specifically those caused by AmpC enzymes versus other carbapenem resistance mechanisms.

    Key Features

    1. Combination Therapy Detection:
      • Detects AmpC-mediated carbapenem resistance using the synergistic activity of Imipenem and Cloxacillin.
    2. Differentiation of Resistance Mechanisms:
      • Helps identify resistance due to porin loss, efflux pumps, or AmpC hyperproduction.
    3. Global Standards Compliance:
      • Designed for use according to CLSI and EUCAST guidelines.
    4. Ease of Use:
      • Compatible with standard disc diffusion methods on Mueller-Hinton Agar.
    5. Enhanced Sensitivity:
      • Provides accurate results for detecting low-level AmpC expression.

    Applications

    • Target Pathogens:
      • Enterobacterales: Escherichia coli, Klebsiella spp., Proteus spp., Serratia spp.
      • Non-fermenters: Pseudomonas aeruginosa, Acinetobacter baumannii.
    • Resistance Mechanisms:
      • AmpC β-lactamase overexpression.
      • Porin loss or reduced permeability.
      • Efflux pump-mediated resistance.

    Technical Specifications

    FeatureDetails
    Active IngredientsImipenem 10 µg, Cloxacillin 500 µg
    Disc ContentCombination of carbapenem and β-lactamase inhibitor
    Disc Diameter6 mm
    Recommended MediaMueller-Hinton Agar
    Incubation Conditions35–37°C for 16–20 hours
    Shelf LifeAs indicated on the packaging
    Storage Conditions-20°C for long-term; 2–8°C for short-term

    Testing Procedure

    1. Sample Preparation:
      • Prepare a bacterial suspension equivalent to 0.5 McFarland Standard.
    2. Inoculation:
      • Spread the suspension evenly over a Mueller-Hinton Agar plate using a sterile swab.
    3. Disc Placement:
      • Place the IMI+CL disc and a standalone Imipenem disc at least 25 mm apart on the agar surface.
    4. Incubation:
      • Incubate at 35–37°C for 16–20 hours.
    5. Result Interpretation:
      • Measure and compare inhibition zones around the IMI+CL disc and the standalone Imipenem disc.

    Interpretation of Results

    ObservationInterpretation
    Zone diameter for IMI+CL > IMI aloneSynergy observed; AmpC-mediated resistance likely
    Reduced zones for both discsLikely porin loss or efflux pump activity
    Normal susceptibility zonesNo AmpC or other carbapenem resistance detected

    Quality Control Data

    Control StrainExpected Results
    Escherichia coli ATCC® 25922No zone enhancement
    Pseudomonas aeruginosa ATCC® 27853No synergy observed
    Klebsiella pneumoniae (AmpC-producing clinical isolate)Zone diameter for IMI+CL > IMI alone

    Advantages

    FeatureBenefit
    Enhanced Detection of AmpCReliable identification of AmpC hyperproducers.
    Synergy TestingDifferentiates between AmpC and other resistance mechanisms.
    Ease of IntegrationCompatible with standard laboratory workflows.
    Cost-effectiveSimple and efficient method for resistance screening.

    References

    1. CLSI (Clinical and Laboratory Standards Institute): M100 Performance Standards for Antimicrobial Susceptibility Testing.
    2. EUCAST (European Committee on Antimicrobial Susceptibility Testing): Breakpoints for Carbapenem Susceptibility.
    3. Studies on Imipenem+Cloxacillin Synergy for detecting AmpC β-lactamase in Enterobacterales.

    Conclusion

    The Liofilchem® Imipenem+Cloxacillin IMI+CL Antimicrobial Susceptibility Discs provide a robust method for identifying AmpC-mediated resistance in clinical microbiology. Their high sensitivity, standardized application, and compatibility with established guidelines make them an essential tool in antimicrobial resistance surveillance.

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