Liofilchem® Imipenem+EDTA IMI+ED Antimicrobial Susceptibility Discs

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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+EDTA IMI+ED Antimicrobial Susceptibility Discs are diagnostic tools designed for the phenotypic detection of metallo-β-lactamase (MBL) production in Gram-negative bacteria. These discs combine imipenem (a carbapenem antibiotic) and EDTA (a chelating agent), allowing the differentiation of MBL-mediated resistance from other carbapenem resistance mechanisms.

    Key Features

    1. Selective Detection of MBL Activity:
      • Effective in identifying resistance due to MBL production by chelating divalent cations required for MBL enzymatic activity.
    2. Dual-Action Testing:
      • Synergistic action of imipenem and EDTA distinguishes MBL-producing strains from other carbapenem-resistant organisms.
    3. Global Compliance:
      • Conforms to international standards, including CLSI and EUCAST guidelines for antimicrobial susceptibility testing.
    4. Versatile Application:
      • Applicable to a wide range of Gram-negative pathogens, including Enterobacterales, Pseudomonas aeruginosa, and Acinetobacter spp..
    5. Simple Laboratory Workflow:
      • Compatible with disc diffusion methods on Mueller-Hinton Agar for routine diagnostic use.

    Applications

    Pathogen GroupTarget SpeciesMechanism Detected
    EnterobacteralesEscherichia coli, Klebsiella spp.Metallo-β-lactamase (MBL) production
    Non-FermentersPseudomonas aeruginosa, Acinetobacter spp.MBL-mediated carbapenem resistance
    OthersProteus mirabilis, Serratia spp.Differentiation from efflux or porin loss

    Technical Specifications

    FeatureDetails
    Active IngredientsImipenem (10 µg), EDTA (500 µg)
    Disc Diameter6 mm
    Recommended MediaMueller-Hinton Agar
    Incubation Conditions35–37°C for 16–20 hours
    Shelf LifeRefer to package labeling
    Storage Conditions-20°C for long-term; 2–8°C for short-term
    Zone InterpretationMeasured in mm, compared with CLSI/EUCAST standards

    Testing Procedure

    1. Preparation:
      • Prepare a bacterial suspension equivalent to 0.5 McFarland Standard.
      • Inoculate the suspension evenly on Mueller-Hinton Agar plates.
    2. Disc Placement:
      • Place an IMI+ED disc alongside a standalone imipenem disc (control) at least 25 mm apart.
    3. Incubation:
      • Incubate plates at 35–37°C for 16–20 hours.
    4. Interpretation:
      • Measure inhibition zones around the discs.
      • Compare the zone diameters of IMI+ED and imipenem-only discs.

    Result Interpretation

    ObservationInterpretation
    Zone diameter for IMI+ED > IMI alonePositive for MBL production
    Reduced zone sizes for both discsNon-MBL carbapenem resistance (e.g., efflux pump)
    Normal susceptibility zonesNo carbapenem resistance detected

    Quality Control Data

    Control StrainExpected Zone Diameter
    Escherichia coli ATCC® 25922≥23 mm (No synergy observed)
    Pseudomonas aeruginosa ATCC® 27853No zone enhancement
    Klebsiella pneumoniae (MBL positive)Zone diameter for IMI+ED > IMI alone
    Proteus mirabilisResistant, no synergy

    Advantages

    FeatureBenefit
    High SpecificityReliable identification of MBL-producing strains.
    Cost-effective DetectionSimple and economical phenotypic testing method.
    Ease of UseCompatible with routine laboratory workflows.
    Broad ApplicabilityCovers both Enterobacterales and non-fermenters.

    Comparison with Other Methods

    ParameterIMI+ED DiscsMolecular Methods
    CostAffordableExpensive
    Time to Results16–20 hoursVaries (24–48 hours typical)
    Ease of UseSimple disc diffusion methodRequires specialized equipment
    ScopeMBL detection onlyDetects multiple resistance genes

    References

    1. CLSI (Clinical and Laboratory Standards Institute): M100 Performance Standards for Antimicrobial Susceptibility Testing.
    2. EUCAST (European Committee on Antimicrobial Susceptibility Testing): Guidelines for phenotypic detection of MBL.
    3. Scientific Literature:
      • "Detection of Carbapenem Resistance in Enterobacteriaceae," Journal of Clinical Microbiology.
      • "Phenotypic Methods for Identifying MBL Production in Pseudomonas aeruginosa," International Journal of Infectious Diseases.

    Conclusion

    The Liofilchem® Imipenem+EDTA IMI+ED Antimicrobial Susceptibility Discs are reliable and cost-effective tools for identifying metallo-β-lactamase-producing organisms. With their high specificity, compatibility with standard laboratory workflows, and adherence to global testing guidelines, they are indispensable for antimicrobial resistance surveillance and clinical diagnostics.

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