Pharmaceutical Microbiology

Principles and methods of different microbiological assay

Introduction to microbiological assay

  • Microbiological assays are analytical methods used to measure the concentration or potency of a substance by its effect on microorganisms.
  • These assays are pivotal in the pharmaceutical industry for the standardization of antibiotics, vitamins, amino acids, and for the assessment of new antibiotics.
  • They rely on the response of microorganisms to specific substances, allowing quantification based on microbial growth inhibition or stimulation.

Principles of Microbiological Assays

  • Biological Activity Measurement

    • Basis: Microbiological assays measure the biological activity of a substance rather than its chemical concentration.
    • Response Relationship: They rely on a linear relationship between the logarithm of the concentration of the substance and the biological response (e.g., inhibition zone size, turbidity).
  • Use of Test Organisms

    • Selection: Specific microorganisms are chosen based on their sensitivity to the substance being assayed.
    • Standardization: Test organisms must be of a standardized strain and in optimal physiological state.
  • Quantitative Analysis

    • Comparison with Standards: The activity of the test sample is compared against a reference standard of known potency.
    • Dose-Response Curve: Constructed to establish the relationship between concentration and response.

Methods of Different Microbiological Assays

  • Microbiological assays can be broadly classified into:
  • Diffusion Methods
  • Turbidimetric (Tube) Methods
  • Bioautographic Methods

1. Diffusion Methods of Microbiological assay

  • These methods involve the diffusion of an antibiotic from a reservoir through a solid or semi-solid medium to inhibit the growth of microorganisms.

A. Cylinder-Plate Method (Cup-Plate Method)

  • Principle:
    • Antibiotic diffuses from a cylindrical cup into the agar medium inoculated with a microorganism.
  • Procedure:
    • Prepare agar plates inoculated with the test organism.
    • Place stainless steel cylinders or cups on the agar surface.
    • Fill cups with known concentrations of standard and test solutions.
    • Incubate plates under suitable conditions.
    • Measure the zones of inhibition around each cup.
  • Application:
    • Used for antibiotics like penicillin.

B. Paper Disk Diffusion Method

  • Principle:
    • Similar to the cylinder-plate method but uses paper disks impregnated with the antibiotic.
  • Procedure:
    • Place paper disks soaked with standard and test solutions on the inoculated agar surface.
    • Incubate and measure inhibition zones.
  • Application:
    • Commonly used for antibiotic susceptibility testing.
  • Advantages of Diffusion Methods
    • Simple and inexpensive.
    • Suitable for substances that diffuse well in agar.
  • Limitations
    • Diffusion rate may vary with molecular size and agar properties.
    • Less precise than turbidimetric methods.

2. Turbidimetric (Tube) Methods of Microbiological assay

    • Principle

      • Based on the inhibition of microbial growth in a liquid medium containing the test substance.
      • The extent of inhibition is measured by the reduction in turbidity compared to controls.
    • Procedure

      • Prepare a series of tubes with varying concentrations of the test and standard solutions.
      • Inoculate each tube with a standardized microbial suspension.
      • Incubate under optimal conditions.
      • Measure turbidity using a spectrophotometer or nephelometer.
    • Advantages

      • Rapid and more precise than diffusion methods.
      • Suitable for substances that do not diffuse well in agar.
    • Limitations

      • Turbidity measurements can be affected by the presence of precipitates or colored substances.
      • Requires careful standardization of inoculum and incubation conditions.

3. Bioautographic Methods of Microbiological assay

    • Principle

      • Combines chromatography and microbiological assay.
      • Used to identify and quantify antimicrobial substances in complex mixtures.
    • Procedure

      • Separate the components of a mixture using chromatography (e.g., TLC).
      • Transfer the chromatogram onto an agar plate inoculated with a test organism.
      • Incubate and observe zones of inhibition corresponding to antimicrobial substances.
    • Application

      • Screening natural products for antibiotic activity.
      • Identifying active components in complex mixtures.

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