Validation Protocol to Determine the Shelf Life of Prepared Microbiological Media : Pharmaguideline
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  • Apr 21, 2013

    Validation Protocol to Determine the Shelf Life of Prepared Microbiological Media

    Learn how to validate the shelf life of prepared microbiological media used in microbiological analysis of samples in Pharmaceutical.

    1.0 INTRODUCTION

    The most important thing is to ensure that various media used during any test, support microbial growth to consider the test results as valid. The ability of the nutritive media to support the microbial growth is mainly influenced by pH, physical description and water content. Thus it is essential to check that, at the time of usage these parameters are unaffected, which can be done by checking the pH and carrying out growth promotion test.

    This protocol provides the procedure to determine the shelf life and consistency in pH of prepared media on storage at 20-25°C and 2-8°C. All media shall be prepared as per the SOP for media preparation and the prepared media shall be tested for growth promotion test per container on opening or when required and pH after sterilization  Representative volumes of all these media shall be then taken out at different storage intervals and tested for growth promotion capability and change in pH.
    1) Initial
    2) After 1 day
    3) After 3 days
    4) After 7 days
    5) After 14 days
    6) After 21 days
    7) After 28 days
    8) After 31 days

    The maximum storage period or shelf life of all these various media shall then be determined based on the results of growth promotion test and physical appearance. Check the maximum storage period over which a medium is well capable of supporting growth of test organism and also shows no variation with respect to pH (at the end of study) shall be taken into consideration for deciding the shelf life of that particular medium.

    2.0 OBJECTIVE

    The objective of this study is to determine the shelf life of prepared microbiological media on storage with respect to change in pH and growth promotion test to ensure that at the time of usage the media has capability to support the microbial growth and are free from any contamination and deformation after storage in defined conditions.

    3.0 SCOPE

    This protocol is applicable for microbiology laboratory in quality control.

    4.0 REFERENCE DOCUMENT

    SOP for media preparation

    5.0 RESPONSIBILITY

    Microbiologist

    6.0 PROCEDURE

    6.1 PREPARATION OF MEDIA
    6.1.1  Media shall be prepared as per the SOP for media preparation.
    6.1.2  Liquid media shall be distributed in parts of 100 ml in 250 ml conical flasks / bottles.
    6.1.3  Solid media shall be poured in to sterilized petridishes after sterilization.
    6.1.4  All the media shall be labelled for name of the medium, date of preparation and signature.
    6.1.5  Media shall be stored in an incubator maintained at 20-25 °C and 2-8°C
    6.2 RECORDING OF pH
    6.2.1  After sterilization of media, pH shall be recorded in the datasheet as ‘INITIAL pH’
    6.2.2  On storage, at different time intervals mentioned in section 1.0, individual liquid media shall be checked for pH.
    6.2.3  For each medium, pH observed at different time intervals shall be recorded in the data sheet.
    6.2.4  Solid media should be checked for pH initially only. 
    6.3 GROWTH PROMOTION TEST
    6.3.1  After preparation and sterilization of all the media, immediately carry out growth promotion test on all of them as per the SOP for growth promotion. Record the results in datasheet.
    6.3.2  On storage, at different time intervals as mentioned in section 1.0, individual media shall be checked for growth promotion.
    6.3.3  Record the results of growth promotion test in datasheet for each medium.
    6.4 CHECKING FOR PHYSICAL APPEARANCE AND CONTAMINATION
    6.4.1  Check the solid agar media visually for dryness.
    Check the solid agar media as well as liquid media visually for any deformation such as a change in color sedimentation, precipitation, for microbial contamination etc.

    7.0 ACCEPTANCE CRITERIA

    The maximum storage period over which a medium comply the following criteria shall be taken into consideration for deciding the shelf life of the particular medium.
    A)  pH may not vary from the given range of pH in Annexure - II
    B)  Growth promotion test shall comply when done initially as well as during the particular storage period.
    i)  Liquid media: Should show growth in the form of turbidity. If liquid medium is opaque, then after incubation in this medium further carryout streaking on selective agar media, where the characteristic growth shall be observed as Annexure – I.
    ii)  General /Enrichment agar media: The total viable count obtained should not be less than + 30 % of the actual count of the respective culture suspension.
    iii)  Selective agar media : Should show characteristic growth comparable to as described in
    Annexure –I.
    C)  The Solid agar media should not get dry. The liquid, as well as solid agar media, should not show any deformation and contamination. 


    ANNEXURE – I
    Sr. No
    Name of the Medium
    Test organism
    Observations
    1
    Bismuth Sulphite agar
    Salmonella species
    Good growth, Black or green colonies.
    2
    Brilliant Green agar

    Salmonella species
    Good growth, Small, Transparent and colorless, or opaque, or white (frequently surrounded by a pink or red zone) colonies.
    3
    Xylose Lysine Deoxycholate agar
    Salmonella species
    Good growth, well-developed, red colonies with or without black centers.
    4
    Triple Sugar Iron agar
    Salmonella species
    Formation of acid and gas in the stab culture (with or without concomitant blackening) and the absence of acidity from the surface growth.
    5
    Mannitol Salt agar

    Staphylococcus aureus
    Good growth, yellow colonies surrounded by yellow zone.
    6
    Vogel - Johnson agar

    Staphylococcus aureus
    Good growth, Black colonies surrounded by yellow zone.
    7
    Braid Parker agar
    Staphylococcus aureus
    Good growth, Black colonies surrounded by clear zone.
    8
    Cetrimide agar
    Pseudomonas aeruginosa
    Good growth, Generally greenish, shows greenish fluorescence when observed under Ultraviolet light
    9
    Pseudomonas agar for  Fluorescein
    Pseudomonas aeruginosa
    Good growth, Generally colorless to yellowish, shows yellowish fluorescence when observed under Ultraviolet light
    10
    Pseudomonas agar for  Pyocyanin
    Pseudomonas aeruginosa
    Good growth, Generally greenish, shows blue fluorescence when observed under Ultraviolet light
    11
    Eosin Methylene Blue agar
    Escherichia coli
    Good growth, Blue-black colonies under transmitted light; with characteristic metallic sheen under reflected light.
    12
    MacConkey agar
    Escherichia coli
    Good growth, Brick-red colonies; may have a surrounding zone of precipitated bile.
    13
    MacConkey broth
    Escherichia coli
    Acid and gas production.
    14
    EE broth
    Escherichia coli
    Good growth with colour change
    15
    M-endo
    Escherichia coli           
    pink to dark red with a green metallic surface sheen
    16
    Giolitti Cantoni broth
    Staphylococcus aureus ATCC 6538
    Good growth
    17
    Cetrimide broth
    Pseudomonas aeruginosa
    Good growth, Generally greenish coloration
    18
    Peptone water
    Bacillus subtilis
    Good growth in the form of turbidity
    19
    Fluid Lactose medium
    Salmonella  species OR Escherichia coli
    Good growth in the form of turbidity
    20
    Soyabean Casein Digest medium

    Bacillus subtilis
          OR
    Escherichia coli
    Good growth in the form of turbidity
    21
    R2A agar
    Bacillus subtilis
         
    The total viable count obtained should not be less than + 30 % of the actual count of the respective culture suspension
    22
    Fluid Thioglycolate medium
    Bacillus subtilis
    Good growth in the form of turbidity
    23
    Soyabean Casein Digest agar

    Bacillus subtilis
    The total viable count obtained should not be less than + 30 % of the actual count of the respective culture suspension
    24
    Sabouraud Dextrose agar
    Candida albicans
    OR
    Aspergillus niger
    The total viable count obtained should not be less than + 30 % of the actual count of the respective culture suspension
    25
    Nutrient agar
    Bacillus subtilis
    The total viable count obtained should not be less than + 30 % of the actual count of the respective culture suspension
    26
    Plate Count agar

    Bacillus subtilis
    The total viable count obtained should not be less than + 30 % of the actual count of the respective culture suspension


                                                                        ANNEXUERE - II

    STORAGE CONDITION
    Date:                                                    Instrument ID:
    S.No
    Name of the Medium
    Test organism
    Inoculum
    used
    (cfu /ml)
    Incubation Temp
    Incubation Period
    Count obtained (cfu/ml)
    1
    RAA





    2
    SDA





    3
    SCA










    STORAGE CONDITION
    Date:                                                    Instrument ID:
    S.No
    Name of the Medium
    Test organism
    Inoculum
    used
    (cfu /ml)
    Incubation Temp
    Incubation Period
    pH
    Observation
    1
    SCM






    2
    FTG






    3
    CMM






    4
    FLM






    5
    TTB






    6
    MCB






    7
    CTB






    8
    SCB






    9
    GCB






    10
    EEB






    11
    RFM






    12
    BSP







    STORAGE CONDITION
    Date:                                                    Instrument ID:
    S.No
    Name of the Medium
    Test organism
    Inoculum
    used
    Incubation Temp
    Incubation Period
    Observation
    1
    MEA





    2
    TSI





    3
    VRB





    4
    CBA





    5
    BPA





    6
    EMB





    7
    MSA





    8
    VJA





    9
    PAP





    10
    PAF





    11
    CTA





    12
    MCA





    13
    BGA





    14
    XLD





    15
    BSA






    Done By:                                                                                                Checked By:

    Date:                                                                                                       Date:
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    1 comment: Post Yours! Read Comment Policy ▼

    1. From where we get the references for hold time study of sterlized media for solid 10 days and liquid 21 days? Like usp,ip,other guideline plz revert its urgent.

      ReplyDelete

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