SOP for Check Suitability of Dissolution Test Apparatus | Pharmaguideline
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  • Apr 17, 2021

    SOP for Check Suitability of Dissolution Test Apparatus

    Standard operating procedure to check the suitability of dissolution test apparatus as per United State Pharmacopeial Convention Inc.

    1.0 OBJECTIVE

    To perform the suitability test as per U.S.P. for reliable and accurate results.

    2.0 SCOPE

    This procedure is applicable to check suitability of dissolution test apparatus, installed in quality control department.

    3.0 RESPONSIBILITY

    3.1 Doing: Technical Assistant
    3.2 Checking: Executive /Manager

    4.0 ACCOUNTABILITY

    Head of the Department

    5.0 PROCEDURE

    5.1 Perform the operational qualification as per reference S.O.P.
    5.2 Use current lot of U.S.P. standard of Prednisone and Salicylic acid tablets for calibration
    5.3 Perform the calibration as per the method given by United States Pharmacopeial Convention Inc. along with reference standard for both disintegrating type and Non disintegrating type.
    5.4 Ensure that the limits of dissolution are within the specified limit.
    5.5 If results found out of limit for RPM, Temperature and alignment parameters, follow the S.O.P. for parameters.
    5.6 Record all the values in the respective annexure I and II.
    5.7 Frequency of calibration :- every six month
    1. First with Salicylic acid tablet
    2. Second with Prednisone tablet

    6.0 ABBREVIATIONS

    6.1 R.P.M.= Rotation per minute
    6.2 ml= milliliter
    6.3 min.= Minute
    6.4 °C= Degree centigrade
    6.5 mg= milligram
    6.6 %= Percentage
    6.7 & = and

    ANNEXURE-I
    QUALITY CONTROL LABORATORY
    SUITABILITY TEST OF DISSOLUTION TEST APPARATUS
                                                                                                                           
    CALIBRATION DATE
    DATE OF LAST CALIBRATION
    DONE
    NEXT DUE FOR
    CALIBRATION

    INSTRUMENT DETAILS
    INSTRUMENT NAME
    INSTRUMENT MAKE
    INSTRUMENT
    IDENTIFICATION NO.

    OBSERVATION
            SUITABILITY TEST FOR BASKET :
    1)  DISINTEGRATION TYPE CALIBRATOR
             NAME OF TABLET :    PREDNISONE 10 mg.
             LOT No.           :  
             DISSOLUTION PARAMETERS :
    DISSOLUTION MEDIUM
    RPM
    TEMPERATURE
    TIME
    KETTLES
    500 ml  Deaerated water

    37°C +  0.5°C
    30 min.
    Glass/ Merlon

    ANNEXURE-I
    QUALITY CONTROL LABORATORY
    UITABILITY TEST OF DISSOLUTION TEST APPARATUS                
                                                                                                                Page 2 of 2
    PREPARATION OF DEARATED WATER :
    Filter the medium through 0.45 micron membrane filter and sonicate for fifteen minutes.
    STANDARD PREPARATION :
    Take 10 mg prednisone (previously dried at 105°C for 3 hours) in to 200 ml volumetric flask and make up the volume with dissolution medium. Dilute 10 ml of this solution to 25 ml with dissolution medium.
    SAMPLE PREPARATION :
    Place one tablet into each of the six bowls and operate the apparatus for 30 minutes. Draw 20 ml of sample from each bowl after 30 minutes, filter with 0.45 micron membrane filter. Discard first few ml of filtrate.
    PROCEDURE :
    Measure the absorbance of standard preparation and test preparation at 242 nm.
    OBSERVATIONS :
    Std. wt. in mg. :______________mg
    Prednisone Lot No.:___________
    Std. Absorbance:______________ Sample Absorbance :___________        
    Balance Id.:__________________ U.V Id. No.:__________________
    Reference std. No.:____________
    Calculation:
     Test abs          Std. Wt. in mg
     -------------X-------------------- X 10
     Std. Abs                   1

     =  -------------X-------------------- X 10

     =------------------ % of label claim.
    Sr. No.
    Tablet No.
    Absorbance
    % of label claim
    Limit
    1
    2
    3
    4
    5
    6
    7
    8
    Average
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