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Elixir Department: SOP for Determination of Alcohol Content – V 2.0

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Elixir Department: SOP for Determination of Alcohol Content – V 2.0

Standard Operating Procedure for Determination of Alcohol Content in Elixir Formulations

Department Elixir Department
SOP No. SOP/ELX/216/2025
Supersedes SOP/ELX/216/2022
Page No. Page 1 of 8
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To define a validated method for the determination of ethanol (alcohol) content in elixir formulations using Gas Chromatography (GC) or specific gravity-based reference method, to ensure regulatory compliance and product quality.

2. Scope

This SOP is applicable to all finished elixir products containing alcohol as a solvent or active component, tested by the QC Laboratory of the Elixir Department.

3. Responsibilities

  • QC Analyst:
    • Prepare and analyze samples using the approved method and record results.
  • QC Supervisor:
    • Verify chromatograms or readings and review accuracy of calculations.
  • QA Officer:
    • Verify compliance with specification and documentation practices.

4. Accountability

The QC Head is accountable for proper execution and documentation of the alcohol determination. The QA Head is responsible for final review and approval.

See also  Elixir Department: SOP for Solubility Profiling of Active Ingredients - V 2.0

5. Procedure

5.1 Method Selection

  1. Alcohol content may be determined by:
    • Gas Chromatography
(preferred method)
  • Specific gravity method using alcoholometry tables (if validated)
  • 5.2 Sample Preparation for GC

    1. Use a clean, dry 10 mL volumetric flask.
    2. Weigh accurately 1 mL of elixir and dilute to volume with methanol (or as per validated method).
    3. Filter if necessary and inject into GC vial.

    5.3 GC Operating Conditions (Example Method)

    • Column: Capillary column (e.g., polyethylene glycol, 30 m x 0.32 mm)
    • Carrier Gas: Nitrogen or helium at appropriate flow
    • Detector: Flame Ionization Detector (FID)
    • Injector Temp: 200°C
    • Detector Temp: 250°C
    • Oven Program: 40°C for 2 min, then increase to 150°C at 10°C/min

    5.4 Standard and Calibration

    1. Prepare standard solutions of ethanol in methanol at concentrations ranging from 1% to 10% v/v.
    2. Inject each standard and plot peak area vs. concentration to create a calibration curve.
    3. Inject test sample and determine ethanol concentration using the calibration curve.

    5.5 Calculation

    Alcohol (%) = (Sample Peak Area ÷ Slope of Calibration Curve) × Dilution Factor

    If using specific gravity method:
    Compare measured specific gravity at 20°C against reference alcohol tables and interpolate the alcohol %.

    5.6 Acceptance Criteria

    1. The result should fall within the approved specification range (e.g., 10.0% – 12.0% v/v or as per batch record).
    2. Deviation from specified range requires batch hold and investigation.

    5.7 Documentation

    1. Record results in the Alcohol Test Logbook (Annexure-1).
    2. Attach chromatograms or gravimetric readings and calculations to the BMR.
    3. Cross-verify peak retention time with the standard.

    6. Abbreviations

    • GC: Gas Chromatography
    • FID: Flame Ionization Detector
    • SOP: Standard Operating Procedure
    • QA: Quality Assurance
    • QC: Quality Control
    • BMR: Batch Manufacturing Record

    7. Documents

    1. Alcohol Test Logbook (Annexure-1)
    2. GC Calibration and Maintenance Log
    3. Batch Manufacturing Record (BMR)

    8. References

    • USP General Chapter <611> – Alcohol Determination
    • 21 CFR Part 211.165 – Testing and Release for Distribution
    • ICH Q2(R1) – Validation of Analytical Procedures

    9. SOP Version

    Version: 2.0

    10. Approval Section

    Prepared By Checked By Approved By
    Signature
    Date
    Name
    Designation
    Department

    11. Annexures

    Annexure-1: Alcohol Test Logbook

    Date Batch No. Sample ID Method Alcohol % (v/v) Specification Tested By Checked By
    11/04/2025 ELX-0425-034 ALC-Test-034 GC 11.3% 10.0% – 12.0% Rajesh Kumar Sunita Reddy

    Revision History:

    Revision Date Revision No. Revision Details Reason for Revision Approved By
    01/01/2024 1.0 Initial Release New SOP QA Head
    11/04/2025 2.0 Added GC method and specific gravity as alternate method Method Standardization QA Head
    See also  Elixir Department: SOP for Recording Parameters in BMR - V 2.0
    Elixers V 2.0 Tags:Elixir colorants, Elixir dosage form, Elixir filtration techniques, Elixir flavoring agents, Elixir formulation, Elixir GMP compliance, Elixir manufacturing process, Elixir manufacturing SOPs, Elixir packaging requirements, Elixir pharmacopoeial standards, Elixir preparation methods, Elixir preservatives, Elixir production equipment, Elixir quality control, Elixir regulatory guidelines, Elixir shelf life, Elixir stability testing, Elixir sterilization methods, Elixir storage conditions, Elixir sweetening agents, Elixir viscosity modifiers, Hydroalcoholic solutions, Medicated elixirs, Non-medicated elixirs, Pharmaceutical elixirs

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    Standard Operating Procedures V 1.0

    • Aerosols
    • Analytical Method Development
    • Bioequivalence Bioavailability Study
    • Capsule Formulation
    • Clinical Studies
    • Creams
    • Data Integrity
    • Dental Dosage Forms
    • Drug Discovery
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    • Raw Material Stores
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    • Tablet Manufacturing
    • Rectal Dosage Forms
    • Transdermal Patches
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    NEW! Revised SOPs – V 2.0

    • Aerosols V 2.0
    • Analytical Method Development V 2.0
    • API Manufacturing V 2.0
    • BA-BE Studies V 2.0
    • Biosimilars V 2.0
    • Capsules V 2.0
    • Creams V 2.0
    • Elixers V 2.0
    • Gels V 2.0
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    • Raw Material Warehouse V 2.0
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