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SOP for Use of Humectants in Lyophilized Products

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SOP for Use of Humectants in Lyophilized Products

Standard Operating Procedure for Use of Humectants in Lyophilized Products

1) Purpose

This SOP outlines the process of incorporating humectants into lyophilized products to ensure moisture retention and stability during storage and reconstitution.

2) Scope

This SOP applies to formulation scientists, production operators, and QA personnel involved in the preparation of lyophilized products requiring humectants.

3) Responsibilities

  • Formulation Scientists: Responsible for selecting humectants based on the moisture retention needs of the formulation.
  • Operators: Responsible for incorporating humectants as outlined in the Batch Manufacturing Record (BMR).
  • QA: Responsible for verifying the incorporation of humectants and ensuring proper documentation.
See also  SOP for Preparation of Lyophilized Formulations for Ophthalmic Use

4) Procedure

4.1 Selection of Humectants

4.1.1 Criteria for Selection

  • 4.1.1.1 Humectants must ensure moisture retention and prevent excessive drying of the lyophilized product. Common agents include glycerol and propylene glycol.

4.2 Incorporation of Humectants

4.2.1 Weighing and Dispensing

  • 4.2.1.1 Weigh the required amount of humectants using a calibrated balance as specified in the BMR.
  • 4.2.1.2 Add the humectants to the formulation solution while stirring to ensure even distribution.

4.2.2 Mixing and Homogenization

  • 4.2.2.1 Stir the solution using a mechanical stirrer to ensure the humectants are evenly distributed throughout the formulation.
  • 4.2.2.2 Homogenize the mixture if necessary to ensure uniformity across the entire batch.
See also  SOP for Preparation of Freeze-Dried Antibiotics

4.3 Filtration and Filling

  • 4.3.1 Filter the solution using a sterile 0.22-micron filter and fill into vials as per the BMR for lyophilization.

4.4 Documentation

Record all steps, including the addition of humectants, filtration, and lyophilization parameters, in the Humectant Incorporation Logbook and ensure QA verification.

5) Abbreviations

  • BMR: Batch Manufacturing Record

6) Documents

  • Humectant Incorporation Logbook

7) References

  • Pharmacopoeial guidelines for the use of humectants in lyophilized products

8) SOP Version

Version 1.0

Annexure

Humectant Incorporation Logbook Template

Date Humectant Name Batch No. Quantity Operator Initials QA Verification
DD/MM/YYYY Humectant Name Batch Number Quantity (grams) Operator Name QA Initials
           


See also  SOP for Incorporation of Stabilizers in Lyophilized Formulations
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Standard Operating Procedures V 1.0

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NEW! Revised SOPs – V 2.0

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