Standard Operating Procedure for Selection of Capsule Size for Formulations
Department | Capsule Manufacturing |
---|---|
SOP No. | SOP/CM/039/2025 |
Supersedes | SOP/CM/039/2022 |
Page No. | Page 1 of 6 |
Issue Date | 01/02/2025 |
Effective Date | 05/02/2025 |
Review Date | 01/02/2026 |
1. Purpose
The purpose of this SOP is to establish the procedure for selecting the appropriate capsule size for different formulations. The goal is to ensure that the selected capsule size accommodates the required dose, ensuring both the stability and ease of administration of the final product.
2. Scope
This SOP applies to the selection of capsule sizes during the development and manufacturing of hard gelatin capsules. The size selection process takes into account the weight and volume of the fill material, as well as regulatory requirements.
3. Responsibilities
- Formulation Development Team: Responsible for providing information regarding the fill material’s properties, including density and required dose, to ensure the correct capsule size is selected.
- Manufacturing Team: Responsible for producing the capsules according to the selected size and ensuring uniformity in capsule weight and content.
- Quality Control (QC) Team: Responsible for verifying that the selected capsule size meets the necessary specifications for weight, volume, and other quality attributes.
- Quality Assurance (QA) Team: Ensures that the size selection process adheres to GMP and regulatory requirements, and reviews the records to confirm compliance.
4. Accountability
The Capsule Manufacturing Supervisor is accountable for overseeing the selection process and ensuring that the selected capsule size is suitable for the formulation. The QA Manager is responsible for reviewing the process and ensuring compliance with regulatory standards.
5. Procedure
5.1 Initial Considerations for Capsule Size Selection
Before selecting a capsule size, the following factors should be considered:
-
Fill Material Properties
- Determine the density, flowability, and compressibility of the fill material (API, excipients, or granules).
- Ensure that the material can be evenly and efficiently encapsulated without causing issues such as clumping or uneven fill distribution.
-
Required Dose
- Consider the dose to be administered. Larger doses may require larger capsule sizes to accommodate the amount of active pharmaceutical ingredient (API) and excipients.
-
Desired Release Profile
- Consider the type of release profile (e.g., immediate, controlled, extended-release) as it may affect the formulation and capsule size selection.
5.2 Capsule Size Chart
The capsule size chart below provides general guidelines for selecting the appropriate size based on the volume and dose requirements:
Capsule Size | Approximate Fill Volume (ml) | Typical Fill Weight (mg) | Recommended Use |
---|---|---|---|
Size 000 | 1.37 | 900 mg | Large doses, typically for powders or granules |
Size 00 | 1.23 | 600 mg | Common for large dose formulations |
Size 0 | 0.91 | 400 mg | Common for moderate dose formulations |
Size 1 | 0.68 | 300 mg | Moderate to small dose formulations |
Size 2 | 0.37 | 200 mg | Small dose formulations, used for pediatric doses |
Size 3 | 0.30 | 150 mg | Small doses, typically for children or elderly patients |
5.3 Calculating the Appropriate Capsule Size
To calculate the appropriate capsule size for a given formulation, follow these steps:
-
Determine the Dose per Capsule
- Calculate the total dose required for a single capsule. This includes both the API and excipients.
-
Calculate the Volume of the Fill Material
- Determine the volume of the fill material by using its bulk density. The formula is:
- Volume = Mass / Density
- Ensure the calculated volume fits within the target capsule size based on the volume chart.
-
Select the Capsule Size
- Select the smallest capsule size that can accommodate the required dose and volume of the fill material, while ensuring optimal encapsulation efficiency and ease of swallowing.
5.4 Adjustments for Difficult Fill Materials
If the fill material is difficult to encapsulate (e.g., it has poor flowability or compressibility), consider the following adjustments:
-
Use of Excipient Modifications
- Modify the excipient blend to improve flowability and compressibility, such as adding glidants or binders.
-
Smaller Fill Quantities
- If the dose is too high for the selected capsule size, consider splitting the dose into two smaller capsules or adjusting the formulation.
-
Capsule Type
- If the standard hard gelatin capsule is unsuitable, consider using alternative capsule types, such as soft gelatin capsules or liquid-filled capsules, to accommodate challenging formulations.
5.5 Documentation and Record-Keeping
Document all capsule size selection processes and decisions as follows:
-
Capsule Size Selection Report
- Document the rationale behind the selected capsule size, including the calculation of volume and dose, and any adjustments made during the process.
-
Batch Records
- Ensure that the selected capsule size is recorded in the batch records for reference during production and quality control.
6. Abbreviations
- SOP: Standard Operating Procedure
- QC: Quality Control
- API: Active Pharmaceutical Ingredient
- GMP: Good Manufacturing Practice
- RH: Relative Humidity
- USP: United States Pharmacopeia
7. Documents
- Capsule Size Selection Report Template (Annexure-1)
- Capsule Size Chart (Annexure-2)
8. References
- USP <711> – Dissolution Testing
- FDA Guidance for Industry: Stability Testing of Drug Products
- International Conference on Harmonization (ICH) Guidelines for Pharmaceutical Development
9. SOP Version
Version: 2.0
10. Approval Section
Prepared By | Checked By | Approved By | |
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Signature | |||
Date | |||
Name | |||
Designation | |||
Department |
11. Annexures
Annexure-1: Capsule Size Selection Report Template
Material | Capsule Size | Required Volume | Calculated Dose | Reason for Size Selection |
---|---|---|---|---|
API A | Size 0 | 1.2 ml | 300 mg | Selected for optimal dose delivery and efficient encapsulation |
Annexure-2: Capsule Size Chart
Capsule Size | Volume (ml) | Fill Weight (mg) |
---|---|---|
Size 000 | 1.37 | 900 mg |
Size 00 | 1.23 | 600 mg |
Revision History:
Revision Date | Revision No. | Revision Details | Reason for Revision | Approved By |
---|---|---|---|---|
01/01/2024 | 1.0 | Initial Version | New SOP Creation | QA Head |
01/02/2025 | 2.0 | Updated capsule size chart | Standardization | QA Head |