Capsules

Study Note on Pharmaceutical Dosage Forms

Based on The Theory and Practice of Industrial Pharmacy Authors: Van B. Hostetler (Part One), J.P. Stanley (Part Two), J.A. Bakan

Introduction to Capsules

Capsules are solid dosage forms in which the drug is enclosed in a soluble shell or container. They are one of the most popular oral dosage forms due to their ease of swallowing, ability to mask unpleasant tastes, and rapid disintegration. Capsules are classified into two main types: hard gelatin capsules and soft gelatin capsules.

Definition: Capsules are solid dosage forms with hard or soft soluble shells made from gelatin or other suitable materials, containing medicinal substances in solid, liquid, or semisolid form.

Hard Gelatin Capsules

Composition and Manufacturing

Hard gelatin capsules consist of two pieces: a body and a cap. They are typically made from gelatin, plasticizers, and coloring agents.

Component Function Percentage
Gelatin Formation of shell 80-85%
Water Plasticizer, processing aid 12-16%
Colorants Identification, opacity 0.5-2%
Opacifiers Light protection 0.2-1%
Preservatives Prevent microbial growth 0.1-0.3%

Manufacturing Process

Hard gelatin capsules are manufactured by dipping stainless steel pins into gelatin solution:

  1. Preparation of Gelatin Solution: Gelatin is dissolved in hot water with additives
  2. Dipping: Stainless steel pins are dipped into gelatin solution
  3. Rotation: Pins are rotated to ensure uniform coating
  4. Drying: Coated pins are dried in controlled humidity and temperature
  5. Stripping: Capsules are stripped from pins
  6. Cutting and Joining: Capsules are cut to length and cap joined to body
  7. Printing: Identification codes are printed
  8. Sorting and Packaging: Capsules are sorted and packaged

Capsule Sizes

Hard gelatin capsules are available in standard sizes:

Capsule Size Volume (mL) Typical Fill Weight (mg)
000 1.37 950-1300
00 0.95 650-900
0 0.68 450-600
1 0.50 300-450
2 0.37 250-350
3 0.30 200-300
4 0.21 120-200
5 0.13 90-150

Formulation of Hard Capsule Contents

Powder Formulations

Most common filling material for hard capsules:

  • Drug Substance: Active pharmaceutical ingredient
  • Diluents: Lactose, microcrystalline cellulose, starch
  • Disintegrants: Croscarmellose sodium, sodium starch glycolate
  • Lubricants: Magnesium stearate, stearic acid
  • Glidants: Colloidal silicon dioxide
  • Wetting Agents: Sodium lauryl sulfate

Liquid and Semisolid Fills

Hard capsules can also contain:

  • Oils: Vegetable oils for lipid-soluble drugs
  • Pastes: Thixotropic semisolids
  • Granules: For improved flow properties
  • Pellets: For modified release

Capsule Filling Methods

  1. Manual Filling: For small batches and clinical trials
  2. Auger Filling: Simple mechanical method
  3. Dosator Method: Piston-type filling
  4. Tamping Filling: Multiple tamping to compress powder
  5. Vacuum Filling: Using vacuum to draw powder into capsules

Important: Powder flow properties are critical for accurate capsule filling. Poor flow can lead to weight variation and content uniformity issues.

Part Two: Soft Gelatin Capsules

Author: J.P. Stanley

Soft Gelatin Capsules

Composition and Properties

Soft gelatin capsules (softgels) are one-piece, hermetically sealed capsules containing liquids, suspensions, or semisolids.

Component Function Typical Content
Gelatin Shell formation 40-50%
Plasticizer Flexibility 20-30%
Water Processing aid 20-30%
Colorants/Opacifiers Appearance, protection 1-2%
Preservatives Stability 0.1-0.2%

Plasticizers for Soft Gelatin Capsules

  • Glycerin: Most common, provides flexibility
  • Sorbitol: Alternative to glycerin
  • Polyethylene Glycol: For special applications
  • Propylene Glycol: Less commonly used

Manufacturing Methods

Soft gelatin capsules are manufactured by three main methods:

1. Plate Process

Traditional method using molds:

  • Gelatin sheets placed between plates with cavities
  • Fill material added
  • Plates pressed together to form capsules
  • Limited production capacity

2. Rotary Die Process

Most common commercial method:

  • Continuous process with rotating dies
  • Two gelatin ribbons formed
  • Fill material injected between ribbons
  • Capsules formed, filled, and sealed simultaneously
  • High production capacity

3. Reciprocating Die Process

Similar to rotary die but with reciprocating motion.

Formulation Considerations for Softgels

Fill Formulations

Softgels can contain various types of fills:

Fill Type Examples Considerations
Oils Vegetable oils, fish oils Most common, good compatibility
Suspensions Drugs in oils or PEG Particle size control needed
Solutions Drugs in PEG, surfactants Improved bioavailability
Pastes Thixotropic mixtures Specialized applications

Compatibility Issues

Important considerations for softgel formulations:

  • Water Migration: Fill should not extract water from shell
  • Solvent Action: Fill should not dissolve gelatin
  • pH Effects: Extreme pH can affect gelatin stability
  • Cross-linking: Aldehydes can cause gelatin cross-linking

Quality Control Tests

  • Shell Thickness: Uniformity of gelatin shell
  • Seal Integrity: Hermetic sealing of capsules
  • Fill Weight: Accurate dosing
  • Disintegration/Dissolution: Release characteristics
  • Stability: Physical and chemical stability
Part Three: Microencapsulation

Author: J.A. Bakan

Microencapsulation

Introduction

Microencapsulation is the process of enclosing microscopic particles or droplets in a coating material to produce microcapsules. These microcapsules can then be filled into capsules or compressed into tablets.

Microcapsule: A small sphere with a uniform coating around it. The material inside the microcapsule is referred to as the core, internal phase, or fill, while the wall is sometimes called a shell, coating, or membrane.

Reasons for Microencapsulation

  • Taste Masking: Bitter drugs can be encapsulated
  • Sustained Release: Controlled drug delivery
  • Stability Improvement: Protection from environment
  • Incompatibility Prevention: Separation of incompatible materials
  • Handling Improvement: Conversion of liquids to solids

Microencapsulation Methods

1. Coacervation/Phase Separation

Most common method for microencapsulation:

  1. Core material dispersed in polymer solution
  2. Phase separation induced by temperature, pH, or solvent addition
  3. Polyter deposits on core material
  4. Shell hardened by cross-linking or temperature change

2. Spray Drying

Rapid and economical method:

  • Core material dispersed in polymer solution
  • Mixture atomized into hot air
  • Solvent evaporates, forming microcapsules
  • Suitable for heat-stable materials

3. Pan Coating

For larger particles (600 microns and above):

  • Core particles tumbled in pan
  • Coating solution applied
  • Drying between applications
  • Multiple layers applied

4. Fluidized Bed Coating

Similar to pan coating but more efficient:

  • Particles fluidized by air
  • Coating solution sprayed
  • Uniform coating achieved
  • Suitable for wide size range

5. Interfacial Polymerization

For producing polymer shells:

  • Reactants meet at interface
  • Polymer forms at droplet surface
  • Produces strong, impermeable shells

Applications of Microencapsulation

Pharmaceutical Applications

Application Purpose Examples
Sustained Release Prolong drug action Antibiotics, analgesics
Taste Masking Improve palatability Antibiotics, vitamins
Stability Improvement Protect from moisture, oxygen Vitamins, enzymes
Targeted Delivery Site-specific release Cancer drugs
Incompatibility Prevention Separate reactive components Aspirin-antacid combinations

Coating Materials

Common materials used for microencapsulation:

  • Natural Polymers: Gelatin, gum arabic, alginates
  • Synthetic Polymers: Polyvinyl alcohol, polyvinyl pyrrolidone
  • Cellulose Derivatives: Ethyl cellulose, cellulose acetate phthalate
  • Waxes: Beeswax, carnauba wax
  • Lipids: Hydrogenated oils, fatty acids

Quality Control: Microcapsules must be evaluated for particle size distribution, drug content, release characteristics, and stability. Specialized equipment such as laser diffraction particle analyzers and dissolution apparatus are used for characterization.

Quality Control of Capsules

General Tests for All Capsules

  • Weight Variation: Individual capsule weights within limits
  • Content Uniformity: Drug content consistency
  • Disintegration Test: Capsules should disintegrate within specified time
  • Dissolution Test: Drug release characteristics
  • Moisture Content: Especially important for gelatin capsules
  • Stability Testing: Under various storage conditions

Specific Tests for Hard Capsules

  • Locking Strength: Capsule cap should not separate from body
  • Empty Capsule Weight: Consistency of shell weight
  • Dimensions: Length and diameter specifications

Specific Tests for Soft Capsules

  • Seal Integrity: No leakage of fill material
  • Shell Thickness: Uniform gelatin shell
  • Fill Volume: Accurate filling
  • Bloom Strength: Gelatin quality

Storage Conditions: Gelatin capsules are hygroscopic and should be stored in tightly closed containers at controlled temperature and humidity to prevent deformation or changes in disintegration time.

Recent Advances and Future Trends

1. Vegetarian Capsules

Alternative to gelatin capsules:

  • Hypromellose (HPMC): Most common vegetarian capsule material
  • Pullulan: Natural polysaccharide
  • Starch: Modified starch capsules
  • Carrageenan: Marine polysaccharide

2. Modified Release Capsules

Capsules designed for controlled release:

  • Enteric-coated capsules
  • Pulsatile release systems
  • Colon-targeted delivery

3. Liquid-Filled Hard Capsules

Combining advantages of hard and soft capsules:

  • Liquid fills in hard capsules
  • Improved bioavailability
  • Wider formulation options

4. Specialty Capsules

  • Inhalation Capsules: For dry powder inhalers
  • Rectal/Vaginal Capsules: For local delivery
  • Effervescent Capsules: Rapid disintegration

Future Directions: Smart capsules with electronic components for tracking, capsules with integrated sensors, and personalized medicine approaches with patient-specific capsule formulations.

Conclusion

Capsules represent a versatile and patient-friendly dosage form with applications ranging from conventional immediate release to sophisticated controlled delivery systems. The choice between hard and soft gelatin capsules depends on the physical and chemical properties of the drug, desired release profile, and manufacturing considerations. Microencapsulation extends the capabilities of capsule technology by enabling taste masking, stability improvement, and modified release. Quality control is essential throughout capsule manufacturing to ensure product safety, efficacy, and consistency. Advances in capsule technology continue to expand the therapeutic possibilities of this important dosage form.

Key Advantage: Capsules offer excellent patient compliance due to ease of swallowing, ability to mask unpleasant tastes, and rapid onset of action compared to some other oral dosage forms.