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Rapidly disintegrating tablets prepared by the wet compression method: mechanism and optimization.
1Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Tempaku-ku, Nagoya, Aichi 468-8503, Japan. d5971101@meijo-u.ac.jp
Journal of Pharmaceutical Sciences
|October 9, 1999
Summary
The wet compression method creates rapidly disintegrating tablets with adequate mechanical strength by optimizing lactose particle size and granule moisture. This technique ensures tablets achieve high tensile strength and quick disintegration times.
Area of Science:
- Pharmaceutical technology
- Materials science
Background:
- Developing rapidly disintegrating tablets with sufficient mechanical integrity is challenging.
- Traditional tablet manufacturing methods may not always achieve desired disintegration and strength properties simultaneously.
Purpose of the Study:
- To investigate the wet compression method for producing rapidly disintegrating tablets with adequate mechanical integrity.
- To determine the influence of various formulation and processing parameters on tablet properties.
Main Methods:
- Tablets were prepared using the wet compression method, involving compression of wet granules followed by drying.
- Lactose of varying particle sizes was used as the excipient, with water as the wetting agent.
- Parameters studied included drying time, compression force, lactose particle size, and granule moisture content.
Main Results:
- Tablet formation and disintegration time were found to be related to the formation of solid bridges between lactose particles.
- Optimizing compression force, lactose particle size, and granule moisture content was crucial for achieving desired tablet properties.
- Tablets meeting tensile strength >0.5 MPa and disintegration time <15 s were successfully produced.
Conclusions:
- The wet compression method is effective for manufacturing rapidly disintegrating tablets with good mechanical integrity.
- Careful optimization of particle size, moisture content, and compression force is key to successful tablet formulation using this method.
- This study provides a viable approach for producing high-quality oral dosage forms with improved patient compliance.