Related Experiment Video
Updated: Aug 5, 2025

Fabricating Superhydrophobic Polymeric Materials for Biomedical Applications
Published on: August 28, 2015
Perspectives on the Wetting of Solids in Pharmaceutical Systems
1Seventh Street Development Group, PO Box 251, Kure Beach, NC, 24889, 765-650-4462, USA. ann.newman@seventhstreetdev.com.
Understanding pharmaceutical solid wettability is key for drug development. Surface properties like energetics, heterogeneities, and pore structure significantly influence how well drug formulations interact with water.
Area of Science:
- Pharmaceutical Sciences
- Materials Science
- Physical Chemistry
Background:
- Wettability of pharmaceutical solids by water is crucial for solid dosage form processing and administration.
- Nonpolar pharmaceutical solids present challenges in achieving adequate wetting.
Purpose of the Study:
- To review and analyze factors influencing the wettability of pharmaceutical solids.
- To emphasize the thermodynamic principles and practical considerations for improving wettability.
Main Methods:
- Thermodynamic analysis of liquid surface tension and solid surface energetics.
- Evaluation of contact angle and solid surface polarity.
- Analysis of various factors affecting surface energetics and structure.
Main Results:
- Ideal wettability depends on liquid surface tension and solid surface energetics (contact angle, polarity).
- Crystal defects, polymorphism, amorphous structures, surface roughness, and pore complexity significantly alter surface energetics.
- Case studies demonstrated wettability in single, binary, and multicomponent pharmaceutical systems.
Conclusions:
- Modifying solid surface energetics, chemical/physical heterogeneities, and pore structure is essential for enhancing pharmaceutical wettability.
- A comprehensive understanding of these factors is critical for successful drug formulation development.
Related Concept Videos
Factors Influencing Drug Absorption: Pharmaceutical Parameters
Theories of Dissolution: The Danckwerts' Model and Interfacial Barrier Model
Factors Affecting Dissolution: Particle Size and Effective Surface Area
Factors Affecting Dissolution: Drug pKa, Lipophilicity and GI pH
A drug's pKa and the pH of the gastrointestinal (GI) tract play crucial roles...
Factors Influencing Drug Absorption: Drug Dissolution
Theories of Dissolution: Diffusion Layer Model
This process starts with a thin layer, saturated with the drug, forming at the interface between the solid and liquid. The solute then diffuses from this layer into the main solution. The Noyes-Whitney equation suggests that the rate of dissolution relies on the diffusion...

