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Amorphous or Crystalline? A Comparison of Particle Engineering Methods and Selection
Sachin G Thakkar, Kristin Fathe, Hugh D C Smyth1
1Division of Pharmaceutics, College of Pharmacy, The University of Texas at Austin, TX 78712, Austin, USA. hugh.smyth@austin.utexas.edu.
This review critically examines particle engineering technologies for crystalline and amorphous particle production. It covers traditional and advanced methods, evaluating their characterization, limitations, and impact on bioavailability.
Area of Science:
- Pharmaceutical Technology
- Materials Science
- Chemical Engineering
Background:
- Particle engineering is crucial for controlling drug properties.
- Crystalline and amorphous forms offer distinct formulation advantages.
- Current technologies require critical evaluation for optimal production.
Purpose of the Study:
- To provide a critical review of particle engineering technologies.
- To discuss methods for producing crystalline and amorphous particles.
- To assess the impact of particle properties on bioavailability.
Main Methods:
- Review of traditional crystallization, supercritical fluid, spray drying, controlled solvent crystallization, and sonocrystallization.
- Presentation of advanced techniques: spray freezing into liquid, thin-film freeze-drying, and PRINT technology.
- Examination of characterization methods and their limitations.
Main Results:
- Detailed comparison of various particle engineering technologies.
- Analysis of the merits and limitations of each method.
- Discussion on the role of particle engineering in enhancing bioavailability.
Conclusions:
- Particle engineering offers diverse strategies for crystalline and amorphous particle production.
- Selection of appropriate technology depends on desired particle properties and formulation goals.
- Understanding technology limitations and characterization is key for successful drug development.
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