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Solid state investigation of mefloquine hydrochloride
Journal of Pharmaceutical and Biomedical Analysis
|July 1, 1994
Summary
Different crystallization conditions yield various mefloquine hydrochloride crystal structures, including hydrates, polymorphs, and solvates. Some forms transform during storage or heat treatment, yielding new crystal structures.
Area of Science:
- Pharmaceutical Chemistry
- Solid-State Chemistry
Background:
- Mefloquine hydrochloride is an antimalarial drug.
- Understanding its solid-state properties is crucial for formulation and stability.
Purpose of the Study:
- To investigate the impact of crystallization conditions on mefloquine hydrochloride's solid forms.
- To characterize the resulting crystal structures and their stability.
Main Methods:
- Crystallization under varied conditions.
- Thermal analysis (e.g., DSC, TGA).
- Infrared (IR) spectroscopy.
- X-ray diffraction (XRD).
Main Results:
- Different crystallization conditions produced distinct crystal structures.
- Identified forms include hydrates (alpha, delta), polymorphs (beta, gamma), and solvates (epsilon - acetone, theta - tetrahydrofuran).
- Alpha, delta, and theta forms transformed during storage; heat treatment of delta, epsilon, and theta yielded a new structure.
Conclusions:
- Mefloquine hydrochloride exhibits polymorphism and solvation, influenced by crystallization parameters.
- The stability of different solid forms varies, with potential for transformation under storage or thermal stress.
- Controlled crystallization and heat treatment can generate novel crystal structures.