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Solvated Crystalline Forms of Nevirapine: Thermoanalytical and Spectroscopic Studies.

Authors :
Chadha, Renu
Arora, Poonam
Saini, Anupam
Jain, Dharamvir
Source :
AAPS PharmSciTech; Sep2010, Vol. 11 Issue 3, p1328-1339, 12p
Publication Year :
2010

Abstract

The study is aimed at exploring the utility of thermoanalytical methods in the solid-state characterization of various crystalline forms of nevirapine. The different forms obtained by recrystallization of nevirapine from various solvents were identified using differential scanning calorimetry and thermogravimetric analysis (TGA). The appearance of desolvation peak accompanied by weight loss in TGA indicated the formation of solvates: hemi-ethanolate (Form I), hemi-acetonitrilate (Form II), hemi-chloroformate (Form III), hemi-THF solvate (Form IV), mixed hemi-ethanolate hemi-hydrate (Form V), and hemi-toluenate (Form VI). The higher desolvation temperatures of all the solvates except toluenate than their respective boiling point indicate tighter binding of solvent. Emphasis has been laid on the determination of heat capacity and heat of solution utilizing microreaction calorimeter to further distinguish the various forms. The enthalpy of solution (Δ H), an indirect measure of the lattice energy of a solid, was well correlated with the crystallinity of all the solid forms obtained. The magnitude of Δ H was found to be −14.14 kJ/mol for Form I and −2.83 kJ/mol for Form V in phosphate buffer of pH 2, exhibiting maximum ease of molecular release from the lattice in Form I. The heat capacity for solvation (Δ C) was found to be positive, providing information about the state of solvent molecules in the host lattice. The solubility and dissolution rate of the forms were also found to be in agreement with their enthalpy of solution. Form (I), being the most exothermic, was found to be the most soluble of all the forms. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15309932
Volume :
11
Issue :
3
Database :
Complementary Index
Journal :
AAPS PharmSciTech
Publication Type :
Academic Journal
Accession number :
55023488
Full Text :
https://doi.org/10.1208/s12249-010-9511-z