Publication Type Journal Article
Title New Thermoresistant Polymorph from CO2 Recrystallization of Minocycline Hydrochloride
Authors Miguel Rodrigues Joao M. Tiago Luis Padrela Henrique A. Matos Teresa G. Nunes Lidia Pinheiro Antonio J. Almeida Edmundo Azevedo
Groups MET BioMol
Journal PHARMACEUTICAL RESEARCH
Year 2014
Month November
Volume 31
Number 11
Pages 3136-3149
Abstract To prepare and thoroughly characterize a new polymorph of the broad-spectrum antibiotic minocycline from its hydrochloride dehydrate salts. The new minocycline hydrochloride polymorph was prepared by means of the antisolvent effect caused by carbon dioxide. Minocycline recrystallized as a red crystalline hydrochloride salt, starting from solutions or suspensions containing CO2 and ethanol under defined conditions of temperature, pressure and composition. This novel polymorph (beta-minocycline) revealed characteristic PXRD and FTIR patterns and a high melting point (of 247 A(0)C) compared to the initial minocycline hydrochloride hydrates (alpha-minocycline). Upon dissolution the new polymorph showed full anti-microbial activity. Solid-state NMR and DSC studies evidenced the higher chemical stability and crystalline homogeneity of beta-minocycline compared to the commercial chlorohydrate powders. Molecular structures of both minocyclines present relevant differences as shown by multinuclear solid-state NMR. This work describes a new crystalline structure of minocycline and evidences the ability of ethanol-CO2 system in removing water molecules from the crystalline structure of this API, at modest pressure, temperature and relatively short time (2 h), while controlling the crystal habit. This process has therefore the potential to become a consistent alternative towards the control of the solid form of APIs.
DOI http://dx.doi.org/10.1007/s11095-014-1406-3
ISBN
Publisher SPRINGER/PLENUM PUBLISHERS
Book Title
ISSN 0724-8741
EISSN 1573-904X
Conference Name
Bibtex ID ISI:000344554000019
Observations
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