Mesoscopic solute-rich clusters in olanzapine solutions
Warzecha, Monika and Safari, Mohammad S. and Florence, Alastair J. and Vekilov, Peter G. (2017) Mesoscopic solute-rich clusters in olanzapine solutions. Crystal Growth and Design. pp. 6668-6676. ISSN 1528-7483 (https://doi.org/10.1021/acs.cgd.7b01299)
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Abstract
An organic molecule may crystallize in numerous distinct lattices, and the slow and unpredictable transitions between multiple crystal forms are a significant concern in its pharmaceutical application. Recent results indicate that the transformation of olanzapine (OZPN) from anhydrous to hydrate crystals is mediated by mesoscopic solute-rich clusters. Here we demonstrate the existence of such clusters in undersaturated OZPN solutions in purely aqueous and mixed EtOH/aqueous solvents. The clusters occupy about 10–8 to 10–7 of the solution volume and capture ca. 10–7 to 10–5 of the dissolved OZPN. The average cluster radius is steady in time at about 35 nm and independent of the OZPN concentration and the solvent composition, whereas the OZPN fraction captured in the clusters is dictated by the solution thermodynamics. Both behaviors are in dire conflict with classical theories of phase transformation and recent aggregation models. They are, however, consistent with the predictions of a model that assumes the formation of OZPN dimers and their decay upon exiting the clusters. We propose that a transient dimer, which may be akin to the centrosymmetric dimer present in all of the 60 known OZPN crystal structures, may underlie cluster formation. The finding of cluster formation in organic systems and the proposed cluster mechanism provide guidance toward enhanced control over nucleation, molecular transitions, and the solid forms in molecular systems.
ORCID iDs
Warzecha, Monika ORCID: https://orcid.org/0000-0001-6166-1089, Safari, Mohammad S., Florence, Alastair J. ORCID: https://orcid.org/0000-0002-9706-8364 and Vekilov, Peter G.;-
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Item type: Article ID code: 62293 Dates: DateEvent26 October 2017Published26 October 2017AcceptedNotes: This document is the Accepted Manuscript version of a Published Work that appeared in final form in Crystal Growth & Design, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.cgd.7b01299. Subjects: Science > Chemistry Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
Technology and Innovation Centre > Continuous Manufacturing and Crystallisation (CMAC)
Strategic Research Themes > Advanced Manufacturing and MaterialsDepositing user: Pure Administrator Date deposited: 09 Nov 2017 10:47 Last modified: 11 Nov 2024 11:50 URI: https://strathprints.strath.ac.uk/id/eprint/62293