AI Article Synopsis

  • The study analyzed metronidazole (MNZ) cocrystal polymorphs with gallic and gentisic acids, exploring how different solvent properties affect their formation.
  • Solvents with higher polarity led to a stable cocrystal form, while less polar solvents produced a metastable form that was only slightly less stable in energy.
  • The researchers also discovered a new high-temperature polymorph of the MNZ-GNT system and found that molecular electrostatic potentials can help in selecting coformers in future cocrystal studies.

Article Abstract

In this study, key features of metronidazole (MNZ) cocrystal polymorphs with gallic acid (GAL) and gentisic acid (GNT) were elucidated. Solvent-mediated phase transformation experiments in 30 solvents with varying properties were employed to control the polymorphic behavior of the MNZ cocrystal with GAL. Solvents with relative polarity (RP) values above 0.35 led to cocrystal I°, the thermodynamically stable form. Conversely, solvents with RP values below 0.35 produced cocrystal II, which was found to be only 0.3 kJ mol less stable in enthalpy. The feasibility of electrospraying, including solvent properties and process conditions required, and spray drying techniques to control cocrystal polymorphism was also investigated, and these techniques were found to facilitate exclusive formation of the metastable MNZ-GAL cocrystal II. Additionally, the screening approach resulted in a new, high-temperature polymorph I of the MNZ-GNT cocrystal system, which is enantiotropically related to the already known form II°. The intermolecular energy calculations, as well as the 2D similarity between the MNZ-GAL polymorphs and the 3D similarity between MNZ-GNT polymorphs, rationalized the observed transition behaviors. Furthermore, the evaluation of virtual cocrystal screening techniques identified molecular electrostatic potential calculations as a supportive tool for coformer selection.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626573PMC
http://dx.doi.org/10.1021/acs.cgd.3c00951DOI Listing

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Article Synopsis
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