Next Article in Journal
Synergistic Effects Between Mixed Plastics and Their Impact on Pyrolysis Behavior and Pyrolysis Products
Next Article in Special Issue
Mixed Halide Isothiocyanate Tin(II) Compounds, SnHal(NCS): Signs of Tetrel Bonds as Bifurcated Extensions of Long-Range Asymmetric 3c-4e Bonds
Previous Article in Journal
Enhancement of Thermochemical Energy Storage by Alkali Metal Chloride Salts-Doped Ca-Based Sorbents: A Combined DFT and Experimental Study
Previous Article in Special Issue
Design, Synthesis and Crystal Structure of a Novel Fluorescence Probe for Zn2+ Based on Pyrano[3,2-c] Carbazole
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Apremilast Cocrystals with Phenolic Coformers

1
Department of Solid State Chemistry, University of Chemistry and Technology, Prague, Technicka 5, 16628 Prague, Czech Republic
2
Chemical Engineering Department, National Research Tomsk Polytechnic University, Lenin Avenue 30, 634050 Tomsk, Russia
*
Author to whom correspondence should be addressed.
Molecules 2024, 29(24), 6060; https://doi.org/10.3390/molecules29246060
Submission received: 31 October 2024 / Revised: 14 December 2024 / Accepted: 17 December 2024 / Published: 23 December 2024

Abstract

Apremilast (APR) is an anti-inflammatory drug commonly used in the treatment of psoriasis. In efforts to enhance its solubility, several cocrystals with similar structural features have been developed. This study investigates the cocrystallization of APR with four phenolic-type coformers: phenol, catechol, pyrogallol, and hydroxyquinol. These coformers differ in the number and position of their hydroxyl groups, with their melting points varying by as much as 100 °C. Four novel cocrystal forms were synthesized, purified, and characterized using X-Ray diffraction and thermal analysis techniques. Surprisingly, the resulting cocrystals exhibited minimal differences in their melting points. The molecular packing of APR appears to limit the network-forming potential of the hydroxyl groups, a conclusion supported by the solved crystal structures, Hirshfeld surface analysis, and differential scanning calorimetry (DSC) results.
Keywords: cocrystals; Apremilast; phenolic compounds; π–π interactions; hydrogen bonds cocrystals; Apremilast; phenolic compounds; π–π interactions; hydrogen bonds

Share and Cite

MDPI and ACS Style

Naumkina, Y.; Kratochvíl, B.; Korotkova, E.; Čejka, J. Apremilast Cocrystals with Phenolic Coformers. Molecules 2024, 29, 6060. https://doi.org/10.3390/molecules29246060

AMA Style

Naumkina Y, Kratochvíl B, Korotkova E, Čejka J. Apremilast Cocrystals with Phenolic Coformers. Molecules. 2024; 29(24):6060. https://doi.org/10.3390/molecules29246060

Chicago/Turabian Style

Naumkina, Yelizaveta, Bohumil Kratochvíl, Elena Korotkova, and Jan Čejka. 2024. "Apremilast Cocrystals with Phenolic Coformers" Molecules 29, no. 24: 6060. https://doi.org/10.3390/molecules29246060

APA Style

Naumkina, Y., Kratochvíl, B., Korotkova, E., & Čejka, J. (2024). Apremilast Cocrystals with Phenolic Coformers. Molecules, 29(24), 6060. https://doi.org/10.3390/molecules29246060

Article Metrics

Back to TopTop