AI Article Synopsis

  • The study explores how solvents like ethanol, acetonitrile, and acetone affect the crystallization of irbesartan (IBS) in combination with 2,3-dibromosuccinic acid to create new pharmaceutical crystals with enhanced properties.
  • The researchers utilized techniques such as single-crystal diffraction and Hirshfeld surfaces analysis to determine the crystal structures and analyze intermolecular interactions, discovering two distinct IBS salts with unique crystallization patterns.
  • Findings indicated that both salts displayed different thermal behaviors, including variations in melting temperature and stability, which were supported by additional characterization methods like FT-IR and NMR.

Article Abstract

The design of new pharmaceutical solids with improved physical and chemical properties can be reached through in-detail knowledge of the noncovalent intermolecular interactions between the molecules in the context of crystal packing. Although crystallization from solutions is well-known for obtaining new solids, the effect of some variables on crystallization is not yet thoroughly understood. Among these variables, solvents are noteworthy. In this context, the present study aimed to investigate the effect of ethanol (EtOH), acetonitrile (MeCN), and acetone (ACTN) on obtaining irbesartan (IBS) crystal forms with 2,3-dibromosuccinic acid. Crystal structures were solved by single-crystal diffraction, and the intermolecular interactions were analyzed using the Hirshfeld surfaces analysis. The characterization of physicochemical properties was carried out by powder X-ray diffraction, Fourier transform infrared spectroscopy (FT-IR), thermal analysis, and solution-state NMR techniques. Two different IBS salts were obtained, one from MeCN and ACTN (compound ) and a different one from EtOH (compound ). The experimental results were in agreement with the findings obtained through quantum mechanics continuum solvation models. Compound crystallized as a monoclinic system 2/, whereas compound in a triclinic system 1̅. In both structures, a net of strong hydrogen bonds is present, and their existence was confirmed by the FT-IR results. In addition, the IBS cation acts as a H-bond donor through the N1 and N6 nitrogen atoms which interact with the bromide anion and the water molecule O1W in compound . Meanwhile, N1 and N6 nitrogen atoms interact with the oxygen atoms provided by two symmetry-related 2,3-dibromo succinate anions in compound . Solution-state NMR data agreed with the protonation of the imidazolone ring in the crystal structure of compound 1. Both salts presented a different thermal behavior not only in melting temperature but also in thermal stability.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089371PMC
http://dx.doi.org/10.1021/acsomega.2c00545DOI Listing

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