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  First Evidence of Polymorphism in Furosemide Solvates

Beloborodova, A. A., Minkov, V. S., Rychkov, D. A., Rybalova, T. V., & Boldyreva, E. V. (2017). First Evidence of Polymorphism in Furosemide Solvates. Crystal Growth & Design, 17(5), 2333-2341. doi:10.1021/acs.cgd.6b01191.

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 Creators:
Beloborodova, Alina A.1, Author
Minkov, V. S.2, Author           
Rychkov, Denis A.1, Author
Rybalova, Tatyana V.1, Author
Boldyreva, Elena V.1, Author
Affiliations:
1external, ou_persistent22              
2High Pressure Group, Max Planck Institute for Chemistry, Max Planck Society, ou_1826289              

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 Abstract: Several polymorphs of solvates of furosemide with dimethyl sulfoxide (DMSO) and dimethylformamide (DMF) have been obtained, and their crystal structures were solved and analyzed. The structures differ from each other in both conformation of the furosemide molecule (particularly with respect to the orientation of the furanylmethylamino fragment) and molecular packing. The arrangement of solvent molecules—DMSO and DMF—is different in different polymorphs: either in the channels or between the layers. Layered polymorphs can be formed on rapid crystallization using water as an antisolvent, whereas a slower crystallization on evaporation promotes the growth of channeled structures. Despite different crystal structures, F-DMSO-I, F-DMSO-II, F-DMSO-III, and F-DMF-II give the same phase on desolvation, namely, furosemide polymorph I, which is the thermodynamic form at ambient conditions.

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 Dates: 2017
 Publication Status: Issued
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 Rev. Type: -
 Identifiers: ISI: 000400802500006
DOI: 10.1021/acs.cgd.6b01191
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Title: Crystal Growth & Design
  Other : Cryst. Growth Des.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 17 (5) Sequence Number: - Start / End Page: 2333 - 2341 Identifier: ISSN: 1528-7483
CoNE: https://pure.mpg.de/cone/journals/resource/110978984570353