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  • Alleso, MortenDepartment of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, and Department of Food Science, Faculty of Life Sciences, University of Copenhagen (författare)

Near-infrared spectroscopy for cocrystal screening : a comparative study with Raman spectroscopy

  • Artikel/kapitelEngelska2008

Förlag, utgivningsår, omfång ...

  • 2008-09-18
  • American Chemical Society (ACS),2008
  • printrdacarrier

Nummerbeteckningar

  • LIBRIS-ID:oai:DiVA.org:ltu-15646
  • https://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-15646URI
  • https://doi.org/10.1021/ac8011329DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:ref swepub-contenttype
  • Ämneskategori:art swepub-publicationtype

Anmärkningar

  • Validerad; 2008; 20081105 (ysko)
  • Near-infrared (NIR) spectroscopy is a well-established technique for solid-state analysis, providing fast, noninvasive measurements. The use of NIR spectroscopy for polymorph screening and the associated advantages have recently been demonstrated. The objective of this work was to evaluate the analytical potential of NIR spectroscopy for cocrystal screening using Raman spectroscopy as a comparative method. Indomethacin was used as the parent molecule, while saccharin and L-aspartic acid were chosen as guest molecules. Molar ratios of 1:1 for each system were subjected to two types of preparative methods. In the case of saccharin, liquid-assisted cogrinding as well as cocrystallization from solution resulted in a stable 1:1 cocrystalline phase termed IND-SAC cocrystal. For L-aspartic acid, the solution-based method resulted in a polymorphic transition of indomethacin into the metastable a form retained in a physical mixture with the guest molecule, while liquid-assisted cogrinding did not induce any changes in the crystal lattice. The good chemical peak selectivity of Raman spectroscopy allowed a straightforward interpretation of sample data by analyzing peak positions and comparing to those of pure references. In addition, Raman spectroscopy provided additional information on the crystal structure of the IND-SAC cocrystal. The broad spectral line shapes of NIR spectra make visual interpretation of the spectra difficult, and consequently, multivariate modeling by principal component analysis (PCA) was applied. Successful use of NIR/PCA was possible only through the inclusion of a set of reference mixtures of parent and guest molecules representing possible solid-state outcomes from the cocrystal screening. The practical hurdle related to the need for reference mixtures seems to restrict the applicability of NIR spectroscopy in cocrystal screening.

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Velaga, SitaramLuleå tekniska universitet,Medicinsk vetenskap(Swepub:ltu)sitvel (författare)
  • Alhalaweh, AmjadLuleå tekniska universitet,Medicinsk vetenskap(Swepub:ltu)amjalh (författare)
  • Cornett, ClausDepartment of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, and Department of Food Science, Faculty of Life Sciences, University of Copenhagen (författare)
  • Rasmussen, Morten A.Department of Food Science, Faculty of Life Sciences, University of Copenhagen (författare)
  • van den Berg, FransDepartment of Food Science, Faculty of Life Sciences, University of Copenhagen (författare)
  • de Diego, Heidi LopezAnalytical R and D, H. Lundbeck A/S (författare)
  • Rantanen, JukkaDepartment of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, University of Copenhagen (författare)
  • Department of Pharmaceutics and Analytical Chemistry, Faculty of Pharmaceutical Sciences, and Department of Food Science, Faculty of Life Sciences, University of CopenhagenMedicinsk vetenskap (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Analytical Chemistry: American Chemical Society (ACS)80:20, s. 7755-77640003-27001520-6882

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