Polymorphism, pseudopolymorphism, and amorphism of hexakis(2,3,6-tri-O-acetyl)--cyclodextrin (TACyD), heptakis(2,3,6-tri-O-acetyl)--cyclodextrin (TACyD), and octakis(2,3,6-tri-O-acetyl)--cyclodextrin (TACyD) were investigated using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), powder X-ray diffractometry (XRPD), Fourier transform infrared spectroscopy (FTIR) and optical microscopy. An anhydrous and a bi-hydrate crystalline forms of TACyD, two monotropic anhydrous polymorphs and three pseudopolymorphs (i.e. methanolate, hydrate, and isopropanolate-hydrate) of TACyD, as well as two monotropic anhydrous polymorphs and isostructural pseudopolymorphs (e.g. hydrate and isopropanolate-hydrate) of TACyD were isolated and characterized. The amorphous forms of each TACyD were also obtained. Thermal data for desolvation of TACyD·2H2O and TACyD·CH3OH were reconciled with their crystal packing features. Melting temperatures and enthalpies of the crystalline forms of each TACyD can be referred to for possible solid-state interactions with drugs.

Polymorphism, pseudopolymorphism and amorphism of peracetylated alpha-, beta- and gamma cyclodextrins

BETTINETTI, GIAMPIERO;SORRENTI, MILENA LILLINA;CATENACCI, LAURA;FERRARI, FRANCA;ROSSI, SILVIA STEFANIA
2006-01-01

Abstract

Polymorphism, pseudopolymorphism, and amorphism of hexakis(2,3,6-tri-O-acetyl)--cyclodextrin (TACyD), heptakis(2,3,6-tri-O-acetyl)--cyclodextrin (TACyD), and octakis(2,3,6-tri-O-acetyl)--cyclodextrin (TACyD) were investigated using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), powder X-ray diffractometry (XRPD), Fourier transform infrared spectroscopy (FTIR) and optical microscopy. An anhydrous and a bi-hydrate crystalline forms of TACyD, two monotropic anhydrous polymorphs and three pseudopolymorphs (i.e. methanolate, hydrate, and isopropanolate-hydrate) of TACyD, as well as two monotropic anhydrous polymorphs and isostructural pseudopolymorphs (e.g. hydrate and isopropanolate-hydrate) of TACyD were isolated and characterized. The amorphous forms of each TACyD were also obtained. Thermal data for desolvation of TACyD·2H2O and TACyD·CH3OH were reconciled with their crystal packing features. Melting temperatures and enthalpies of the crystalline forms of each TACyD can be referred to for possible solid-state interactions with drugs.
2006
Chemistry & Analysis covers research on natural and laboratory syntheses, chemical structure, structure-function relationship, isolation and analyses of biologically significant molecules, medicinal and food chemistry. Technical material describing crucial chemical methods in biochemical analysis and research is also placed in this category. Resources covering general biochemistry and natural metabolic pathways are excluded.
Esperti anonimi
Inglese
Internazionale
STAMPA
41
4
1205
1211
7
Sistemi microparticellari per il rilascio controllato sito-specifico di antinfettivi glicopeptidici
Peracetylated cyclodextrins; Differential Scanning Calorimetry; Thermogravimetric Analysis; Powder Xray diffractometry; Fourier Transform Infrared Spectroscopy
no
5
info:eu-repo/semantics/article
262
Bettinetti, Giampiero; Sorrenti, MILENA LILLINA; Catenacci, Laura; Ferrari, Franca; Rossi, SILVIA STEFANIA
1 Contributo su Rivista::1.1 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/133803
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