Thermal properties of hot-stage extrudates of itraconazole and eudragit E100 - Phase separation and polymorphism

Solid dispersions of itraconazole and eudragit E 100 were prepared by hot-stage extrusion. Analysis of the physical structure revealed the existence of different phases, depending on the manufacturing condition. Extrudates prepared at 453 K existed as a molecular dispersion of itraconazole in eudrag...

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Veröffentlicht in:Journal of thermal analysis and calorimetry 2002-01, Vol.68 (2), p.591-601
Hauptverfasser: Six, Karel, Leuner, C, Dressman, J, Verreck, G, Peeters, J, Blaton, Norbert, Augustijns, Patrick, Kinget, Renaat, Van den Mooter, Guy
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container_end_page 601
container_issue 2
container_start_page 591
container_title Journal of thermal analysis and calorimetry
container_volume 68
creator Six, Karel
Leuner, C
Dressman, J
Verreck, G
Peeters, J
Blaton, Norbert
Augustijns, Patrick
Kinget, Renaat
Van den Mooter, Guy
description Solid dispersions of itraconazole and eudragit E 100 were prepared by hot-stage extrusion. Analysis of the physical structure revealed the existence of different phases, depending on the manufacturing condition. Extrudates prepared at 453 K existed as a molecular dispersion of itraconazole in eudragit E100 when the drug concentration did not exceed ca. 13% mass/mass. At higher concentrations, a second phase consisting of pure glassy itraconazole emerged. In other dispersions prepared at 413 K, the second phase consisted of pure crystalline itraconazole. The difference can be attributed to the relation of the process-temperature to the melting point. Heating of both dispersions induced cold crystallization. Extrudates prepared at 453 K showed comparable behavior before and after milling, with the exception that unmilled dispersions with a drug load of greater than or equal to60% mass/mass recrystallized upon heating into a polymorphic modification of itraconazole (T-m = 431 K). Upon further heating the polymorph recrystallized to the stable crystalline form (T-m = 441 K).
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Analysis of the physical structure revealed the existence of different phases, depending on the manufacturing condition. Extrudates prepared at 453 K existed as a molecular dispersion of itraconazole in eudragit E100 when the drug concentration did not exceed ca. 13% mass/mass. At higher concentrations, a second phase consisting of pure glassy itraconazole emerged. In other dispersions prepared at 413 K, the second phase consisted of pure crystalline itraconazole. The difference can be attributed to the relation of the process-temperature to the melting point. Heating of both dispersions induced cold crystallization. Extrudates prepared at 453 K showed comparable behavior before and after milling, with the exception that unmilled dispersions with a drug load of greater than or equal to60% mass/mass recrystallized upon heating into a polymorphic modification of itraconazole (T-m = 431 K). 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title Thermal properties of hot-stage extrudates of itraconazole and eudragit E100 - Phase separation and polymorphism
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