Co-amorphous systems consisting of indomethacin and the chiral co-former tryptophan: Solid-state properties and molecular mobilities

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Co-amorphous systems consisting of indomethacin and the chiral co-former tryptophan : Solid-state properties and molecular mobilities. / Holzapfel, Katharina; Rades, Thomas; Leopold, Claudia S.

In: International Journal of Pharmaceutics, Vol. 636, 122840, 2023.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Holzapfel, K, Rades, T & Leopold, CS 2023, 'Co-amorphous systems consisting of indomethacin and the chiral co-former tryptophan: Solid-state properties and molecular mobilities', International Journal of Pharmaceutics, vol. 636, 122840. https://doi.org/10.1016/j.ijpharm.2023.122840

APA

Holzapfel, K., Rades, T., & Leopold, C. S. (2023). Co-amorphous systems consisting of indomethacin and the chiral co-former tryptophan: Solid-state properties and molecular mobilities. International Journal of Pharmaceutics, 636, [122840]. https://doi.org/10.1016/j.ijpharm.2023.122840

Vancouver

Holzapfel K, Rades T, Leopold CS. Co-amorphous systems consisting of indomethacin and the chiral co-former tryptophan: Solid-state properties and molecular mobilities. International Journal of Pharmaceutics. 2023;636. 122840. https://doi.org/10.1016/j.ijpharm.2023.122840

Author

Holzapfel, Katharina ; Rades, Thomas ; Leopold, Claudia S. / Co-amorphous systems consisting of indomethacin and the chiral co-former tryptophan : Solid-state properties and molecular mobilities. In: International Journal of Pharmaceutics. 2023 ; Vol. 636.

Bibtex

@article{86d769051c62461eb0e148a97f04efc9,
title = "Co-amorphous systems consisting of indomethacin and the chiral co-former tryptophan: Solid-state properties and molecular mobilities",
abstract = "In this study the influence of an enantiomeric co-former and the preparation method on the solid-state properties and physical stability of co-amorphous systems were investigated. Co-amorphous systems consisting of indomethacin (IND) and chiral tryptophan (TRP) as co-former in its two enantiomeric forms, as racemate, and as conglomerate (equimolar mixture of D- and L-TRP) were prepared. Co-amorphization was achieved by ball milling (BM) and spray drying (SD). The effects of chirality and preparation method on the solid-state properties and physical stabilities of the systems were investigated by XRPD, FTIR and mDSC. Differences in the BM process were caused by the enantiomeric properties of the co-former: The IND/TRP conglomerate (IND/TRPc) turned co-amorphous after 60 min. In contrast, co-amorphization of IND/L-TRP and IND/D-TRP required 80 min of ball milling, respectively, and the co-amorphous IND/TRP racemate (IND/TRPr) was obtained only after 90 min of ball milling. Although the intermolecular interactions of the co-amorphous systems prepared by BM and SD were similar (determined by FTIR), the Tg values differed (∼87 °C for the ball milled and ∼62 °C for the spray dried systems). The physical stabilities of the ball milled co-amorphous systems varied between 3 and 11 months if stored at elevated temperature and dry conditions, with the highest stability for the IND/TRPc system and the lowest stability for the IND/TRPr system, and these differences correlated with the calculated relaxation times. In contrast, all spray dried systems were stable only for 1 month and their relaxation times were similar. It could be shown that the chirality of a co-former and the preparation method influence the solid-state properties, thermal properties and physical stability of IND/TRP systems.",
keywords = "Chirality, Co-amorphous, Glass transition temperature, Intermolecular interactions, Molecular mobility, Physical stability",
author = "Katharina Holzapfel and Thomas Rades and Leopold, {Claudia S.}",
note = "Funding Information: The authors would like to thank Isabelle Nevoigt and Stefan Bleck for performing the XRPD and the mDSC measurements, respectively. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. ",
year = "2023",
doi = "10.1016/j.ijpharm.2023.122840",
language = "English",
volume = "636",
journal = "International Journal of Pharmaceutics",
issn = "0378-5173",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Co-amorphous systems consisting of indomethacin and the chiral co-former tryptophan

T2 - Solid-state properties and molecular mobilities

AU - Holzapfel, Katharina

AU - Rades, Thomas

AU - Leopold, Claudia S.

N1 - Funding Information: The authors would like to thank Isabelle Nevoigt and Stefan Bleck for performing the XRPD and the mDSC measurements, respectively. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

PY - 2023

Y1 - 2023

N2 - In this study the influence of an enantiomeric co-former and the preparation method on the solid-state properties and physical stability of co-amorphous systems were investigated. Co-amorphous systems consisting of indomethacin (IND) and chiral tryptophan (TRP) as co-former in its two enantiomeric forms, as racemate, and as conglomerate (equimolar mixture of D- and L-TRP) were prepared. Co-amorphization was achieved by ball milling (BM) and spray drying (SD). The effects of chirality and preparation method on the solid-state properties and physical stabilities of the systems were investigated by XRPD, FTIR and mDSC. Differences in the BM process were caused by the enantiomeric properties of the co-former: The IND/TRP conglomerate (IND/TRPc) turned co-amorphous after 60 min. In contrast, co-amorphization of IND/L-TRP and IND/D-TRP required 80 min of ball milling, respectively, and the co-amorphous IND/TRP racemate (IND/TRPr) was obtained only after 90 min of ball milling. Although the intermolecular interactions of the co-amorphous systems prepared by BM and SD were similar (determined by FTIR), the Tg values differed (∼87 °C for the ball milled and ∼62 °C for the spray dried systems). The physical stabilities of the ball milled co-amorphous systems varied between 3 and 11 months if stored at elevated temperature and dry conditions, with the highest stability for the IND/TRPc system and the lowest stability for the IND/TRPr system, and these differences correlated with the calculated relaxation times. In contrast, all spray dried systems were stable only for 1 month and their relaxation times were similar. It could be shown that the chirality of a co-former and the preparation method influence the solid-state properties, thermal properties and physical stability of IND/TRP systems.

AB - In this study the influence of an enantiomeric co-former and the preparation method on the solid-state properties and physical stability of co-amorphous systems were investigated. Co-amorphous systems consisting of indomethacin (IND) and chiral tryptophan (TRP) as co-former in its two enantiomeric forms, as racemate, and as conglomerate (equimolar mixture of D- and L-TRP) were prepared. Co-amorphization was achieved by ball milling (BM) and spray drying (SD). The effects of chirality and preparation method on the solid-state properties and physical stabilities of the systems were investigated by XRPD, FTIR and mDSC. Differences in the BM process were caused by the enantiomeric properties of the co-former: The IND/TRP conglomerate (IND/TRPc) turned co-amorphous after 60 min. In contrast, co-amorphization of IND/L-TRP and IND/D-TRP required 80 min of ball milling, respectively, and the co-amorphous IND/TRP racemate (IND/TRPr) was obtained only after 90 min of ball milling. Although the intermolecular interactions of the co-amorphous systems prepared by BM and SD were similar (determined by FTIR), the Tg values differed (∼87 °C for the ball milled and ∼62 °C for the spray dried systems). The physical stabilities of the ball milled co-amorphous systems varied between 3 and 11 months if stored at elevated temperature and dry conditions, with the highest stability for the IND/TRPc system and the lowest stability for the IND/TRPr system, and these differences correlated with the calculated relaxation times. In contrast, all spray dried systems were stable only for 1 month and their relaxation times were similar. It could be shown that the chirality of a co-former and the preparation method influence the solid-state properties, thermal properties and physical stability of IND/TRP systems.

KW - Chirality

KW - Co-amorphous

KW - Glass transition temperature

KW - Intermolecular interactions

KW - Molecular mobility

KW - Physical stability

U2 - 10.1016/j.ijpharm.2023.122840

DO - 10.1016/j.ijpharm.2023.122840

M3 - Journal article

C2 - 36921746

AN - SCOPUS:85150301164

VL - 636

JO - International Journal of Pharmaceutics

JF - International Journal of Pharmaceutics

SN - 0378-5173

M1 - 122840

ER -

ID: 341261412