Peer-Reviewed Journal Details
Mandatory Fields
Gniado, K,MacFhionnghaile, P,McArdle, P,Erxleben, A
2018
January
International Journal Of Pharmaceutics
The natural bile acid surfactant sodium taurocholate (NaTC) as a coformer in coamorphous systems: Enhanced physical stability and dissolution behavior of coamorphous drug-NaTc systems
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Amorphous Crystallization inhibition Dissolution studies Spectroscopy CO-AMORPHOUS SIMVASTATIN CITRIC-ACID MECHANICAL ACTIVATION CRYSTAL-STRUCTURES SOLID DISPERSIONS BINARY-SYSTEMS AMINO-ACIDS INDOMETHACIN STATE FORMULATIONS
535
132
139
The amorphization of 18 different drugs on milling with one mole equivalent sodium taurocholate (NaTC) was investigated. In all cases the X-ray powder pattern showed an amorphous halo after milling at room temperature or after cryomilling and 14 of the 18 coamorphous drug-NaTC systems were physically stable for between one to eleven months under ambient storage conditions. In three cases, namely carbamazepine-NaTC, indomethacin-NaTC and mefenamic acid-NaTC, significant dissolution advantages over the crystalline drugs were observed, both for the freshly prepared samples and after storage for seven months. To understand the increased physical stability, infrared-, near-infrared and Raman spectroscopic studies were carried out. The effectiveness of NaTC as a coformer in a diverse range of coamorphous systems is attributed to its awkward molecular shape that hampers recrystallization and phase separation and its propensity to form a range of similar, yet different drug-coformer hydrogen bonding arrangements.
10.1016/j.ijpharm.2017.10.049
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