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@article{1800801, author = {Muselík, Jan and Urbanova, M. and Bartonickova, E. and Palovcik, J. and Vetchý, David and Czernek, J. and Janisova, L. and Velychkivska, N. and Franc, Aleš and Brus, J.}, article_location = {BASEL}, article_number = {9}, doi = {http://dx.doi.org/10.3390/pharmaceutics13091364}, keywords = {warfarin; solid-state NMR; polymorphism; stability; particle size; bioavailability; generic substitution}, language = {eng}, issn = {1999-4923}, journal = {Pharmaceutics}, title = {Structural Changes of Sodium Warfarin in Tablets Affecting the Dissolution Profiles and Potential Safety of Generic Substitution}, url = {https://www.mdpi.com/1999-4923/13/9/1364/htm}, volume = {13}, year = {2021} }
TY - JOUR ID - 1800801 AU - Muselík, Jan - Urbanova, M. - Bartonickova, E. - Palovcik, J. - Vetchý, David - Czernek, J. - Janisova, L. - Velychkivska, N. - Franc, Aleš - Brus, J. PY - 2021 TI - Structural Changes of Sodium Warfarin in Tablets Affecting the Dissolution Profiles and Potential Safety of Generic Substitution JF - Pharmaceutics VL - 13 IS - 9 SP - 1-19 EP - 1-19 PB - MDPI SN - 19994923 KW - warfarin KW - solid-state NMR KW - polymorphism KW - stability KW - particle size KW - bioavailability KW - generic substitution UR - https://www.mdpi.com/1999-4923/13/9/1364/htm N2 - At present, the risk of generic substitutions in warfarin tablets is still being discussed. The aim of this study was to assess whether API interactions with commonly used excipients may affect the safety of generic replacement of warfarin sodium tablets. These interactions were observed during an accelerated stability study, and the effect of the warfarin solid phase (crystalline/amorphous form) as well as the API particle size distribution was studied. Commercial tablets and prepared tablets containing crystalline warfarin or amorphous warfarin were used. In addition, binary mixtures of warfarin with various excipients were prepared. The structural changes before and after the stability study were monitored by dissolution test in different media, solid-state NMR spectroscopy and Raman microscopy. During the stability study, the conversion of the sodium in warfarin to its acid form was demonstrated by some excipients (e.g., calcium phosphate). This change in the solid phase of warfarin leads to significant changes in dissolution, especially with the different particle sizes of the APIs in the tablet. Thus, the choice of suitable excipients and particle sizes are critical factors influencing the safety of generic warfarin sodium tablets. ER -
MUSELÍK, Jan, M. URBANOVA, E. BARTONICKOVA, J. PALOVCIK, David VETCHÝ, J. CZERNEK, L. JANISOVA, N. VELYCHKIVSKA, Aleš FRANC a J. BRUS. Structural Changes of Sodium Warfarin in Tablets Affecting the Dissolution Profiles and Potential Safety of Generic Substitution. \textit{Pharmaceutics}. BASEL: MDPI, 2021, roč.~13, č.~9, s.~1-19. ISSN~1999-4923. Dostupné z: https://dx.doi.org/10.3390/pharmaceutics13091364.
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