TY - JOUR
T1 - Difluprednate
T2 - More than meets the eye
AU - Giacobbe, Carlotta
AU - Palmisano, Giovanni
AU - Giovenzana, Giovanni B.
AU - Giovannelli, Lorella
AU - Negri, Roberto
AU - Masciocchi, Norberto
N1 - Publisher Copyright:
© 2014 Elsevier B.V..
PY - 2015/1/5
Y1 - 2015/1/5
N2 - Difluprednate, a FDA approved topical corticosteroid indicated for the treatment of inflammation and pain associated with ocular surgery, affords three polymorphic crystal forms (one hexagonal, sg. P65, and two distinct orthorhombic, both sg.'s P212121, phases), whose preparation, thermal stability ranges, crystal structures and stereochemical preferences are here reported. Using DSC, single-crystal structural analysis and less conventional ab-initio X-ray powder diffraction methods, the rich structural and thermal behavior of three difluprednate polymorphs have been clarified, and the validity of previous complex and sometimes contradicting literature reports has been challenged. Complementary solution state NMR provided 1H, 13C and 19F chemical shifts full assignment of the corresponding signals. These results allow us to precisely describe the selective isolation pathways toward three distinct crystal phases, and to define their structural and analytical data necessary for identification and easy and accurate quantification, by modern Rietveld analysis, of complex difluprednate polymorphic mixtures, often obtained as a result of poorly controlled (co)-precipitation methods.
AB - Difluprednate, a FDA approved topical corticosteroid indicated for the treatment of inflammation and pain associated with ocular surgery, affords three polymorphic crystal forms (one hexagonal, sg. P65, and two distinct orthorhombic, both sg.'s P212121, phases), whose preparation, thermal stability ranges, crystal structures and stereochemical preferences are here reported. Using DSC, single-crystal structural analysis and less conventional ab-initio X-ray powder diffraction methods, the rich structural and thermal behavior of three difluprednate polymorphs have been clarified, and the validity of previous complex and sometimes contradicting literature reports has been challenged. Complementary solution state NMR provided 1H, 13C and 19F chemical shifts full assignment of the corresponding signals. These results allow us to precisely describe the selective isolation pathways toward three distinct crystal phases, and to define their structural and analytical data necessary for identification and easy and accurate quantification, by modern Rietveld analysis, of complex difluprednate polymorphic mixtures, often obtained as a result of poorly controlled (co)-precipitation methods.
KW - Crystal structure
KW - Difluprednate
KW - Phase transitions
KW - Polymorphism
KW - Powder diffraction
UR - http://www.scopus.com/inward/record.url?scp=84908430618&partnerID=8YFLogxK
U2 - 10.1016/j.jpba.2014.09.028
DO - 10.1016/j.jpba.2014.09.028
M3 - Article
SN - 0731-7085
VL - 102
SP - 305
EP - 313
JO - Journal of Pharmaceutical and Biomedical Analysis
JF - Journal of Pharmaceutical and Biomedical Analysis
ER -