Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jorma Haarala"'
Autor:
Bert van Veen, Jorma Haarala, Inna Miroshnyk, Anna Shevchenko, Lars-Olof Pietilä, Sabiruddin Mirza, Jouko Yliruusi, Erkki Kolehmainen, Nonappa, Jukka Salmia, Kai Sinervo
Publikováno v:
Crystal Growth and Design. 13(11):4877-4884
The cocrystal formation potential of itraconazole, a potent antifungal drug, with C2–C10 aliphatic dicarboxylic acids has been investigated. Using two experimental screening techniques (solvent-assisted grinding and evaporation-based crystallizatio
Publikováno v:
Crystal Growth & Design. 13:346-351
Exact knowledge of the crystal structure of drugs and lead compounds plays a significant role in the fields of crystal engineering, docking, computational modeling (drug–receptor interactions), and rational design of potent drugs in pharmaceutical
Autor:
Hélder A. Santos, Bert van Veen, Kristýna Jelínková, Kaisa Syrjänen, Luis M. Bimbo, Jouko Yliruusi, Inna Miroshnyk, Anna Shevchenko, Jorma Haarala, Juha Kiesvaara
Publikováno v:
International Journal of Pharmaceutics. 436:403-409
Cocrystallization and salt formation have been shown to entail substantial promise in tailoring the physicochemical properties of drug compounds, in particular, their dissolution and hygroscopicity. In this work, we report on the preparation and comp
Autor:
Arto Tolvanen, Jouko Yliruusi, Saara Tiittanen, Karjalainen Arto Johannes, Mäkelä Mikko, David Din Belle, Veli Pekka Tanninen, Anna Shevchenko, Jorma Haarala, Inna Miroshnyk
Publikováno v:
Organic Process Research & Development. 15:666-672
The need for effective solid-form screening approaches, especially designed for the early discovery phases, is well recognized within the pharmaceutical industry. Here we report on the early polymorphism and solvatomorphism evaluation of a new drug c
Publikováno v:
Analytica Chimica Acta. 542:178-185
A constrained total-line-shape (CTLS) fitting strategy for organic impurity analysis from 1H NMR spectra was developed and assessed by studying two examples. In general, total-line-shape fitting allows integration of overlapping lines without sufferi
Publikováno v:
Archiv der Pharmazie. 321:103-106
Decompositions of dithranol and butantrone (10-butyryldithranol) were studied in buffer solutions. Half lives at pH 9.4, 7.4 and 6.5 were 0.6, 1.2 and 3.0 h for dithranol, and 1.3, 15 and 30 h for butantrone, respectively. 1,8-Dihydroxyanthraquinone
Publikováno v:
ChemInform. 19
Decompositions of dithranol and butantrone (10-butyryldithranol) were studied in buffer solutions. Half lives at pH 9.4, 7.4 and 6.5 were 0.6, 1.2 and 3.0 h for dithranol, and 1.3, 15 and 30 h for butantrone, respectively. 1,8-Dihydroxyanthraquinone
Autor:
Harry G. Brittain
Profiles of Drug Substances, Excipients, and Related Methodology, Volume 44, presents comprehensive reviews of drug substances and additional materials, with critical review chapters that summarize information related to the characterization of drug