crystal solvates
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2020 ◽  
Vol 43 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Jonathan O. Bauer

AbstractStructural investigations of molecular crystal solvates can provide important information for the targeted crystallization of particular inclusion compounds. Here, the crystal structure of the first ether solvate of hexaphenyldistannane [(Ph3Sn)2 • 2 THF] is reported. Structural features in terms of host-guest interactions and in the context of the previously reported polymorphs and solvates of (Ph3Sn)2 are discussed.



2019 ◽  
Vol 19 (7) ◽  
pp. 3660-3669 ◽  
Author(s):  
Ivan V. Fedyanin ◽  
Konstantin A. Lyssenko ◽  
Leonid L. Fershtat ◽  
Nikita V. Muravyev ◽  
Nina N. Makhova


INDIAN DRUGS ◽  
2018 ◽  
Vol 55 (05) ◽  
pp. 31-36
Author(s):  
P. M. Walvekar ◽  

Fluconazole (anhydrate) is an anti-fungal agent which exists in various polymorphic forms. The present study is an attempt to obtain crystal solvates of fluconazole using various solvents and study its effect on polymorphic transformation and its implication on solubility and dissolution. fluconazole exhibits polymorphism and is poorly soluble in water, hence attempt was made to improve its solubility and dissolution. Crystal solvates of fluconazole were prepared in different solvents viz acetonitrile, methanol, propan-2-d and n-butanol. Polymorphic transformations were ascertained by subjecting the crystal solvates of fluconazole to BCS solubility, dissolution, FTIR, optical microscopy, DSC, SEM and X-ray powder diffraction (XRPD). Results indicated that the crystal solvates of propan-2-ol exhibited improved solubility and dissolution compared to other crystal solvates and pure drug. BCS based intrinsic solubility studies revealed that crystal solvates of propan-2-ol exhibited highest solubility at pH 1.2. FTIR studies revealed that the functional groups of fluconazole were found to be unaltered. Optical microscopy and scanning electron microscopy studies revealed morphological changes of crystal solvates, which indicates polymorphic changes of fluconazole. DSC of crystal solvates obtained from propan-2-ol revealed change to hydrate form, whereas XRPD study revealed crystal solvates of propan-2-ol were more crystalline in nature when compared with that of the pure drug.



2017 ◽  
Vol 251 ◽  
pp. 858-868 ◽  
Author(s):  
A.A. Ksenofontov ◽  
G.B. Guseva ◽  
E.V. Antinа ◽  
I.A. Khodov ◽  
A.I. Vyugin


2016 ◽  
Vol 126 (3) ◽  
pp. 1481-1490 ◽  
Author(s):  
G. B. Guseva ◽  
A. A. Ksenofontov ◽  
E. V. Antina ◽  
A. I. Vyugin ◽  
V. P. Barannikov


2016 ◽  
Vol 69 (5) ◽  
pp. 901-914 ◽  
Author(s):  
G. B. Guseva ◽  
A. A. Ksenofontov ◽  
E. V. Antina ◽  
V. P. Barannikov ◽  
A. I. Vyugin


2015 ◽  
Vol 60 (3) ◽  
pp. 379-382 ◽  
Author(s):  
A. S. Vashurin ◽  
T. V. Tikhomirova ◽  
V. E. Maizlish
Keyword(s):  


2014 ◽  
Vol 88 (10) ◽  
pp. 1726-1731 ◽  
Author(s):  
V. V. Aksenova ◽  
R. M. Nikonova ◽  
V. L. Lad’yanov ◽  
V. V. Mukhgalin


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