Pharmaceutical cocrystals comprise one active pharmaceutical ingredient (API) and at least one small molecule excipient coformer. While solvent evaporation and mechanochemistry are the preferred methods for their synthesis, some cocrystals are known to form spontaneously at ambient conditions when powders of input materials are mixed-a process not yet fully understood. Aqueous humidity is also known to accelerate spontaneous cocrystal formation. We report here the extent of spontaneous cocrystallization for 14 cocrystal systems, at four levels of humidity. The binary cocrystals in our study consist of a model API (caffeine, theophylline, nicotinamide) and a small chain diacid coformer (oxalic acid, malonic acid, maleic acid, fumaric acid, s...
The cocrystallization of caffeine and urea was monitored and analyzed using infrared spectroscopy, R...
7The inability to obtain a crystal form that has previously been reliably prepared is an important c...
Tablets containing a theophylline–glutaric acid (TG) cocrystal dissociated rapidly forming crystalli...
Caffeine–glutaric acid cocrystal polymorphs, Form I and Form II, are presented as a model system to ...
ABSTRACT: A systematic crystal engineering study was performed on the model pharmaceutical compound ...
We demonstrate the utility of freeze-drying as a general method for cocrystal synthesis as well as f...
Post-synthesis (de)hydration techniques were used here to explore further hydrated forms of ionic co...
Previously reported methods for co-crystal synthesis have employed a variety of strategies and these...
Caffeine–oxalic acid cocrystal, widely reported to be stable under high humidity, dissociated in the...
Solid-state cocrystallisation is of contemporary interest, because it offers an easy and efficient w...
Phase diagrams of cocrystals often show a highly unsymmetrical nature. The solvent has an important ...
Phase diagrams of cocrystals often show a highly unsymmetrical nature. The solvent has an important ...
In recent years, there has been an increasing interest in cocrystallization of active pharmaceutical...
Caffeine and maleic acid can form various cocrystal forms, which is a potential route to avoiding hy...
Solid-state cocrystallization is of contemporary interest because it offers an easy and efficient wa...
The cocrystallization of caffeine and urea was monitored and analyzed using infrared spectroscopy, R...
7The inability to obtain a crystal form that has previously been reliably prepared is an important c...
Tablets containing a theophylline–glutaric acid (TG) cocrystal dissociated rapidly forming crystalli...
Caffeine–glutaric acid cocrystal polymorphs, Form I and Form II, are presented as a model system to ...
ABSTRACT: A systematic crystal engineering study was performed on the model pharmaceutical compound ...
We demonstrate the utility of freeze-drying as a general method for cocrystal synthesis as well as f...
Post-synthesis (de)hydration techniques were used here to explore further hydrated forms of ionic co...
Previously reported methods for co-crystal synthesis have employed a variety of strategies and these...
Caffeine–oxalic acid cocrystal, widely reported to be stable under high humidity, dissociated in the...
Solid-state cocrystallisation is of contemporary interest, because it offers an easy and efficient w...
Phase diagrams of cocrystals often show a highly unsymmetrical nature. The solvent has an important ...
Phase diagrams of cocrystals often show a highly unsymmetrical nature. The solvent has an important ...
In recent years, there has been an increasing interest in cocrystallization of active pharmaceutical...
Caffeine and maleic acid can form various cocrystal forms, which is a potential route to avoiding hy...
Solid-state cocrystallization is of contemporary interest because it offers an easy and efficient wa...
The cocrystallization of caffeine and urea was monitored and analyzed using infrared spectroscopy, R...
7The inability to obtain a crystal form that has previously been reliably prepared is an important c...
Tablets containing a theophylline–glutaric acid (TG) cocrystal dissociated rapidly forming crystalli...