Towards more efficient screening of pharmaceutical cocrystals

N Issa - 2011 - discovery.ucl.ac.uk
Pharmaceutical cocrystals are formed between active pharmaceutical ingredients (APIs) and
coformers that are biologically safe. Cocrystals are of considerable relevance to the …

Co-crystal solubility and thermodynamic stability

L Roy, MP Lipert… - Pharmaceutical salts and …, 2012 - books.google.com
Co-crystal-solution phase interactions have a major impact on our ability to understand and
engineer co-crystal solubility. Recent advances in crystal engineering, in combination with …

[HTML][HTML] Model-based solvent selection for the synthesis and crystallisation of pharmaceutical compounds

MH Muhieddine, SK Viswanath, A Armstrong… - Chemical Engineering …, 2022 - Elsevier
The pharmaceutical industry needs design tools to identify greener and more resource-
efficient process routes. Current model-based solvent selection methodologies often focus …

Rational coformer or solvent selection for pharmaceutical cocrystallization or desolvation

YA Abramov, C Loschen, A Klamt - Journal of pharmaceutical sciences, 2012 - Elsevier
It is demonstrated that the fluid-phase thermodynamics theory conductor-like screening
model for real solvents (COSMO-RS) as implemented in the COSMOtherm software can be …

Cocrystal solubility advantage and dose/solubility ratio diagrams: a mechanistic approach to selecting additives and controlling dissolution–supersaturation …

KL Cavanagh, G Kuminek… - Molecular …, 2020 - ACS Publications
Two of the main questions regarding cocrystal selection and formulation development are
whether the will be stable and how fast can it dissolve the drug dose. Dissolving the drug …

Cocrystals: design, properties and formation mechanisms

N Rodríguez-Hornedo, SJ Nehm… - Encyclopedia of …, 2007 - api.taylorfrancis.com
The design of pharmaceutical crystals that possess different molecular components is
valuable to control pharmaceutical properties of solids without changing the covalent bonds …

Engineering Cocrystal and Cocrystalline Salt Solubility by Modulation of Solution Phase Chemistry.

L Roy - 2013 - deepblue.lib.umich.edu
There is increasing interest in cocrystal and cocrystalline salts as alternate pharmaceutical
solid forms because they provide a range of physicochemical and biopharmaceutical …

[HTML][HTML] In silico screening of dicarboxylic acids for cocrystallization with phenylpiperazine derivatives based on both cocrystallization propensity and solubility …

P Cysewski - Journal of Molecular Modeling, 2017 - Springer
In silico screening was performed to search for binary solids in which a phenylpiperazine-
derivative drug was cocrystallized with a dicarboxylic acid. The phenylpiperazine derivative …

[图书][B] Modeling and simulation of antisolvent crystallization: mixing and control

XY Woo - 2007 - core.ac.uk
In the pharmaceutical industry, both company internal and regulatory authorities impose
stringent requirements on the product quality, which includes crystal size distribution, of …

Phase behaviour and crystal nucleation in complex multicomponent system

OH Olalere - 2019 - stax.strath.ac.uk
The continuing research and use of co-crystallisation for separation, purification and
modification of pharmaceutical materials in multiple industrial sectors can be attributed to the …