High-throughput crystallization: polymorphs, salts, co-crystals and solvates of pharmaceutical solids.

By S. Morissette, O. Almarsson, M. Peterson, J. Remenar, Michael J. Read, A. Lemmo, Steve Ellis, M. Cima, C. Gardner. Advanced Drug Delivery Reviews, 2004

676 citations recorded by the source corpus.

Subfields: Biomedical Engineering, Materials Chemistry, Spectroscopy

View Paper: https://www.semanticscholar.org/paper/3692f90b3f7404d71c5f86c159447895030a50e7

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In Materials Chemistry

1. Christopher J. H. Porter
2. W. Charman
3. S. Charman
4. H. Williams
5. R. Shanker
6. Natalie L. Trevaskis
7. Colin W. Pouton

In Spectroscopy

1. Christopher J. H. Porter
2. W. Charman
3. S. Charman
4. H. Williams
5. R. Shanker
6. Natalie L. Trevaskis
7. Colin W. Pouton

Citations in the corpus

• Strategies to Address Low Drug Solubility in Discovery and Development (2013, background): “Consequently, several studies have presented highthroughput screening approaches to cocrystal synthesis and physicochemical characterization (Remenar et al., 2003a; Morissette et al., 2004; Seefeldt et al., 2007; Zhang et al., 2007; Childs et al., 2008; Lu et al., 2008; Kojima et al., 2010).”