The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Fast Dissolving Curcumin Cocrystals
Abstract
Curcumin is the principal curcuminoid of the popular Indian spice turmeric. Despite the diverse pharmacological activities of this bioactive phenol, its application as a drug is severely limited by poor aqueous solubility. We report novel cocrystals of curcumin ( 1 ) with resorcinol and pyrogallol obtained by liquid-assisted grinding. Curcumin–resorcinol ( 1a ) (1:1) and curcumin–pyrogallol ( 1b ) (1:1) were characterized by X-ray diffraction, thermal analysis, FT-IR, FT-Raman, and solid-state 13 C NMR spectroscopy. The 1:1 cocrystal stoichiometry is sustained by O–H···O hydrogen bonds between the phenolic OH groups of the coformers to the carbonyl group of curcumin. The melting point of the cocrystals is in between that of curcumin and the coformer and the lower melting cocrystal 1b is more soluble than higher melting 1a . The dissolution rates of curcumin–resorcinol ( 1a ) and curcumin–pyrogallol ( 1b ) in 40% EtOH–water are ∼5 and ∼12 times faster than that for curcumin.
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Cites
OLEX2 : a complete structure solution, refinement and analysis program
Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K., & Puschmann, H. (2009) · Journal of Applied Crystallography · doi:10.1107/s0021889808042726 · Cited by 32,811
Bioavailability of curcumin: Problems and promises
Anand, P., Kunnumakkara, A. B., Newman, R. A., & Aggarwal, B. B. (2007) · Molecular Pharmaceutics · doi:10.1021/mp700113r · Cited by 5,543
Amidon, G. L., Lennernäs, H., Shah, V. P., & Crison, J. R. (1995) · Pharmaceutical Research · doi:10.1023/a:1016212804288 · Cited by 5,430
Can the pharmaceutical industry reduce attrition rates?
Kola, I., & Landis, J. (2004) · Nature Reviews Drug Discovery · doi:10.1038/nrd1470 · Cited by 4,167
Cited by
Creating Cocrystals: A Review of Pharmaceutical Cocrystal Preparation Routes and Applications
Karimi-Jafari, M., Padrela, L., Walker, G. M., & Croker, D. M. (2018) · Crystal Growth & Design · doi:10.1021/acs.cgd.8b00933 · Cited by 667
Pharmaceutical cocrystals and poorly soluble drugs
Thakuria, R., Delori, A., Jones, W., Lipert, M. P., Roy, L., & Rodríguez-Hornedo, N. (2013) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2012.10.043 · Cited by 614
Eutectics as improved pharmaceutical materials: design, properties and characterization
Cherukuvada, S., & Nangia, A. (2014) · Chem. Commun. · doi:10.1039/c3cc47521b · Cited by 296
Self-citation
Metadata
- Authors
- Sanphui, P., Goud, N. R., Khandavilli, U. B. R., & Nangia, A.
- Venue
- Crystal Growth & Design
- Publisher
- American Chemical Society (ACS)
- Published
- 2011-08-05
- Volume
- 11
- Issue
- 9
- Pages
- 4135-4145
- ISSN
- 1528-7483 (ISSN-L)
- 1528-7505
- OpenAlex
- W2318047941
- Cited by
- 253
- References
- 4
- FWCI
- 7.76
- Type
- journal article
- Language
- en
- Open access
- closed
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