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* Papers with Sirius co-authors


Fan, Y. Yang, M. Wang, Y. Li, Y.  Zhou, Y. Chen, X. Shan, L. Wei, J. Gao, C., Preformulation characterization and in vivo absorption in beagle dogs of JFD, a novel anti-obesity drug for oral delivery. Drug Development and Industrial Pharmacy, 2015, 41(5), 801-811

* Bergstrom, C. A.; Holm, R.; Jorgensen, S. A.; Andersson, S. B.; Artursson, P.; Beato, S.; Borde, A.; Box, K.; Brewster, M.; Dressman, J.; Feng, K. I.; Halbert, G.; Kostewicz, E.; McAllistar, M.; Muenster, U.; Thinnes, J.; Taylor, R.; Mullertz, A., Early pharmaceutical profiling to predict oral drug absorption: Current status and unmet needs. Eur J Pharm Sci 2013.

* Lennernas, H.; Aarons, L.; Augustijns, P.; Beato, S.; Bolger, M.; Box, K.; Brewster, M.; Butler, J.; Dressman, J.; Holm, R.; Julia Frank, K.; Kendall, R.; Langguth, P.; Sydor, J.; Lindahl, A.; McAllister, M.; Muenster, U.; Mullertz, A.; Ojala, K.; Pepin, X.; Reppas, C.; Rostami-Hodjegan, A.; Verwei, M.; Weitschies, W.; Wilson, C.; Karlsson, C.; Abrahamsson, B., Oral biopharmaceutics tools - Time for a new initiative - An introduction to the IMI project OrBiTo. Eur J Pharm Sci 2013.

* Heikal, A. Box, K. Rothnie, A. Storm, J. Callaghan, R. Allen, M. The stabilisation of purified, reconstituted P-glycoprotein by freeze drying with disaccharides. Cryobiology, Volume 58, Issue 1, February 2009, 37-44

* Huque, F T T. Box, K. Platts, J A. Comer, J. Permeability through DOPC/dodecane membranes: measurement and LFER modelling. Eur. J. Pharm. Sci. 2004, 23(3), 223-232

Clarke, E.D. Delaney, J.S. Physical and molecular properties of agrochemicals: an analysis of screen inputs, hits, leads and products. Chimia (Aarau), 2003 (57) pp 731-734

* Abraham, M.H. Ibrahim, A. Zissimos, A M. Zhao, Y.H. Comer, J. Reynolds, D P. Application of hydrogen bonding calculations in property based drug design. Drug Discov. Today. 2002, 7(20), 1056-106

* A.M. Zissimos, M.H. Abraham, M.C. Barker, K.J. Box, K.Y. Tam, Journal of the Chemical Society, Perkin Transactions 2 2002 1-9. Calculation of Abraham Descriptors from solvent-water partition coefficients in four different systems; evaluation of different methods of calculation.

Y.H. Zhao, J. Le, M.H. Abraham, A. Hersey, P.J.J. Eddershaw, C.N. Luscombe, D. Boutina, G. Beck, B. Sherborne, I. Cooper, J.A. Platts, J. Pharm. Sci. 2001, (90(6)), 749-784; Evaluation of human intestinal absorption data and subsequent derivation of a quantitative structure-activity relationship (QSAR) with the Abraham descriptors.

* K.Y. Tam, Computers & Chemistry, 1999, 23(5), 415-419. BUFMAKE: a computer program to calculate the compositions of buffers of defined buffer capacity and ionic strength for ultra-violet spectrophotometry.

* J.E.A. Comer and C. Hibbert, J. Automatic Chem., 1997, 19(6), 213-224. pH electrode performance under automated management conditions.

* A. Avdeef and A.R. Chemotti, J. Chem. Soc. Dalton Trans. 1991, 1189-94; Cadmium binding by biological ligands 4.