Tel: +61 3 990 39682
Fax: +61 3 9903 9583
Email: Suzanne.Caliph@monash.edu
Web: http://www.pharm.monash.edu.au/research/mips/d4/index.html
Position
Lecturer
Faculty of Pharmacy and Pharmaceutical Sciences
Drug Delivery, Disposition and Dynamics
Monash Institute of Pharmaceutical Sciences
Caliph, S.M., Trevaskis, N., Charman, W.N., Porter, C.J., 2012, Intravenous dosing conditions may affect systemic clearance for highly lipophilic drugs: implications for lymphatic transport and absolute bioavailability studies, Journal of Pharmaceutical Sciences [P], vol 101, issue 9, Wiley-Blackwell, Malden, Massachusetts USA, pp. 3540-3546.
Caliph, S.M., Faassen, W.A., Vogel, G.M., Porter, C.J., 2009, Oral bioavailability assessment and intestinal lymphatic transport of org 45697 and org 46035, two highly lipophilic novel immunomodulator analogues, Current Drug Delivery [P], vol 6, issue 4, Bentham Science Publishers Ltd, The Netherlands, pp. 359-366.
Edwards, G.A., Porter, C.J.H., Caliph, S.M., Khoo, S., Charman, W.N., 2001, Animal models for the study of intestinal lymphatic drug transport, Advanced Drug Delivery Reviews, vol 50, Elsevier Science BV, The Netherlands, pp. 45-60.
Caliph, S.M., Charman, W.N., Porter, C.J.H., 2000, Effect of short-, medium-, and long-chain fatty acid based vehicles on the absolute oral bioavailability and intestinal lymphatic transport of halofantrine and assessment of mass balance in lymph-cannulated and non-cannulated rats, Journal of Pharmaceutical Sciences, vol 89 issue 8, John Wiley & Sons Inc., New York NY USA, pp. 1073-1084.
Porter, C.J.H., Caliph, S.M., Charman, W.N., 1997, Differences in pre- and post-prandial plasma lipid profiles affect the extraction efficiency of a model highly lipophilic drug from beagle dog plasma, Journal of Pharmaceutical and Biomedical Analysis, vol 16, Elsevier Science, Netherlands, pp. 175-180.
Jones, K.M., Larson, I.C., Weaver, D., Caliph, S.M., 2005, The adventures of Trev the tablet: replacing practical classes and lectures using an online game scenario, Proceedings of the Australasian Society for Computers in Learning in Tertiary Education Conference, 04 December 2005 to 07 December 2005, AJET, Brisbane Qld Australia, pp. 309-312.
Caliph, S.M., Charman, W.N., Porter, C.J.H., 1998, The bioavailabiliity of a highly lipophilic compound after oral administration in lipidic and lipid free formulations: Assessment in lymph fistulated and non-lymph fistulated rat models, Proceedings of ASCEPT: Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists, Hobart Tas, 13-16 December 1998, Australasian Soc of Clinical & Exp Pharm & Toxicol, Sydney NSW Australia, p. 63.
Caliph, S.M., Charman, W.N., Porter, C.J.H., 1997, The effect of medium and long chain lipids on the lymphatic transport and bioavailability of halofantrine, a highly lipophilic drug, after oral administration to conscious rats, Australasian Pharmaceutical Science Association 1997 Conference, Sydney Australia, 26-28 November, APSA 1997 Organising Committee, Sydney NSW Australia, p. 53.
Affiliations with institutes
Drug Delivery, Disposition and Dynamics
Monash Institute of Pharmaceutical Sciences
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