C J Porter

发表

Transport and absorption of drugs via the lymphatic system.

C. Porter, W. Charman, C J Porter, 2001, Advanced drug delivery reviews.

In vitro assessment of oral lipid based formulations.

C. Porter, W. Charman, C J Porter, 2001, Advanced drug delivery reviews.

Physiochemical and physiological mechanisms for the effects of food on drug absorption: the role of lipids and pH.

J. Dressman, C. Porter, W. Charman, 1997, Journal of pharmaceutical sciences.

The polyoxyethylene/polyoxypropylene block co‐polymer Poloxamer‐407 selectively redirects intravenously injected microspheres to sinusoidal endothelial cells of rabbit bone marrow

S. Davis, L. Illum, L Illum, 1992, FEBS letters.

Intestinal lymphatic drug transport: an update.

C. Porter, W. Charman, C J Porter, 2001, Advanced drug delivery reviews.

Animal models for the study of intestinal lymphatic drug transport.

G. Edwards, C. Porter, W. Charman, 2001, Advanced drug delivery reviews.

A physicochemical basis for the effect of food on the absolute oral bioavailability of halofantrine.

C. Porter, W. Charman, C J Porter, 1996, Journal of pharmaceutical sciences.

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.

C. Porter, W. Charman, C J Porter, 2000, Journal of pharmaceutical sciences.

Association of halofantrine with postprandially derived plasma lipoproteins decreases its clearance relative to administration in the fasted state.

G. Edwards, C. Porter, W. Charman, 1998, Journal of pharmaceutical sciences.

The formulation of Halofantrine as either non-solubilizing PEG 6000 or solubilizing lipid based solid dispersions: physical stability and absolute bioavailability assessment.

C. Porter, W. Charman, S. Khoo, 2000, International journal of pharmaceutics.

LIPID-BASED FORMULATIONS FOR ORAL ADMINISTRATION: OPPORTUNITIES FOR BIOAVAILABILITY ENHANCEMENT AND LIPOPROTEIN TARGETING OF LIPOPHILIC DRUGS

C. Porter, W. Charman, C J Porter, 2001, Journal of receptor and signal transduction research.

Non-phagocytic uptake of intravenously injected microspheres in rat spleen: influence of particle size and hydrophilic coating.

S. Davis, C. Porter, L. Illum, 1991, Biochemical and biophysical research communications.