Definition of a Physiologic Pharmacokinetic Model of Cutaneous Drug Distribution Using the Isolated Perfused Porcine Skin Flap
- 1 July 1989
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 78 (7) , 550-555
- https://doi.org/10.1002/jps.2600780708
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Determination of Doxycycline in Bovine Tissues and Body Fluids by High-Performance Liquid Chromatography Using Photodiode Array Ultraviolet-Visible DetectionJournal of Pharmaceutical Sciences, 1989
- The use of mass balance principles to describe regional drug distribution and eliminationJournal of Pharmacokinetics and Biopharmaceutics, 1988
- Area method for the estimation of partition coefficients for physiological pharmacokinetic modelsJournal of Pharmacokinetics and Biopharmaceutics, 1987
- On the definition of viability in isolated perfused skin preparationsBritish Journal of Dermatology, 1987
- Structural identifiability of “first-pass” modelsJournal of Pharmacokinetics and Biopharmaceutics, 1987
- The isolated perfused porcine skin flap (IPPSF) I. A novel in vitro model for percutaneous absorption and cutaneous toxicology studiesFundamental and Applied Toxicology, 1986
- Physiological model for the pharmacokinetics ofcis-dichlorodiammineplatinum(II) (DDP) in the tumored ratJournal of Pharmacokinetics and Biopharmaceutics, 1985
- Physiologic Pharmacokinetic Models: Relevance, Experience, and Future TrendsDrug Metabolism Reviews, 1984
- Physiologically Based Pharmacokinetic Modeling: Principles and ApplicationsJournal of Pharmaceutical Sciences, 1983
- Sequential Organ First-Pass Effects: Simple Methods for Constructing Compartmental Pharmacokinetic Models from Physiological Models of Drug Disposition by Several OrgansJournal of Pharmaceutical Sciences, 1982