Graphical process design tools for iontophoretic transdermal drug-delivery devices
Document Type
Article
Publication Date
9-1-2012
Abstract
A graphical procedure was proposed for the optimum design of transdermal drug-delivery systems enhanced by iontophoresis. Contour plots displayed the relationships among steady-state plasma level, current density and initial drug concentration in a vehicle. This information was combined with a closed-form expression of the process time constant, estimated as the medicament in the blood reaches a plateau after application of the electric field. Analysis was conducted using Laplace-transformed variables and did not require time-domain solutions. Simulation results show that a current density of 0.044mA/cm2 and a loading of 3500μg/ml of dexamethasone sodium m-sulfobenzoate were necessary to achieve an equilibrium plasma concentration of 1.254ng/cm3 with a time constant of 8.34h. © 2011 Elsevier Ireland Ltd.
Identifier
84863869783 (Scopus)
Publication Title
Computer Methods and Programs in Biomedicine
External Full Text Location
https://doi.org/10.1016/j.cmpb.2011.01.004
e-ISSN
18727565
ISSN
01692607
PubMed ID
21345513
First Page
447
Last Page
455
Issue
3
Volume
107
Recommended Citation
Simon, Laurent, "Graphical process design tools for iontophoretic transdermal drug-delivery devices" (2012). Faculty Publications. 18118.
https://digitalcommons.njit.edu/fac_pubs/18118
