Two-dimensional transport analysis of transdermal drug absorption with a non-perfect sink boundary condition at the skin-capillary interface
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Publication:2637586
Recommendations
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Cites work
- A repeated-dose model of percutaneous drug absorption
- An analytical solution for percutaneous drug absorption: application and removal of the vehicle
- Flux tracking in drug delivery
- scientific article; zbMATH DE number 898088 (Why is no real title available?)
- Repeated applications of a transdermal patch: Analytical solution and optimal control of the delivery rate
- Timely drug delivery from controlled-release devices: dynamic analysis and novel design con\-cepts
Cited in
(14)- On the effusion time of drugs from the open pore of a spherical vesicle
- A network model of successive partitioning-limited solute diffusion through the stratum corneum
- Analysis of the absorption kinetics following dermal exposure to large doses of volatile organic compounds
- Meshless modeling of coupled transdermal pharmacokinetics with analytical validation
- A geometrical model of dermal capillary clearance
- Probabilistic modeling of percutaneous absorption for risk-based exposure assessments and transdermal drug delivery
- An analytical solution for percutaneous drug absorption: application and removal of the vehicle
- A two-phase two-layer model for transdermal drug delivery and percutaneous absorption
- An analytical approach to study the drug diffusion through transdermal drug delivery system
- scientific article; zbMATH DE number 7750596 (Why is no real title available?)
- Effects of epidermal turnover on the dynamics of percutaneous drug absorption
- Transport mechanisms in oral transmucosal drug delivery: implications for pain management
- Analysis of heat-aided membrane-controlled drug release from a process control perspective
- Prediction of \textit{in-vivo} iontophoretic drug release data from \textit{in-vitro} experiments-insights from modeling
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