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Related Concept Videos

Diffusion01:21

Diffusion

Diffusion is a type of passive transport. In passive transport, a substance tends to move from an area of high concentration to an area of low concentration until the concentration is equal across the space. For example, take the diffusion of substances through the air. When someone opens a perfume bottle in a room filled with people, the perfume is at its highest concentration in the bottle and is at its lowest at the edges of the room. The perfume vapor will diffuse, or spread away, from the...
Diffusion01:12

Diffusion

Diffusion is the passive movement of substances down their concentration gradients—requiring no expenditure of cellular energy. Substances, such as molecules or ions, diffuse from an area of high concentration to an area of low concentration in the cytosol or across membranes. Eventually, the concentration will even out, with the substance moving randomly but causing no net change in concentration. Such a state is called dynamic equilibrium, which is essential for maintaining overall...
Transdermal Drug Delivery Systems01:18

Transdermal Drug Delivery Systems

Transdermal drug delivery systems (TDDS) enable the controlled release of drugs across the skin into systemic circulation. They are particularly advantageous for drugs with short half-lives or narrow therapeutic indices, as they maintain consistent plasma concentrations and reduce the risk of subtherapeutic or toxic levels.TDDS are categorized into monolithic, reservoir, and mixed systems. Monolithic systems embed the drug in a polymer matrix, where diffusion governs release. Reservoir systems...
Physiological Pharmacokinetic Models: Blood Flow-Limited Versus Diffusion-Limited Models00:57

Physiological Pharmacokinetic Models: Blood Flow-Limited Versus Diffusion-Limited Models

Physiological pharmacokinetic models, often called flow-limited or perfusion models, typically assume a swift drug distribution between tissue and venous blood, creating a rapid drug equilibrium. This premise is based on the idea that drug diffusion is extremely fast, and the cell membrane presents no barrier to drug permeation. In this scenario, where no drug binding occurs, the drug concentration in the tissue equals that of the venous blood leaving the tissue. This greatly simplifies the...
Passive Diffusion: Overview and Kinetics01:17

Passive Diffusion: Overview and Kinetics

Passive diffusion is a critical process that allows small lipophilic drugs to cross the cell membrane along a concentration gradient. This mechanism's efficiency depends on four primary factors: the membrane's surface area, the drug's lipid-water partition coefficient, the concentration gradient, and the membrane's thickness.
When administered orally, drugs establish a substantial concentration gradient between the gastrointestinal (GI) lumen and the bloodstream, expediting their diffusion into...
Protein Diffusion in the Membrane01:24

Protein Diffusion in the Membrane

Proteins show rotational as well as lateral diffusion across the membrane. The lateral diffusion of proteins was confirmed through the cell fusion experiment where mouse and human cells were fused, resulting in hybrid cells. When the human and mouse cells fused, the specific membrane proteins on human and mouse cells were marked with the red and green-fluorescent markers, respectively. Initially, the red and green fluorescence was located on the respective hemisphere of the cell. As time...

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Related Experiment Video

Updated: Jun 22, 2026

A Method for Determination and Simulation of Permeability and Diffusion in a 3D Tissue Model in a Membrane Insert System for Multi-well Plates
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A Method for Determination and Simulation of Permeability and Diffusion in a 3D Tissue Model in a Membrane Insert System for Multi-well Plates

Published on: February 23, 2018

Diffusion through skin and model systems.

A Dyer1, G G Hayes, J G Wilson

  • 1Department of Pure and Applied Chemistry, University of Salford, Salford M5 4WT.

International Journal of Cosmetic Science
|May 27, 2009
PubMed
Summary
This summary is machine-generated.

Researchers developed a new method to study molecular diffusion through skin using radioactive tracers. This approach calculates the self-diffusion coefficient (D*) and analyzes its changes with temperature and membrane type.

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Improving 2D and 3D Skin In Vitro Models Using Macromolecular Crowding
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Improving 2D and 3D Skin In Vitro Models Using Macromolecular Crowding

Published on: August 22, 2016

Area of Science:

  • Biophysics
  • Materials Science
  • Pharmacokinetics

Background:

  • Understanding molecular diffusion through biological barriers like skin is crucial for drug delivery and toxicology.
  • Existing methods for measuring diffusion coefficients can be complex and time-consuming.

Purpose of the Study:

  • To introduce a novel experimental and mathematical approach for investigating diffusion through skin.
  • To determine the self-diffusion coefficient (D*) of molecules across skin and model membranes.
  • To analyze the influence of temperature, skin type, and membrane composition on diffusion parameters.

Main Methods:

  • Utilizing a self-exchange experimental setup with radioactively labeled compounds.
  • Employing a new mathematical solution to compute the self-diffusion coefficient (D*).
  • Conducting experiments across various skin types and synthetic model membranes.
  • Performing thermal analyses to complement diffusion studies.

Main Results:

  • Successfully computed the self-diffusion coefficient (D*) for molecules diffusing through skin and model membranes.
  • Demonstrated variations in self-diffusion parameters influenced by temperature, skin type, and model membrane properties.
  • Provided insights into the thermal behavior affecting diffusion.

Conclusions:

  • The novel self-exchange method offers a robust approach to quantify molecular diffusion through skin.
  • Temperature and membrane characteristics significantly impact self-diffusion coefficients.
  • This method can be valuable for predicting drug permeation and understanding skin barrier function.