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Related Concept Videos

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...
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...
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...
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...
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...
Physiological Pharmacokinetic Models: Assumption with Protein Binding01:13

Physiological Pharmacokinetic Models: Assumption with Protein Binding

Physiological models with protein binding in pharmacokinetics offer a sophisticated approach to understanding drug disposition. These models consider drug-protein interactions, enabling them to effectively predict drug concentrations in different organs and tissues. This precision aids in accurate drug dosing, providing a significant advantage over conventional models. A key process within these models is equilibration, which ensures that drug concentrations achieve a steady state within the...

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Related Experiment Video

Updated: Jun 19, 2026

Setting-up an In Vitro Model of Rat Blood-brain Barrier (BBB): A Focus on BBB Impermeability and Receptor-mediated Transport
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Setting-up an In Vitro Model of Rat Blood-brain Barrier (BBB): A Focus on BBB Impermeability and Receptor-mediated Transport

Published on: June 28, 2014

Extracellular diffusion and permeability effects on NO-RBCs interactions using an experimental and theoretical model.

Prabhakar Deonikar1, Mahendra Kavdia

  • 1Biomedical Engineering Program, College of Engineering, University of Arkansas, 223 Engineering Hall, Fayetteville, AR 72701, USA.

Microvascular Research
|October 20, 2009
PubMed
Summary

This study quantifies nitric oxide (NO) and red blood cell (RBC) interactions using a novel bioreactor. Findings reveal that NO concentration and hematocrit significantly influence NO-RBC reactions, impacting NO transport crucial for vasodilation.

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16:26

Setting-up an In Vitro Model of Rat Blood-brain Barrier (BBB): A Focus on BBB Impermeability and Receptor-mediated Transport

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Published on: August 22, 2016

Area of Science:

  • Physiology
  • Biochemistry
  • Biophysics

Background:

  • Nitric oxide (NO) is a critical vasodilator regulating vascular homeostasis.
  • Red blood cells (RBCs) play a key role in NO transport and bioavailability.
  • Understanding NO-RBC interactions is vital for physiological and pathological processes.

Purpose of the Study:

  • To quantitatively analyze the effect of NO concentration and hematocrit on NO-RBC interactions.
  • To determine the NO-RBC reaction rate constant and predict NO concentrations at the RBC membrane.
  • To investigate the influence of extracellular resistance and RBC membrane permeability on NO transport.

Main Methods:

  • Designed a bioreactor to control NO concentration in the headspace for in vitro NO-RBC interaction studies.
  • Measured nitrite and total nitrogen species (NOx) using chemiluminescence assay.
  • Developed a mathematical model to simulate NO biotransport and estimate reaction kinetics and membrane permeability.

Main Results:

  • Nitrite and NOx levels increased with higher headspace NO concentrations.
  • Nitrite concentrations decreased with increasing hematocrit, while total NOx increased.
  • Modeling estimated the effective reaction rate constant (k(eff)) between 2.32 x 10(4) and 1.08 x 10(6) M(-1) s(-1).
  • Physiologically relevant NO levels require membrane permeability between 0.0415-0.4 cm/s.
  • Extracellular resistance significantly impacts NO uptake by RBCs, especially at higher hematocrit.

Conclusions:

  • Both unstirred layers and RBC membrane properties significantly affect NO transport to RBCs.
  • The study provides crucial insights into the quantitative aspects of NO-RBC interactions.
  • Identified optimal membrane permeability ranges for maintaining adequate NO levels in vascular tissues.