Translation of two aggregated low-density lipoproteins within blood plasma: a mathematical model

Maria Hadjinicolaou1, Eleftherios Protopapas

  • 1School of Science and Technology, Hellenic Open University, 11 Sahtouri str., Patras, Greece, GR-26 222, hadjinicolaou@eap.gr.

Insights

This study models aggregated low-density lipoproteins (LDLs) in blood plasma to understand atherosclerosis. The mathematical approach provides insights into lipoprotein precipitation for concentration measurement.

Area of Science:

  • Biophysics
  • Fluid Dynamics
  • Cardiovascular Science

Background:

  • Arteriosclerosis involves artery wall thickening, while atherosclerosis restricts blood flow and elevates pressure.
  • Low-density lipoproteins (LDLs) aggregation is a key factor in atherosclerosis development.

Purpose of the Study:

  • To develop a mathematical model simulating the movement of two aggregated LDLs in blood plasma.
  • To provide a foundational understanding for lipoprotein precipitation methods used in concentration measurement.

Main Methods:

  • Modeling aggregated LDLs as inverted oblate spheroids.
  • Applying creeping flow, Kelvin inversion, and semi-separation of variables in spheroidal coordinates.
  • Deriving a stream function using a series expansion of Gegenbauer functions.

Main Results:

  • An analytical solution for the translation of two aggregated LDLs was obtained.
  • The solution describes the fluid dynamics of aggregated LDLs in plasma.

Conclusions:

  • The mathematical model offers insights into the behavior of aggregated LDLs.
  • This work is a crucial first step for improving lipoprotein concentration measurement through chemical precipitation.

Related Concept Videos

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...
362
The Fluid Mosaic Model01:34

The Fluid Mosaic Model

The fluid mosaic model was first proposed as a visual representation of research observations. The model comprises the composition and dynamics of membranes and serves as a foundation for future membrane-related studies. The model depicts the structure of the plasma membrane with a variety of components, which include phospholipids, proteins, and carbohydrates. These integral molecules are loosely bound, defining the cell’s border and providing fluidity for optimal function.
186.3K
Three-Compartment Open Model01:06

Three-Compartment Open Model

The three-compartment open model is a pharmacokinetic model used to describe the distribution and elimination of drugs following extravascular administration. It comprises a central compartment representing the plasma and two peripheral compartments. The highly perfused peripheral compartment represents organs and tissues with a rich blood supply, such as the liver, kidneys, and lungs. The scarcely perfused peripheral compartment represents tissues with lower blood supply, such as adipose...
1.2K
Two-Compartment Open Model: Extravascular Administration01:12

Two-Compartment Open Model: Extravascular Administration

The two-compartment model for extravascular administration represents a drug's absorption and distribution process. It features a central compartment, where the drug is first absorbed, and a peripheral compartment, which illustrates the drug's distribution throughout the body. The rate of change in drug concentration in the central compartment is calculated by three exponents: absorption, distribution, and elimination.
The absorption exponent (ka) indicates the speed at which the drug...
871
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...
474
Physiological Pharmacokinetic Models: Incorporating Hepatic Transporter-Mediated Clearance01:07

Physiological Pharmacokinetic Models: Incorporating Hepatic Transporter-Mediated Clearance

Drug transporters are critical in drug absorption, distribution, and excretion processes. They should be included in physiological-based pharmacokinetic (PBPK) models, which help predict human drug disposition. However, predicting this is challenging during drug development, especially when liver transport is involved. However, with a realistic representation of body transport processes, an accurate model may be possible.
A recent model describes pravastatin's hepatobiliary excretion,...
385