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March 30, 2026Chaos Theory and Applications0 citationsOpen Access

Drug Delivery to the Bloodstream within the Cardiovascular System using Caputo-Fabrizio Fractional Derivatives

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MYMohamed YaceenaB.S. Abdur Rahman Crescent Institute of Science & TechnologySUSheik UdumanB.S. Abdur Rahman Crescent Institute of Science & TechnologyS-Shyamsunder -SRM University

Key Points

  • The research aims to extend a compartmental model to improve understanding of drug distribution in the cardiovascular system.
  • Developed a fractional-order model based on the third compartmental model with the Caputo-Fabrizio derivative.
  • Used fixed-point theorem under Lipschitz conditions to establish existence and uniqueness of solutions.
  • Applied Laplace transform techniques to obtain an analytic model solution.
  • Conducted MATLAB simulations to analyze the impact of fractional order on drug concentrations.
  • The fractional-order model demonstrated a memory effect slowing concentration decay.
  • Results indicated that lower fractional orders could lead to increased residual drug levels.
  • Model insights could improve dosing strategies and reduce residue accumulation.

Abstract

We present a fractional-order extension of the third compartmental model of (Khanday et al. 2017) to study drug distribution after oral and intravenous administration. The Caputo–Fabrizio (CF) fractional derivative order (0 γ 1) replaces the integer-order time derivatives in the original model, which provides a non-singular memory kernel suitable for modeling biological processes with finite memory. We first establish the existence and uniqueness of solutions for the fractional model using a fixed-point theorem under mild Lipschitz conditions. An analytic representation of the model solution is then obtained via Laplace transform techniques adapted to the CF operator. Numerical results (MATLAB simulations) illustrate how the fractional order γ and key rate parameters shape arterial, tissue, and venous concentrations. In particular, γ 1 introduces a memory effect that slows concentration decay and may increase residual drug levels, and discusses the implications for dosing and residue accumulation. Finally, we discuss limitations, key model parameters with physical units, and directions for further validation with experimental pharmacokinetic data.

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Cite This Study

Yaceena et al. (2026) studied this question.

synapsesocial.com/papers/69c9c5c5f8fdd13afe0bddc3https://doi.org/10.51537/chaos.1655908
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