Influence of system formulation on the release of encapsulated food active compounds. Analysis based on a
Jesica D Oroná1, Ignacio Niizawa1, Juan Manuel Peralta2
1Instituto de Desarrollo Tecnológico para la Industria Química (INTEC), Universidad Nacional del Litoral - CONICET, Güemes 3450, S3000GLN Santa Fe, Argentina.
Abstract:
Encapsulation technology is used in the food industry mainly to protect unstable active compounds and allow their controlled release at a specific site. The release is strongly influenced by the structure of the encapsulating matrix (e.g., its formulation). In this study, the influence of alginate-based particle formulation (matrix) on astaxanthin (active compound) release was experimentally evaluated and theoretically analyzed using a mechanistic mathematical model. Particles were obtained by external ionic gelation using gelling solutions with different calcium concentrations (25.75 mM, 250 mM, 474.25 mM) and equal curing time (30 min). The theoretical analysis of the active release from the encapsulation systems studied showed good agreement with the experimental data (MAPE < 15 %). The model assumes that water diffusion, active dissolution and diffusion, and matrix swelling and erosion occur simultaneously. Analysis of the dimensionless model parameters and theoretical profiles of the volume-averaged fractions of released active, absorbed water, remaining polymer, and developed matrix stress showed that for higher calcium concentrations in the gelling medium, water uptake and matrix erosion were slower, swelling had a greater effect, and the matrix exhibited more elastic behavior. The results highlight the potential of the proposed model as a valuable tool for the design and optimization of encapsulation systems.
Related Concept Videos
Pharmacokinetic Models: Overview
There are three primary types of models: empirical, compartment, and physiological. Empirical models, with minimal...
Model Approaches for Pharmacokinetic Data: Compartment Models
Two primary types of compartment models are recognized: mammillary and catenary. The more...
One-Compartment Open Model for IV Bolus Administration: Estimation of Elimination Rate Constant, Half-Life and Volume of Distribution
Parameters Affecting Nonlinear Elimination: Zero-Order Input, First-Order Absorption and Two-Compartment Model
When a drug is administered through a constant intravenous infusion and eliminated via nonlinear pharmacokinetics, it follows zero-order input. For example, oral drugs undergo first-order absorption upon administration and are eliminated through nonlinear pharmacokinetics.
In the case of subcutaneously administered drugs,...
Physiological Pharmacokinetic Models: Assumption with Protein Binding
Pharmacokinetic Models: Comparison and Selection Criterion
Physiological models take a detailed approach by considering specific molecular processes. They can predict drug distribution, metabolism, and elimination changes, providing a comprehensive understanding of how drugs interact with the body.


