Table 3.
Models | Advantages | Disadvantages |
---|---|---|
In vitro models | ||
Simulation of gastrointestinal transformation | Similar to the physiological processes in the human body Suitable for high-throughput format Ability of testing a specific mechanisms of action Focus on small number of components Validation with reference material |
No hormonal and nervous control Lack of feedback mechanisms Absence of mucosal cell activity Deficiency of complexity of peristaltic movements, and involvement of the local immune system Homeostatic mechanisms are not present Difficult to achieve the anaerobic assay conditions |
Caco-2 cells | Reproducibility of results Provides information about efficiency of digestion, absorption Ability of studying transport mechanisms Phenotypically similar to absorptive epithelial cells Suitable for high-throughput format |
Human colonic adenocarcinoma origin Higher TEER value than human intestine Lack of mucin, microflora, biofilms, and epithelial cell types Variation of efflux transporters expression levels Incapability of simulating the changes of pH |
In vivo models | In vivo condition Well-known biology Selection of specific subjects Better-understanding kinetic of mycotoxins |
High-throughput limitation Extremely complex functional systems Influence of different factors-phenotypic variation Lack of certified reference standards Ethical issues and high cost Time consuming and labor intensive |
TEER: Transepithelial electrical resistance.