Barrier assays are an important tool for in vitro drug development and drug safety testing, e.g. assessing the absorption of a drug candidate through the intestinal wall or the corrosion of chemical compounds on skin.
Barrier assays have a long history and a whole range has been developed to respond to the needs of small academic labs all the way to large pharmaceutical toxicity departments. But where small-scale studies can use in vivo animal studies or ex vivo human tissue for the greatest degree of physiological relevance, large-scale studies have to rely on assays of much lesser complexity, such as Caco2 monolayers or PAMPA for intestinal permeability, to streamline workflows, keep costs down or comply with regulations to decrease animal testing.
Image: Caco2 cells co-cultured with CCD-18co fibroblasts in Alvetex Scaffold, forming a full-thickness model of intestinal mucosa.
Bio-Engineered Tissue Models
Enter bio-engineered 3D tissues models. 3D cell culture scaffolds restore the Z-dimension which is missing in flat-surface cell culture and allows for the building of mucosal and sub-mucosal compartments in a single model. As a result, the epithelial layer can benefit from paracellular signalling from fibroblasts grown in 3D, with endogenously-deposited ECM. The epithelial cells mature better and their morphology and functionality end up being much closer to in vivo compared to conventional culture on flat surfaces.
Watch a video on the features of 3D vs 2D culture:
Physiologically-Relevant Barrier Assays
- Invasiveness of early-stage melanoma in a full-thickness skin model
- Barrier integrity against SDS challenge in a full-thickness skin model
- Infection of Influenza viral particles in a full-thickness airway epithelium model
Alvetex is a great substrate for building barrier assays:
- 200 microns thickness — mimics in vivo passive diffusion metrics
- large pore-based structure — encourages cell migration, multilayering and true three-dimensionality
- insert formats — compatible with 6-well and 12-well plates
- inertness and chemical composition — precludes any exogenous signalling
In addition, Alvetex has been used for more unconventional applications of barrier assays, such as the activation of immune cells after their migration through an epithelium. Actual migration through an epithelium was required, so traditional paracrine co-culture models would have been inadequate, but using the barrier assay improved the functionality of the cells-of-interest prior to the main test of their efficacy. It is a clever solution to the problem of getting more physiologically-relevant cells without having to alter the set-up of an already-established assay system.
Increasing the complexity of established assays is always a challenge, but the rewards gained from greater physiological relevance are worth the effort, both in terms of better disease understanding and to avoid costly drug failures at late pipeline stages.
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