Drug Discovery Assay – reference number: B109
|Assay Type:||GI Tract|
|Tissue:||Human Diseased (IBD) Gastrointestinal Mucosa|
|Study Type:||Ussing chamber|
This assay assesses the permeability of test articles across human diseased (Ulcerative colitis and Crohn’s) gastrointestinal mucosa.
The intestines are essential for the digestion of food and the absorption of fluid and electrolytes. Changes in the anatomy or function of the intestines can lead to disorders such as Irritable Bowel Syndrome (IBS), Crohn’s, Ulcerative Colitis and diarrhoea.
Figure 1: Graph showing relationship between Ussing Papp and Human Absorption in intestinal resections. The Papp values were calculated as a mean of four baths from each donor and then plotted against the reference data.The absorption profile for the healthy donor was comparable to the reference data, whilst data for the Ulcerative Colitis patients varied from the reference data.
The specific results that will be provided are on the permeability of test articles across human gastrointestinal mucosa.
6 weeks from sample receipt for n = 3 donors.
Test article(s) to be provided by the Sponsor in storable aliquots at required test concentrations with information on diluent vehicle used. Stock solutions are prepared in distilled water unless otherwise requested. Bath volumes are 25mL; sponsor to provide sufficient test article to run the entire study.
This assay assesses the permeability of test articles across human diseased gastrointestinal mucosa.
No specific exclusion criteria are in place other than to reject macroscopically diseased/necrotic tissue. Furthermore, tissues which do not have a satisfactory potential difference or transepithelial resistance will be excluded.
All GI mucosal tissues are initially processed through standardisation and qualification procedures to ensure functionality, prior to starting the study protocol.
Prior to mounting the mucosa in the Ussing Chambers, the potential difference of the electrodes and the resistance due to the PSS will be offset prior to the experiment. This will ensure that any electrical measurements obtained will be solely tissue derived.
Following mounting of the mucosa the tissue will be allowed to equilibrate before measurements of the tissues potential difference are made. If the tissue potential difference is satisfactory then the tissue will be placed under voltage clamp and the transepithelial resistance measured.
Tissue will be allowed to equilibrate under voltage clamp conditions before any experimental work is started.
Mucosal samples which pass the qualification pass/fail criteria will then progress to the study protocol.
To assess the permeability of each test article, a single concentration of test article will be added to the apical chamber and samples taken from the apical and basolateral chambers at various time points between 0 and 120 minutes. Reference control compounds can also be run to allow direct comparison with test articles. An example of the conditions assessed for 3 test articles are detailed below (each condition will be run in duplicate mucosal tissues):
End point analysis can either be carried out in-house, outsourced or bath samples can be sent back to the sponsor.
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