Changes in the permeability of the small intestine can result in under-absorption of nutrients or the converse, over-absorption of the intestinal contents. Either condition can be described as malabsorption, although this term is more commonly used in the case of under-absorption of nutrients. A number of investigators have suggested that over-absorption syndromes (increased gut permeability) are significantly underdiagnosed. This may be important, for example, in cases of food intolerance, where derivatives of maldigested food may be absorbed through the gut wall and into the circulation, resulting in characteristic hypersensitivity symptoms [1,2]. Synonyms: PEG test, leaky gut test

Patient Instructions:

The patient should fast for 3 hours before starting the test. Water intake during the first 2 hours of the 6 hour urine collection should be limited to 250 mL. Water consumption during the remainder of the test should be moderate. The PEG test, which is a measure of mucosal permeability, should not be performed if the patient has gastroenteritis or is suffering from any other cause of intestinal hurry, as this will invalidate the urinary reference interval for the recovery of PEG. The sample required for the gut permeability profile is a 6 hour urine collection after a 3 gram oral dose of PEG. A 20 mL aliquot of urine may be sent for analysis if the volume of the total collection can be accurately measured. Postal samples must reach Biolab within 3 days of collection.

Clinical Indications:

The use of PEG 400 as a probe for the investigation of intestinal permeability was first proposed by Chadwick, Philips and Hoffman in 1977 [3]. The rationale was that PEG (polyethylene glycol) contains a mixture of inert, water-soluble molecules of different sizes, whose absorption is independent of dosage, displaying decreasing mucosal transport with increasing molecular size. PEG 400 is also nontoxic, not degraded by intestinal bacteria, not metabolised by tissues, and rapidly excreted in the urine. PEG is polymerised ethylene oxide and is not the substance - ethylene glycol – which is found in anti-freeze. The decreasing absorption of increasing molecular weights of PEG can be explained on the basis of the notional hydrogen bonding capacity of each molecule. Evaluation of this theoretical measure of the oil-water partitioning character of a molecule shows that PEGs, and other low molecular weight molecules used as intestinal probes, may pass through the intestinal cell membranes by a mechanism involving passive diffusion alone. However, a three-mechanism model of intestinal penetration has also been proposed [4].Other factors that may influence the urinary excretion of PEG include its space of distribution in the body, the permeability profile of the kidney [5] and the luminal flow rate in the intestine [4].

Sample Collection Instructions:


Sample Report:

Sample Requirements:

Aliquot of 6hr urine collection, labelled clearly with collection volume

Postal Samples:


1. Mackie RM. Intestinal permeability and atopic disease. Lancet 1981;I:155. 2. Jackson PG, Lessof MH, Baker RWR and Ferrett J. Intestinal permeability in patients with eczema and food allergy. Lancet 1981;1:1285-1286. 3. Chadwick VS, Phillips SF, Hofmann AF. Measurement of intestinal permeability using low molecular weight polyethylene glycols (PEG 400). I. Chemical analysis and biological properties of PEG 400. Gatroenterology 1977;73:241-246. 4. Lloyd JB. Intestinal permeability to polyethyleneglycol and sugars: a re-evaluation. Clin. Sci. 1998;95:107-110. 5. Blatzinger JG, Rommel K, Ecknauer R. Elimination of low molecular weight polyethylene glycol 400 in the urine following an oral load, as a measure of intestinal permeability. J. Clin. Chem. Clin. Biochem. 1981;19:265-266. 6. Sivakumaran T, Jenkins RT, Walker WHC et al. Simplified measurement of polyethylene glycol 400 in urine. Clin. Chem. 1982;28(12):2452-2453