1,4-Benzenedisulfonic acid, 2,2'-[1,2-ethenediylbis[(3-sulfo-4,1-phenylene)imino[6-[bis(2-hydroxypropyl)amino]-1,3,5-triazine-4,2-diyl]imino]]bis-, sodium salt (1:6)

Basic toxicokinetics

Administrative data

Endpoint:

basic toxicokinetics

Type of information:

migrated information: read-across from supporting substance (structural analogue or surrogate)

Adequacy of study:

weight of evidence

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Basic data given: comparable to guidelines/standards

Data source

Reference

Reference Type:

publication

Title:

Metabolic Behaviour of Water-Soluble Fluorescent Whitening Agents in the Rat and Bean Plant

Author:

W. Muecke, G. Dupuis, H.O. Esser

Year:

1975

Bibliographic source:

Environmental Quality and Saftety, Supplement, Vol 4, 174-179

Materials and methods

Objective of study:

toxicokinetics

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 417 (Toxicokinetics)

GLP compliance:

not specified

Test material

Test material information

Constituent 1

Reference substance name:

Disodium 4,4'-bis[[6-anilino-4-[(2-hydroxyethyl)methylamino]-1,3,5-triazin-2-yl]amino]stilbene-2,2'-disulphonate

EC Number:

237-600-9

EC Name:

Disodium 4,4'-bis[[6-anilino-4-[(2-hydroxyethyl)methylamino]-1,3,5-triazin-2-yl]amino]stilbene-2,2'-disulphonate

Cas Number:

13863-31-5

IUPAC Name:

disodium 2,2'-ethene-1,2-diylbis[5-({4-anilino-6-[(2-hydroxyethyl)(methyl)amino]-1,3,5-triazin-2-yl}amino)benzenesulfonate]

Details on test material:

- Specific activity (if radiolabelling): 10.5 µCi/mg

Radiolabelling:

yes

Remarks:

C14

Test animals

Species:

rat

Strain:

SIV 50

Sex:

male/female

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

water

Details on exposure:

PREPARATION OF DOSING SOLUTIONS: test substance was dissolved in water

Duration and frequency of treatment / exposure:

treatment: once
sample preparation 96 hours later

Doses / concentrations

Remarks:

Doses / Concentrations:
4

Control animals:

no

Details on dosing and sampling:

PHARMACOKINETIC STUDY (Absorption, distribution, excretion)
- Tissues and body fluids sampled: urine, faeces, expired CO2, blood, liver, kidney, brain, muscle, fat, cage washes
- Time and frequency of sampling: tissues and blood after 96 hours; urine, faeces and expired air see result table 1

Results and discussion

Toxicokinetic / pharmacokinetic studies

Details on absorption:

The results indicate (see Details on excretion) that test substance is not absorbed from the gut of the rat and probably passes through the gut tightly bound to cellulose in the gut contents. The rate of excretion is probably only dependent on the rate at which the gut contents pass through the gastro-intestinal tract.

Details on distribution in tissues:

The animals were killed 96 hours after dosing and samples of blood, muscle, fat, brain, liver and kidney examined for residual radioactivity. The average residue in all tissues of both sexes was less, than 0.005 ppm test substance equivalents (limit of quantitative determination).

Details on excretion:

More than 90% of the administered radioactivity was excreted within 48 hours of dosing. The faeces being the main, and practically only route of elimination. Little or no radioactivity was found in the urine and expired air. The faeces were lyophilized, ground to a fine powder, and exhaustively extracted in a Soxhlet apparatus, first with methanol and second with water. Practically no radioactivity was extracted with these solvents. This is not entirely suprising as this compound is known to bind very tightly to cellulose and is probably bound to the same substance in the rat faeces.

Metabolite characterisation studies

Metabolites identified:

no