Sodium 2-[(2-aminoethyl)amino]ethanesulphonate

Eye irritation

Administrative data

Endpoint:

eye irritation

Remarks:

other: in vitro test

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: GLP guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2012

Report date:

2012

Materials and methods

Principles of method if other than guideline:

The HCE model is currently involved in the eye irritation validation conducted by COLIPA following ECVAM guidelines. Furthermore, it is routinely used by the major Cosmetic and Pharmaceutical companies, and has already been prevalidated in 2004 (van Goethem et. al., Tox in Vitro 20, 2006, 1-17). This model is recognized as the model of choice and scientifically relevant as documented by several publications (Cotovio et. al., Tox. in Vitro, 24, 2010, 523-537).

GLP compliance:

yes (incl. QA statement)

Test material

Test material information

Constituent 1

Reference substance name:

Sodium 2-[(2-aminoethyl)amino]ethanesulphonate

EC Number:

252-173-9

EC Name:

Sodium 2-[(2-aminoethyl)amino]ethanesulphonate

Cas Number:

34730-59-1

Molecular formula:

C4H12N2O3S.Na

IUPAC Name:

sodium 2-(2-aminoethylamino)ethanesulfonate

Test animals / tissue source

Species:

other: Assessment of ocular irritation potential of the test substance by determination of its cytotoxic effect on a human corneal epithelium (HCE) model (exposure 60 min./rt followed by 16 hours incubation at 37 °C, subsequently MTT).

Details on test animals or tissues and environmental conditions:

The experiment was carried out on a Human Corneal Epithelial (HCE) Model, which is standardized and commercially available (SkinEthic, France). Inserts were of 0.5 cm² size. When cultivated at the air-liquid interface in a chemically defined medium, the immortalized human cornea epithelial cells from the cell line HCE reconstruct a corneal epithelial tissue (mucosa), without a stratum corneum, ultra-structurally (tissue morphology and thickness) similar to the corneal mucosa of the human eye.

Test system

Vehicle:

unchanged (no vehicle)

Controls:

other: as negative control: Phosphate Buffered Saline (PBS, 30 µL)

Amount / concentration applied:

30 µl per insert

Duration of treatment / exposure:

60 min./room temperature

Observation period (in vivo):

post-exposure incubation: 16 hours (37°C, 5% CO2, maximum humidity)

Details on study design:

The irritation potential of the test item is assessed by determination of its cytotoxic effect on an reconstructed human ocular epithelia. The test principle is based on the MTT assay reflecting the cell viability after exposure of the cornea equivalent to topically applied test item.
Tests were performed in triplets. The test item was applied at a 100% concentration, i.e. 30 mg per insert (plus 30 µl PBS to moisten and ensure good contact to the tissue), for 60 min at room temperature. After the exposure period the inserts were washed carefully with PBS. After a post-exposure incubation of 16 hours in the incubator (37 +/- 2 °C, 5 % CO2, maximum humidity) MTT reduction was performed. Cell viability was measured by the amount of MTT reduction, i.e. an OD value following exposure to the negative or positive control substances or the test item.

Positive control: 1H-1,2,4-Triazole-3-thiol (30 mg, plus 30 µl PBS for moistening)

Results and discussion

Any other information on results incl. tables

A test substance is predicted to be an ocular irritant if the mean relative tissue viability (%) exposed to the test substance is ≤ 50 %.

Sample No.	Test item	%Viability
1 -3	negative control PBS	100.00
4 -6	positive control 1H-1,2,4 -Triazole-3 -thiol	22.63
16 -18	test substance	0.60

The test item was detected as irritant to the cornea epithelium in this test model.

Applicant's summary and conclusion

Interpretation of results:

other: irritant property

Executive summary:

An in vitro study for assessing ocular irritation of substances using a human corneal epithelial (HCE) cell model was conducted. This model is routinely used by the major Cosmetic and Pharmaceutical companies, and has already been prevalidated in 2004 (van Goethem et. al., Tox in Vitro 20, 2006, 1-17). The undiluted test item was applied topically to the reconstructed HCE tissue, i.e. 30 µl per insert. After an exposure period of 60 minutes (room temperature) and a subsequent 16 hours post-treatment incubation period (37°C) the cell viability was 0.6 % as measured by a MTT conversion assay. As a substance is predicted to be an irritant to the eye if the cell viability (%) is < 50 %, it is concluded for the test substance investigated that it is an ocular irritant under the conditions of this in vitro assay.