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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Eye irritation

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Administrative data

Endpoint:
eye irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data
Justification for type of information:
Data is from peer reviewed journal.

Data source

Reference
Reference Type:
publication
Title:
Case report of test chemical
Author:
Singalavanija et al.,
Year:
2000
Bibliographic source:
Retina,; 2000

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: as mentioned below
Principles of method if other than guideline:
The clinical manifestations, toxic dosage of iodate, and ocular changes in five patients who had taken a test chemical overdose were analyzed. Electroretinography, visual evoked potential (VEP), and fundus fluorescein angiography (FA) were performed to study retinal function and changes.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Potassium iodate
EC Number:
231-831-9
EC Name:
Potassium iodate
Cas Number:
7758-05-6
Molecular formula:
HIO3.K
IUPAC Name:
potassium iodate
Details on test material:
- Name of test material (as cited in study report): Potassium iodate
- Substance type: Inorganic
- Physical state: Solid

Test animals / tissue source

Species:
human
Details on test animals or tissues and environmental conditions:
TEST ANIMALS
- Age at study initiation:22-65 yrs.

Test system

Vehicle:
not specified
Controls:
not specified
Amount / concentration applied:
KIO3 solution at a concentration between 187 and 470 mg/kg body weight was ingested.
Duration of treatment / exposure:
2 - 12 hours
Observation period (in vivo):
3 months
Number of animals or in vitro replicates:
Two men and three women

Results and discussion

In vivo

Results
Irritation parameter:
other: Retinal pigment epithelial (RPE) window defects
Basis:
mean
Time point:
other: 2-12 hours
Score:
20
Max. score:
80
Reversibility:
not specified
Remarks on result:
other: Two men and three women (age 22-65 years) ingested KIO3 solution at a concentration between 187 and 470 mg/kg body weight. Visual acuity ranged from light perception with projection to counting fingers and decreased from 2 to 12 hours after ingestion.

Applicant's summary and conclusion

Interpretation of results:
Category 2 (irritating to eyes) based on GHS criteria
Conclusions:
The test chemical can produce retinal toxicity that damages RPE and photoreceptor cells. The recovery of retinal function depends on the amount of chemical absorption, the regeneration of RPE, and the recovery function of photoreceptor cells. On the basis of observed effects, the test chemical can be considered as irritating to the human eyes.
Executive summary:

The clinical manifestations, toxic dosage of iodate, and ocular changes in five patients who had taken a overdose of test chemical were analyzed. Electroretinography, visual evoked potential (VEP), and fundus fluorescein angiography (FA) were performed to study retinal function and changes.

Two men and three women (age 22-65 years) ingested test chemical solution at a concentration between 187 and 470 mg/kg body weight. Visual acuity ranged from light perception with projection to counting fingers and decreased from 2 to 12 hours after ingestion. Fundus FA showed bilateral extensive areas of retinal pigment epithelial (RPE) window defects, and electroretinography and VEP showed marked impairment of retinal function. Visual acuity improved from counting fingers to 20/80 in 3 months.

The test chemical can produce retinal toxicity that damages RPE and photoreceptor cells. The recovery of retinal function depends on the amount of chemical absorption, the regeneration of RPE, and the recovery function of photoreceptor cells.

On the basis of observed effects, the test chemical can be considered as irritating to the human eyes.