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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Repeated dose toxicity: other routes

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Administrative data

Endpoint:
sub-chronic toxicity: other route
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Descriptions of these studies were limited in detail and only the eyes were examined

Data source

Reference
Reference Type:
publication
Title:
Ocular effects of oral and dermal application of dimethyl sulfoxide in animals
Author:
Rubin LF and Barnett KC
Year:
1967
Bibliographic source:
Ann. N.-Y. Acad. Sci., 141, 333-345

Materials and methods

Principles of method if other than guideline:
Method: other
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Dimethyl sulfoxide
EC Number:
200-664-3
EC Name:
Dimethyl sulfoxide
Cas Number:
67-68-5
Molecular formula:
C2H6OS
IUPAC Name:
dimethyl sulfoxide
Details on test material:
Test compound: Dimethylsulfoxyde (spectrograde DMSO)
CAS no.: 67-68-5
Source: no data
Batch : no data
Purity : no data

Test animals

Species:
rabbit
Strain:
New Zealand White
Sex:
male/female

Administration / exposure

Route of administration:
other: dermal to normal and abraded skin
Vehicle:
water
Details on exposure:
50% and 90% solution of DMSO in water were applied 5 days weekly to the skin of 2 series of 5 groups of 6 male and 6 female rabbits (3 months old) at the dose levels of 0, 3 and 9 ml/kg/d. In one series solutions were applied on the intact skin and the other on the abraded skin.
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
22 weeks
Frequency of treatment:
5 days/week
Doses / concentrations
Remarks:
Doses / Concentrations:
1.65 and 3 g/kg/d (as 50% or 90% DMSO solutions)
No. of animals per sex per dose:
4 rabbits per group
Control animals:
yes, concurrent vehicle
Details on study design:
Post-exposure period: none

Examinations

Observations and examinations performed and frequency:
The rabbits were examined opthalmoscopically in the 22nd dose-week, slit lamp biomicroscopy was done as well.

Results and discussion

Results of examinations

Clinical signs:
not examined
Mortality:
not examined
Body weight and weight changes:
not examined
Food consumption and compound intake (if feeding study):
not examined
Food efficiency:
not examined
Water consumption and compound intake (if drinking water study):
not examined
Ophthalmological findings:
effects observed, treatment-related
Haematological findings:
not examined
Clinical biochemistry findings:
not examined
Urinalysis findings:
not examined
Behaviour (functional findings):
not examined
Organ weight findings including organ / body weight ratios:
not examined
Gross pathological findings:
not examined
Histopathological findings: non-neoplastic:
not examined
Histopathological findings: neoplastic:
not examined
Details on results:
Lenticular changes were observed in rabbits receiving daily dermal applications of 9 ml/kg, 50% and 90% DMSO, after 15-20 weeks. After 22 weeks these changes were observed in all rabbits receiving 9 ml/kg 90% DMSO and some receiving the smallest dose administered, 3 ml/kg DMSO.
There were no data reported on local skin effects.

Effect levels

Dose descriptor:
LOAEL
Effect level:
1 650 mg/kg bw/day
Sex:
male/female

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion