Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Developmental toxicity / teratogenicity

Currently viewing:

Administrative data

Endpoint:
developmental toxicity
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Well-documented study. The study allows the derivation of a NOAEL value for effects of Ca on developmental toxicity in rats and mice.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1974
Report date:
1974

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 414 (Prenatal Developmental Toxicity Study)
Deviations:
no
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Calcium oxide
EC Number:
215-138-9
EC Name:
Calcium oxide
Cas Number:
1305-78-8
Molecular formula:
CaO
IUPAC Name:
oxocalcium
Details on test material:
- Name of test material (as cited in study report): FDA 73-41 (calcium oxide)
- Physical state: solid
No further details are given.

Test animals

Species:
mouse
Strain:
CD-1
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Housing: Mice were housed in groups in disposable plastic cages.
- Diet: ad libitum
- Water: ad libitum; tap water

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 23 - 27
- Humidity (%): 64 - 78

No further details are given.

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Details on exposure:
no detailed data given
Analytical verification of doses or concentrations:
not specified
Details on analytical verification of doses or concentrations:
no detailed data given
Details on mating procedure:
The female mice were mated with young adult males.
- Impregnation procedure: cohoused
- If cohoused:
- M/F ratio per cage: One male was not permitted to impregnate more than one female per group.
- Length of cohabitation: no data
- Proof of pregnancy: vaginal plug referred to as day 0 of pregnancy
No further details are given.
Duration of treatment / exposure:
Beginning on Day 6 and continuing through Day 15 of gestation, the females were dosed with the indicated dosages.
Frequency of treatment:
daily
Duration of test:
until Day 17 of pregnancy
No. of animals per sex per dose:
mated: 25 to 26 mice
prgnant: 17 to 21 mice
Control animals:
yes
yes, sham-exposed
Details on study design:
no data available

Examinations

Maternal examinations:
CAGE SIDE OBSERVATIONS: Yes
- Time schedule: daily
- Cage side observations checked in table were included.

DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: All animals were observed daily for appearance and behavior.

BODY WEIGHT: Yes
- Time schedule for examinations: Average body weight was determined on days 0, 6, 11, 15 and 17

FOOD CONSUMPTION AND COMPOUND INTAKE (if feeding study): Yes
- Time schedule: All animals were observed daily with particular attention to food consumption and weight.

WATER CONSUMPTION AND COMPOUND INTAKE (if drinking water study): No data

POST-MORTEM EXAMINATIONS: Yes
- Sacrifice on gestation day # 17
- Organs examined: The urogential tract of each dam was examined in detail for anatomical normality.

Ovaries and uterine content:
The ovaries and uterine content was examined after termination: Yes
Examinations included:
- Gravid uterus weight: No data
- Number of corpora lutea: Yes
- Number of implantations: Yes
- Number of early resorptions: Yes
- Number of late resorptions: Yes
Fetal examinations:
- External examinations: Yes
- Soft tissue examinations: Yes
- Skeletal examinations: Yes
- Head examinations: Yes
Statistics:
no data given
Indices:
no data given
Historical control data:
no data given

Results and discussion

Results: maternal animals

Maternal developmental toxicity

Details on maternal toxic effects:
Maternal toxic effects:no effects

Details on maternal toxic effects:
The administration of up to 440 mg/kg bw/d of CaO to pregnant mice for 10 consecutive days had no clearly discernible effect on maternal survival.

Effect levels (maternal animals)

Dose descriptor:
NOAEL
Effect level:
>= 440 mg/kg bw/day
Based on:
test mat.
Basis for effect level:
other: maternal toxicity

Results (fetuses)

Details on embryotoxic / teratogenic effects:
Embryotoxic / teratogenic effects:no effects

Details on embryotoxic / teratogenic effects:
The administration of up to 440 mg/kg bw/d of CaO to pregnant mice for 10 consecutive days had no clearly discernible effect on foetal survival.

Effect levels (fetuses)

Dose descriptor:
NOAEL
Effect level:
>= 440 mg/kg bw/day
Based on:
test mat.
Sex:
not specified
Basis for effect level:
other: developmental toxicity

Overall developmental toxicity

Developmental effects observed:
not specified

Applicant's summary and conclusion

Conclusions:
The administration of up to 440 mg/kg (body weight) of the test material to pregnant mice for 10 consecutively days had no clearly discernible effect on nidation or on maternal or fetal survival. The number of abnormalities seen in either soft or skeletal tissues of the test groups did not differ from the number occuring sponaneously in the sham-treated controls.