Cerium

Acute Toxicity: inhalation

Administrative data

Endpoint:

acute toxicity: inhalation

Type of information:

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

Adequacy of study:

key study

Study period:

January 1993

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: GLP OECD TG 403-compliant study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1993

Report date:

1993

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 403 (Acute Inhalation Toxicity)

GLP compliance:

yes

Test type:

standard acute method

Limit test:

yes

Test material

Test material information

Constituent 1

Reference substance name:

Dicerium tricarbonate

EC Number:

208-655-6

EC Name:

Dicerium tricarbonate

Cas Number:

537-01-9

IUPAC Name:

dicerium tricarbonate

Test animals

Species:

rat

Strain:

Wistar

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Biological Research Laboratory Ltd., 4414 Fuellinsdorf, Switzerland
- Age at study initiation: 10 (males) / 12 (females) weeks old
- Weight at study initiation: 184.8 - 192.0 g (males) / 183.8 - 195.6 g (females)
- Fasting period before study: no
- Housing: by groups of 5 in makrolon type-4 cages (59 x 38.5 x 20 cm)
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: 7 days


ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 +/- 3
- Humidity (%): 50 +/- 20
- Air changes (per hr): 10 to 15
- Photoperiod (hrs dark / hrs light): 12 / 12


IN-LIFE DATES: From: 04 January 1993 To: 25 January 1993

Administration / exposure

Route of administration:

inhalation: aerosol

Type of inhalation exposure:

nose only

Vehicle:

other: unchanged (no vehicle)

Details on inhalation exposure:

GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: piston/brush-feed aerosol generator (RBG 1000, Palas GmbH, 7500 Karlsruhe 1, Germany)
- Exposure chamber volume: not specified
- Method of holding animals in test chamber: individual macrolon restraining tubes positioned radially around exposure chamber
- Source and rate of air: compressed air at 1.0 L/min/animal
- Method of conditioning air: filtering + Ni63 charge neutralizer
- System of generating particulates/aerosols: piston/stainless steel brush
- Method of particle size determination: aerosol concentration monitored using a RAM-1 light scattering type monitor / particle size distribution determined once during exposure using a Mercer 7 stage cascade impactor
- Treatment of exhaust air: not specified
- Temperature, humidity, oxygene concentration: 22.1°C, 5.0%, 20.9%, respectively


TEST ATMOSPHERE
- Brief description of analytical method used: aerosol concentration monitored by light scattering / particle size distribution determined by cascade impaction
- Samples taken from breathing zone: yes
- Particle size distribution (cumulative %):
< 0.325 µ = 3%
< 0.715 µ = 5.1%
< 1.06 µ = 16.7%
< 1.6 µ = 43.9%
< 2.13 µ = 64.6%
< 3 µ = 85.4%
< 4.6 µ = 94.1%
> 4.6 µ = 100%


- MMAD (Mass median aerodynamic diameter) / GSD (Geometric st. dev.):

- Rationale for the selection of the starting concentration:

Analytical verification of test atmosphere concentrations:

yes

Remarks:

aerosol concentration monitored by light scattering

Duration of exposure:

4 h

Concentrations:

5.047 +/- 0.93 mg/L air (mean +/- SD)

No. of animals per sex per dose:

5

Control animals:

no

Details on study design:

- Duration of observation period following administration: 15 days
- Frequency of observations and weighing:
Mortality: once per hour during exposure, once after exposure on day 1, twice daily thereafter
Clinical signs: once per hour during exposure, once after exposure on day 1, once daily thereafter
Body weight: before exposure on day 1 and on days 8 and 15
- Necropsy of survivors performed: yes
- Other examinations performed: lungs, trachea, larynx and nasopharyngeal tissues preserved for histopathology

Statistics:

LOGIT-Model (not applied due to absence of deaths)

Results and discussion

Effect levels

Effect levels 1

Sex:

male/female

Dose descriptor:

LC0

Effect level:

5.05 mg/L air (analytical)

Exp. duration:

4 h

Effect levels 2

Sex:

male/female

Dose descriptor:

LC50

Effect level:

> 5.05 mg/L air (analytical)

Exp. duration:

4 h

Mortality:

No mortality occurred during the exposure and observation periods

Clinical signs:

other: Labored breathing and ruffled fur were noted in 2 males just after exposure. This persisted in one male for up to 24 hours after exposure.

Body weight:

No significant changes in body weight were seen when compared to controls

Gross pathology:

At necropsy, the lungs of all animals were incompletely collapsed with diffuse whitish foci

Applicant's summary and conclusion

Interpretation of results:

not classified

Remarks:

Migrated information Criteria used for interpretation of results: other: Annex VI Directive 67/748/EEC or UN/EU GHS

Conclusions:

Inhalation LC50 washigher than 5.05 mg/L for male and female rats exposed for 4 hours

Executive summary:

In an acute inhalation toxicity study (RCC Project No. 330974), one group of 10 to 12-week old Wistar rats (5/sex) was exposed by nose-only inhalation route to Cerium Oxide for 4 hours at a mean gravimetric concentration of 5.05 mg/L, and observed for 15 days. Mortality and clinical signs were checked during and just after exposure, and daily for 15 days. Body weight was recorded prior to exposure and on days 8 and 15.

 

No mortality occurred during the exposure and observation periods. Labored breathing and ruffled fur were noted in 2 males just after exposure. This persisted in one male for up to 24 hours after exposure. No significant changes in body weight were seen when compared to controls. At necropsy, the lungs of all animals were incompletely collapsed with diffuse whitish foci.

 

Therefore, the inhalation LC50 was higher than 5.05 mg/L for males and females exposed for 4 hours. No classification for acute inhalation toxicity is warranted based on the absence of mortality at the concentration tested, according to the criteria of Annex VI Directive 67/748/EEC or UN/EU GHS.

 

This study is classified as acceptable. It satisfies the OECD 403 guideline requirements for acute inhalation toxicity.