White mineral oil (petroleum)

Toxicity to reproduction

Administrative data

Endpoint:

one-generation reproductive toxicity

Remarks:

based on test type (migrated information)

Type of information:

migrated information: read-across based on grouping of substances (category approach)

Adequacy of study:

key study

Study period:

1985-06-18 to 1985-11-25

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: This study is classified as reliable with restrictions because although it closely follows OECD Guideline 415, no GLP statement was provided in the study report and only data on pregnant females and pups were provided.

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1987

Report date:

1987

Materials and methods

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 415 [One-Generation Reproduction Toxicity Study (before 9 October 2017)]

GLP compliance:

not specified

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

8042-47-5

Cas Number:

8042-47-5

IUPAC Name:

8042-47-5

Constituent 2

Reference substance name:

80SUS white mineral oil

IUPAC Name:

80SUS white mineral oil

Test material form:

other: Oily liquid

Details on test material:

- Name of test material (as cited in study report): Stock 461 (80" White Oil)
- Substance type: white mineral oil
- Physical state: liquid
- Composition of test material, percentage of components: 60% paraffins, 40% naphthenes
- Density: 0.88 g/mL

Test animals

Species:

rat

Strain:

Sprague-Dawley

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Charles River Breeding Laboratories, Lakeview, New Jersey, United States
- Age at study initiation: (P) 7 wks
- Weight at study initiation: not reported
- Fasting period before study: not reported
- Housing: cages with stainless steel floors and Beta Chip Bedding for nesting material for presumed-pregnant females
- Use of restrainers for preventing ingestion (if dermal): yes, Elizabethan-style collars
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: approximately three weeks


ENVIRONMENTAL CONDITIONS: not reported

IN-LIFE DATES: From: 1985-06-18 To: 1985-11-25

Administration / exposure

Route of administration:

dermal

Vehicle:

unchanged (no vehicle)

Details on exposure:

TEST SITE
- Area of exposure: intact, dorsal skin
- % coverage: not reported
- Type of wrap if used: none
- Time intervals for shavings or clippings: just prior to the first test material application and weekly thereafter


REMOVAL OF TEST SUBSTANCE
- Washing (if done): excess material was removed with a gauze pad
- Time after start of exposure: 4 hours


TEST MATERIAL
- Amount(s) applied (volume or weight with unit): applied as mg/kg
- Concentration (if solution): not reported
- Constant volume or concentration used: not reported


VEHICLE not reported


USE OF RESTRAINERS FOR PREVENTING INGESTION: yes

Details on mating procedure:

- M/F ratio per cage: 1:1
- Length of cohabitation: not reported
- Proof of pregnancy: female positive for sperm plug and spermatozoa were considered at day 0 of gestation
- No male replacements were made after unsuccessful mating
- Further matings after two unsuccessful attempts: not reported
- After successful mating each pregnant female was caged (how): individually
- Any other deviations from standard protocol: not reported

Analytical verification of doses or concentrations:

not specified

Details on analytical verification of doses or concentrations:

No data provided

Duration of treatment / exposure:

Animals were treated throughout pre-mating (approximately 10 weeks), mating (approximately 3 weeks), and post-mating (gestation days 0 through 20 for females, 9 weeks post-mating for males)

Frequency of treatment:

5 days/week except during gestation when females were treated daily

Details on study schedule:

- Age at mating of the mated animals in the study: approximately 17 weeks

Doses / concentrations

Remarks:

Doses / Concentrations:
0, 125, 500, 2000 mg/kg/day
Basis:

No. of animals per sex per dose:

20 females per dose, 10 males per dose

Control animals:

yes

Details on study design:

no data provided

Positive control:

none

Examinations

Parental animals: Observations and examinations:

CAGE SIDE OBSERVATIONS: Yes
- Time schedule: daily
- Cage side observations included: changes in appearance, behaviour, excretory function, ill-health, and mortality


DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: daily; Females were observed for pathosis, abortion, premature delivery, and mortality.


BODY WEIGHT: Yes
- Time schedule for examinations: once per week during premating phase; not measured during mating phase; presumed-pregnant females were measured in days 0, 3, 6, 10, 13, 16, 18 of gestation, and days 0, 4, 7, 10, 14, and 21 post-partum (lacation).


FOOD CONSUMPTION AND COMPOUND INTAKE (if feeding study):
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes
- Compound intake calculated as time-weighted averages from the consumption and body weight gain data: No data

Oestrous cyclicity (parental animals):

Estrous was determined in five female rats from the untreated control, vehicle control, and 2000 mg/kg-day group for two weeks prior to mating until breeding via examination of vaginal lavage fluid.

Sperm parameters (parental animals):

Data from male animals was not reported in the study.

Litter observations:

STANDARDISATION OF LITTERS
- Performed on day 4 postpartum: yes
- If yes, maximum of 8 pups/litter (4/sex/litter as nearly as possible); excess pups were killed and discarded.


PARAMETERS EXAMINED
The following parameters were examined in [F1] offspring:
number and sex of pups, stillbirths, live births, postnatal mortality, presence of gross anomalies, weight gain, physical or behavioural abnormalities, other: number of open eyelids for each pup was recorded on day 10 and continued daily until both eyes were open; righting reflex was examined on post-partum day 14.


GROSS EXAMINATION OF DEAD PUPS:
yes, for external and internal abnormalities; possible cause of death was not determined for pups born or found dead.

Postmortem examinations (parental animals):

Females were sacrificed on gestation day day 25 if they did not deliver pups or on postpartum day 21 if they did deliver pups. Thoracic and abdominal cavities were examined for gross morphologic changes. Uterus and ovaries were grossly examined and fixed in formalin. The number of implantation sites was recorded.

Postmortem examinations (offspring):

Thoracic and abdominal cavities were examined for gross morphologic changes.

Statistics:

ANOVA, group comparisons using Fisher's Exact or Dunnett's Test

Reproductive indices:

number of implantation sites

Offspring viability indices:

Live birth index, 4-day survival index, and 21-day survival index were measured.

Results and discussion

Results: P0 (first parental generation)

General toxicity (P0)

Clinical signs:

effects observed, treatment-related

Body weight and weight changes:

no effects observed

Food consumption and compound intake (if feeding study):

no effects observed

Organ weight findings including organ / body weight ratios:

no effects observed

Histopathological findings: non-neoplastic:

no effects observed

Other effects:

no effects observed

Reproductive function / performance (P0)

Reproductive function: oestrous cycle:

no effects observed

Reproductive function: sperm measures:

not specified

Reproductive performance:

no effects observed

Details on results (P0)

CLINICAL SIGNS AND MORTALITY (PARENTAL ANIMALS)
Clinical signs in females included slight dermal irritation (erythema, flaking, scabs) at the site of application

BODY WEIGHT AND FOOD CONSUMPTION (PARENTAL ANIMALS)
No signficant effects on body weight and food consumption were observed in treated females at any dose level.

TEST SUBSTANCE INTAKE (PARENTAL ANIMALS)
No significant effect on test substance intake was observed in treated females at any dose level.

REPRODUCTIVE FUNCTION: ESTROUS CYCLE (PARENTAL ANIMALS)
No significant effect on estrous cycle was observed in treated females at any dose level.

REPRODUCTIVE FUNCTION: SPERM MEASURES (PARENTAL ANIMALS)
Sperm measures were not included in this study report.

REPRODUCTIVE PERFORMANCE (PARENTAL ANIMALS)
No signficant effect on reproductive performance was observed in treated females at any dose level.

ORGAN WEIGHTS (PARENTAL ANIMALS)
No signficant effect on organ weights was observed in treated females at any dose level.

GROSS PATHOLOGY (PARENTAL ANIMALS)
No signficant effect on gross pathology was observed in treated females at any dose level.

HISTOPATHOLOGY (PARENTAL ANIMALS)
Histopathology was not included in this study report.

OTHER FINDINGS (PARENTAL ANIMALS): none reported

Effect levels (P0)

Dose descriptor:

NOAEL

Effect level:

>= 2 000 mg/kg bw/day

Sex:

female

Basis for effect level:

other: No adverse effects on reproductive parameters

Results: F1 generation

General toxicity (F1)

Clinical signs:

no effects observed

Mortality / viability:

no mortality observed

Body weight and weight changes:

no effects observed

Sexual maturation:

not examined

Organ weight findings including organ / body weight ratios:

not specified

Gross pathological findings:

no effects observed

Histopathological findings:

no effects observed

Details on results (F1)

VIABILITY (OFFSPRING)
No adverse effects were observed.

CLINICAL SIGNS (OFFSPRING)
No adverse effects were observed.

BODY WEIGHT (OFFSPRING)
No adverse effects were observed.

SEXUAL MATURATION (OFFSPRING)
No adverse effects were observed.

ORGAN WEIGHTS (OFFSPRING)
No adverse effects were observed.

GROSS PATHOLOGY (OFFSPRING)
No adverse effects were observed.

HISTOPATHOLOGY (OFFSPRING)
Histopathology results were not reported.

OTHER FINDINGS (OFFSPRING): No significant effect was observed on righting reflex or eyelid opening.

Effect levels (F1)

Dose descriptor:

NOAEL

Generation:

F1

Effect level:

>= 2 000 mg/kg bw/day

Sex:

male/female

Basis for effect level:

other: No adverse effects on reproductive parameters.

Overall reproductive toxicity

Reproductive effects observed:

not specified

Applicant's summary and conclusion

Conclusions:

Dermal administration of white mineral oil had no adverse effects on reproductive parameters or development of pups in a one-generation study. Therefore, the NOAEL is greater than or equal to 2000 mg/kg/day for both the parental and F1 generation.

Executive summary:

In a one-generation reproduction study, white mineral oil was administered dermally to Sprague-Dawley rats (10/dose for males, 20/dose for females) at dose levels of 0, 125, 500, or 2000 mg/kg bw/day at a frequency of 5 days/week during premating and daily during gestation (for females).

 

No mortality was observed in any treatment groups. No treatment-related changes in body weight gain or food consumption were observed in the females of the parental generation. No adverse effects were noted in the number of implantation sites per dam, litter size, or length of gestation in treated animals. Treatment-related clinical signs included erythema, scabs, and flaking at application site at all dose levels. No signs of gross toxicity were observed at necropsy. The parental systemic NOAEL is greater than or equal to 2000 mg/kg bw/day for females. Data on males were not provided in this study report.

 

The offspring exhibited no significant differences in body weight gain, eyelid disjunction, righting reflex, or viability in treated groups versus control.  No treatment-related signs of gross pathology were noted at necropsy. The offspring NOAEL is greater than or equal to 2000 mg/kg bw/day.

 

This study received a Klimisch score of 2 and is classified as reliable with restrictions because, although it closely follows OECD Guideline 415, no GLP statement was provided in the study report and only data on pregnant females and pups were provided.