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Diss Factsheets

Administrative data

Endpoint:
developmental toxicity
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2020-04-17 to to 2021-02-08
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2021
Report date:
2021

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
other: OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developme ntal Toxicity Screening Test)
Version / remarks:
2016
Deviations:
no
Qualifier:
according to guideline
Guideline:
other: EPA OPPTS 870.3650, Combined Repeated Dose Toxicity Study with the Reproduction/Deve lopmental Toxicity Screening Test
Version / remarks:
2000
GLP compliance:
yes
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,1,5,5,5-hexamethyl-3,3-bis[(trimethylsilyl)oxy]trisiloxane
EC Number:
222-613-4
EC Name:
1,1,5,5,5-hexamethyl-3,3-bis[(trimethylsilyl)oxy]trisiloxane
Cas Number:
3555-47-3
Molecular formula:
C12H36O4Si5
IUPAC Name:
tetratrimethylsilyl silicate
Test material form:
liquid

Test animals

Species:
rat
Strain:
Wistar
Remarks:
This animal model has been proven to be susceptible to the effects of reproductive toxicants.
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Charles River Deutschland, Sulzfeld, Germany
- Age at study initiation: Males: 10 to 11 weeks old; Females: 11 to 12 weeks old
- Weight at study initiation: Males: 250 to 325 g; Females: 194 to 244 g
- Fasting period before study: No
- Housing: Main animals were randomly group housed (up to five animals of the same sex and same dosing group together) in Makrolon polycarbonate cages on arrival and during the pre-mating period. Main males and females were cohabitated on a 1:1 basis in Makrolon plastic cages during the mating phase. Main males and females were housed in Makrolon plastic cages during the post-mating phase, with a maximum of five/cage for males and individually for females. During the lactation phase, pups were housed with the dam in Makrolon plastic cages except during locomotor activity monitoring of the dams. Each cage was clearly labeled with a colour-coded cage card indicating Test Facility Study No., group, animal number(s), and sex.
- Diet: ad libitum, except during locomotor activity
- Water: ad libitum, except during locomotor activity
- Acclimation period: Males: six days before commencement of dosing; Females: 7 days prior to start of the pretest period

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 to 22°C
- Humidity (%): 46 to 78%
- Air changes: 10 per hour minimum
- Photoperiod: 12-hour light/12-hour dark

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Details on exposure:
PREPARATION OF DOSING SOLUTIONS: The test item was administered as received. An adequate amount of the test item was dispensed into daily aliquots, which were stored the same as for the bulk test item until use. Test item dosing formulations were kept at room temperature until dosing. If practically possible, the dosing formulations and vehicle were continuously stirred until and during dosing. Adjustment was made for specific gravity of the test item (0.87). No correction was made for the purity/composition of the test item.

Analytical verification of doses or concentrations:
no
Details on mating procedure:
- M/F ratio per cage: 1:1
- Length of cohabitation: until evidence of mating (maximum of 14 days)
- Proof of pregnancy: vaginal plug / sperm in vaginal smear referred to as day 0 post-coitum
- After successful mating each pregnant female was caged (how): individually, in Makrolon plastic cages (MIII type, height 18 cm).
Duration of treatment / exposure:
At least 29 days. Main males and Recovery males were treated for 29 days including a minimum of 14 days prior to mating and during the mating period for Main males. Females that delivered offspring were treated for two weeks prior to mating, during mating, during post-coitum, and at least 13-15 days of lactation (for 52-65 days). Females that failed to deliver pups were treated for 41-52 days. Recovery females were treated during the same period as Main females, until at least the first scheduled necropsy of Main females (55 days).
Frequency of treatment:
Daily, 7 days a week
Duration of test:
Exposure period: Premating (14 days), mating, gestation, and postpartum days 13-15 for a maximum of 65 days depending on duration of mating/gestation phase
Doses / concentrationsopen allclose all
Dose / conc.:
0 mg/kg bw/day (actual dose received)
Remarks:
Group 1
Dose / conc.:
100 mg/kg bw/day (actual dose received)
Remarks:
Group 2
Dose / conc.:
300 mg/kg bw/day (actual dose received)
Remarks:
Group 3
Dose / conc.:
1 000 mg/kg bw/day (actual dose received)
Remarks:
Group 4
No. of animals per sex per dose:
15 males and females for Group 1 and 4 (water and 100 mg/kg/day of undiluted test item, respectively ); 10 males and 10 females for Group 2 and 3 (300 and 1000 mg/kg/day of undiluted test item, respectively)
Control animals:
yes
Details on study design:
- Dose selection rationale: Based on the results of a 14-day Dose Range Finder (Test Facility Reference No. 20226169)
- Rationale for animal assignment : random
- Fasting period before blood sampling for clinical biochemistry: Yes for main and recovery males, not for main females
- Rationale for selecting satellite groups: The recovery animals, euthanised following a 14-day treatment-free recovery period, were used to study the potential reversibility of possible toxic effects and were not mated.
- Post-exposure recovery period in satellite groups: Yes

Examinations

Maternal examinations:
CAGE SIDE OBSERVATIONS: Yes
- Time schedule: All animals were observed for general health/mortality and moribundity twice daily, in the morning and at the end of the working day. Animals were not removed from the cage during observation, unless necessary for identification or confirmation of possible findings. Cage debris of pregnant females was examined for evidence of premature delivery and pregnant females were examined to detect signs of difficult or prolonged parturition or deficiencies in maternal care.

DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: 1. Once daily, beginning during the first administration of the test item and lasting throughout the dosing and recovery periods up to the day prior to necropsy. During the dosing period, these observations were performed after dosing at no specific time point, but within a similar time period after dosing for the respective animals. The time of onset, grade and duration of any observed sign was recorded. Signs were graded for severity and the maximum grade was predefined at 1, 2, 3 or 4. Grades were coded as slight (grade 1), moderate (grade 2), severe (grade 3) and very severe (grade 4). For certain signs, only its presence (grade 1) or absence (grade 0) was scored.
2. Arena observations were also conducted beginning before the first administration of the test item and then once weekly throughout treatment and recovery. These observations were conducted after dosing.

Oestrous cycles were evaluated by examining the vaginal cytology of samples obtained by vaginal lavage. Daily vaginal lavage was performed for all females (Main and Recovery) during 14 days prior to treatment (pretest period) and the first 14 days of treatment. For Main females, daily vaginal lavage was continued during mating until evidence of copulation was observed.

BODY WEIGHT: Yes
- Time schedule for examinations: Animals were weighed individually on the first day of treatment (prior to dosing), and weekly thereafter. Mated Main females were weighed on Days 0, 4, 7, 11, 14, 17, and 20 post-coitum and during lactation on PND 1, 4, 7, and 13. A terminal weight was recorded on the day of scheduled necropsy.

FOOD CONSUMPTION: Yes
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes
Food consumption was quantitatively measured weekly, except for Main males and Main females which were housed together for mating and for Main females without evidence of mating. Food consumption of mated Main females was measured on Days 0, 4, 7, 11, 14, 17, and 20 post-coitum and during lactation on PND 1, 4, 7, and 13.

WATER CONSUMPTION : Yes
- Time schedule for examinations: Subjective appraisal was maintained during the study, but no quantitative investigation was introduced as no effect was suspected.

HAEMATOLOGY: Yes
- Time schedule for collection of blood: On the day of scheduled necropsy in main and recovery animals
- Anaesthetic used for blood collection: Yes (isoflurane)
- Animals fasted: Yes for main and recovery males, not for main females
- How many animals: All animals except for animals which were found dead or died during the blood sampling procedure
- Parameters checked in table were examined: yes, see table 1

CLINICAL CHEMISTRY: Yes
- Time schedule for collection of blood: On the day of scheduled necropsy in main and recovery animals
- Animals fasted: Yes for main and recovery males, not for main females
- How many animals: All animals except for animals which were found dead or died during the blood sampling procedure
- Parameters checked in table were examined.: yes, see table 1

URINALYSIS: No

FUNCTIONAL OBSERVATIONAL BATTERY: Yes
- Time schedule for examinations: Functional tests were performed on the five selected Main malesand all Recovery males during Week 4 of treatment and the five selected Main females during the last week of lactation (i.e. PND 6-13), and all Recovery females were tested on the first day a Main female was tested. These tests were performed after completion of clinical observations (including arena observation, if applicable).
- Battery of functions tested: Hearing ability, Pupillary reflex, statis righting reflex, Fore-and hind-limb grip strenght, locomotor activity.
As the above-mentioned measurements did not reveal test item-related effects, the functional observation tests were not performed at the end of the recovery phase.

POST-MORTEM EXAMINATIONS: Yes
- Sacrifice on PND 14-16 for main females which delivered.
- Organs examined: Histopathologic examination was performed on an extensive list of organs and tissues from five selected Main Group 1 and 4 animals as well as the lung from selected Main Group 2 and 3 and Recovery Group 1 and 4 rats and all organs with macroscopic findings from all rats. The reproductive organs were examined from all males that failed to sire and all females that failed to deliver healthy pups.

Ovaries and uterine content:
The ovaries and uterine content was examined after termination: Yes
Examinations included:
- Gravid uterus weight: Yes
- Number of corpora lutea: Yes
- Number of implantations: Yes
- Number of early resorptions: Yes
- Number of late resorptions: No data
Fetal examinations:
Number and sex of pups, stillbirths, live births, postnatal mortality, presence of gross anomalies, weight gain, physical abnormalities, anogenital distance (AGD), pup weight on the day of AGD, presence of nipples/areolae in male pups. Blood was collected from two pups per litter, and the thyroid from two pups per litter (if possible one male and one female pup) was preserved in 10% buffered formalin. The pups selected for blood sampling were the same pups as selected for thyroid preservation.
Statistics:
Mean values of the following were evaluated appropriately: body weights and body weight gain, food consumption and relative food consumption, grip fore and grip hind, total movements and ambulations, haematology and serum chemistry, terminal organ weights and body weight ratios, precoital time, implantation sites, gestation length, deads pups and living pups, litter weight, ratio of live births/litter size, anogenital distance and nipple retention, thyroid hormone values and thyroidweight, litter sex ratio, mating, fertility and gestation index.
Indices:
Gestation, viability and lactation indices

Results and discussion

Results: maternal animals

General toxicity (maternal animals)

Clinical signs:
effects observed, non-treatment-related
Description (incidence and severity):
No test item-related clinical signs were noted during daily detailed clinical observations or during weekly arena observations.
Any clinical signs noted during the treatment period occurred within the range of background findings to be expected for rats of this age and strain which are housed and treated under the conditions in this study and did not show any apparent dose-related trend. At the incidence observed, these were considered to be unrelated to treatment.
Mortality:
mortality observed, non-treatment-related
Description (incidence):
No mortality occurred during the study period that was considered to be related to treatment with the
test item.
Female No. 59 (control) died at blood sampling on the day of scheduled necropsy. No clinical signs were noted. Slightly low body weight gain was recorded on the days preceding its death. At necropsy many reddish foci on the thymus were recorded. As this was a control animal which died during the blood sampling procedure, this death was considered not treatment-related.
Female No. 80 (300 mg/kg/day) was found dead on Day 15 post-coitum. No clinical signs or body weight changes were noted on the days preceding death. At macroscopy reddish fluid in the trachea, not collapsed lungs and reddish discoloration of the lungs were recorded, suggesting that death was related to the gavage procedure.
Body weight and weight changes:
no effects observed
Description (incidence and severity):
Body weights and body weight gain of treated animals up to 1000 mg/kg/day remained in the same range as controls over the treatment period (Main and Recovery animals) and in the recovery period thereafter (Recovery animals only).
Food consumption and compound intake (if feeding study):
no effects observed
Description (incidence and severity):
Food consumption before or after correction for body weight was similar to the control level over the treatment period up to 1000 mg/kg/day (Main and Recovery animals) and in the recovery period thereafter (Recovery animals only).
Food efficiency:
not examined
Water consumption and compound intake (if drinking water study):
no effects observed
Ophthalmological findings:
not examined
Haematological findings:
no effects observed
Description (incidence and severity):
No statistically significant changes were recorded at the end of the treatment period. Any statistically significant differences recorded at the end of the recovery period (but not at the end of the treatment period) were considered not related to treatment with the test item. Coagulation parameters of treated rats were considered not to have been affected by treatment with the test item.
Clinical biochemistry findings:
effects observed, non-treatment-related
Description (incidence and severity):
No toxicologically relevant changes were noted in clinical biochemistry parameters after treatment with the test item up to 1000 mg/kg/day.
Any (statistically significant) changes noted were considered to be unrelated to treatment based on the small magnitude of change and/or as these changes occurred in the absence of a dose-related trend, or were recorded at the end of the recovery period only. Thyroid hormone analyses: Serum levels of T4 in Main males (F0-generation) were considered unaffected by treatment with the test item up to 1000 mg/kg/day.
Urinalysis findings:
not examined
Behaviour (functional findings):
effects observed, non-treatment-related
Description (incidence and severity):
Hearing ability, pupillary reflex, static righting reflex and grip strength were normal in all examined animals.
Motor activity in males at end of treatment was similar between control and treated animals.
Motor activity in Main females at end of treatment was increased at 300 and 1000 mg/kg/day, for total movements as well as and ambulations. As this difference was caused by one animal in each group (Nos. 84 and 88), this was considered not toxicologically relevant.
In Recovery females at the end of treatment total movements and ambulations were similar between treated and control animals.
A similar motor activity habituation profile with a decreasing trend in activity over the duration of the test period was noted in all groups and sexes.
Immunological findings:
not examined
Organ weight findings including organ / body weight ratios:
effects observed, non-treatment-related
Description (incidence and severity):
There were no test item-related alterations in organ weights.
In Main females lower absolute thyroid gland weights were recorded at the end of treatment starting at 100 mg/kg/day. These were considered the result of relatively high control values and not related to treatment with the test item.
Statistically significant changes in Main animals at the end of treatment were noted in seminal vesicles in males (lower relative to body weight at 100 and 300 mg/kg/day) and liver of females (higher relative to body weight at 300 mg/kg/day). These weight changes were considered to be of no toxicological significance as they occurred in the absence of a dose related trend.
Statistically significant changes in Recovery animals at the end of recovery were noted in the adrenal gland of females (lower absolute and relative to body weight at 1000 mg/kg/day) and kidney of females (lower relative to body weight at 1000 mg/kg/day). These weight changes were considered to be of no toxicological significance as they occurred in recovery animals only.
Gross pathological findings:
effects observed, treatment-related
Description (incidence and severity):
There were gross observations in the lungs of test item-treated animals at the end of the treatment period. Gray-white focus/foci were recorded in the lungs of 3/10 males at 100 mg/kg/day, in 1/10 males at 300 mg/kg/day and in 2/10 females at 1000 mg/kg/day. In 1/10 males at 300 mg/kg/day a hardened, discolored lung lobe was recorded. The microscopic correlate for these necropsy findings was multifocal granulomatous inflammation.
The remainder of the recorded macroscopic findings were within the range of background gross observations encountered in rats of this age and strain.
Neuropathological findings:
not examined
Histopathological findings: non-neoplastic:
effects observed, treatment-related
Description (incidence and severity):
There were microscopic observations of note in the lungs of some animals after treatment with the test item at all dose levels.
At the end of the treatment period, main finding in the lungs of both sexes consisted of granulomatous inflammation (varying from minimal to marked degree). This was recorded in three males and two females at 100 mg/kg/day, two males and two females at 300 mg/kg/day and in one male and three females at 1000 mg/kg/day. The multifocal granulomatous inflammatory processes contained multinucleated foreign body giant cells, a varying amount of vacuolated material (mainly in macrophages
) and granulocytic inflammatory cells. This inflammatory process was seen in one or more lung lobes and was in most cases located close to the main stem bronchi.
Additional findings in the lungs included, alveolar (vacuolated) macrophage aggregations (varying from minimal to marked degree) and an increased incidence and severity of perivascular/peribronchial mixed inflammatory cell infiltrate (minimal to slight degree). There was no dose relationship for the incidences and severities of these lung alterations.
After the 14-day treatment-free recovery period two males and three females of the 1000 mg/kg/day group showed granulomatous inflammation (minimal-slight). The alveolar (vacuolated) macrophage aggregations and/or perivascular/peribronchial mixed inflammatory cell infiltrates were recorded for some animals but didn’t exceed a minimal degree. The alterations in the lungs of the recovery animals were recorded at lower severities compared to the animals at the end of the treatment period, suggesting partial, ongoing recovery. These alterations were attributed to aspiration of non-lethal amounts of test item formulation resulting in local inflammatory lesions in the lungs.
Histopathological findings: neoplastic:
no effects observed
Other effects:
not specified

Maternal developmental toxicity

Number of abortions:
no effects observed
Description (incidence and severity):
Examination of cage debris of pregnant females revealed no signs of abortion or premature birth.
Pre- and post-implantation loss:
no effects observed
Description (incidence and severity):
The total number of offspring born compared to the total number of uterine implantations was considered not to be affected by treatment with the test item.
Post-implantation survival index was 94, 95, 74 and 95% for the control, 100, 300 and 1000 mg/kg/day groups, respectively.
The low post-implantation survival index at 300 mg/kg/day was considered a result of the death of Female No. 80 during the post-coitum period. When this animal was not taken into
account, the post-implantation survival index was 92%. For Female Nos. 68 (100 mg/kg/day) and 92 (1000 mg/kg/day), the number of pups was
slightly higher than the number of implantations. This phenomenon is observed from time to time and is caused by normal resorption of these areas during lactation. No toxicological
relevance was attached to this finding in the current study.
Total litter losses by resorption:
no effects observed
Description (incidence and severity):
Litter size was considered not affected by treatment.
Live litter sizes were 12.6, 11.4, 11.0 and 10.7 living pups/litter for the control, 100, 300 and 1000 mg/kg/day groups, respectively.
Slightly lower mean number of living pups recorded at 100, 300 and 1000 mg/kg/day were considered the results of a slightly high control value.
Early or late resorptions:
no effects observed
Dead fetuses:
no effects observed
Description (incidence and severity):
The number of live offspring on Day 1 after littering compared to the total number of offspring born was unaffected by treatment.
The live birth index was 100% for the control, 100, 300 and 1000 mg/kg/day groups.
Changes in pregnancy duration:
no effects observed
Description (incidence and severity):
Gestation index and duration of gestation were considered not to be affected by treatment with the test item. Mean duration of gestation was 21.3, 21.3, 21.5 and 21.5 days, in order of ascending dose level.
Except for one female in the control group (Female No. 51, one implantation only) and one female at 300 mg/kg/day (Female No. 80, found dead on post-coitum Day 15), all pregnant
females had live offspring. Females No. 78, 83 and 85 at 300 mg/kg/day were not pregnant. The gestation index was 90, 100, 86 and 100% for the control, 100, 300 and 1000 mg/kg/day groups, respectively.
Changes in number of pregnant:
no effects observed
Description (incidence and severity):
There were 1/10 couples of the control group (Male No. 1 and Female No. 51), 2/10 couples at 100 mg/kg/day (Male Nos. 19, 20 and Female Nos. 69, 70) and 3/10 couples at 300
mg/kg/day day (Male Nos. 28, 33, 35 and Female Nos. 78, 83, 85) with no offspring. No abnormalities were seen in the reproductive organs, which could account for their lack of
offspring. As Female Nos. 78, 83 and 85 at 300 mg/kg/day were not pregnant and Female No. 80 was found dead during the post-coitum period, developmental data was available of only six females in the mid dose group.
Other effects:
not specified

Effect levels (maternal animals)

open allclose all
Key result
Dose descriptor:
NOAEL
Remarks:
Maternal developmental effects
Effect level:
> 1 000 mg/kg bw/day (actual dose received)
Based on:
test mat.
Remarks on result:
not determinable due to absence of adverse toxic effects
Dose descriptor:
NOAEL
Remarks:
Maternal general toxicity (systemic effects)
Effect level:
> 1 000 mg/kg bw/day (actual dose received)
Based on:
test mat.
Basis for effect level:
other: No systemic parental toxicity was observed up to 1000 mg/kg/day
Remarks on result:
not determinable due to absence of adverse toxic effects

Maternal abnormalities

Key result
Abnormalities:
no effects observed

Results (fetuses)

Fetal body weight changes:
no effects observed
Description (incidence and severity):
Body weights of pups were considered not to be affected by treatment with the test item.
Reduction in number of live offspring:
no effects observed
Description (incidence and severity):
The number of live offspring on Day 1 after littering compared to the total number of offspring born was unaffected by treatment.
The live birth index was 100% for the control, 100, 300 and 1000 mg/kg/day groups.
Changes in sex ratio:
no effects observed
Description (incidence and severity):
Sex ratio was considered not to be affected by treatment with the test item.
Changes in litter size and weights:
no effects observed
Description (incidence and severity):
Litter size was considered not affected by treatment.
Live litter sizes were 12.6, 11.4, 11.0 and 10.7 living pups/litter for the control, 100, 300 and 1000 mg/kg/day groups, respectively.
Slightly lower mean number of living pups recorded at 100, 300 and 1000 mg/kg/day were considered the results of a slightly high control value
Changes in postnatal survival:
no effects observed
Description (incidence and severity):
The number of live offspring on Day 4 before culling compared to the number of offspring on Day 1 was considered not affected by treatment.
Viability indices were 100, 99, 100 and 99% for the control, 100, 300 and 1000 mg/kg/day groups, respectively.
There were two pups missing between PND 2 and 3 (Pup No. 5 of Litter No. 74 of the 100 mg/kg/day group and Pup No. 4 of Litter No. 88 of the 1000 mg/kg/day group). For pup No. 5 of Litter No. 74 pale appearance was recorded at first litter check. Pups missing were most likely cannibalized. No toxicological relevance was attributed to these dead/missing
pups since the mortality incidence did not show a dose-related trend and remained within the
range considered normal for pups of this age.
External malformations:
no effects observed
Description (incidence and severity):
No clinical signs occurred among pups that were considered to be related to treatment with the test item. The nature and incidence of clinical signs remained within the range considered normal for pups of this age and were therefore considered not to be toxicologically relevant.
Skeletal malformations:
not specified
Visceral malformations:
not specified
Other effects:
no effects observed
Description (incidence and severity):
Serum T4 levels in male and female PND 14-16 pups were considered not to be affected by treatment up to 300 mg/kg/day.
The number of live offspring on Day 13 after littering compared to the number of live offspring on Day 4 (after culling) was considered not to be affected by treatment. In the control group and at 300 and 1000 mg/kg/day, no pups were found dead/missing between lactation Days 5 and 13, resulting in a lactation index of 100%. For the 100 mg/kg/day group, the lactation index was 98%.
One pup of the 100 mg/kg/day group (Pup No. 1 of Litter No. 71) was missing on PND 5. Pups missing were most likely cannibalized. No toxicological relevance was attributed to these dead/missing pups since the mortality incidence did not show a dose-related trend and remained within the range considered normal for pups of this age.

Effect levels (fetuses)

Key result
Dose descriptor:
NOAEL
Effect level:
>= 1 000 mg/kg bw/day (actual dose received)
Based on:
test mat.
Sex:
male/female
Remarks on result:
not determinable due to absence of adverse toxic effects

Fetal abnormalities

Key result
Abnormalities:
no effects observed

Overall developmental toxicity

Key result
Developmental effects observed:
no

Any other information on results incl. tables

Table 3: Correlation of Histopathology Findings with In-Life Reason for Males that Failed to Sire and Females that

Failed to Deliver Healthy Pups.

 Group Dose level (mg/kg bw/day)  No. Female/Male  In-life reason Histopathology 
 1  0  51/01  Not mated  No histopathological correlate
 2 100 

69/19

70/20 

Not pregnant

Not pregnant 

No histopathological correlate

No histopathological correlate

 3 300 

78/28

83/33

85/35 

Not pregnant

Not pregnant

Not pregnant 

No histopathological correlate

No histopathological correlate

No histopathological correlate

 4  1000  -  -   -

Applicant's summary and conclusion

Conclusions:
In a combined repeated dose oral toxicity study with the reproduction/developmental toxicity screening test with the registered substance 1,1,1,5,5,5-hexamethyl-3,3-bis[(trimethylsilyl)oxy]trisiloxane, conducted according to OECD Test Guideline 422 and in compliance with GLP, a NOAEL for maternal and foetal developmental effects was concluded to be > 1000 mg/kg bw/day based on no treatment-related effects observed in any of the developmental parameters evaluated.