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EC number: 231-308-5 | CAS number: 7491-09-0
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
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- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
![](https://echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Endpoint summary
Administrative data
Description of key information
Repeated dose toxicity was tested in various species, including rats, dogs, rabbits and monkeys. The NOAEL of 1000 mg/kg bw/day obtained in the key study in rats on docusate sodium was confirmed to be consistent with data from docusate sodium and category members in supporting studies in rats; other data from other species were of limited reliability and relevance and therefore not taken into account.
The NOAEL of 1000 mg/kg bwt/day for docusate sodium will be used to read across to Potassium 1,2-bis(2-ethylhexyloxycarbonyl)ethanesulphonate CAS No 7491-09-0, 0 as in the body the test substance will dissociate and exposure will be to the same test substance the sodium and potassium ion not affecting possible toxicity.
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Link to relevant study records
- Endpoint:
- sub-chronic toxicity: oral
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- 2016-2017
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Justification for type of information:
- Data has been read across from a structurally identical substance forming a salt with sodium instead of potassium. This is not expected to chenge the toxicological properties in a significant way. See further discussion in the read across justification attached.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 408 (Repeated Dose 90-Day Oral Toxicity Study in Rodents)
- Version / remarks:
- Adopted 21st September 1998
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.26 (Sub-Chronic Oral Toxicity Test: Repeated Dose 90-Day Oral Toxicity Study in Rodents)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Limit test:
- no
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No.of test material: SD6073132, Manufacturer: Cytec-Solvay Group Willow Island Plant, #1 Heilman Avenue, Willow Island, WV 26134, USA
- Expiration date of the lot/batch: July 31, 2019 (3 years from date of manufacturing)
- Purity test date: August 4, 2016
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: At +10°C to +25°C
- Stability under test conditions: The analysis of the left-over-diet (food which has been available to the animals for 6 to 7 days) revealed a stability of the test item in the test item-diet mixture. The measured concentrations ranged from 88.4% to 110.1% (low dose), from 82.0% to 102.5% (intermediate dose) and from 87.1% to 112.9% (high dose) in test weeks 1, 4, 8 and 13. - Species:
- rat
- Strain:
- other: Crl:CD(SD)
- Details on species / strain selection:
- Selected because of its proven suitability in toxicology studies and to comply with regulatory requirements for testing in a rodent animal species.
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Laboratories, Research Models and Services, Germany GmbH, Sandhofer Weg 7, 97633 Sulzfeld, Germany
- Age (at 1st dosing): Males: 65 days; Females: 65 days
- Body weight (at 1st dosing): Males: 282.6 – 332.8 g; Females: 207.0 - 260.5 g
- Housing: The animals were kept singly in MAKROLON cages (type III plus) with a basal surface of approx. 39 cm x 23 cm and a height of approx. 18 cm. Granulated textured wood (Granulat A2, J. Brandenburg, 49424 Goldenstedt, Germany) was used as bedding material for the cages. The cages were changed and cleaned once a week.
- Diet (e.g. ad libitum): Commercial ssniff®-R/M-H V1530 diet (ssniff® Spezialdiäten GmbH, 59494 Soest, Germany) served as food.This diet was offered without Docusate Sodium to group 1 and with Docusate Sodium to groups 2, 3 and 4 ad libitum. food residue was removed and weighed weekly.
- Water (e.g. ad libitum): Drinking water was offered ad libitum.
- Acclimation period: 6 days
DETAILS OF FOOD AND WATER QUALITY:
Periodic analysis of the food for contaminants based on EPA/USA1 is conducted at least twice a year by LUFA-ITL (Landwirtschaftliche Untersuchungs- und Forschungsanstalt, Institut für Tiergesundheit und Lebensmittelqualität GmbH, 24107 Kiel, Germany.). Certificates of analysis of the composition and for contaminants were provided by the manufacturer and are included in the raw data.
Samples of drinking water are taken periodically by the Wasserwerk Wankendorf and periodic analyses are performed by LUFA-ITL according to the 'Deutsche Trinkwasserverordnung 2001' [German Regulations on drinking water 2001] (Version from August 02, 2013, revised on November 18, 2015.
In addition, drinking water samples taken at LPT are analysed by LUFA-ITL once a year for means of bacteriological investigations according to the 'Deutsche Trinkwasserverordnung 2001, Anlage 1' [German Regulations on drinking water 2001, Addendum 1].
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22°C ± 3°C (maximum range)
- Humidity (%): 55% ± 10% (maximum range). Deviations from the maximum range caused for example during cleaning procedures are dealt with in SOPs.
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES:
From: Start of the exposure period May 23, 2017
To: Termination of the in-life period:September 18, 2017
Dissection of main study animals August 21, 2017
Dissection of recovery animals September 18, 2017 - Route of administration:
- oral: feed
- Details on route of administration:
- According to expected route of exposure and international guidelines.
- Vehicle:
- unchanged (no vehicle)
- Remarks:
- in diet
- Details on oral exposure:
- DIET PREPARATION
- Rate of preparation of diet (frequency): The test item-diet mixtures were freshly prepared once a week.
- Mixing appropriate amounts with (Type of food): The appropriate amount of pre-cooled (+2°C to +8°C) test item (based on the most recently recorded food consumption and body weights) was chopped or shredded into small pieces and weighed into a glass container. Some of the test item and of also pre-cooled diet were mixed with an impact mill to produce a premix. This process was repeated until the whole quantity of test compound was distributed in the diet. Then the premix was added to the diet, mixed with a mixer (Röhnradmischer; Typ ELTE 650; J. Engelsmann AG, Ludwigshafen, Germany) for 15 minutes and then transferred to a closable bucket. Each bucket was labelled with study number, group number, sex, and dose.
To maintain a constant dose level in relation to the animals body weight, the concentration in the diet was adjusted based on the mean group food consumption per sex. The concentration was adjusted weekly using the food consumption values from the previous week.
The total weekly intake of the test item was calculated and reported as daily average for the respective week.
- Storage temperature of food: stored at +10°C to +25°C. - Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- For the determination of the Docusate Sodium concentration in the exposure diets (groups 1 to 4), samples of approximately 10 g were taken at the following times and stored at -20°C or colder until analysis at LPT.
Exposure diet analysis:
Determination Test week Handling of samples per Number of samples
sex and dosage (in total 3 (including control)
dosages and 1 control) per sex# total
Concentration 1 One sample from each of 10 20
and 4 three areas (top, middle and 10 20
homogeneity 8 bottom) of the bucket## 10 20
13 10 20
Concentration 1 Left-over diet food which 4 8
and stability 4 has been available to the 4 8
(left-over diet) 8 animals for 7 days 4 8
13 Left-over diet food which 4 8
has been available to the
animals for 6 days
Total number of samples: 56 112
#: Due to gender dependent body weight gain, the test item concentrations were calculated and mixed separately for males and females.
##: Only one sample from the control.
The samples were labelled with study number, test species, sex, type of sample, concentration, test week, location (top/middle/bottom), and date.
The samples were analysed for Docusate Sodium according to the HPLC-UV method for the determination of the test item in diet-mixture samples validated at LPT (LPT validation study no. 34903). The results of the validation confirmed that the method employed was suitable for the determination and quantification of Docusate Sodium in diet-mixture samples (diet: ssniff® R/M-H V1530).
The mean test item intake per week ranged from 84 to 117 and 78 to 117 mg/kg bw/day for the male and female animals treated with a nominal dose level of 100 mg Docusate Sodium/kg bw/day via the diet, respectively, from 250 to 351 and 237 to 350 mg/kg bw/day for the male and female animals treated with a nominal dose level of 300 mg Docusate Sodium/kg bw/day via the diet, respectively, and from 854 to 1239 and 811 to 1369 mg/kg bw/day for the male and female animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet, respectively.
The results of the analysis revealed that the test item-diet mixtures were correctly prepared and were very homogenous. The measured concentrations ranged from 81.6% to 119.4% (low dose), from 83.4% to 115.8% (intermediate dose) and from 91.9% to 111.6% (high dose) in test weeks 1, 4, 8 and 13.
The results were within the admissible limits of 80% to 120% for a test item-diet mixture preparation.
The analysis of the left-over-diet (food which has been available to the animals for 6 to 7 days) revealed a stability of the test item in the test item-diet mixture. The measured concentrations ranged from 88.4% to 110.1% (low dose), from 82.0% to 102.5% (intermediate dose) and from 87.1% to 112.9% (high dose) in test weeks 1, 4, 8 and 13.
No Docusate Sodium could be detected in any of the control samples. - Duration of treatment / exposure:
- 90 test days, 28 additional days for the animals scheduled for the recovery period
- Frequency of treatment:
- daily in diet
- Dose / conc.:
- 0 mg/kg bw/day (nominal)
- Remarks:
- Control (Group 1; standard diet)
- Dose / conc.:
- 100 mg/kg bw/day (nominal)
- Remarks:
- Docusate Sodium (Group 2)
- Dose / conc.:
- 300 mg/kg bw/day (nominal)
- Remarks:
- Docusate Sodium (Group 3)
- Dose / conc.:
- 1 000 mg/kg bw/day (nominal)
- Remarks:
- Docusate Sodium (Group 4)
- No. of animals per sex per dose:
- Main study: 10 per sex per group (80 in total)
Recovey animals: 5 per sex per group for groups 1, 3 and 4 (30 in total)
Additionally, 10 spare animals (5 males and 5 females) were reserved for possible replacement during the adaptation period, however, not used. - Control animals:
- yes, plain diet
- Details on study design:
- - Dose selection rationale: The dose levels for this study were selected in agreement with the Sponsor based on available data and the results of a preliminary 14-day dose-range finding study
(LPT study report no. 34271):
The doses administered via the diet in the dose-range finding study 34271 ranged from 821 to 1414 mg/kg bw/day, depending on the daily food intake of the animals. No deaths and no signs of toxicity were noted. No influence was observed on the body weight, the body weight gain, and the food and drinking consumption. No test item-related findings were noted at macroscopic inspection at necropsy. The male animals revealed increased kidney and liver weights on test day 15.
After consideration of these data nominal dose levels of 100, 300 and 1000 mg Docusate Sodium/kg bw/day via the diet were selected for this 90-day toxicity study.
- Rationale for animal assignment (if not random): The animals were allocated to the 4 test groups based on body weight by means of a computerised randomisation program. Animals with a body weight at the extremes of the weight distribution were excluded and replaced by healthy spare animals. Animal replacement after the first dosing was not planned nor did it occur.
- Rationale for selecting satellite groups: 5 animals/sex/group were allocated to groups 1, 3 and 4 at the start of the experiment for 28 days recovery after 90 days of dosing
- Post-exposure recovery period in satellite groups: 28 days
- Section schedule rationale (if not random): Starting on test day 91 the main study animals were dissected following a randomisation scheme. Animals allocated to the recovery period were dissected on test day 119. - Observations and examinations performed and frequency:
- CAGE SIDE OBSERVATIONS: Yes
- Time schedule: The animals were observed individually at least once daily.
Animals were checked regularly throughout the working day from 7.00 a.m. to 3.45 p.m. On Saturdays and Sundays animals were checked regularly from 7.00 a.m. to 11.00 a.m. with a final check performed at approximately 3.30 p.m.
- Cage side observations included any signs of behavioural changes, reaction to treatment or illness: yes.
skin/fur, eyes, mucous membranes, respiratory and circulatory systems, somatomotor activity and behaviour patterns.
The onset, intensity and duration of any signs observed were recorded.
Dated and signed records of appearance, change and disappearance of clinical signs were maintained on clinical history sheets for individual animals.
Checks were made early in the morning and again in the afternoon of each working day to look for dead or moribund animals. This would have allowed post mortem examination to be carried out during the working period of that day. On Saturdays and Sundays a similar procedure was followed except that the final check was carried out at approximately 4:00 p.m.
However, no premature deaths occurred in this study.
DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: Additionally, once before the first exposure (to allow for within-subject comparisons) and once a week thereafter (always on the first day of the test week), detailed clinical observations were made in all animals. In test week 13 these observations were performed prior to any laboratory investigations. These observations were made outside the home cage in a standard arena and at the same time of day, each time.
Signs noted included changes in skin, fur, eyes, mucous membranes, occurrence of secretions and excretions and autonomic activity (e.g. lacrimation, pilo-erection, pupil size, unusual respiratory pattern).
Changes in gait, posture and response to handling as well as the presence of clonic or tonic movements, stereotypies (e.g. excessive grooming, repetitive circling) or bizarre behaviour (e.g. self-mutilation, walking backwards) were also recorded.
BODY WEIGHT: Yes
- Time schedule for examinations: The weight of each rat was recorded at the time of group allocation, on the day of commencement of treatment and once a week thereafter always on the same day of the week throughout the experimental period.
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
The quantity of food left by individual animals was recorded on a weekly basis throughout the experimental period. The food intake per rat (g/rat/week) was calculated using the total amount of food given to and left by each rat in each group on completion of a treatment week.
The relative food consumption (in g/kg bw/day) was calculated as follows:
Relative food consumption = Total food given (g) - Total food left (g)
(g/kg bw/day) Number of animal days# × Body weight (kg)
# The term 'animal days' counts one animal day for each animal alive for a whole day; it is assumed that on the day of death an animal does not eat.
- Compound intake calculated as time-weighted averages from the consumption and body weight gain data: Yes
Individual test item intake was calculated on a weekly basis throughout the experimental period based on concentration in the diet, individual food intake and body weight.
FOOD EFFICIENCY: no (not required)
WATER CONSUMPTION AND COMPOUND INTAKE INTAKE (no drinking water study): Yes
- Time schedule for examinations: The drinking water consumption was monitored daily by visual appraisal throughout the study.
OPHTHALMOSCOPIC EXAMINATION: Yes.
- Time schedule for examinations: Examinations were performed on all animals at study initiation (on test day 7), at the end of the main study (on test day 87 in test week 13) and at the end of the
recovery period (on test day 116 in test week 17).
- Dose groups that were examined: on all animals
The eyes were examined with a HEINE ophthalmoscope.
After examination of the pupillary reflex, mydriasis was produced by instillation of STULLN®10 eye drops onto the cornea. The following ocular structures were then examined: Adnexa oculi (i.e. lids, lacrimal apparatus), conjunctiva; Cornea, anterior chamber; Lens, vitreous body, fundus (retina, optic disc)
HAEMATOLOGY: Yes
- Time schedule for collection of blood:
At the end of the treatment period (on the first day of dissection, test day 91) for all animals
At the end of the recovery period (on the day of dissection, test day 119) for all recovery animals
- Anaesthetic used for blood collection: Yes, light ether anaesthesia
- Animals fasted: Yes, fasted overnight
- How many animals: all animals/all recovery animals
- Parameters examined: Haemoglobin content, Erythrocytes, Leucocytes, Reticulocytes, Platelets, Haematocrit, Differential blood count (relative), Differential blood count (absolute), Mean corpuscular volume, Mean corpuscular haemoglobin, Mean corpuscular haemoglobin concentration
CLINICAL CHEMISTRY: Yes
- Time schedule for collection of blood:
At the end of the treatment period (on the first day of dissection, test day 91) for all animals
At the end of the recovery period (on the day of dissection, test day 119) for all recovery animals
- Animals fasted: Yes, fasted overnight
- How many animals: all animals/all recovery animals
- Parameters examined: Albumin, Globulin, Albumin/globulin ratio, Bile acids, Bilirubin (total), Cholesterol (total), Creatinine, Glucose, Protein (total), Triglycerides, Urea (in blood), Calcium, Chloride, Potassium, Sodium, Alanine amino-transferase (ALAT), Alkaline phosphatase (aP), Aspartate dehydrogenase (ASAT), Lactate dehydrogenase (LDH), Gamma-glutamyl-transferase (Gamma-GT), coagulation (TPT, aPTT).
URINALYSIS: Yes
- Time schedule for collection of urine:
At the end of the treatment period (on test days 90 to 91) for all animals
At the end of the recovery period (on test days 118 to 119) for all recovery animals
- Metabolism cages used for collection of urine: Yes. The urine was collected for 16 hours in an URIMAX funnel cage. The collection of urine was terminated immediately prior to starting the blood withdrawals for the haematological and clinical chemistry examinations.
- Animals fasted: Yes, fasted overnight
- Parameters examined: Volume, Osmolality, pH, Specific gravity.
Protein, Glucose, Bilirubin, Urobilinogen, Ketones, Haemoglobin (approx. Values), Nitrite.
Microscopic examinations of urine samples were carried out by centrifuging samples and spreading the resulting deposit on a microscopic slide. The deposits were examined for the presence of the following parameters: Epithelial cells, Leucocytes, Erythrocytes, Organisms, Further constituents (i.e. sperm, casts), Crystalluria.
The colour and turbidity of the urine were examined visually.
NEUROBEHAVIOURAL EXAMINATION: Yes
- Time schedule for examinations:
Neurological screening: In test weeks 13 and 17 (before any blood sampling for laboratory examinations), screening of sensory reactivity to stimuli of different types (e.g. auditory, visual and proprioceptive stimuli) (based on GAD), as well as the assessment of grip strength (MEYER) and motor activity assessment were conducted in all animals approximately 2 hours after dosing outside the home cage.
- Dose groups that were examined: all animals
- Battery of functions tested:
Observational screening
*Righting reflex: The animal was grasped by its tail and flipped in the air (approx. 60 cm) above the cart surface so that it turned head over heels. The normal animal should land squarely on its feet, in this case zero (0) points were scored. If it landed on its side, 1 point was scored; if it landed on its back, 2 points were scored. This test was repeated five times and the total scores were recorded.
*Body temperature: An electronic probe thermometer (with a blunt probe) was used to take a rectal temperature, being allowed to equilibrate for 30 seconds before the reading was recorded.
*Salivation: The animals were observed for discharge of clear fluid from mouth, most frequently seen as beads of moisture on lips in rats. Normal state is to see none, in which case a zero (0) was recorded. If present, a plus sign (+) was recorded.
*Startle response: With the animal on the cart, the metal cage was struck with the blunt probe. The normal animal should exhibit a marked but short-lasting response, in which case a zero (0) was recorded. If there was no response, a plus sign (+) was recorded.
*Respiration: While at rest on the cart, the animal's respiration cycle was observed and evaluated in terms of a scale from 1 (reduced) to 5 (increased), with 3 being normal.
*Mouth breathing: Rats are normally obligatory nose-breathers. Each animal was observed, whether or not it was breathing through its mouth. If the rat was breathing through its nose, a zero (0) was recorded. Mouth breathing was documented by a plus sign (+).
*Urination: When an animal was removed from its cage, the pan beneath the animal's cage was examined while returning the animal to its cage. The signs of urination were evaluated on a scale of 0 (lacking) to 5 (polyurea) with 3 being normal.
*Convulsions: If clonic or tonic convulsions were observed, their intensity was graded on a scale of 1 (minor) to 5 (marked) and the type was recorded. In the normal animal no, convulsions should be observed, in which case a score of zero (0) was recorded.
*Pilo-erection: The fur of the animal's back was observed, whether it was raised or elevated. In the normal animal no pilo-erection should be observed and a score of zero (0) was recorded. If pilo-erection was present, a plus sign (+) was recorded.
*Diarrhoea: In examining the pan beneath an animal's cage, it was noted if there were any signs of loose or liquid stools. Normal state is for there to be none (0), in case of diarrhoea the intensity was recorded on a scale of 1 (slight) to 5 (much increased).
*Pupil size: It was determined if the pupils were constricted or dilated and the observations were evaluated in terms of a scale from 1 (constricted) to 5 (dilated), with 3 being normal.
*Pupil response: The beam of light from the pen light was played across the eyes of the animal and the changes in pupil size were noted. In the normal animal, the pupil is constricted when the beam is on it and then dilates back to normal when the light is removed, whereby a score of zero (0) was recorded. If there was no pupil response, a minus sign was recorded.
*Lacrimation: The animal was observed for the secretion and discharge of tears. In rats the tears contain a reddish pigment. No discharge is normal, whereby a score of zero (0) was recorded. If a discharge was present, a plus sign was recorded.
*Impaired gait: The occurrence of abnormal gait was evaluated. The most frequent impairments are waddling (W), hunched gait (H), or ataxia (A, the inability of all the muscles to act in unison). The extent of any impairment was recorded on a scale of 1 (slight) to 5 (marked). A normal gait was documented by a score of zero (0).
*Stereotypy
Each animal was evaluated for stereotypic behaviour (isolated motor acts or partial sequences of more complex behavioural patterns, occurring out of context and with an abnormal high frequency). These were graded on a scale of 0 (absent = normal) to 5 (marked).
*Toe pinch: The blunt probe was used to bring pressure to bear on one of the digits of the hind limb. This should evoke a response from the normal animal. The response or lack thereof was graded on a scale from 1 (absent) to 5 (exaggerated) with 3 being the normal response.
*Tail pinch: The toe pinch procedure was utilized with the animal's tail instead of its hind limb and was graded on the same scale of 1 to 5 with 3 being the normal response.
*Wire maneuver
The animal was placed on the metal rod suspended parallel to the cart approximately 60 cm above the cart's surface. The animal's ability to move along the rod was evaluated. If impaired, a score of from 1 (slightly impaired) to 5 (unable to stay on wire) was recorded. Normal movement was documented by a score of zero (0).
*Hind leg splay: Using an ink pad, the hind paws were marked with ink. The rat was then held 30 cm above a sheet of blotting paper on the cart. The animal was dropped and the distance between the prints of the two hind paws was measured.
*Positional passivity: The animal was observed after being placed in an awkward position, such as on the edge of the top of the wire-bottomed cage on the cart surface. If the animal immediately moved into a normal position, a score of zero (0) was recorded. If not, a score was recorded on a scale of 1 (slightly impaired) to 5 (cataleptic).
*Tremors: Periods of continued fine movements, usually starting in the limbs (and perhaps limited to them). The normal case is to have none, in which case a score of zero (0) was recorded. If tremors were present, they were graded on a scale of 1 (slight and infrequent) to 5 (continuous and marked).
*Positive geotropism: The animal was placed on the inclined (at an angle of approx. 30°) top surface of the wire cage with its head facing downward. It should turn 180° and face 'uphill', in which case a score of zero (0) was recorded. If this did not occur, a negative sign was recorded.
*Limb rotation: One of the animal's hind limbs was taken and moved through its normal plane of rotation. In the normal state, it should rotate readily but there should be some resistance. The variations from normal were from no resistance (1) to markedly increased resistance or rigidity (5), with 3 being normal.
*Auditory function: Each animal was placed in a container and observed for Preyer's reflex (twitching of the pinna) in response to a high frequency sound stimulus. The stimulus was repeated, if necessary, up to 3 times. A normal response was recorded with a plus sign (+). If there was no response a zero (0) was recorded.
Functional tests
*Grip strength: Prior to testing, the gauge (Chatillon, Model DPP - 1.0 kg) was calibrated with a set of known weights and the apparatus was adjusted for the size of the animal (about 1 cm clearance on both sides of the animal). After the strain gauge had been zeroed and set in the record mode, the animal was placed into the trough with the forepaws inside the triangular grasping ring. Using one hand, the animal was grasped about 2.5 cm of the way up toward the base of the tail and steadily pulled (approx. 2.5 cm/sec) away from the ring until the grip was broken. The animal continued to be pulled along the trough until the hind limbs grasp the T-bar.
The trial was completed when grip of the hind limbs was broken. Three successive readings were taken for each animal with an intertrial interval long enough to record the data and zero both meters for the next trial.
*Locomotor activity: The motility was measured using the TSE InfraMot system8. The infrared sensor was mounted on top of the home cage and any movements were measured for the duration of 12 minutes by sensing the body heat image, i.e. the infrared radiation, and its spatial displacement over time.
Any movements within the cage, even brief movement events of only a few milliseconds duration, were detected and included in the activity data.
IMMUNOLOGY: No - Sacrifice and pathology:
- GROSS PATHOLOGY: Yes
Starting on test day 91 the main study animals were dissected following a randomisation scheme. Main study animals not dissected on test day 91 were dosed on test day 91 and dissected on test day 92. Animals allocated to the recovery period were dissected on test day 119.
The animals were euthanized by carbon dioxide (CO2) inhalation, exsanguinated by cutting the aorta abdominalis, weighed, dissected and inspected macroscopically under the direction of a pathologist.
All superficial tissues were examined visually and by palpation and the cranial roof was removed to allow observation of the brain, pituitary gland and cranial nerves.
After ventral midline incision and skin reflection, all subcutaneous tissues were examined. The condition of the thoracic viscera was noted with due attention to the thymus, lymph nodes and heart.
The abdominal viscera were examined before and after removal, the urinary bladder was examined externally and by palpation. The gastro-intestinal tract was examined as a whole and the stomach and caecum were incised and examined.
The lungs were removed and all pleural surfaces examined under suitable illumination. The liver and the kidneys were examined. Any abnormalities in the appearance and size of the gonads, adrenal glands, uterus, intra-abdominal lymph nodes and accessory reproductive organs were recorded.
HISTOPATHOLOGY: Yes.
The following organs or parts of organs with the exception of the eyes and testes of all animals were fixed in 7% buffered formalin. The eyes were preserved in Davidson's solution and the testes in modified Davidson's solution for optimum fixation.
Adrenal gland (2), Aorta abdominalis, Bone (os femoris with joint), Bone marrow (os femoris), Brain (3 levels: cerebrum, cerebellum,medulla/pons), Caecum, Epididymis (2), Eye with optic nerve and Harderian gland (2), Gross lesions observed, Heart (left and right ventricle, septum), Intestine, large (colon, rectum), Intestine, small (duodenum, jejunum, ileum, including Peyer´s patches), Swiss roll Method, Kidney and ureter (2), Liver (2 lobes), Lungs (with mainstem bronchi and bronchioles (preserved by inflation with fixative and then immersion)), Lymph node (1, cervical), Lymph node (1, mesenteric), Mammary gland), Muscle (skeletal, leg), Nerve (sciatic), Ovary and oviducts (2), Pancreas, Pituitary, Prostate and seminal vesicles with coagulating glands, Salivary glands (mandibular, parotid, sublingual), Skin (left flank), Spinal cord (3 sections: cervical, midthoracic, lumbar), Spleen, Stomach, Testis (2), Thymus, Thyroid (2) (including parathyroids), Tissue masses or tumours, (including regional lymph nodes), Tongue (including base), Trachea (including larynx), Urinary bladder, Uterus (including cervix), Vagina
The afore-listed organs of all groups 1 and 4 main study and recovery animals were examined histologically after preparation of haematoxylin-eosin stained paraffin sections. In addition, frozen sections of the heart, liver and one kidney were made, stained with Oil Red O and examined as well.
Parathyroids cannot always be identified macroscopically. They were examined microscopically if in the plane of section and in all cases where they were noted as grossly enlarged. - Other examinations:
- ORGAN WEIGHTS:
The weights of the following organs of all animals were determined before fixation:
Adrenal gland (2), Brain, Epididymis (2), Heart, Kidney (2), Liver, Ovary (2), Spleen, Testicle (2), Thymus, Uterus (including cervix), As a whole: Prostate and seminal vesicles with coagulating glands.
Paired organs were weighed individually and identified as left or right.
The relative organ weight [g/kg bw] was calculated as follows:
relative organ weight [g/kg bw] = absolute organ weight [g]
animal weight at dissection [kg] - Statistics:
- Data for toxicology and pathology were captured, as far as possible; using the departmental computerized systems (Provantis® Integrated Preclinical Software, version 9.4.0, Instem LSS Ltd., Stone, Staffordshire ST15 0SD, United Kingdom).
Raw data not fully compatible with the computerized systems were maintained on paper according to appropriate SOPs.
The test item groups 2 to 4 were compared to the control group 1.
The following statistical methods were used:
Multiple t-test based on DUNNETT, C. W. New tables for multiple comparisons with a control. Biometrics, 482-491 (September 1964): Body weight / Food consumption /Haematology / Coagulation /Clinical chemistry / Urinalysis / Relative and absolute organ weights (p ≤ 0.05 and p ≤ 0.01)
Exact test of R. A. FISHER (if applicable): Histopathology (p ≤ 0.05)
The following settings were used for the statistical evaluation of the parametrical values captured by Provantis:
Homogeneity of variances and normality of distribution were tested using the BARTLETT’s and SHAPIRO-WILKS test. In case of heterogeneity and/or nonnormality of distribution, stepwise transformation of the values into logarithmic or rank values was performed prior to ANOVA. If the ANOVA yielded a significant effect (p ≤ 0.05), intergroup comparisons with the control group was made by the DUNNETT’s test (p ≤ 0.01 and p ≤ 0.05).
The following statistical methods were used for the data not captured with the Provantis system:
STUDENT's t-test:
Numerical functional tests: Body temperature / Hind leg splay / Grip strength / Spontaneous motility (p ≤ 0.05 and p ≤ 0.01)
The following limits were used:
p = 0.05 / 0.01 ^ t = 2.0484 / 2.7633 (for 28 degrees of freedom)
p = 0.05 / 0.01 ^ t = 2.0687 / 2.8073 (for 23 degrees of freedom)
p = 0.05 / 0.01 ^ t = 2.3060 / 3.3554 (for 8 degrees of freedom)
These statistical procedures were used for all data. - Clinical signs:
- no effects observed
- Description (incidence and severity):
- All parameters of the detailed clinical observations of all animals scheduled for the control or treatment groups were in the normal range at pre-dose examination on test day 1. All male and female control animals revealed normal values for each parameter set examined throughout the course of the study. None of the animals treated with nominal dose levels of 100, 300 or 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days revealed any changes in external appearance, body posture, movement and coordination capabilities in test weeks 1 to 13.
- Mortality:
- no mortality observed
- Description (incidence):
- None of the male and female rats died or had to be sacrificed prematurely after repeated oral administration of nominal dose levels of 100, 300 or 1000 mg Docusate Sodium/kg bw/day via the diet during the 90-day treatment period or during the 28-day treatment-free recovery period.
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- The body weight of the male animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days was slightly reduced by 6% to 11% compared to the control group as of test day 36. The body weight gain from start (test day 1) to the end of test day 90 was 59% compared to 75% of the animals of the control group. Body weight at autopsy was slightly reduced by 12% compared to the control group. The female animals were not affected.
No test item-related influence was noted on the body weight, body weight gain and body weight at autopsy of the male and female animals previously treated with nominal dose levels of 300 or 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days compared to the control group during the 28-day treatment-free recovery period. - Food consumption and compound intake (if feeding study):
- effects observed, treatment-related
- Description (incidence and severity):
- The relative food consumption of the male and female rats treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days was increased compared to the control group starting in test week 2. The increase versus control group reached 51% in males and 21% in females.
The relative food consumption of the male and female rats previously treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days dropped again to or slightly above the values consumed by the control group during the 28-day treatment-free recovery period, however, the male animals still revealed a slightly increased food consumption by 11% at the end of the recovery period compared to the control group.
The calculation of the test item intake via the diet revealed a dose-dependent exposure of the male and female animals to the test item. The mean test item intake per week ranged from 84 to 117 and 78 to 117 mg/kg bw/day for the male and female animals treated with a nominal dose level of 100 mg Docusate Sodium/kg bw/day via the diet, respectively, from 250 to 351 and 237 to 350 mg/kg bw/day for the male and female animals treated with a nominal dose level of 300 mg Docusate Sodium/kg bw/day via the diet, respectively, and from 854 to 1239 and 811 to 1369 mg/kg bw/day for the male and female animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet, respectively. - Food efficiency:
- not examined
- Water consumption and compound intake (if drinking water study):
- no effects observed
- Description (incidence and severity):
- The visual appraisal of the drinking water consumption did not reveal any test item-related influence in any of the dose groups.
- Ophthalmological findings:
- effects observed, non-treatment-related
- Description (incidence and severity):
- No test item-related changes were noted. The changes noted in the left eye of 1 of 10 male animals treated with a nominal dose level of 100 mg Docusate Sodium/kg bw/day via the diet (slight congestion of iris vessels, slight myosis and no pupil reflex) in test week 1 are considered to be incidental findings due to the low number of animals affected. No changes of the eyes were noted for this animal in test week 13.
- Haematological findings:
- effects observed, non-treatment-related
- Description (incidence and severity):
- No test item-related changes were noted. Statistically significant differences in haematological parameters compared to the control which are not considered to be test item-related were: decreased reticulocytes (high dose males), decreased platelets (mid dose males), increased thromboplastin time (high dose females), decreased thromboplastin time (high dose males), decreased activated partial thromboplastin time (high dose males). The slight alteration in comparison to control animals is without any biological relevance for all these parameters.
- Clinical biochemistry findings:
- effects observed, non-treatment-related
- Description (incidence and severity):
- No test item-related changes were noted. Statistically significant differences in clinical chemistry parameters compared to
the control which are not considered to be test item-related were: decreased albumin (high dose females; test day 119), decreased bilirubin (mid and high dose males and females; test day 91); decreased protein (high dose females; test day 119), increased ALAT (mid and high dose males and increased Gamma-GT (high dose females; test day 119). The slight alteration in comparison to control animals is without any biological relevance for all these above parameters. The increased bile acids (mid and low dose females) were due to the relative low or high value observed for the control group. - Urinalysis findings:
- effects observed, non-treatment-related
- Description (incidence and severity):
- No test item-related changes were noted. The statistical significance of the differences in urinary parameters compared to
the control which are not considered to be test item-related were: increased specific gravity ( mid dose males; test day 91) and decreased pH (mid dose males; test day 91). Both parameters were lacking dose dependence and the slight alteration in comparison to control animals is without any biological relevance. For the increased urine volume in the high dose females on test day 119, the slight alteration in comparison to control animals is without any biological relevance. - Behaviour (functional findings):
- effects observed, non-treatment-related
- Description (incidence and severity):
- The neurological screening performed at the end of the treatment period in test week 13 did not reveal any test item-related influence in the male and female rats treated with nominal dose levels of 100, 300 or 1000 mg Docusate Sodium/kg bw/day via the diet, neither on any of the parameters examined during the functional observation tests nor on the fore- and hind limb grip strength or on the spontaneous motility. Furthermore, no test item-related influence was noted in the rats previously treated with 1000 mg Docusate Sodium/kg bw/day via the diet at the end of the recovery period in test week 17.
Statistically significant differences in neurological parameters compared to the control which are not considered to be test item-related are: increased body temperature (high dose males), increased forelimb grip strength (mid dose and high dose females), increased hind limb grip strength (mid dose and high dose females). The slight alteration in comparison to control animals is without any biological relevance and/or lacking dose dependence. - Immunological findings:
- not examined
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Description (incidence and severity):
- Slightly increased relative and/or absolute liver weights were noted for the male and female animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days compared to the control group on test day 91/92 (up to 18% increase in relative liver weiight n males and females) . The organ weight changes are considered to be test item-related.
Treatment period: Statistically significant differences in relative and absolute organ weights compared to the control which are not considered to be test item-related were: increased relative brain weight high dose males; test day 91/92), decreased absolute heart weight (high dose males; test day 91/92), decreased absolute right ovary weight ( high dose females; test day 91/92) and decreased absolute spleen weight (high dose males; test day 91/92). For all the above parameters the slight alteration in comparison to control animals is without any biological relevance. The increased absolute thymus weight (mid dose femlaes; test day 91/92) was lacking dose dependence.
Recovery period: The liver weights of the male and female animals previously treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet were not test item-relatedly increased compared to the control group at the end of the 28-day treatment-free recovery period. Statistically significant differences in relative and absolute organ weights compared to the control which are not considered to be test item-related (lacking dose dependence) were: increased relative right adrenal gland weight, increased absolute right adrenal gland weight and increased absolute brain weight in the mid dose females on test day 119. - Gross pathological findings:
- effects observed, non-treatment-related
- Description (incidence and severity):
- No test item-related changes were noted.
Treatment period: Macroscopic changes were noted in the duodenum (dilated), kidneys (cysts) and thymus (reddened / red foci) in individual animals of the test item-treated groups. These changes are considered to be incidental findings due to the low number of animals affected.
Recovery period: Macroscopic changes were noted in the kidneys (cyst), lungs (partly reddened), ovary (cyst filled with clear liquid) and thymus (reddened) in individual animals of the previously test item-treated groups. These changes are considered to be incidental findings due to the low number of animals affected. - Neuropathological findings:
- no effects observed
- Histopathological findings: non-neoplastic:
- effects observed, non-treatment-related
- Description (incidence and severity):
- The histological examination of rat organs did not reveal any morphological changes in the animals treated with a nominal dose level of 1000 mg Docusate
Sodium/kg bw/day via the diet for 90 days which are considered to be related to the administration of the test item. No test item-related changes were noted in the rat organs at the end of the 28-day treatment-free recovery period.
A few minor microscopic changes were recorded for the organs and tissues examined in this study. However, the type, incidence and severity of all
microscopic findings observed did not indicate any relationship to the treatment with the test item. All changes noted are regarded as spontaneous and to be within the normal background pathology commonly seen in rats of this strain and age. - Histopathological findings: neoplastic:
- no effects observed
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- > 1 000 mg/kg bw/day (nominal)
- Based on:
- act. ingr.
- Remarks:
- Docusate Sodium
- Sex:
- male/female
- Basis for effect level:
- other: No haematological, biochemical or histopathological changes or any other noteworthy changes were observed
- Critical effects observed:
- not specified
- Conclusions:
- The experimental no-observed-adverse-effect level (NOAEL) was above 1000 mg Docusate Sodium/kg bw/day (nominal dose), by daily oral administration via the diet, in particular, as no haematological, biochemical or histopathological changes or any other noteworthy changes were observed.
- Executive summary:
The aim of this repeated dose toxicity study was to obtain information on the toxicity of Docusate Sodium administered daily via the diet to rats for 90 consecutive days and to assess the reversibility of any effects at the end of a 28-day recovery period.
The test item supplied was mixed to the diet by LPT. Rats were treated with Docusate Sodium at nominal dose levels of 100, 300 and 1000 mg/kg bw/day. The control animals received standard diet only. Mean actual dose levels of 105, 313 and 1066 mg Docusate Sodium/kg bw/day for the low, intermediate and high dosed males and 107, 319 and 1069 mg Docusate Sodium/kg bw/day for the low, intermediate and high dosed females were achieved during the 90-day treatment period. None of the animals died or had to be sacrificed prematurely.
The body weight of the male animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days was slightly reduced compared to the control group. The female animals were not affected. The relative food consumption of the male and female rats treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days was increased compared to the control group starting in test week 2. The relative and/or absolute liver weights of the male and female animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet were slightly increased compared to the control group at the end of the 90-day treatment period.
No test item-related changes were observed for the behaviour or external appearance of the animals, the detailed clinical observations, the neurological screening, the drinking water consumption, for any of the haematological, clinical chemical and urinary parameters, the eyes or optic region, the auditory acuity, and at macroscopic inspection at necropsy at any dose level. The histopathological examination of the animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet did not reveal any test item-related morphological changes, neither at the end of the 90-day treatment period nor at the end of the 28-day treatment-free recovery period.
At the end of the 28-day treatment-free recovery period, the values for relative food consumption of the previously high dosed animals were in the range or slightly above the values consumed by the control group, the body weight of the previously high dosed male animals had completely recovered to the values of the control group, and the liver weights of the previously high dosed male and female animals were not test item-relatedly increased compared to the control group.
The experimental NOAEL was above 1000 mg Docusate Sodium/kg bw/day (nominal dose), by daily oral administration via the diet, in particular, as no haematological, biochemical or histopathological changes or any other noteworthy changes were observed.
- Endpoint:
- short-term repeated dose toxicity: oral
- Type of information:
- read-across based on grouping of substances (category approach)
- Adequacy of study:
- supporting study
- Study period:
- 2017
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: The study is a 14-day dose range finding study for the OECD 408 study, therefore it is only supportive.
- Justification for type of information:
- Data has been read across from a structurally identical substance forming a salt with sodium instead of potassium. This is not expected to chenge the toxicological properties in a significant way. See further discussion in the read across justification attached.
- Reason / purpose for cross-reference:
- read-across: supporting information
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 408 (Repeated Dose 90-Day Oral Toxicity Study in Rodents)
- Version / remarks:
- adopted September 21, 1998
- Deviations:
- yes
- Remarks:
- on 14 days dosing in limited No.of animals
- GLP compliance:
- yes (incl. QA statement)
- Limit test:
- yes
- Species:
- rat
- Strain:
- other: Crl:CD(SD)
- Details on species / strain selection:
- Crl:CD(SD) rat was selected because of its proven suitability in toxicology studies and to comply with regulatory requirements for testing in a rodent animal species.
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Laboratories, Research Models and Services, Germany GmbH, Sandhofer Weg 7, 97633 Sulzfeld, Germany
- Age (at 1st dosing): Males: 64 days; Females: 64 days
- Weight (at 1st dosing): Males: 334.3 - 354.1 g; Females: 216.7 - 246.4 g
- Housing: The animals were kept singly in MAKROLON cages (type III plus) with a basal surface of approx. 39 cm × 23 cm and a height of approx. 18 cm. Granulated textured wood (Granulat A2, J. Brandenburg, 49424 Goldenstedt, Germany) was used as bedding material for the cages. The cages were changed and cleaned once a week.
- Diet (e.g. ad libitum): A certified commercial diet (ssniff® R/M-H V1534, ssniff Spezialdiäten GmbH, 59494 Soest, Germany) served as food. The food was offered ad libitum. Food residue was removed and weighed.
- Water (e.g. ad libitum): Drinking water (tap water) was offered ad libitum.
- Acclimation period: 5 days
DETAILS OF FOOD AND WATER QUALITY:
Periodic analysis of the food for contaminants based on EPA/USA (Proposed Health Effects Test Standards for Toxic Substances Control Act Test Rules, Federal Register 44, 27334 - 27375, May 1979.) is conducted at least twice a year by LUFA-ITL (Landwirtschaftliche Untersuchungs- und Forschungsanstalt, Institut für Tiergesundheit und Lebensmittelqualität GmbH, 24107 Kiel, Germany.). Certificates of analysis of the composition and for contaminants were provided by the manufacturer and included in the raw data.
Samples of drinking water are taken by Wasserwerk Wankendorf and periodic analyses are performed by LUFA-ITL according to the 'Deutsche Trinkwasserverordnung 2001' [German Regulations on Drinking Water 2001: Version from August 02, 2013, revised on November 18, 2015]. In addition, drinking water samples taken at LPT are analyzed by LUFA-ITL once a year for means of bacteriological investigations according to the 'Deutsche Trinkwasserverordnung 2001, Anlage 1' [German Regulations on Drinking Water 2001, Addendum 1].
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22°C ± 3°C (maximum range)
- Humidity (%): 55% ± 15% (maximum range); Deviations from the maximum range caused for example during cleaning procedures were dealt with in SOPs.
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES:
From: Start of dosing January 09, 2017
To: Termination of the in-life period January 23, 2017 - Route of administration:
- other: Group 1 and 2 : oral by gavage; Group 3 : oral via diet
- Details on route of administration:
- According to international guidelines.
- Vehicle:
- other: Group 1 and 2: tap water; Group 3: diet
- Details on oral exposure:
- PREPARATION OF DOSING SOLUTIONS:
Group 2 (oral administration via gavage): Administration volume was 20 mL/kg bw/day.
The administration formulations were prepared one day before each administration day. The test item was chopped or shredded into small pieces. The pieces were placed in the vehicle and the mixture was continuously agitated overnight to facilitate dissolution. The formulations of appropriate concentrations were administered orally at a constant daily volume. The administration formulation was continuously agitated by stirring throughout the entire administration procedure.
The amount of test item administered to the animals of group 2 (gavage dosing) was daily adjusted to the current body weight of the animals.
DIET PREPARATION
Group 3 (oral administration via the diet):
- Rate of preparation of diet (frequency): The administration formulation was prepared weekly.
- Mixing appropriate amounts with (Type of food): The appropriate amount of test item (based on the most recently recorded food consumption and body weight) were chopped or shredded into small pieces and weighed into a glass container. A portion of the test item and a portion of diet were mixed with an impact mill to produce a pre-mix. The process was repeated until the whole quantity of test item was distributed in the diet. The pre-mix was added to the diet, mixed with a mixer (Rhönradmischer, type ELTE 650, J. Engelsmann AG, Ludwigshafen, Germany) for 15 minutes, and then transferred to a closable bucket. Each bucket was labelled with group, sex and dose.
To maintain a constant dose level in relation to the body weight of the animals of group 3 (diet dosing), the concentration in the diet was adjusted based on the weekly mean group food consumption per sex. The concentration was adjusted weekly using the food consumption value from the previous week. For test week 1, the food consumption determined during the adaptation period was used.The start concentration in the diet was selected based on LPT's historical background data of food consumption of rats.
- Storage temperature of food: Not provided. - Analytical verification of doses or concentrations:
- yes
- Remarks:
- For each test item mixed with a vehicle, tests by appropriate analytical methods will be carried out in the 90-day study (LPT Study No. 34272) to determine the concentration, homogeneity and, if needed, stability of the test item in the formulations.
- Details on analytical verification of doses or concentrations:
- See main study (90 day study) 34272.
The administration formulation was prepared weekly. The appropriate amount of test item (based on the most recently recorded food consumption and body weight) were chopped or shredded into small pieces and weighed into a glass container. A portion of the test item and a portion of diet were mixed with an impact mill to produce a pre-mix. The process was repeated until the whole quantity of test item was distributed in the diet. The pre-mix was added to the diet, mixed with a mixer (Rhönradmischer, type ELTE 650, J. Engelsmann AG, Ludwigshafen, Germany) for 15 minutes, and then transferred to a closable bucket. Each bucket was labelled with group, sex and dose. The total daily intake per animal and the average daily intake per group of the test item were calculated. - Duration of treatment / exposure:
- Group 1: 15 days
Group 2: maximally 10 days (termination of group 2 for animal welfare reasons on test day 10 due to pronounced toxicity). Dose reduction as of test day 5 due to mortality.
Group 3: 15 days (360 hours) - Frequency of treatment:
- Group 1 and 2: Once daily
Group 3: Test item-diet ad libitum (continuous) - Dose / conc.:
- 0 mg/kg bw/day (actual dose received)
- Remarks:
- control group by gavage
- Dose / conc.:
- 1 000 mg/kg bw/day (actual dose received)
- Remarks:
- test group by gavage. Dose reduction to 500 mg/kg bw/day as of test day 5 due to mortality.
- Dose / conc.:
- 1 000 mg/kg bw/day (nominal)
- Remarks:
- test group via diet. The actual individual dose for the animals of group 3 varied from 821 to 1414 mg/kg bw, depending on the individual daily food intake, thus ranging from 82% to 141% of the nominal dose, across male and female animals and test weeks 1 and 2.
- No. of animals per sex per dose:
- 5/sex/dose
Additionally, 6 spare animals (3 males and 3 females) were available for possible replacement during the adaptation period. However, no replacements were necessary. - Control animals:
- yes, concurrent vehicle
- Details on study design:
- - Dose selection rationale: The dose levels applied in this study had been selected in agreement with the Sponsor based on available toxicological data.
- Rationale for animal assignment (if not random): The animals were allocated to 3 test groups by means of a computer generated randomization program (Provantis® Integrated preclinical software, version 9.4.0, Instem LSS Ltd., Stone,Staffordshire ST15 0SD, United Kingdom) - Observations and examinations performed and frequency:
- CAGE SIDE OBSERVATIONS: Yes
- Time schedule: The animals were checked regularly throughout the working day from 7.00 a.m. to 3.45 p.m. by cageside observations. On Saturdays and Sundays, the animals were checked regularly from 7.00 a.m. to 11.00 noon with a final check performed at approximately 3.30 p.m.
Cageside observations included skin/fur, eyes, mucous membranes, respiratory and circulatory systems, somatomotor activity and behavior patterns. The onset, intensity and duration of any signs observed were recorded.
Further checks were made early in the morning and again in the afternoon of each working day to look for dead or moribund animals. On Saturdays and Sundays a similar procedure was followed with a final check at approximately 4.00 p.m. These provisions allowed for post mortem examinations to be carried out during the working period of the respective day, and to record premortal symptoms in detail.
- Dated and signed records of appearance, change and disappearance of clinical signs of individual animals were maintained on clinical history sheets.
DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: The animals were observed individually before and after dosing at each time of dosing for any signs of behavioral changes, reaction to treatment or illness.
BODY WEIGHT: Yes
- Time schedule for examinations: The animals were weighed daily including the day of sacrifice. Individual body weights were recorded.
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.
The quantity of food left by individual animals was recorded on a weekly basis throughout the experimental period. The food intake per animal (g/animal/week) was determined using the total amount of food given to and left by each animal in each group on completion of a treatment week.
The relative food consumption (in g/kg bw/day) was calculated as follows:
Relative food consumption (g/kg bw/day) = Total food given (g) - Total food left (g) / Number of animal days# × Body weight (kg)
# The term 'animal days' counts one animal day for each animal alive for a whole day; it is assumed that on the day of death an animal does not eat.
- Compound intake calculated as time-weighted averages from the consumption and body weight gain data: Yes
The actual individual test item intake (in mg/kg bw/day) was calculated for the animals of group 3 based on the actual test item concentration in the diet, the food consumption per day and the individual body weights on a weekly basis.
WATER CONSUMPTION: Yes
- Time schedule for examinations: The drinking water consumption was monitored daily by visual appraisal throughout the study.
OPHTHALMOSCOPIC EXAMINATION: No
BLOOD COLLECTION AND EXAMINATION: Yes (for pharmacokinetics)
- Time schedule for collection of blood:
Group 2: 2 hours following the last administration on test day 5 (male animal) or 10 (female animals)
Group 3: 2 hours after removal of the diet on test day 15
- Anaesthetic used for blood collection: Yes, isoflurane.
- Animals fasted:
Group 2: No
Group 3: 2 hours before blood colletion
- How many animals:
Group 2: 4 (1 M and 3 F)
Group 3: 10 (5 M and 5 F)
- Parameters examined: The aim of the study is to determine the concentrations of docusate sodium USP applied once daily to CD® rats by oral administration (diet vs. gavage) up to 15 days.
URINALYSIS: No
NEUROBEHAVIOURAL EXAMINATION: No
IMMUNOLOGY: No - Sacrifice and pathology:
- GROSS PATHOLOGY: Yes.
On test day 15 (approximately 2 hours after the last dosing or after removal of the diet and after the last blood sampling) all animals were euthanised by carbon dioxide (CO2) inhalation, exsanguinated by cutting the aorta abdominalis, dissected, weighed, and inspected macroscopically.
All superficial tissues were examined visually and by palpation. The cranial roof was removed to allow observation of the brain, pituitary gland and cranial nerves. After ventral midline incision and skin reflection, all subcutaneous tissues were examined. The condition of the thoracic viscera was noted with due attention to the thymus, the lymph nodes and the heart.
The abdominal viscera were examined before and after removal, the urinary bladder was examined externally and by palpation. The gastro-intestinal tract was examined as a whole and the stomach and caecum were incised and examined. The lungs were removed and all pleural surfaces were examined under suitable illumination. The liver and the kidneys were examined. Any abnormalities in the appearance and size of the gonads, adrenal glands, uterus, intra-abdominal lymph nodes and accessory reproductive organs were recorded.
The prematurely deceased animals (Group 2) nos. 11 m, 13 m, 14 m, 15 m, 18 f, and 20 f were examined as soon as possible after the animals had been found dead. For the prematurely terminated animals nos. 12, 16, 17, and 19 the examinations were performed immediately after sacrifice.
HISTOPATHOLOGY: No - Other examinations:
- The organs listed in the text table below were weighed:
Adrenal gland (2), Brain, Epididymis (2), Heart, Kidney (2), Liver, Ovary, Spleen, Testicle (2), Thymus, Uterus including cervix, Prostate and seminal vesicles with coagulating glands (as a whole).
The paired organs were identified as left or right and weighed individually.
The organ weights of the animals which had died or were sacrificed prematurely were recorded but are not included in mean value comparisons. - Statistics:
- Toxicology and pathology data for were captured, as far as possible, using the departmental computerized systems (Provantis® Integrated preclinical software, version 9.4.0, Instem LSS Ltd., Stone, Staffordshire ST15 0SD, United Kingdom). Raw data not fully compatible with the computerized systems were maintained on paper according to appropriate SOPs.
The test item-treated groups 2 and 3 were compared with the control group 1.
The statistical methods described below were used for the data captured with the Provantis system:
-Multiple t-test based on DUNNETT, C. W. New tables for multiple Comparisons with a control Biometrics, 482-491 (Sept 1964)
-Body weight / Food consumption / Relative and absolute organ weights (p ≤ 0.05 and p ≤ 0.01).
Homogeneity of variances and normality of distribution were tested using BARTLETT's test and the SHAPIRO-WILKS test. In case of heterogeneity and/or non-normality of distribution, stepwise transformation of the values into logarithmic or rank values was performed prior to ANOVA. If the ANOVA yielded a significant effect (p ≤ 0.05), intergroup comparisons with the control group were made by DUNNETT's test (see above). - Clinical signs:
- effects observed, treatment-related
- Description (incidence and severity):
- Group 3: No signs of toxicity were noted.
Group 2: The male animal no. 12 and the female animals (nos. 16, 17, and 19) that were treated orally with 1000/500 mg/kg bw/day via gavage and did not die prematurely, revealed signs of toxicity similar to those of the prematurely deceased animals until their respective premature sacrifice:
Piloerection, slight to extreme salivation, and slightly to moderately reduced motility were noted for all male and female animals (nos. 12, 16, 17, and 19) on up to 9 days, starting on test day 2. Salivation and reduced motility started within 5 minutes of administration and typically lasted 20 to 60 minutes. In addition, individual female animals revealed gasping, breathing sounds, ptosis, and a moistened anus on several days, starting on test day 8. All findings are considered to be test item-related. - Mortality:
- mortality observed, treatment-related
- Description (incidence):
- Group 3: No deaths were noted for the animals treated with 1000 mg/kg bw/day (nominal dose) via the diet.
Group 2: One of 5 male animals (no. 15) treated orally with 1000 mg/kg bw/day was found dead during test day 4. Due to the death of this animal, the dosage was reduced to 500 mg/kg bw/day as of test day 5, except for the male animal no. 12 that was once more dosed with 1000 mg/kg bw on test day 5 and euthanized following blood withdrawal 2 h after dosing. However, another male animal (no. 11) and 2 of 5 female animals (nos. 18 and 20) were found dead in the morning of test day 5, i.e. before the dose reduction became effective. Two additional male animals treated with the reduced dose of 500 mg/kg bw/day via gavage as of test day 5 were found dead on test days 7 and 9.
All premature deaths are considered to be test item-related. The female animals nos. 16, 17, and 19 which received a dose of 500 mg/kg bw/day as of test day 5 were prematurely sacrificed for animal welfare reasons on test day 10. - Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- Group 3: No test-item related influence was noted.
Group 2: The body weight of the male animals treated orally with 1000/500 mg/kg bw/day via gavage was reduced compared to the control group as of test day 2, reaching a decrease by 39.1% on test day 7 for the only remaining animal. The female animals were slightly less affected, the decrease in body weight amounted up to 18.5% in comparison to the control group. Actually, a body weight loss was noted for all male and female animals compared to the animals' respective start body weight on test day 1 as of test day 2. The reduced body weight noted for group 2 is considered to be test item-related. - Food consumption and compound intake (if feeding study):
- effects observed, treatment-related
- Description (incidence and severity):
- Group 3: No test-item related influence was noted. The actual individual dose, depending on the daily food intake of the animals, varied from 821 to 1414 mg/kg bw/day, thus ranging from 82% to 141% of the nominal dose, across male and female animals and test weeks 1 and 2.
Group 2: For the male animals treated orally with 1000/500mg/kg bw/day via gavage, the food consumption in test week 1 could only be calculated for animal no. 13 that was still alive on test day 8. The food intake of animal no. 13 was reduced by 78.6% compared to the mean value of the control group in test week 1.
The mean food consumption of the three surviving female animals (nos. 16, 17, and 19) was reduced by 36.8% compared to control group in test week 1 (statistically significant at p ≤ 0.01); all three animlals were still consuming feed.The reduced food consumption noted for group 2 is considered to be test item-related. - Food efficiency:
- not examined
- Water consumption and compound intake (if drinking water study):
- not examined
- Description (incidence and severity):
- The drinking water consumption was monitored daily by visual appraisal throughout the study.
- Ophthalmological findings:
- not examined
- Haematological findings:
- not examined
- Clinical biochemistry findings:
- not examined
- Urinalysis findings:
- not examined
- Behaviour (functional findings):
- not examined
- Immunological findings:
- not examined
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Description (incidence and severity):
- Group 3: No test-item related influence was noted on the organ weights of the female animals treated with 1000 mg/kg bw/day (nominal dose) via the diet on test day 15. Increased relative and absolute kidney (+12.1-14.4%) and liver (+31-32%) weights were noted for the male animals treated with 1000 mg/kg bw/day (nominal dose) via the diet on test day 15 . The organ weight changes in the male animals are considered to be test item-related.
Group 2: Considering the slightly younger age of the prematurely deceased and prematurely sacrificed animals, there appeared to be no effect on relative and absolute organ weights that could clearly be attributed to the test item. Due to the different days on which the organs were sampled, the effects on organs weights can not be evaluated. - Gross pathological findings:
- effects observed, treatment-related
- Description (incidence and severity):
- Group 3: No test-item related changes were noted.
Group 2: The male animal no. 12 and the female animals (nos. 16, 17, and 19) which were treated orally with 1000/500 mg/kg bw/day via gavage and did not die prematurely revealed macroscopic findings similar to those of the prematurely deceased animals at macroscopic inspection at necropsy following their respective premature sacrifice:
For the male animal no. 12, a hemorrhagic nose and snout, a moistened anus and genital area, reddened walls of the gastro-intestinal tract, a dark stained liver, and a reddened brain were noted. The female animals (nos. 16, 17, and 19) revealed rough fur, reddened walls of the gastro-intestinal tract, and a dark stained
liver. Additionally, a moistened anus and genital area was noted for animal no. 19.
All macroscopic findings noted are considered to be test item-related. - Neuropathological findings:
- not examined
- Histopathological findings: non-neoplastic:
- not examined
- Histopathological findings: neoplastic:
- not examined
- Other effects:
- effects observed, treatment-related
- Description (incidence and severity):
- Pharmacookinetics (Bioanalysis):
Blood samples processed for plasma by LPT were dispatched for analysis to Prolytic GmbH on January 25, 2017. The bioanalysis of the plasma samples was performed at the Test Site under the responsibility of the PI according to the bioanalytical Phase Plan 17008. The bioanalytical phase report issued by the Test Site is given in Appendix 4 of the report. - Details on results:
- Bioanalysis revealed that the animals were exposed to Docusate sodium. The following plasma levels were noted per route of administration:
Blood samples processed for plasma by LPT were dispatched for analysis to Prolytic GmbH on January 25, 2017. The bioanalysis of the plasma samples was performed at the Test Site under the responsibility of the PI according to the bioanalytical Phase Plan 17008. The bioanalytical phase report issued by the Test Site is given in Appendix 4 of the report.
Bioanalysis revealed that the animals were exposed to Docusate sodium. The following plasma levels were noted per route of administration:
Oral administration via the diet: 310 ng/mL to 2528 ng/mL (1263 ng/mL ±1050)
Oral administration via gavage: 238 ng/mL to 1121 ng/mL (508 ng/mL ±295) - Dose descriptor:
- other: maximum tolerated dose
- Effect level:
- 1 000 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Remarks on result:
- other: dietary administration
- Critical effects observed:
- yes
- Lowest effective dose / conc.:
- 1 000 mg/kg bw/day (nominal)
- System:
- urinary
- Organ:
- kidney
- Treatment related:
- yes
- Critical effects observed:
- yes
- Lowest effective dose / conc.:
- 1 000 mg/kg bw/day (nominal)
- System:
- hepatobiliary
- Organ:
- liver
- Treatment related:
- yes
- Conclusions:
- Based on the present results, oral administration of Docusate Sodium via the diet is the recommended route of administration for a repeated dose oral taxicity study in rats .
The following nominal dose levels are suggested:
Group 1: 0 mg Docusate Sodium/kg b.w./day, p.o. (control)
Group 2:100 mg Docusate Sodium/kg b.w./day, p.o. (low dose)
Group 3:300 mg Docusate Sodium/kg b.w./day, p.o. (intermediate dose)
Group 4:1000 mg Docusate Sodium/kg b.w./day, p.o. (high dose) - Executive summary:
The aim of this dose-range-finding study was to select the dose levels for a study with repeated oral administration of the test item Docusate Sodium USP in rats. The following main study will be carried out according to current OECD guideline 408.
A nominal dose level of 1000 mg Docusate Sodium USP/kg bw was administered orally once daily either via gavage or via the diet.
The actual doses for the oral administration via the diet ranged from 821 to 1414 mg/kg bw/day, depending on the daily food intake of the animals. No deaths and no signs of toxicity were noted. No influence was observed on the body weight, the body weight gain, and the food and drinking consumption. No test item-related findings were noted at macroscopic inspection at necropsy. The male animals revealed increased kidney (up to 14% increase) and liver weights (up to 32% increase) on test day 15.
Oral administration via gavage of 1000 mg Docusate Sodium USP/kg bw/day led to the premature death of 4 of 5 male and 2 of 5 female animals. The remaining animals were prematurely sacrificed on test day 5 (1 male animal) or on test day 10 (3 female animals) for animal welfare reasons.
All deceased male and female animals revealed premortal symptoms in form of piloerection, slight to moderate salivation, and slightly to extremely reduced motility.
Further, a hemorrhagic nose/snout, breathing sounds, pultaceous feces, and a moisted anus were observed for individual animals. Similar findings were noted for the prematurely sacrificed animals.
The macroscopic inspection at necropsy revealed a hemorrhagic or reddened nose and/or snout, a moistened anus and genital area, and reddened walls in the gastrointestinal tract for all prematurely deceased male and female animals. Further findings included undescended testes, a dark stained liver, a reddened thymus, yellowish stained indurations in the urinary bladder, and a greyish/greenish covering of the stomach wall in individual animals. Similar findings were noted for the prematurely sacrificed animals.
The body weight of the male animals was severely reduced in comparison to the control group. The female animals were slightly less affected. All animals revealed a body weight loss compared to their respective start body weight.
The food intake was reduced compared to the mean value of the control group.
Bioanalysis revealed that the animals were exposed to Docusate sodium.
Referenceopen allclose all
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEL
- 1 000 mg/kg bw/day
- Study duration:
- subchronic
- Species:
- rat
- Quality of whole database:
- Reliable as study is new fully guideline and GLP compliant study on the read across substance docusate sodium
Repeated dose toxicity: inhalation - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: inhalation - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
A key dietary 90 -day subchronic toxicity study with Docusate Sodium was performed in rats, followed by a 28 -day recovery period (Hansen, 2017). Mean actual dose levels of 105, 313 and 1066 mg /kg bw/day in males and 107, 319 and 1069 mg bw/day in females were achieved for the low, intermediate and high dose levels, respectively. None of the animals died or had to be sacrificed prematurely. The body weight of the male animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days was slightly reduced compared to the control group. The female animals were not affected. The relative food consumption of the male and female rats treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet for 90 days was increased compared to the control group starting in test week 2. The relative and/or absolute liver weights of the male and female animals treated with a nominal dose level of 1000 mg Docusate Sodium/kg bw/day via the diet were slightly increased compared to the control group at the end of the 90-day treatment period. No test item-related changes were observed for the behaviour or external appearance of the animals, the detailed clinical observations, the neurological screening, the drinking water consumption, for any of the haematological, clinical chemical and urinary parameters, the eyes or optic region, the auditory acuity, and at macroscopic inspection at necropsy at any dose level. The histopathological examination of the animals treated with a nominal dose level of 1000 mg/kg bw/day via the diet did not reveal any test item-related morphological changes, neither at the end of the 90-day treatment period nor at the end of the 28-day treatment-free recovery period.
At the end of the 28-day treatment-free recovery period, the values for relative food consumption of the previously high dosed animals were in the range or slightly above the values consumed by the control group, the body weight of the previously high dosed male animals had completely recovered to the values of the control group, and the liver weights of the previously high dosed male and female animals were not test item-relatedly increased compared to the control group.
The experimental NOAEL was above 1000 mg Docusate Sodium/kg bw/day (nominal dose), by daily oral administration via the diet, in particular, as no haematological, biochemical or histopathological changes or any other noteworthy changes were observed.
A dose-range-finding study (Hansen, 2018) was done to select the route and dose levels for a study for the above study. A nominal dose level of 1000 mg Docusate Sodium USP/kg bw was administered orally once daily either via gavage or via the diet. The actual doses for the oral administration via the diet ranged from 821 to 1414 mg/kg bw/day, depending on the daily food intake of the animals. No deaths and no signs of toxicity were noted. No influence was observed on the body weight, the body weight gain, and the food and drinking consumption. No test item-related findings were noted at macroscopic inspection at necropsy. The male animals revealed increased kidney (up to 14% increase) and liver weights (up to 32% increase) on test day 15. Oral administration via gavage of 1000 mg Docusate Sodium USP/kg bw/day led to the premature death of 4 of 5 male and 2 of 5 female animals. The remaining animals were prematurely sacrificed on test day 5 (1 male animal) or on test day 10 (3 female animals) for animal welfare reasons. All deceased male and female animals revealed premortal symptoms in form of piloerection, slight to moderate salivation, and slightly to extremely reduced motility. Further, a hemorrhagic nose/snout, breathing sounds, pultaceous feces, and a moisted anus were observed for individual animals. Similar findings were noted for the prematurely sacrificed animals.
The macroscopic inspection at necropsy revealed a hemorrhagic or reddened nose and/or snout, a moistened anus and genital area, and reddened walls in the gastrointestinal tract for all prematurely deceased male and female animals. Further findings included undescended testes, a dark stained liver, a reddened thymus, yellowish stained indurations in the urinary bladder, and a greyish/greenish covering of the stomach wall in individual animals. Similar findings were noted for the prematurely sacrificed animals.
The body weight of the male animals was severely reduced in comparison to the control group. The female animals were slightly less affected. All animals revealed a body weight loss compared to their respective start body weight. The food intake was reduced compared to the mean value of the control group. Bioanalysis revealed that the animals were exposed to Docusate sodium. Based on the present results, oral administration of Docusate Sodium via the diet is the recommended route of administration for a repeated dose oral taxicity study in rats . The following nominal dose levels are suggested: 0 - 100 - 300 - 1000 mg/kg bw/day via the diet.
A supporting study for oral subchronic toxicity was performed in rats with Docusate sodium (Cytec, Plank 1969a). The validity of the study was supported by additional audits on the raw data and histopathological evaluation, however the study was changed from key to supporting data based on the new key study provided above. Although deficiencies were detected compared to current standards, the study was concluded to be valid and reliable. A group of 40 albino rats (20 males and 20 females) was fed with 1% test substance mixed into the diet, compared to a control group. There were no significant differences in body weights, haematology, clinical blood chemistry, urinalysis and organ weights. No deaths or abnormal behavioral reactions occurred; no gross pathological findings were noted. Administration of 1% docusate sodium in the diet (10.000 ppm equivalent to approximately 750 mg/kg body weight/day) for 90 days in rats did not result in any relevant changes in the subchronic toxicity study. The NOAEL was therefore established at 750 mg/kg bw/day.
In that same study, various category members/structural analogues were tested as supporting information at the same doses: Sodium Diamylsulfosuccinate, Sodium Dicyclohexylsulfosuccinate, Diisobutylsulfosuccinate, Sodium Dihexylsulfosuccinate, Sodium Di- (tridecyl) sulfosuccinate (Cytec, Plank 1969b). Five groups of 40 albino rats were fed with 1% test substance mixed into the diet and examined for the same parameters as listed above, compared to a control group. With the exception of an evaluation of both SGPT (serum glutamic pyruvic transaminase) and SAP (serum alkaline phosphatase) values among males fed CAS 2673-22-5 and smaller absolute liver weights among males fed CAS 127-39-9, no significant differences in clinical blood chemistry studies and absolute organ weights have been detected. Administration of 1% in the diet (10,000 ppm equivalent to approximately 750 mg/kg body weight/day) for 90 days in rats did not result in any relevant changes in the subchronic toxicity study. The NOAEL was 750 mg/kg bw/day for the various category members.
In a supporting study, groups of 10 (5 male & 5 female) Wistar rats were treated for 6 months at concentrations of 0.25, 0.5, 0.75, 1.0 and 1.25 g/kg diet, corresponding to doses of 190, 370, 550, 750 and 870mg/kg bw/day. Occasional spells of diarrhea occurred in some animals, particularly at the higher doses. Neither the total red cell, total white cell, nor the differential counts of rats was affected by the continued administration . The dose level of 750 mg/kg was confirmed as NOAEL (Literature, Benaglia et al. 1943).
Other studies were also available from literature in various species (Literature, Benaglia et al. 1943 and Case et al., 1977) in dogs, rabbits and Rhesus monkeys. The other species were considered to be less appropriate due to the gastrointestinal tensio-active local irritation by which systemic effects could not be fully evaluated. The NOAEL of 750 mg/kg bw/day in rats was selected as main endpoint, as this was confirmed in various studies and with different category substances.
In summary, repeated dose toxicity was tested in various species, including rats, dogs, rabbits and monkeys. The NOAEL of 1000 mg/kg bw/day obtained in the key study in rats was confirmed to be relevant and consistent.
Justification for classification or non-classification
As the NOAEL is higher than treshold levels given in the classification guidelines, there is no indication for classification.
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