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EC number: 215-185-5 | CAS number: 1310-73-2
- 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
- Nanomaterial porosity
- 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
Repeated dose toxicity: oral
Administrative data
- Endpoint:
- chronic toxicity: oral
- Type of information:
- other: Data sharing dispute
- Adequacy of study:
- key study
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- other: No standard test guideline followed. No test concentrations noted or measured, only pH values.
Data source
Reference
- Reference Type:
- publication
- Title:
- Systemic and local effects of long-term exposure to alkaline drinking water in rats
- Author:
- Merne M.E.T., Syrjänen KJ, Syrjänen SM
- Year:
- 2 001
- Bibliographic source:
- Int. J. Exp. Path. 82, 231-219
Materials and methods
- Principles of method if other than guideline:
- To assess the systemic (organ) and local (oral mucosal) effects of alkalinity, drinking water supplemented with Ca(OH)2 or NaOH to adjust pH to 11.2 or 12 was administered to rats (n=36) for 52 weeks.
- GLP compliance:
- no
- Limit test:
- no
Test material
- Reference substance name:
- Sodium hydroxide
- EC Number:
- 215-185-5
- EC Name:
- Sodium hydroxide
- Cas Number:
- 1310-73-2
- Molecular formula:
- HNaO
- IUPAC Name:
- sodium hydroxide
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Long-Evans
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Age at study initiation: in groups 1, 2 and 3, the experiment was started when the rats were 12 weeks old, and in grouops 4 and 5 at the age of 6 weeks
- Housing: rats were housed in solid-polycarbonate bottom metal wire cages with alderwood bedding in groups of three.
- Diet (e.g. ad libitum): the animals were provided with standard laboratory animal feed (SDS, RM3, Essex, UK).
- Water (e.g. ad libitum): water was always available ad libitum. The water given to the rats in the study groups was modified to meet the criteria of the study design
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-22°C
- Humidity (%): (relative), 45-55%
- Photoperiod (hrs dark / hrs light): 12-h light and 12-h dark cycle
Administration / exposure
- Route of administration:
- oral: drinking water
- Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- the duration of the experiment in all groups was one year (52 weeks)
- No. of animals per sex per dose:
- group 1 (control, pH 7): 6 females, 6 males
group 2 (Ca(OH)2, pH 11.2): 6 females, 6 males
group 3 (NaOH, pH 11.2) : 6 females, 6 males
group 4 (Ca(OH)2, pH 12): 3 females, 3 males
group 5 (NaOH, pH 12): 3 females, 3 males - Control animals:
- yes, concurrent vehicle
Examinations
- Sacrifice and pathology:
- After completion of the study, the rats were killed using carbon dioxide, and necropsy samples were taken from the oral buccal mucosa, palate, tongue, oesophagus, stomach, intestines, liver, and kidney. in groups 4 and 5, additional samples were obtained from the salivary glands (parotis, submandibularis, sublingualis), masseter muscle, thyroid, hypothalamus, and overay or testes. The samples were fixed in 10% neutral formalin, embedded in paraffin, cut into 5-µm sections, and stained with haema
toxylin and eosin for routine light microscopic evaluation. All biopsy samples were examined by a board-certified pathologist (KS), blinded for all other data. - Other examinations:
- All animals were weighed at the completion of the experiment
- Statistics:
- Kruskall-Wallis test
Results and discussion
Results of examinations
- Clinical signs:
- no effects observed
- Mortality:
- no mortality observed
- Body weight and weight changes:
- effects observed, treatment-related
- Food efficiency:
- effects observed, treatment-related
- Water consumption and compound intake (if drinking water study):
- effects observed, treatment-related
- Ophthalmological findings:
- not examined
- Haematological findings:
- not examined
- Clinical biochemistry findings:
- not examined
- Urinalysis findings:
- not examined
- Behaviour (functional findings):
- not examined
- Organ weight findings including organ / body weight ratios:
- not examined
- Gross pathological findings:
- not examined
- Histopathological findings: non-neoplastic:
- not examined
- Histopathological findings: neoplastic:
- not examined
- Details on results:
- CLINICAL SIGNS AND MORTALITY: All animals survived the experiment and remained in good condition until the end of the experiment. However, female rats, especially in Group 2 but also in Group 4 and 5, had dull-appearing and thin fur in patches at the end of the experiment. Some light-brownish discoloration of the oral mucosa was seen in Group 2 rats.
BODY WEIGHT AND WEIGHT GAIN: The mean weight of the rats in the experimental groups was lower (1-29%) than that of control animals. The lowest bodyweight was observed in rats receiving Ca(OH)2 and in those with exposure starting at low age (6 weeks). Thus, the weights of the rats in experimental groups differed statistically significantly from the controls in the following groups: female rats of group 2, female rats of Group 4, female and male rats of group 5
FOOD EFFICIENCY: food intake was equal in the study and control rats
WATER CONSUMPTION AND COMPOUND INTAKE (if drinking water study): water intake was monitored intermittently in all groups, showing no differences between groups.
HISTOPATHOLOGY:
NON-NEOPLASTIC: No histological changes attributable to alkaline exposure occurred in the oral mucosa or other tissues studied. Alkaline exposure did not affect cell proliferation in the oral epithelium, as shown by the equal expression did not affect cell proliferation in the oral epithelium, as shown by the equal expression of PCNA in groups. The up-regulation of HSP70 protein expression in the oral mucosa of rats exposed to alkaline water, especially Ca(OH)2 treated rats, may indicate a protective response. Intercellular adhesion molecule-1 (ICAM-1) positivity was lost in6/12 rats treated with Ca(OH)2 with pH 11.2, and loss of CD44 expression was seen in 3/6 rats in both study groups exposed to alkaline water with pH 12.
Effect levels
- Remarks on result:
- other: no details reported
Target system / organ toxicity
- Critical effects observed:
- not specified
Any other information on results incl. tables
The results suggest that the oral mucosa in rats is resistant to
the effects of highly alkaline drinking water. The observed effects on
growth can be explained by NaOH neutralising the acid in the stomach
which decreases the digestion and the absorption of the food. Oral
studies with high concentrations of the substance are corrosive or
irritating, while at low concentrations the hydroxide will be
neutralised in the stomach by gastric juice, which has a very low pH.
Furthermore it should be realised that oral exposure to NaOH is
negligible under normal handling and use conditions. Weight of animals
before testing is not described.
Applicant's summary and conclusion
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