Ferbam

Repeated dose toxicity: oral

Administrative data

Endpoint:

sub-chronic toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Study period:

not mentioned

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

comparable to guideline study with acceptable restrictions

Data source

Reference

Reference Type:

publication

Title:

Oral toxicity of ferric dimethyl-dithiocarbamate (ferbam) and tetramethylthiuram disulfide (thiram) in rodents

Author:

Lee C.-C. et al.

Year:

1978

Bibliographic source:

Journal of Toxicology and Environmental Health 4 (1), 93-106

Materials and methods

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 408 (Repeated Dose 90-Day Oral Toxicity Study in Rodents)

Deviations:

yes

Remarks:

only male rats

GLP compliance:

not specified

Test material

Test material information

Constituent 1

Reference substance name:

Ferbam

EC Number:

238-484-2

EC Name:

Ferbam

Cas Number:

14484-64-1

Molecular formula:

C9H18FeN3S6

IUPAC Name:

iron(3+) tris(dimethyldithiocarbamate)

Test material form:

solid: particulate/powder

Details on test material:

The test material contained 76% ferbam, the remaining constituents were inert material added by the manufacturers to make dry powders for spray suspensions.
The test item contained 13.1% iron, and in addition also 0.242% lead and very small amounts of cobalt, nickel, thallium, selenium, or mercury.

Test animals

Species:

rat

Strain:

other: CD strain

Sex:

male

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Charles River Breeding Laboratory, Wilmington, Massachusetts
- Females (if applicable) nulliparous and non-pregnant: [yes/no] no females
- Age at study initiation: young rats
- Weight at study initiation: 120 - 190 g
- Housing: The rats were housed, two per cage, in plastic cages with filter tops in temperature- and humidity-controlled quarters on a 12-h light cycle. Hardwood bedding material was used.
- Diet (e.g. ad libitum): Wayne Laboratory Animaf Dieis, Allied Mills, Chicago.
- Water (e.g. ad libitum): no details given
- Acclimation period: no details given

DETAILS OF FOOD AND WATER QUALITY: Regular chow was analyzed for metals, trace elements, and various pesticides. The diets were prepared every 2-3 wk.

ENVIRONMENTAL CONDITIONS
- Photoperiod (hrs dark / hrs light): 12-h light cycle

Administration / exposure

Route of administration:

oral: feed

Details on route of administration:

Regular chow was analyzed for metals, trace elements, and various pesticides. The diets were prepared every 2-3 wk. Ferbam was found to be stable in the diets at room temperature for 8 wk.

Vehicle:

unchanged (no vehicle)

Details on oral exposure:

- PREPARATION OF DOSING SOLUTIONS:

- DIET PREPARATION
- Rate of preparation of diet (frequency): The diets were prepared every 2-3 wk.
- Mixing appropriate amounts with (Type of food): powdered regular rodent chow
- Storage temperature of food: room temperature

Analytical verification of doses or concentrations:

not specified

Details on analytical verification of doses or concentrations:

Food intake was measured throughout the study.

Duration of treatment / exposure:

13 weeks

Frequency of treatment:

Daily

Doses / concentrations

Doses / concentrations 1

Dose / conc.:

23 mg/kg bw/day (nominal)

Doses / concentrations 2

Dose / conc.:

66 mg/kg bw/day (nominal)

Doses / concentrations 3

Dose / conc.:

109 mg/kg bw/day (nominal)

Doses / concentrations 4

Dose / conc.:

331 mg/kg bw/day (nominal)

No. of animals per sex per dose:

20 male rats per dose

Control animals:

yes, plain diet

Positive control:

not specified

Examinations

Observations and examinations performed and frequency:

CAGE SIDE OBSERVATIONS: Yes
- Time schedule: daily

DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: checked daily for behavioural changes and adverse effects

BODY WEIGHT: Yes
- Time schedule for examinations: weekly

FOOD CONSUMPTION AND COMPOUND INTAKE (if feeding study):
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes
- Compound intake calculated as time-weighted averages from the consumption and body weight gain data: Not specified

FOOD EFFICIENCY:
- Body weight gain in kg/food consumption in kg per unit time X 100 calculated as time-weighted averages from the consumption and body weight gain data: Not specified

OPHTHALMOSCOPIC EXAMINATION: No

HAEMATOLOGY: Yes
- Time schedule for collection of blood: at termination
- Anaesthetic used for blood collection: Not specified
- Animals fasted: Not specified
- How many animals: 12 rats of each group
- Parameters examined: total red blood cells, white blood cell and reticulocyte counts, differential leukocyte count, hematocrit, and hemoglobin

CLINICAL CHEMISTRY: Yes
- Time schedule for collection of blood: at termination
- Animals fasted: Not specified
- How many animals: 12 rats of each group
- Parameters examined: fasting glucose, serum glutamic oxaloacetic transaminase (SGOT), serum glutamic pyruvic transaminase (SGPT), alkaline phosphatase, and blood urea nitrogen (BUN)

URINALYSIS: No

NEUROBEHAVIOURAL EXAMINATION: Yes
- Time schedule for examinations: observed daily

OTHER: organ weights, microscopic examination

Sacrifice and pathology:

GROSS PATHOLOGY: Yes
The liver, spleen, kidneys, adrenals, thyroids, and gonads were removed and weighed; organ weight/body weight ratios were calculated.

HISTOPATHOLOGY: Yes
The liver, spleen, kidneys, adrenals, thyroids, gonads, heart, lung, salivary gland, pancreas, fundic and pyloric stomach, intestines, urinary bladder, accessory sex organs, diaphragm and gracilis muscle, rib bone with marrow smears, pituitary, and brain were stained with hematoxylin and eosin (H&E) for microscopic examination.

Statistics:

Differences between treated and control groups were tested for significance according to Dunnett's (1955) multiple comparison procedure.

Results and discussion

Results of examinations

Clinical signs:

effects observed, treatment-related

Description (incidence and severity):

Six deaths occurred in rats fed 109 mg/kg'd between the 3d and 5th wk. In a fourth group, 331 mg/kg*d ferbam killed all 20 rats during the 1st wk.

Mortality:

mortality observed, treatment-related

Description (incidence):

Six deaths occurred in rats fed 109 mg/kg'd between the 3d and 5th wk. In a fourth group, 331 mg/kg*d ferbam killed all 20 rats during the 1st wk.

Body weight and weight changes:

effects observed, treatment-related

Description (incidence and severity):

Ferbam intake of 23, 66, or 109 mg/kg*d significantly reduced the weight gain and food consumption of male rats.

Food consumption and compound intake (if feeding study):

effects observed, treatment-related

Description (incidence and severity):

Ferbam intake of 23, 66, or 109 mg/kg*d significantly reduced the weight gain and food consumption of male rats.

Food efficiency:

not specified

Ophthalmological findings:

not examined

Haematological findings:

no effects observed

Clinical biochemistry findings:

no effects observed

Urinalysis findings:

not examined

Behaviour (functional findings):

not examined

Immunological findings:

not examined

Organ weight findings including organ / body weight ratios:

no effects observed

Gross pathological findings:

no effects observed

Neuropathological findings:

not examined

Histopathological findings: non-neoplastic:

effects observed, treatment-related

Description (incidence and severity):

Rats in the two high-dose groups had golden pigmentation of the reticuloendothelial (R-E) cells of the spleen and mesenteric lymph nodes.

Histopathological findings: neoplastic:

no effects observed

Effect levels

1

Key result

Dose descriptor:

NOAEL

Effect level:

66 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

male

Basis for effect level:

body weight and weight gain

clinical biochemistry

clinical signs

food consumption and compound intake

gross pathology

haematology

histopathology: neoplastic

histopathology: non-neoplastic

mortality

organ weights and organ / body weight ratios

2

Dose descriptor:

LOAEL

Effect level:

109 mg/kg bw/day (nominal)

Based on:

test mat.

Sex:

male

Basis for effect level:

histopathology: non-neoplastic

mortality

Target system / organ toxicity

Critical effects observed:

not specified

Any other information on results incl. tables

Summary of subactute toxicities of ferbam in rats.

	23 mg/kg*d	66 mg/kg*d	109 mg/kg*d	331 mg/kg*d
Total weight gain, % of control	90	79	58
Average feed intake, % of control	91	83	63
Number of deaths	0	0	6	20
Clinical chemistry	-	-	-
Lesions
- Spleen, lymph node	-	-	+	+
- Testes	-	-	-	-

Applicant's summary and conclusion

Conclusions:

The most obvious effect of ferbam in rats was the reduced weight gain. This was significant in males fed ferbam at all dosages (23, 66, and 109 mg/kg'd) for 13 wk. Food consumption was reduced and paralleled the reduced weight gain, thus the depressed weight gain could be a result of decreased palatability of the ferbam-containing feed. Ferbam intake of 109 mg/kg*d killed 6 of 20 rats between the 3d and 5th wk and 331 mg/kg-d killed all rats during the 1st wk. No adverse effects on clinical chemistry parameters or examined organs were observed in rats treated with 66 mg/kg*d. Based on mortality and lesions in spleen and lymph nodes observed in rats fed 109 mg/kg*d ferbam, a NOAEL of 66 mg/kg*d can be derived.

Executive summary:

The subchronic oral toxicity of the test item ferbam was studied in male rats. Administration of ferbam in the diet for 13 weeks reduced weight gain, parraleled with reduced food consumption. Ferbam intake of 109 mg/kg*d killed 6 of 20 rats between the 3d and 5th wk and 331 mg/kg-d killed all rats during the 1st wk. No adverse effects on clinical chemistry parameters or examined organs were observed in rats treated with 66 mg/kg*d. Based on mortality and lesions in spleen and lymph nodes observed in rats fed 109 mg/kg*d ferbam, a NOAEL of 66 mg/kg*d can be derived.