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Ecotoxicological information

Long-term toxicity to fish

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Administrative data

Link to relevant study record(s)

Reference
Endpoint:
fish early-life stage toxicity
Type of information:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Study period:
2008-2009
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Justification for type of information:
Sorafenib tosylate was used as an analogue.
Reason / purpose for cross-reference:
read-across: supporting information
Qualifier:
according to guideline
Guideline:
OECD Guideline 210 (Fish, Early-Life Stage Toxicity Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Analytical monitoring:
yes
Vehicle:
yes
Test organisms (species):
Pimephales promelas
Test type:
flow-through
Water media type:
freshwater
Limit test:
no
Total exposure duration:
33 d
Duration:
28 d
Dose descriptor:
EC10
Effect conc.:
0 mg/L
Nominal / measured:
meas. (arithm. mean)
Conc. based on:
test mat.
Basis for effect:
mortality

Fish larvae hatched 4 days after the introduction of the eggs in all test solutions. The hatching success was > 66 % in all test and control solutions. The number of dead fish increased with increasing concentration. From the second highest concentration on, fish growth (weight and length) decreased. The NOEC and LOEC for weight and length was 2.4 µg/L and 14.8 µg/L, respectively, for survival the NOEC was < 1.0 µg/L and the LOEC was  1.0 µg/L and for hatchability NOEC and LOEC were 14.8 µg/L.


In order to define a threshold for toxic effects, the EC10 for weight and length inhibition was determined with 0.47 µg/L and 0.32 µg/L, respectively, for survival (28 dph) was 0.17 µg/L.

Validity criteria fulfilled:
yes
Conclusions:
The results of this study showed that Sorafenib tosylate has effects on growth and survival of fish
(fathead minnow) at concentrations from 1.0 µg/L onwards. Thus, the overall no observed effect concentration (NOEC) was <1.0 µg/L, the lowest observable effect concentration (LOEC) was 1.0 µg/L. The lowest EC10 for survival was 0.17 µg/L.
Executive summary:

The eggs and larvae were exposed to three test solutions of sorafenibtosylate with nominal


concentrations of 6, 17 and 50 µg (nominal) per liter tap water and additionally to a vehicle


(dimethylformamide, DMF) and a control for a period of 28 days post hatch (ph). For the


preparation of the stock solution, the test substance was dissolved in DMF.


The stock solution was mixed with tap water and delivered continuously to the tanks.


Mortalities and visible abnormalities were recorded daily over the exposure phase. Hatching


success and survival were recorded during the first phase of embryonic development as well as


growth and survival during the larval stage until the end of the exposure period. The


hydrographic parameters were recorded weekly.


The oxygen concentration in the test vessels was >60 % of air saturation value, the


temperature was maintained at 24 ± 2 ºC and the pH-value between 6.5 and 8.5.


Samples for the concentration analysis in the test solutions were taken at the start of the exposure


and weekly thereafter. The determination of Sorafenib tosylate in the test solutions was carried


out by HPLC/MS.


The endpoint survival was statistically evaluated by the computer program


TOXRat Professional XT, length and weight was evaluated by PROVANTIS (NOEC, LOEC)


and TOXRat Professional XT (ECx).


Then analytical results gave mean measured concentrations of 1, 2.4 and 14.8 µg/L.


Hatching and short-term survival (day 5 ph) was not affected by the test substance while


mortality of the larvae (day 28 ph) increased clearly with increasing concentration of


sorafenibtosylate. Additionally, the growth of the treated fish decreased with increasing


concentration of the test substance.


A significant substance-related effect on growth and survival of the treated fish compared to the


control could be observed. The NOEC (survival) was <1.0 µg/L and the LOEC (survival) was


1.0 µg/L, the EC10 for survival was 0.17 µg/L. The NOEC for length and weight was 2.4 µg/L,


the LOEC was 14.8 µg/L. The EC10 was 0.47 µg/L for weight and 0.32 µg/L for length.


Accordingly, 0.17 µg/L was the toxicity threshold for sorafenib tosylate.

Description of key information

A guideline study according to OECD Guideline 210 (Fish, Early-Life Stage Toxicity Test) was performed under GLP to assess the long-term toxicity of Sorafenib tosylate to fish Pimephales promelas. The eggs and larvae were exposed to three test solutions with nominal concentrations of 6, 17 and 50 µg (nominal) per liter tap water and additionally to a vehicle (dimethylformamide, DMF) and a control for a period of 28 days post hatch (ph). For the preparation of the stock solution, the test substance was dissolved in DMF. The stock solution was mixed with tap water and delivered continuously to the tanks. Mortalities and visible abnormalities were recorded daily over the exposure phase. Hatching success and survival were recorded during the first phase of embryonic development as well as growth and survival during the larval stage until the end of the exposure period. Samples for the concentration analysis in the test solutions were taken at the start of the exposure. The analytical results by HPLC/MS gave mean measured concentrations of 1, 2.4 and 14.8 µg/L. A significant substance-related effect on growth and survival of the treated fish compared to the control could be observed. The NOEC (survival) was <1.0 µg/L and the LOEC (survival) was 1.0 µg/L, the EC10 for survival was 0.17 µg/L. The NOEC for length and weight was 2.4 µg/L, the LOEC was 14.8 µg/L. The EC10 was 0.47 µg/L for weight and 0.32 µg/L for length. Accordingly, 0.17 µg/L was the toxicity threshold for the test substance.

Key value for chemical safety assessment

Fresh water fish

Fresh water fish
Dose descriptor:
LC10
Effect concentration:
0 mg/L

Additional information