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Diss Factsheets

Toxicological information

Skin sensitisation

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Administrative data

Endpoint:
skin sensitisation: in vitro
Type of information:
experimental study
Adequacy of study:
key study
Study period:
2 October 2018 - 31 January 2019
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2019
Report date:
2019

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 442C (In Chemico Skin Sensitisation: Direct Peptide Reactivity Assay (DPRA))
Deviations:
yes
Remarks:
See Deviations text below.
GLP compliance:
yes (incl. QA statement)
Type of study:
other: DPRA

Test material

Constituent 1
Chemical structure
Reference substance name:
Methyl dihydrogen phosphate
EC Number:
212-379-1
EC Name:
Methyl dihydrogen phosphate
Cas Number:
812-00-0
Molecular formula:
CH5O4P
IUPAC Name:
methyl dihydrogen phosphate
Test material form:
liquid
Specific details on test material used for the study:
Batch 34448
Purity 67.9 - 71.2% Methyl dihydrogen phosphate
Expiry 30 March 2022

In vitro test system

Details on the study design:
Preparation of test item
The concentration of the test item to be used was determined based on the molecular weight (MW) 96 g/mol and the purity, the purity value 67.9-71.2 % was treated as 67.9 %. The target weight (± 10 %) of the test item was calculated. 100 mM test item solution was prepared by dissolving 42.3 mg and 42.5 mg test item in 3 mL of the solvent acetonitrile for the Cys-peptide and Lys-peptide, respectively.

HPLC was used for the measurement of peptide depletion of the Cys-peptide and the Lys-Peptide.

Positive control
Positive controls were treated identically as the test item. The following positive controls were used:
• Cinnamaldehyde (CAS 104-55-2, food grade ≥95 %, batch no. MKBT8955V) was used as 100 mM (± 10 %) solution in acetonitrile for the Cys-peptide.
• 2,3-Butanedione (CAS 431-03-8, ≥99 %, batch no. BCBS3560V) was used as 100 mM (± 10 %) solution in acetonitrile for the Lys-peptide

As cinnamaldehyde mixed with the lysine peptide turned turbid in all experiments performed during the implementation phase, it was considered unsuitable as positive control. Instead, the proficiency chemical 2,3-Butanedione was used as positive control showing mid-range depletion for the lysine peptide.

Solvent controls
For both peptides, four sets of solvent controls using acetonitrile instead of test item stock solution were prepared in triplicate. Set A was analysed together with the peptide calibration standards, sets B1 and B2 were analysed at the start and end of the analysis sequence and were used as stability control for the peptide over the total analysis time. Set C was incubated and analysed together with the samples and was used for calculation of the peptide depletion.


Co-elution control
Sample prepared from the respective peptide buffer and the test item, but without peptide.

Test solutions
Dilution buffers
• 2 mL Acetonitrile were mixed with 8 mL phosphate buffer, pH 7.498 (Peptide dilution buffer C)
• 2 mL Acetonitrile were mixed with 8 mL ammonium acetate buffer, pH 10.204 (Peptide dilution buffer K)

Peptide stock solutions
The peptide stock solutions were freshly prepared for each assay.
• 0.667 mM Cys-Peptide solution was prepared by dissolving 20.0 mg of the peptide in 40 mL phosphate buffer, pH 7.498. (batch no. 20181024)
• 0.667 mM Lys-Peptide solution was prepared by dissolving 25.9 mg of the peptide in 50 mL ammonium acetate buffer, pH 10.204. (batch no.20181009)

Peptide calibration standards
From each peptide stock solution, the following calibration standards were prepared in the appropriate dilution buffer: 0.534 / 0.267 / 0.1335 / 0.0667 / 0.0334 / 0.0167 mM Peptide. Calibration samples were analysed before the samples containing the test item. Blank dilution buffer was also measured.

Test item samples
Samples were prepared in triplicate for each peptide. The Cys-peptide samples were prepared in 1:10 molar ratio (0.5 mM peptide: 5 mM test item), the Lys-peptide samples in 1:50 molar ratio (0.5 mM peptide and 25 mM test item) using the stock solutions. A final volume of 1 mL per sample was prepared for each sample.


Incubation
The positive control, solvent control sets C, and test item samples were incubated in closed amber glass HPLC vials in an incubation chamber at 25.0 °C for 22 h and 5 minutes for the Cys-peptide and 22 h for the Lys-peptide, respectively. All three replicates for the Cys-peptide were turbid after incubation. They were centrifuged (10 min, 400 g) and only the clear supernatant was used for the measurement. None of the replicates for the Lys-peptide were turbid after incubation.

According to the test guideline, the reactivity is classified as “high”, “moderate”, “low” or “minimal” using the Cysteine 1:10/Lysine 1:50 prediction model shown in the table below.

Results and discussion

Positive control results:
The mean peptide-depletion of the positive control 2,3 butanedione for the Lys-peptide was marginal out of the range of historical data, but nevertheless the value 40.25 % was within the range given in the OECD442C.

In vitro / in chemico

Resultsopen allclose all
Key result
Group:
test chemical
Run / experiment:
mean
Parameter:
lysine depletion
Value:
0 %
Key result
Group:
test chemical
Run / experiment:
mean
Parameter:
cysteine depletion
Value:
0 %
Other effects / acceptance of results:
No observations arousing doubts concerning the accuracy of the results and the validity of the study were made.

Any other information on results incl. tables

Calculated peptide depletion values for the Cys-Peptide

 Sample name     Depletion (%)      
 Single  Mean  SD
 Positive control Rep 1  75.44  76.14        0.94      
 Positive control Rep 2  75.77
 Positive control Rep 3  77.21
 Test item Rep 1  0.00 (-1.07)  0.00        0.00      
 Test item Rep 2  0.00 (-1.34)
 Test item Rep 3  0.00 (-1.23)

Negative depletion values were considered as “zero” when calculating the mean.

Calculated peptide depletion values for the Lys-Peptide

 Sample name     Depletion (%)      
 Single  Mean  SD
 Positive control Rep 1  38.14    40.25  3.99
 Positive control Rep 2  37.76
 Positive control Rep 3  48.46
 Test item Rep 1  0.00 (-3.33)  0.00        0.00   
 Test item Rep 2  0.00 (-0.73)
 Test item Rep 3  0.00 (-0.92)

Negative depletion values were considered as “zero” when calculating the mean.

Applicant's summary and conclusion

Conclusions:
The mean peptide depletion in the Cys-peptide and Lys-peptide assay was 0.00 %, therefore the test item was classified with:

DPRA Prediction: Negative Reactivity class: Minimal
Executive summary:

DPRA Prediction: Negative Reactivity class: Minimal