1-isoctyloxycarbonyl ethylated 2,4,6 tris (2,4- hydroxyphenyl) -1,3,5 triazine derivatives

Skin sensitisation

Administrative data

Endpoint:

skin sensitisation: in vivo (LLNA)

Type of information:

experimental study

Adequacy of study:

key study

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: GLP and guideline conform study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2003

Report date:

2003

Materials and methods

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)

Deviations:

no

GLP compliance:

yes

Type of study:

mouse local lymph node assay (LLNA)

Test material

Test material information

Constituent 1

In vivo test system

Test animals

Species:

mouse

Strain:

CBA

Sex:

female

Details on test animals and environmental conditions:

TEST ANIMALS
- Source: Harian Netheriands B.V. Postbus6174 NL - 5960 AD Horst / The Netheriands
- Age at study initiation: 8-12 weeks
- Weight at study initiation: 19-24g
- Housing: In groups of four in Makrolon type-3 cages with standard softwood bedding ("Lignocel", Schill AG, CH-4132 Muttenz).
- Diet (e.g. ad libitum): Pelleted standard Kliba 3433, batch no. 84/02 mouse maintenance diet (Provimi Kliba AG, CH-4303 Kaiseraugst) available ad libitum. Results of analyses for contaminants are archived at RCC.
- Water (e.g. ad libitum): Community tap water from Itingen, available ad libitum. Results of representative bacteriological, chemical and contaminant analyses are archived at RCC.
- Acclimation period: 04-JUN-2003 to 10-JUN-2003

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22+/- 3
- Humidity (%): 30-70
- Air changes (per hr): 10-15
- Photoperiod (hrs dark / hrs light): 12

IN-LIFE DATES:
Experimental Starting Date 04-JUN-2003
Experimental Completion Date 18-JUN-2003
Delivery of Animals 04-JUN-2003
Acclimatization 04-JUN-2003 to 10-JUN-2003
Treatment (epicutaneous) 11 -JUN-2003 to 13-JUN-2003
Treatment (intravenous) 16-J U N-2003
Observation 04-JUN-2003 to 16-JUN-2003
Termination 18-JUN-2003

Study design: in vivo (LLNA)

Vehicle:

acetone/olive oil (4:1 v/v)

Concentration:

5%, 10% and 25%

No. of animals per dose:

4

Details on study design:

RANGE FINDING TESTS:
- Irritation: In a non-GLP conform pre-test in two mice, test item concentrations of 5 %, 10 %, 25 % and 50 % (w/w) were tested on one ear each. No irritation effects were observed at concentrations of 5 %, 10 % and 25 % after a single application.

MAIN STUDY
ANIMAL ASSIGNMENT AND TREATMENT
- Name of test method:
- Criteria used to consider a positive response: The proliferative capacity of pooled lymph node cells was determined by the incorporation of ^Hmethyl thymidine measured in a p-scintillation counter.

TREATMENT PREPARATION AND ADMINISTRATION:
The test item was placed into a glass beaker on a tared Mettler balance and the vehicle
(acetone:olive oil, 4:1 (v/v)) was quantitatively added. The weight/weight dilutions were
prepared individually using a magnetic stirrer as homogenizer. Homogeneity of the test item
in the vehicle was maintained during treatment with the magnetic stirrer.
The preparations were made freshly before each dosing occasion.
To determine the highest non-irritant and technically applicable test item concentration, a
non-GLP pretest was performed in two mice with concentrations of 5 %, 10 %, 25 % and
50 % (w/w) (pretest excluded from Statement of Compliance).
The test item in the main study was assayed at three consecutive concentrations. The top
dose is the highest technically achievable concentration whilst avoiding systemic toxicity and
excessive local irritation. No severe irritant effects were tolerated choosing the test
concentrations.
Concentrations were in terms of material as supplied.

TREATMENT PROCEDURES
TOPICAL APPLICATION
Each test group of mice was treated by topical (epidermal) application to the dorsal surface
of each ear lobe (left and right) with different test item concentrations of 5 %, 10 % and 25 %
(w/w) in acetone:olive oil, 4:1 (v/v). The application volume, 25 pi, was spread over the entire
dorsal surface ( 0 - 8 mm) of each ear lobe once daily for three consecutive days. A further
group of mice was treated with an equivalent volume of the relevant vehicle alone (control
animals). A hair dryer was used to dry the ear's surface as quickly as possible to avoid loss
of test item applied.

ADMINISTRATION OF 3H-METHYL THYMIDINE*
3H-methyl thymidine (3HTdR) was purchased from Amersham International (Amersham
product code no. TRA 310; specific activity, 2 Ci/mmol; concentration, 1 mCi/ml).
Five days after the first topical application, all mice were administered with 250 pi of
79.5 pCi/ml 3HTdR (equal to 19.9 pCi 3HTdR) by intravenous injection via a tail vein.

DETERMINATION OF INCORPORATED 3HTDR*
Approximately five hours after treatment with 3HTdR all mice were euthanized by
intraperitoneal injection of VETANARCOL (Veterinaria AG, Zurich).
The draining lymph nodes were rapidly excised and pooled for each experimental group
(8 nodes per group). Single cell suspensions (phosphate buffered saline) of pooled lymph
node cells were prepared by gentle mechanical disaggregation through stainless steel gauze
(200 pm mesh size). After washing two times with phosphate buffered saline (approx. 10 ml)
the lymph node cells were resuspended in 5 % trichloroacetic acid (approx. 3 ml) and
incubated at approximately +4 °C for at least 18 hours for precipitation of macromolecules.
The precipitates were then resuspended in 5 % trichloroacetic acid (1 ml) and transferred to
glass scintillation vials with 10 ml of 'Ultima Gold' scintillation liquid and thoroughly mixed.
The level of 3HTdR incorporation was then measured on a P-scintillation counter. Similariy,
background 3HTdR levels were also measured in two 1ml-aliquots of 5 % trichloroacetic acid.
The p-scintillation counter expresses 3HTdR incorporation as the number of radioactive
disintegrations per minute (DPM).

Positive control substance(s):

hexyl cinnamic aldehyde (CAS No 101-86-0)

Statistics:

The mean values and standard deviations were calculated in the body weight tables.

Results and discussion

Positive control results:

The test item ALPHA-HEXYLCINNAMALDEHYDE was found to be a sensitizer and an EC3 value of 7.08 % (w/v) was derived.

In vivo (LLNA)

Results

Results 1

Parameter:

SI

Remarks on result:

other: see above or in summary

Results 2

Parameter:

other: disintegrations per minute (DPM)

Remarks on result:

other: see Remark

Remarks:

concentration (%) dpm S.I. 0 (backgroundI, II) 0, 1 - 0 (control group) 5191 - 5 5848 1.1 10 4202 0.8 25 10298 2.0

Applicant's summary and conclusion

Interpretation of results:

not sensitising

Remarks:

Migrated information

Conclusions:

In this study STIMULATION INDICES of 1.1, 0.8 and 2.0 were determined with the test item at concentrations of 5 %, 10 % and 25 % (w/w) in acetone:olive oil, 4:1 (v/v). A test item is regarded as a sensitizer in the LLNA if the exposure to one or more test concentrations resulted in 3-fold or greater increase in incorporation of 3HTdR compared with concurrent controls, as indicated by the STIMULATION INDEX (S.I.).
The test item was found to be a non-sensitizer when tested at up to concentration of 25 % (w/w) in acetone:olive oil, 4:1 (v/v).

Executive summary:

In order to study a possible contact allergenic potential of the test item, three groups each of four female mice were treated daily with the test item at concentrations of 5%, 10% and 25% (w/w) in acetone:olive oil, 4:1 (v/v) by topical application to the dorsum of each ear lobe (left and right) for three consecutive days. A control group of four mice was treated with the vehicle (acetone:olive oil, 4:1 (v/v)) only. Five days after the first topical application the mice were injected intravenously into a tail vein with radio-labelled thymidine (3H-methyl thymidine). Approximately five hours after intravenous injection, the mice were sacrificed, the draining auricular lymph nodes excised and pooled per group. Single cell suspensions of lymph node cells were prepared from pooled lymph nodes which were subsequently washed and incubated with trichloroacetic acid overnight. The proliferative capacity of pooled lymph node cells was determined by the incorporation of 3Hmethyl thymidine measured in a p-scintillation counter.

No test item-related clinical signs were observed. All treated animals survived the scheduled study period. A test item is regarded as a sensitizer in the LLNA if the exposure to one or more test concentrations resulted in 3-fold or greater increase in incorporation of 3HTdR compared with concurrent controls, as indicated by the STIMULATION INDEX (S.I.).

	Test item concentration % (w/w)	S.I.
Group 2	5	1.1
Group 3	10	0.8
Group4	25	2.0
No dose-response relation was observed.