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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Exposure related observations in humans: other data

Administrative data

Endpoint:
exposure-related observations in humans: other data
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Basic data given

Data source

Reference
Reference Type:
publication
Title:
Percutanous absorption of azelaic acid in humans
Author:
Taeuber U., Weiss C. and Matthes H.
Year:
1992
Bibliographic source:
Exp Dermatol. 1992 Nov;1(4):176-9

Materials and methods

Type of study / information:
Six healthy male volunteers received a single topical treatment with 5 g of an anti-acne cream containing 20% azelaic acid (AzA) onto the face, the chest and the upper back. One week later 1 g of AzA was given orally to the same subjects as aqueous microcrystalline suspension. Following the two treatments the renal excretion of the unchanged compound was measured
Endpoint addressed:
basic toxicokinetics
Principles of method if other than guideline:
Excretion of azelaic acid was analyzed in urine after dermal application of six healthy male volunteers with a singlel treatment with 5 g of an anti-acne cream containing 20% azelaic acid and after oral application.
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
Azelaic acid
EC Number:
204-669-1
EC Name:
Azelaic acid
Cas Number:
123-99-9
IUPAC Name:
azelaic acid

Method

Ethical approval:
confirmed and informed consent free of coercion received
Details on study design:
Six healthy male volunteers received a single topical treatment with 5 g of an anti-acne cream containing 20% azelaic acid (AzA) onto the face, the chest and the upper back. One week later 1 g of AzA was given orally to the same subjects as aqueous microcrystalline suspension. Following the two treatments the renal excretion of the unchanged compound was measured
Exposure assessment:
measured
Details on exposure:
TYPE OF EXPOSURE:
- Dermal: 1 g azelaic acid in 5 g cream (Skinoren, Schering AG) was applied to ca. 5 cm2 skin. 2 g to chest, 2 g onto the back and 1 g to the face.
One hour after application, the skin areas treated on the back and chest were covered with cotton tissue fixed with adhesive tape. After 24 h of exposure, the covering material was removed and the treated areas were washed with 25 ml of ethanol 70% (v /v)
- Oral: 1 week after dermal application subjects received 100 ml of an aqueous micro-crystalline suspension containing 1 g azelaic acid in the morning before the breakfast was served

TYPE OF EXPOSURE MEASUREMENT: Biomonitoring (urine) by HPLC

EXPOSURE PERIOD:
- Dermal: 24 hours
- Oral: single application

POSTEXPOSURE PERIOD:
- Dermal: up to 3 days
- Oral: up to 4 days

Results and discussion

Results:
After dermal application of 5 g of cream containing 20% of Azelaic acid at a skin area dose of 5 mg /cm2 maximum concentrations 7.8 ± 3.2 µg/ ml (11.29 ± 0.5% of the dose applied) have been measured in the urine within the first 24 h. During the 2nd and 3rd d 0.76 +0.49% and 0.12 + 0.15% of the dose, respectively, was excreted unchanged with the urine. The total amount of Azelaic acid excreted unchanged with the urine within 3 d was determined to 2.2 ± 0.7% of the dose.
After oral administration a mean concentration of Azelaic acid of 424 + 104 µg/ml was found in the 0-24 h urine samples, corresponding to 61.2+ 8.8% of the dose administered. Excretion was complete within 24 h.

Any other information on results incl. tables

Urinary excretion of unchanged azelaic acid alter oral and dermal administration of 1 g azelaic acid to 6 male volunteers. Percentage of dose per fraction:

Time post aplication Subjects
1 2 3 4 5 6 mean ± SD
Oral 0 - 24 h 49.4 59.5 72.5 65.7 53.4 66.9 61.2 ± 0.88
24 -48 h 0 0 0 0 0 0 0.0 ± 0.0
Dermal 0 - 24 h 0.68 1.52 1.01 1.73 2.06 0.75 1.29 ± 0.56
24 -48 h 0.48 1.01 1.46 0 0.75 0.83 0.76 ± 0.49
48 - 72 h 0.17 0.37 0.19 0 0 0 0.12 ± 0.15
72 - 96 h 0 0 0.49 0 1.01 0 0.25 ± 0.42

Applicant's summary and conclusion