کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5861174 1562709 2016 16 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Catch-up validation study of an in vitro skin irritation test method based on an open source reconstructed epidermis (phase I)
موضوعات مرتبط
علوم زیستی و بیوفناوری علوم محیط زیست بهداشت، سم شناسی و جهش زایی
پیش نمایش صفحه اول مقاله
Catch-up validation study of an in vitro skin irritation test method based on an open source reconstructed epidermis (phase I)
چکیده انگلیسی


- An in vitro skin irritation test based on the open source reconstructed epidermis (OS-REp) was developed.
- Open source means freely available protocols for tissue construction and test performance without legal restrictions.
- A catch-up validation study with 20 reference chemicals was conducted in 3 laboratories.
- Cross-contamination of OS-REp tissues with volatile irritants was identified as reason for initial low specificity.
- After re-testing with improved experimental set-up 93% overall sensitivity, 70% specificity and 82% accuracy were achieved.

We have developed a new in vitro skin irritation test based on an open source reconstructed epidermis (OS-REp) with openly accessible protocols for tissue production and test performance. Due to structural, mechanistic and procedural similarity, a blinded catch-up validation study for skin irritation according to OECD Performance Standards (PS) was conducted in three laboratories to promote regulatory acceptance, with OS-REp models produced at a single production site only. While overall sensitivity and predictive capacity met the PS requirements, overall specificity was only 57%. A thorough analysis of the test results led to the assumption that some of the false-positive classifications could have been evoked by volatile skin-irritating chemicals tested in the same culture plate as the non-irritants falsely predicted as irritants. With GC/MS and biological approaches the cross-contamination effect was confirmed and the experimental set-up adapted accordingly. Retesting of the affected chemicals with the improved experimental set-up and otherwise identical protocol resulted in correct classifications as non-irritants. Taking these re-test results into account, 93% overall sensitivity, 70% specificity and 82% accuracy was achieved, which is in accordance with the OECD PS. A sufficient reliability of the method was indicated by a within-laboratory-reproducibility of 85-95% and a between-laboratory-reproducibility of 90%.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Toxicology in Vitro - Volume 36, October 2016, Pages 238-253
نویسندگان
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