The International EU/COLIPA In Vitro Phototoxicity Validation Study: Results of Phase II (Blind Trial). Part 1: The 3T3 NRU Phototoxicity Test
- PMID: 20654413
- DOI: 10.1016/s0887-2333(98)00006-x
The International EU/COLIPA In Vitro Phototoxicity Validation Study: Results of Phase II (Blind Trial). Part 1: The 3T3 NRU Phototoxicity Test
Abstract
To date, no standardized international guideline for the testing of chemicals for phototoxic potential has been accepted for regulatory purposes. In 1991, the European Commission (EC), represented initially by the Directorate General XI and later by ECVAM (the European Centre for the Validation of Alternative Methods) and COLIPA (the European Cosmetic, Toiletry and Perfumery Association), agreed to establish a joint EU/COLIPA programme on the development and validation of in vitro phototoxicity tests. The first phase (phase I, 1992-93) was designed as a prevalidation study, to identify in vitro test procedures and test protocols for a formal validation trial under blind conditions. In the second phase (phase II, 1994-95), the formal validation study, the most promising in vitro phototoxicity tests were validated with 30 carefully selected test chemicals in 11 laboratories in a blind trial. The 3T3 mouse fibroblast neutral red uptake phototoxicity test (3T3 NRU PT) was performed as a core test in nine laboratories, since it provided the best results in phase I of the study. The purpose of phase II was to confirm the reliability and relevance of the in vitro tests for predicting phototoxic effects and for identifying phototoxic chemicals. In phase II the phototoxic potential of test chemicals in the 3T3 NRU PT test was either assessed by determining the phototoxicity factor (PIF) by using a cut-off value of 5 as in phase I of the study, or by determining the mean photo effect (MPE) by using a cut-off value of 0.1, as recently proposed by Holzhütter (1997). Results obtained with both approaches in the 3T3 NRU PT test in phase II were reproducible in the nine laboratories, and the correlation between in vitro and in vivo data was very high. Therefore, ECVAM and COLIPA conclude from this formal validation trial under blind conditions that the 3T3 NRU PT test is a scientifically validated in vitro test which is ready to be considered for regulatory purposes for assessing the phototoxic potential of chemicals. A draft OECD Guideline for "In Vitro Phototoxicity Testing", incorporating the standard protocol of the 3T3 NRU PT test, will be submitted to the OECD test guidelines programme in due course.
Similar articles
-
A Study on UV Filter Chemicals from Annex VII of European Union Directive 76/768/EEC, in the In Vitro 3T3 NRU Phototoxicity Test.Altern Lab Anim. 1998 Sep-Oct;26(5):679-708. Altern Lab Anim. 1998. PMID: 26042493
-
The 3T3 neutral red uptake phototoxicity test: practical experience and implications for phototoxicity testing--the report of an ECVAM-EFPIA workshop.Regul Toxicol Pharmacol. 2012 Aug;63(3):480-8. doi: 10.1016/j.yrtph.2012.06.001. Epub 2012 Jun 9. Regul Toxicol Pharmacol. 2012. PMID: 22687423
-
The red blood cell phototoxicity test (photohaemolysis and haemoglobin oxidation): EU/COLIPA validation programme on phototoxicity (phase II).Altern Lab Anim. 2001 Mar-Apr;29(2):145-62. doi: 10.1177/026119290102900208. Altern Lab Anim. 2001. PMID: 11262760
-
Lessons learned from validation of in vitro toxicity test: from failure to acceptance into regulatory practice.Toxicol In Vitro. 2001 Aug-Oct;15(4-5):585-90. doi: 10.1016/s0887-2333(01)00070-4. Toxicol In Vitro. 2001. PMID: 11566595 Review.
-
Validation successes: chemicals.Altern Lab Anim. 2002 Dec;30 Suppl 2:33-40. doi: 10.1177/026119290203002S05. Altern Lab Anim. 2002. PMID: 12513649 Review.
Cited by
-
The effect of injection using narrow-bore needles on mammalian cells: administration and formulation considerations for cell therapies.J Pharm Pharmacol. 2015 May;67(5):640-50. doi: 10.1111/jphp.12362. Epub 2015 Jan 26. J Pharm Pharmacol. 2015. PMID: 25623928 Free PMC article.
-
Exploration of alternative test methods to evaluate phototoxicity of ophthalmic agents by using Statens Seruminstitut Rabbit Cornea cell lines and 3D human reconstituted cornea models.PLoS One. 2018 May 21;13(5):e0196735. doi: 10.1371/journal.pone.0196735. eCollection 2018. PLoS One. 2018. PMID: 29782497 Free PMC article.
-
Hydroxypropyl Cellulose Hydrogel Containing Origanum vulgare ssp. hirtum Essential-Oil-Loaded Polymeric Micelles for Enhanced Treatment of Melanoma.Gels. 2024 Sep 29;10(10):627. doi: 10.3390/gels10100627. Gels. 2024. PMID: 39451280 Free PMC article.
-
Assessment of Developmental Toxicants using Human Embryonic Stem Cells.Toxicol Res. 2013 Dec 31;29(4):221-7. doi: 10.5487/TR.2013.29.4.221. Toxicol Res. 2013. PMID: 24578791 Free PMC article. Review.
-
Determination of the Phototoxicity Potential of Commercially Available Tattoo Inks Using the 3T3-neutral Red Uptake Phototoxicity Test.Turk J Pharm Sci. 2022 Feb 28;19(1):70-75. doi: 10.4274/tjps.galenos.2021.86344. Turk J Pharm Sci. 2022. PMID: 35227052 Free PMC article.
LinkOut - more resources
Full Text Sources
Other Literature Sources