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dc.contributor.author배옥남-
dc.date.accessioned2018-03-29T06:33:06Z-
dc.date.available2018-03-29T06:33:06Z-
dc.date.issued2016-05-
dc.identifier.citationJOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, v. 80, Page. 82-89en_US
dc.identifier.issn1056-8719-
dc.identifier.issn1873-488X-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1056871916300533-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/53723-
dc.description.abstractAssessment of eye irritation potential is important to human safety, and it is necessary for various cosmetics and chemicals that may contact the human eye. Until recently, the Draize test was considered the standard method for estimating eye irritation, despite its disadvantages such as the need to sacrifice many rabbits for subjective scoring. Thus, we investigated the cytotoxicity and inflammatory response to standard eye irritants using SV40 T-transformed human corneal epithelial (SHCE) cells as a step toward development of an animal-free alternative eye irritation test. MTT and NRU assays of cell viability were performed to investigate the optimal experimental conditions for SHCE cell viability when cells were exposed to sodium dodecyl sulfate (SDS) as a standard eye irritant at 6.25 x 10(-3) to 1 x 10(-1)%. Additionally, cell viability of SHCE cells was examined in response to six potential eye irritants, benzalkonium chloride, dimethyl sulfoxide, isopropanol, SDS, Triton X-100 and Tween 20 at 5 x 10(-3) to 1 x 10(-1)%. Finally, we estimated the secretion level of cytokines in response to stimulation by eye irritants in SHCE cells. SHCE cells showed a good response to potential eye irritants when the cells were exposed to potential irritants for 10 min at roomtemperature (RT), and cytokine production increased in a concentration-dependent manner, indicating that cytotoxicity and cytokine secretion from SHCE cells may be well correlated with the concentrations of irritants. Taken together, these results suggest that SHCE cells could be an excellent alternative in vitro model to replace in vivo animal models for eye irritation tests. (C) 2016 Elsevier Inc. All rights reserved.en_US
dc.description.sponsorshipThis research was supported by a grant (13172MFDS987) from the Ministry of Food and Drug Safety, Republic of Korea. In addition, this work was supported by Priority Research Centers Program through NRF funded by the Ministry of Education, Science and Technology (2015R1A6A1A04020885).en_US
dc.language.isoen_USen_US
dc.publisherELSEVIER SCIENCE INCen_US
dc.subjectEye irritationen_US
dc.subjectSHCE cellsen_US
dc.subjectCorneal cellsen_US
dc.subjectIn vitro alternativeen_US
dc.subjectSV40 T antigenen_US
dc.titleApplication of SV40 T-transformed human corneal epithelial cells to evaluate potential irritant chemicals for in vitro alternative eye toxicityen_US
dc.typeArticleen_US
dc.relation.volume80-
dc.identifier.doi10.1016/j.vascn.2016.05.013-
dc.relation.page82-89-
dc.relation.journalJOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS-
dc.contributor.googleauthorKim, Cho-Won-
dc.contributor.googleauthorPark, Geon-Tae-
dc.contributor.googleauthorBae, Ok-Nam-
dc.contributor.googleauthorNoh, Minsoo-
dc.contributor.googleauthorChoi, Kyung-Chul-
dc.relation.code2016008520-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF PHARMACY[E]-
dc.sector.departmentDEPARTMENT OF PHARMACY-
dc.identifier.pidonbae-
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COLLEGE OF PHARMACY[E](약학대학) > PHARMACY(약학과) > Articles
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