A COMPARISON STUDY OF FOUR IN VITRO PHOTOTOXICITY SYSTEMS.
- TR Number: 126
- Authors: Rachui, S.R., Robertson, W.D., Duke, M.A., Allen, R. Stephens & Associates, Inc.
Four in vitro phototoxicity systems were evaluated to determine how closely each method would reproduce the others. Eleven materials were used to evaluate these methods. All eleven materials were run in each system. Phototoxicity was evaluated using the Mattek EPI-100 dermal construct, the Advanced Tissues Sciences’ model 2K1300 dermal construct, and a monolayer of neonatal fibroblasts. The protocol used for these three systems was similar and used cytotoxicity as an endpoint for phototoxicity. The fourth system evaluated used yeast as an indicator of phototoxicity with and an endpoint being zones of inhibition which were generated in response to a phototoxic material. Each of these methods utilized UVA to stimulate phototoxic responses from the materials. Each of these systems have specific advantages and disadvantages. In general, it appears the three dimensional systems are more consistent predictors of phototoxicity. The monolayer system, on the other hand, may be the most sensitive of the models while the yeast method offers a rapid, inexpensive means of screening materials prior to proceeding to more expensive and time consuming testing.
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- Absorption
- Antimicrobial
- Buccal delivery
- Genotoxicity
- Mucosal delivery
- Reproducibility - skin tissue models
- UV protection
- Corneal Drug Delivery
- UV damage
- transporters
- Regulatory Approval
- Review Article
- Drug delivery
- Infectious disease research
- Buccal drug delivery
- Pharmacotoxicology
- Nasal absorption
- Nanotechnology
- Aging
- Respiratory Disease
- Bacterial infection
- Pollution
- Mildness Testing
- Barrier Disruption
- Irritation
- Infection
- Mucosal irritation
- Psoriasis
- Vaginal irritation
- Respiratory immunotoxicity
- Human-on-a-chip
- Atopic Dermatitis
- DNA Damage
- Colitis
- Drug ADME
- Hair Growth
- Permeation
- Infections
- Cosmetics
- Metabolism
- Mucous
- Respiratory infection
- Viral Infection
- Melanogenesis
- Antiviral
- Gastrointestinal Disease
- Hazard assessment
- Biomedical Devices
- Skin irritation
- Toxicity
- Cytokine analysis
- Immulogical research
- Nanoparticle toxicology/penetration
- Respiratory toxicology
- MMPs
- Intestinal Permeation
- Bacterial colonization
- Translational toxicology
- Dry skin
- drug skin compatibility
- Allergenicity
- Antioxidants
- Drug absorption
- Immunologicaal research
- Toxicology
- Skin cancer
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- Electrolyzed Water
- Transbuccal drug delivery
- XtraMild skin mildness testing
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- Protein Expression
- Immunological Research
- Apoptosis
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- Microbicides
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- bacterial vaginosis
- ADME
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- Microphysiological system
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- Skin
- Oral Disease Research
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- Tumor invasion
- Probiotic
- Intestinal infection
- Skin re-epithelization
- Crohn's Disease
- Inflammatory response
- UV toxicity
- Basic respiratory research
- Genomics
- STD infection
- Reproducibility - eye (ocular) tissue model
- UV light
- Irritation>Eye Irritation OECD TG 492
- Skin differentiation
- Barrier repair
- Inflamed Bowel Disease
- Visible Light
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