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New Photosensitization and Alternative Phototoxicity Methods. George L. DeGeorge, Ph.D., DABT MB Research Laboratories. 3T3 NRU Phototoxicity Test. Seed 96 well plates with 3T3 cells. Plate A. Plate B. Dose 2 plates with 8 conc. of TA Incubate 37 º C, 5% CO 2 , 1 hr.
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New Photosensitization and Alternative Phototoxicity Methods George L. DeGeorge, Ph.D., DABT MB Research Laboratories
3T3 NRU Phototoxicity Test Seed 96 well plates with 3T3 cells Plate A Plate B Dose 2 plates with 8 conc. of TAIncubate 37ºC, 5% CO2, 1 hr Plate A: Expose to UVA 5 J/cm2/50 mins Plate B: Keep in the dark, 50 mins Return to 37ºC CO2 incubator for 24 hrs Add Neutral Red media; incubate 3 hrs; Rinse & Fix Read at 540 nm, PIF ratio = IC50Dark / IC50UVA If PIF > 6 then +phototoxin
3T3 NRU Phototoxicity Test • IC50: The concentration of test material which reduces cell viability to 50% compared to untreated controls • Calculation of Photo-Irritation Factor (PIF) PIF = IC50dark / IC50UVA (>6 = +phototoxin)
In Vitro/Alternatives • 3T3 NRU Phototoxicity Assay– (OECD) • Other applicable cell types • Primary Human Keratinocytes • Melanocytes • Langerhans Cells • In Ovo Phototoxicity Assays • 3-D human tissue constructs
Solar Simulator SOL 500 Bulb:400W Metal Halide “S” Bulb Dimensions:34 x 30 x 40cm Weight: 11 kg Spectral Distributions Possible With H1 Filter: UVA+VIS+IR With H2 Filter: UVB + UVA + VIS + IR With NO Filter: UVC+UVB+UVA+VIS+IR
3T3 NRU Phototoxicity Assay • Evaluates photo-cytotoxicity • Mouse Fibroblast Cell Lines • OECD Guideline (TG 432) • New Required Test; No Animal PT Test
EpiDerm™: Human Skin Equivalent • Normal Human Keratinocytes • Stratified, Differentiated Morphology with Barrier Function • Cell culture inserts – allow topical application • Normal Ceramide and Lipid Profile • Ultrastructure of Intercellular Lamellar Lipid Sheets Histological Cross Section of EpiDerm 200. Mag = 440X Transmission Electron Micrograph of Intercellular Lamellar Lipid Sheets: Broad-Narrow-Broad-Spacing (150K X) Courtesy of MatTek Corp.
The Air/Liquid Interface (ALI) Tissue Culture Technique Tissue Culture Well Culture Insert ALI Tissue Membrane Medium Courtesy of MatTek Corp.
EpiDerm Phototoxicity Assay If: Viability (no UVR) – Viability (+UVR) > 30% Then:Phototoxic If: Viability difference is < 30% Then:Non-phototoxic • Allows Topical Dosing • TA need not be Aqueous-Soluble • Human Keratinocyte-based Tissues
Based on modified CAM-VA Eggs dosed i.a., i.v., air sac, or topically Functional hepatic and CV systems Pre-phototoxins such as 5-ALA (PPIX) and Nabumetone (via P450) can be characterized. In Ovo Phototoxicity Assay (IOPA)
Photosensitization Assays • Photo-LLNA: Uses mice instead of GP • Validation by ECVAM and ICCVAM • EPA and OECD list as “Default preferred method”
Basic Photo-LLNA SI and SIUVA < 3 SI or SIUVA≥ 3 SIUVA / SI ≥ 1.25 Apply Test Substance to Mouse Ears (+/– UVA) (+/– UVA) Inject Thymidine / BrdU Excise Nodes Analyze Proliferating LNC (Calculate SIs) Sensitizer Negative Photoallergen
Tiered Strategy for Sensitization Testing Using the Enhanced Photo-LLNA SI and SIUVA < 3 SI or SIUVA≥ 3 Apply Test Substance to Mouse Ears (+/– UVA) (+/– UVA) Inject Thymidine / BrdU Excise Nodes Analyze Proliferating LNC (Calculate SIs) Ear Swelling >25% Irritating ?(Ear Swelling) Immunophenotyping %B220+ or B:T Cell Ratio negative >25% NO equivocal Activation Markers: %CD69+, %I-Ak+ >25% negative SIUVA>25% vs. SI Irritating Sensitizer Irritant Sensitizer Negative Photoallergen SIUVA>25% vs. SI
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