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MB Research Laboratories New Photosensitization and Alternative Phototoxicity Methods George L. DeGeorge, Ph.D., DABT MB Research Laboratories
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Read OD at 540 nm 3T3 NRU Phototoxicity Test Seed 96 well plates with 3T3 cells Dose 2 plates with 8 conc. of TA Incubate 37ºC, 5% CO 2, 1 hr Plate A: Expose to UVA 5 J/cm 2 /50 mins Plate B: Keep in the dark, 50 mins Add Neutral Red media; incubate 3 hrs; Rinse & Fix Return to 37ºC CO 2 incubator for 24 hrs Plate BPlate A Determine IC 50UVA and IC 50Dark Calculate PIF ratio; if >6 then + phototoxin
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MB Research Laboratories 3T3 NRU Phototoxicity Test IC 50 : The concentration of test material which reduces cell viability to 50% compared to untreated controls –Determined for +UV and –UV cultures Calculation of Photo-Irritation Factor (PIF) –PIF = IC 50 (-UV)/IC 50 (+UV)
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MB Research Laboratories 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
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MB Research Laboratories With H1 Filter: UVA+VIS+IR With H2 Filter: UVB + UVA + VIS + IR With NO Filter: UVC+UVB+UVA+VIS+IR Spectral Distributions Possible Weight: 11 kg Dimensions: 34 x 30 x 40cm Bulb: 400W Metal Halide “S” Bulb SOL 500 Solar Simulator
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MB Research Laboratories 3T3 NRU Phototoxicity Assay Evaluates photo-cytotoxicity Mouse Fibroblast Cell Lines OECD Guideline (TG 432) New Required Test; No Animal PT Test
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MB Research Laboratories 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 Transmission Electron Micrograph of Intercellular Lamellar Lipid Sheets: Broad- Narrow-Broad-Spacing (150K X) Histological Cross Section of EpiDerm 200. Mag = 440X Courtesy of MatTek Corp.
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MB Research Laboratories The Air/Liquid Interface (ALI) Tissue Culture Technique Tissue Culture Well Culture Insert ALI Tissue Medium Membrane Courtesy of MatTek Corp.
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MB Research Laboratories EpiDerm Phototoxicity Assay Allows Topical Dosing TA need not be Aqueous- Soluble Human Keratinocyte-based Tissues If: Viability (no UVR) – Viability (+UVR) > 30% Then: Phototoxic If: Viability difference is < 30% Then: Non-phototoxic
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MB Research Laboratories In Ovo Phototoxicity Assay (IOPA) 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.
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MB Research Laboratories Photosensitization Assays Photo-LLNA: Uses mice instead of GP Validation by ECVAM and ICCVAM EPA and OECD list as “Default preferred method”
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MB Research Laboratories Negative SI and SI UVA < 3 SI or SI UVA ≥ 3 Photoallergen SI UVA / SI ≥ 1.25 Apply Test Substance to Mouse Ears (+/– UVA) Inject Thymidine / BrdU Excise Nodes Analyze Proliferating LNC (Calculate SIs) Sensitizer (+/– UVA) Basic Photo-LLNA
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MB Research Laboratories Irritating Sensitizer Irritant Negative SI and SI UVA < 3 SI or SI UVA ≥ 3 negative Ear Swelling >25% >25% Photoallergen Apply Test Substance to Mouse Ears (+/– UVA) Inject Thymidine / BrdU Excise Nodes Analyze Proliferating LNC (Calculate SIs) Irritating ? (Ear Swelling) Sensitizer Activation Markers: % CD69+, %I-A k + Immunophenotyping % B220+ or B:T Cell Ratio equivocal (+/– UVA) Tiered Strategy for Sensitization Testing Using the Enhanced Photo-LLNA SI UVA >25% vs. SI NO
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MB Research Laboratories In Vivo and In Vitro Solutions THANK YOU MB Research Laboratories 1765 Wentz Road, PO Box 178, Spinnerstown, PA 18968 Tel: 215-536-4110Fax: 215-536-1816Email: mbinfo@mbresearch.com
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