Dermatology in vitro Assays |
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Melanin synthesis with the co-culture of Nornal Human |
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Keratinocytes (NHK) and Melanocytes (NHM) |
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Keratinocyte assays with conditioned PBMC medium |
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Oxidative stress assays on Human Dermal Fibroblasts |
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Normal Human Epidermal Keratinocytes (NHEK) qPCR |
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Normal Human Epidermal Keratinocytes (NHEK) |
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proliferation assay |
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Dermatology in vivo Models |
Atopic Dermatitis (AD) |
Contact hypersensitivity (CHS) |
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Tofacitinib Effects in OXA Induced AD in |
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FITC induced CHS in Balb/c mice |
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Balb/c Mice |
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Temovate Effects in DNFB Induced AD in |
Psoriasis |
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Balb/c Mice |
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Imiquimod induced psoriasis in Balb/c |
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DNCB Induced AD in Balb/c Mice |
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mice |
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House Dust Mite (DFE) Induced AD in |
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IL-23 Induced Psoriasis-like Inflammation |
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Balb/c Mice |
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in Balb/c mice |
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PMA induced AD/ear edema in |
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male/female mice |
ITCH Models |
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AEW/Chloroquine induced ITCH in |
Delayed Type Hypersensitivity (DTH) |
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C57BL/6 mice |
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Rodents (mice and rats) |
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Histamine induced ITCH in C57BL/6 mice |
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OXA induced DTH in Balb/c mice/Wistar |
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Rats |
Histamine Wheal Model |
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DNFB induced DTH in Balc/c mice |
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KLH induced DTH in Balb/c mice |
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mBSA induced DTH in C57BL/6J mice |
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Representative in vitro Assays |
Case 1: Melanin Synthesis Assay using Normal Human Keratinocytes (NHK) and Melanocytes (NHM) |
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The NHK-NHM co-culture screening assay provides a useful tool to compare the activity of known modulators of melanogenesis and to perform structure-activity studies with newly |
identified modulators to improve their activity. |
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Changes in the rate of melanin synthesis will be measured on the basis of 14C-thiouracil incorporation into newly synthesized melanin. |
Changes in 3H-leucine incorporation will be taken as an indication of cytotoxicity or induction of proliferation. |
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Case 2: Keratinocytes qPCR study |
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To identify suitable NHEK functional assay readout as measurement of compound effect on |
keratinocyte and skin barrier function |
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Expression levels of several genes in normal human epidermal keratinocyte (NHEK) increased after PMA |
treatment for 48 hours. |
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Representative in vivo Case Studies |
Case 1: Tofacitinib Effects in Oxa Induced Atopic Dermatitis Mice Model |
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Sensitization: 10ul of 5% Oxa in acetone/olive |
oil (4/1) on back skin of animal. |
Challenging: mice were treated topically with 100ul of 0.1% Oxa in acetone/olive oil (4/1) |
on back flanks (once every two days). |
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Note: Tofacitinib significantly decreased OXA induced skin thickness increase, skin TNFα |
expression increase and skin pathology composite score and epidermal thickness increase |
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Case 2: Compound Effects in DNFB Induced Atopic Dermatitis Mice Model |
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DNFB induced AD model were well established in Balb/c mice |
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Temovate significantly decreased DNFB induced ear thickness and weight increase and |
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skin pathology composite score increase and pidermal thickness increase |
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We collaborated with several companies for efficacy and MOA studies. |
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Case 3: Compound Efficacy in DNCB Induced Atopic Dermatitis Mice Model |
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DNCB induced atopic dermatitis model was well established at HDB |
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CompX significantly decreased DNCB induced skin thickness and clinical score increase |
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We collaborated with several companies for efficacy studies. |
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Case 4: Compound Effects in House Dust Mite (DFE) Induced Atopic Dermatitis Mice Model |
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House dust mite and DNCB induced atopic dermatitis model was successfully |
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established at HDB |
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Dex at 1mpk p.o/qd significantly decrease house dust mite and DNCB induce ear |
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thickness and dermatitis score increase |
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Dex at 1mpk p.o/qd significantly decrease house dust mite and DNCB induced ear |
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TNFa/IL-13 gene expression increase |
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Several on-going studies for several clients |
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Connect with us for more information |
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