Anti-oxidant effect proved by Nitric oxide assay, DPPH assay

Psoronorm cell repair oil decreases cell senescence which leads to DNA damage in response to elevated reactive oxygen species (ROS). This benefit is desired for Psoriatic skin.

DPPH ASSAY

Psoronorm cell repair oil IC 50 value at 50 mg/ml
Absorbic acid (positive control) IC 50 value at 1.52 mg/ml

Inhibits DPPH with IC 50 value of 50 mg/ml

INHIBITION OF NITRIC OXIDE (NO) PRODUCTION

Test Details % of Nitrate Production
Only LPS (Positive Control) 73
LPS + 50 mg of Psoronorm cell repair oil 39
Untreated cells 22

Inhibits the production of NO with IC 50 value of 39 mg/ml


Elastase inhibition assay,collagenase inhibition assay,anti glycation assay, Prove that Psoronorm cell repair oil


  • Acts against Elastase and Collagenase enzymes which worsen dry skin conditions.
  • Possess Anti - glycation effect to retard free radicals and inflammatory responses of the skin.

Ellastase Assay

Conc of Product mg/ml % inhibition of Elastase
50 18
40 11

Anti-glycation Assay

Psoronorm cell repair oil 75 mg/ml
Arbutin (positive control) 2.0 mg/ml

Possess Anti - glycation effect to retard free radicals and inflammatory responses of the skin.

Collagenase inhibition Assay

Products Concentration % inhibition of collagenase
Psoronorm cell repair oil 50 mg/ml 11 %
Epi gallo catechin gallate (positive control) 250 um (0.114 mg/ml) 40 %

Showed collagenase inhibition at 50 mg/ml



Prolonged use of cell repair oil is proven to be safe as established by fibrobalst toxicity assay and zein protein hydrolysis assay.

Fibroblast toxicity test- MTT assay

Cell repair oil inhibited fibroblast by 9% at 50 mg/ml.

Zein protein hydrolysis assay

Cell repair oil hydrolyzed zein protein by 9% as against SLS at 90%


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