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The cytotoxic effects of each compound were expressed as IC 50 values, which represent the drug concentrations required to cause 50% tumour cell growth inhibition, and calculated with GraphPad Prism Software version 5.02 (GraphPad Inc., La Jolla, CA, USA)

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As a fragment of gastric juice protective protein, it maintains biological activity at pH below 2.0, confirmed in in vitro stability tests

established that alpha-MSH C-terminal fragments, including the KPV sequence, reduce contact hypersensitivity and produce meaningful anti-inflammatory effects in dermal models.6 Conditions Under Investigation In preclinical models, KPV has shown relevance to: Eczema and atopic dermatitis conditions driven by dysregulated Th2 immune responses and skin barrier failure Psoriasis characterized by keratinocyte hyperproliferation and NF-B overactivation Contact hypersensitivity where KPV's ability to modulate immune cell activation in dermal tissue has been demonstrated directly Wound healing where suppression of excess inflammation supports tissue repair rather than hindering it No large-scale human trials exist for dermatological applications yet