Ingredients: Water, Butylene Glycol, 1,2-Hexanediol, Glycerin, Niacinamide, Hydrogenated Coconut Oil, Hydrolyzed Sodium Hyaluronate(9,749 ppm), Cetearyl Alcohol, Glutathione(6,000 ppm), Glyceryl Stearates, Hydrogenated Lecithin, C14-22 Alcohols, Polyglyceryl-10 Stearate, Cetearyl Olivate, Methyl Glucose Sesquistearate, Isoamyl Laurate, Carbomer, Sorbitan Olivate, Polyglyceryl-4 Caprate, Tromethamine, Sodium Hyaluronate(1,000 ppm), Thujopsis Dolabrata Branch Extract, Betaine, Abies Sibirica Oil, Cryptomeria Japonica Leaf Extract, Citrus Junos Peel Oil, Phyllostachys Pubescens Shoot Bark Extract, Chamaecyparis Obtusa Leaf Extract, C12-20 Alkyl Glucoside, Hydrolyzed Hyaluronic Acid(700 ppm), Hyaluronic Acid(700 ppm), Xanthan Gum, Pentylene Glycol, Adenosine, Disodium EDTA, Maltodextrin, Hydrolyzed Gardenia Florida Extract, Glyceryl Glucoside, Ethylhexylglycerin, Glucose, Silybum Marianum Extract, Polyglyceryl-10 Laurate, Dimethylsilanol Hyaluronate(300 ppb), Copper Tripeptide-1, Acetyl Hexapeptide-8, Cyanocobalamin, Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1, Palmitoyl Pentapeptide-4, Pyridoxine HCl, Hydroxypropyltrimonium Hyaluronate(50 ppb), Potassium Hyaluronate(35 ppb), Sodium Acetylated Hyaluronate(15 ppb), Riboflavin, Fragrance, Citronellol, Geraniol, Hexyl Cinnamal, Hydroxycitronellal, Limonene, Linalool Product Details: Brand: MediPeel Skin Type: All Skin Type

Wetenschappelijke studies richten zich onder andere op celmigratie, fibroblastgerelateerde processen, angiogenese-gerelateerde mechanismen, cytoskeletorganisatie en intracellulaire signalering binnen gecontroleerde laboratoriummodellen
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Corticosteroid and NAC nasal douching significantly reduced symptom severity more than two-fold, resolved mucosal edema, and restored mucociliary function in recurrent acute rhinosinusitis patients compared to steroid with ambroxol, leading to better long-term satisfaction (121)
In addition, the presence of immunosuppressive cytokines, such as transforming growth factor- (TGF-) and IL-10, contribute to the resistance of prostate cancer to immune checkpoint inhibitors by constructing an immunosuppressive tumor microenvironment and inhibiting the function of effector T cells (49)
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