Regenerative Exosome Science · GMP Manufactured

Aging & Sun Damage

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Skin Concern · Aging & Sun Damage

Aging & sun damage — firming & photo-repair

Stimulate collagen and elastin production, lift sagging skin and repair the accumulated damage of sun exposure and time.

Aged and sun-damaged skin is losing collagen faster than it builds it, while years of UV exposure have injured the cells that keep skin firm. MYS-Exo exosomes work on both fronts — switching production back on in the fibroblast, inhibiting the enzymes that break collagen down, and repairing UV-induced cellular damage.

Aging & Sun Damage

Stimulate collagen and elastin production, lift sagging skin and repair the accumulated damage of sun exposure and time.

1 week

Skin feels firmer, superficial dry lines soften

3–4 weeks

Fine lines fade, facial contour gets lifted

8–12 weeks

Skin elasticity improves significantly, aging slows down

How to use: Use consistently for long-term results. Apply on face and neck; daily sunscreen is essential.

Targeting principle & mechanism

Core functional proteins: TGF-β1/3, bFGF, VEGF, HGF, elastin, procollagen, MMP-1 inhibitors, HSP70

Targets: Dermal fibroblasts, elastic-fibre cells, photo-aged / aging areas

  1. Activates the TGF-β/Smad pathway to continuously generate collagen, elastin and fibronectin, thickening the dermis and firming sagging.
  2. Inhibits MMP-1 collagenase, reducing collagen loss and slowing skin laxity.
  3. VEGF boosts dermal blood supply, improving dullness from late nights, dry lines and static fine lines.
  4. Antioxidant repair of UV-induced cellular DNA damage, slowing photo-aging.
  5. Rebuilds the dermal–epidermal junction (DEJ), softening nasolabial folds, eye-area fine lines and laxity creases.

How exosomes target the skin

Core functional proteins: CD9 / CD63 / CD81 tetraspanins, integrins, ICAM adhesion proteins, chemokine receptor CXCR4

Targets: Full-thickness damaged / problem skin areas and their target cells

  1. Targeted recognition: the exosome membrane carries a molecular “postal code” that binds matching ligands on cells in the problem area, actively grabbing the lesion while barely retaining on healthy skin.
  2. Transdermal delivery: the 30–150 nm nanoscale matches stratum-corneum gaps; with its phospholipid bilayer it enters cells intact via both passive penetration and active endocytosis, without being broken down.
  3. Intracellular release: once inside the cell the membrane fuses and ruptures, releasing functional proteins that directly regulate cell genes and signalling pathways — improving skin from the root.

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