PCL Power Booster: Advanced Dermal Matrix Restorer
Clinical-grade biostimulator formulated with 20% active Polycaprolactone (PCL) microspheres suspended in a carboxymethyl cellulose (CMC) gel carrier. Engineered for subdermal injection to induce targeted neocollagenesis (Type I and III) and restore volume in areas of severe facial lipoatrophy.
Clinical Efficacy Metrics
+68% Type I Collagen
Confirmed via punch biopsy at week 8 post-treatment. Sustained synthesis maintained through month 12. [1]
+52% Elastin Synthesis
Measured by histological analysis. Significant improvement in dermal elasticity matrix and tensile strength. [1]
12-15 Month Longevity
Controlled polymer degradation pathway ensures steady neocollagenesis before complete bio-resorption into CO2 and H2O.
[1] Journal of Aesthetic Dermatology, “Efficacy of 20% PCL Microspheres in Dermal Restructuring,” Vol. 16, 2023.
Technical Specifications & Protocol
Composition Data
• PCL Concentration: 20% w/v
• PCL Particle Size: 25-50 μm (optimized to prevent phagocytosis)
• Carrier Gel: PBS-based CMC (Carboxymethyl Cellulose)
• pH Level: 6.8 – 7.2
• Sterilization: 0.22μm terminal filtration
Administration Protocol
• Depth: Deep dermal / Subdermal plane
• Device: 25G or 27G microcannula required
• Dosage: 0.05ml – 0.1ml per injection point
• Regimen: 3 sessions spaced 4 weeks apart
• Storage: 2°C to 25°C. Do not freeze.
Strict Medical Notice
Supply restricted exclusively to licensed medical practitioners. Contraindicated for patients with history of severe allergies, autoimmune disease, or active dermal inflammation. Do not inject into the glabella or periorbital regions to prevent vascular occlusion. Ensure comprehensive aspiration protocols prior to injection. Individual neocollagenesis rates fluctuate based on patient age and metabolic status.

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