Protection
- Phospholipids shield from acid and enzymatic degradation.
- Enhanced chemical stability under stress conditions.
Nanostructured QuanticSphere™ delivery stabilizes curcuminoids, promotes membrane interaction, and sustains exposure at nutritionally feasible doses.
Maintains ~40-fold higher concentration at 8 hr vs raw curcumin.
Value Proposition
Pharmacokinetics
Faster onset, sustained plasma exposure, enhanced absorption, superior clinical potential.
Mechanisms
Down-regulates NF-κB/COX-2 and cytokines (TNF-α, IL-1β, IL-6).
Direct ROS scavenging and Nrf2 activation elevate endogenous defenses.
Modulates PI3K/AKT and MAPK pathways; supportive epigenetic effects.
Vesicles protect curcuminoids, adhere/fuse with enterocytes, and enable controlled release → higher plasma exposure with excellent GI tolerance.
Dosing
Supports long-term antioxidant and anti-inflammatory tone with minimal GI load.
Optional co-actives per clinician judgment.
For symptomatic OA, metabolic inflammation, or neuroinflammatory contexts.
Reassess at 8–12 weeks under clinician guidance.
Formulated with GRAS-status phospholipids. Evaluate potential interactions when adding absorption enhancers or co-actives.
Comparison
Category | Standard Curcumin | Q-Curviva™ (QuanticSphere™) |
---|---|---|
Peak Plasma (Cmax) | ≈ 67 ng/mL @ 1000 mg | ≈ 308 ng/mL @ 350 mg |
Total Exposure (AUC₀–last) | ≈ 698 ng·h/mL | ≈ 2 582 ng·h/mL |
Typical Daily Dose | 1000–2000 mg | 100–150 mg |
GI Tolerability | High-dose GI upset more common | Phospholipid matrix, gut-friendly profile |
Next steps
Request the full white paper, PK appendix, COAs, and sample protocols.
Based on September 2025 dossier and internal PK study.
Clinically engineered multi-pathway therapeutic system for osteoarthritis.
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