
Hermetica Superfood Encyclopedia
Legacy index-continuity record: the score and narrative are provisional and must not be represented as validated or human-approved.
Review flags: AWAITING_SEMANTIC_VALIDATION
Spirulina phycocyanin (C-PC) is a blue pigment protein from Spirulina platensis containing tetrapyrrole chromophores that provide potent antioxidant activity. It works by scavenging free radicals through its phycocyanobilin prosthetic groups and modulating immune cell activity via NF-κB pathway regulation.

Reported Benefits (Provisional)
Origin & History

Spirulina Phycocyanin is a pigment-protein complex derived from the blue-green algae Spirulina. It is extracted through a process that preserves its bioactive properties.
Research Narrative (Provisional)
Scientific investigations, including in vitro and in vivo studies, have highlighted phycocyanin's antioxidant and anti-inflammatory properties. Some clinical trials suggest potential benefits in boosting immune function and reducing oxidative stress.
Preparation & Dosage
Dosage guidance is withheld because the publication gate has not recorded adequate support for this profile.
Nutritional Profile
Spirulina Phycocyanin (C-PC) is a water-soluble biliprotein pigment-protein complex constituting approximately 15–25% of the dry weight of Spirulina (Arthrospira platensis) biomass. Key bioactive compounds: C-Phycocyanin protein (~620 kDa hexameric form) with covalently attached phycocyanobilin (PCB) chromophores at approximately 1–2 chromophores per α-subunit and 2–3 per β-subunit, yielding roughly 5–8% PCB by weight of the holoprotein. Protein content of purified C-PC is >95% by weight, composed of α (~18.5 kDa) and β (~21.5 kDa) subunits in equimolar ratios; amino acid profile is rich in essential amino acids including leucine (~7–9%), valine (~5–6%), and lysine (~4–5%). Micronutrients present in trace amounts from co-extraction include iron (0.5–2.0 mg/g of crude extract), selenium (0.01–0.05 mg/g), zinc (0.1–0.5 mg/g), and chromium (trace). Vitamins are minimal in purified C-PC but crude spirulina-derived extracts may carry residual B-vitamins (B12 analog at ~0.5–2.0 µg/g, though largely pseudovitamin B12 with limited bioavailability). The primary bioactive chromophore phycocyanobilin (a linear tetrapyrrole structurally analogous to biliverdin) is responsible for the majority of antioxidant and anti-inflammatory activity, with concentrations of approximately 40–80 mg per gram of purified C-PC. C-PC exhibits strong absorbance at 615–620 nm with a purity ratio (A620/A280) of ≥0.7 for food-grade, ≥3.9 for analytical-grade. Bioavailability notes: C-PC is orally bioavailable but susceptible to proteolytic degradation in the GI tract, reducing effective absorption of the intact holoprotein to an estimated 20–40%; however, the released phycocyanobilin chromophore retains bioactivity and is absorbed more readily. Encapsulation or enteric coating can improve bioavailability by 2–3 fold. C-PC is heat-sensitive (degradation begins above 45–50°C at neutral pH) and most stable at pH 5.0–7.0. Caloric contribution is negligible at typical supplemental doses (100–500 mg/day). No significant lipid, carbohydrate, or dietary fiber content in purified preparations.
Reported Mechanism (Provisional)
C-phycocyanin contains phycocyanobilin prosthetic groups that directly scavenge hydroxyl radicals, superoxide anions, and peroxyl radicals. It inhibits pro-inflammatory NF-κB signaling while activating Nrf2-mediated antioxidant response pathways. The protein also modulates macrophage polarization toward anti-inflammatory M2 phenotypes and enhances natural killer cell activity.
Clinical Narrative (Provisional)
Small-scale human studies (20-60 participants) show C-phycocyanin supplementation at 200-400mg daily reduces oxidative stress markers by 20-30% within 4-8 weeks. Animal studies demonstrate enhanced immune cell proliferation and reduced inflammatory cytokines, but large-scale randomized controlled trials are limited. Most evidence comes from in vitro studies showing strong radical scavenging activity. More robust human clinical data is needed to confirm therapeutic applications.
Also Known As
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