How to extract beta-carotene from microalgae?

Aug 15, 2025 Legg igjen en beskjed

Extracting -carotene from microalgae is an important development direction for natural pigments and functional ingredients.

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Utilizes the high permeability and solubility of CO₂ under supercritical conditions (high pressure and specific temperature) to selectively extract -carotene.

 

  • Dry and pulverize microalgae (such as Dunaliella salina) to disrupt the cell walls.

Pressure: 30–40 MPa (30 MPa for Dunaliella salina, 40 MPa for other microalgae)

Temperature: 45–60℃ (45℃ for Dunaliella salina; 60℃ for Scenedesmus almeriensis)

CO₂ Flow Rate: 10 L/h (Dunaliella salina) or 1 g/min (for other algae)

Time: 5–6 hours.

  • Add an entrainer (such as ethanol) to increase the solubility of -carotene in CO₂.

 

  • Extraction yield reaches up to 95.09% (salina), and the cis-isomer ratio reaches 82%, indicating higher activity.
  • No solvent residue, high product purity, and compliance with food/pharmaceutical standards.

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Aqueous Two-Phase Extraction (ATPS)

 

A hydrophilic solvent (alcohol) is used to form a two-phase system with salt/sugar, enriching -carotene in the organic phase.

 

  • Ethanol-Acetone/Ammonium Sulfate System (for Spirulina):

15% (ethanol + acetone) + 24% ammonium sulfate;

6% solid-liquid ratio, pH 8.0, extraction at 30℃, extraction yield 94.55%.

  • Ethanol-n-Butanol System:

8.2% ethanol + 36% n-butanol, solid-liquid ratio 1:20, ultrasonication for 3 minutes, yield 3.13 mg/g.

  • Tert-Butanol-Maltose System:

Ultrasound-assisted extraction (90 W, 5 min), yield 3.19 mg/g.
 

Ultrasound-Assisted Solvent Extraction

 

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Ultrasonic cavitation destroys the microalgae cell wall, accelerating solvent penetration.

Petroleum ether-acetone, methanol-acetone, or tetrahydrofuran;

n-Butanol-ethanol mixture (reduces the use of toxic solvents).

Ultrasound Power: 90–325 W;

Time: 3–5 minutes (excessive use may cause isomerization).

Enzyme-Assisted Extraction

 

Cellulase and pectinase hydrolyze the microalgae cell wall to release intracellular components.

 

  • Microalgae slurry is pretreated with an enzyme solution (pH 4.5–5.0) at 40–50℃;
  • Secondary extraction is performed with an organic solvent (e.g., n-hexane).

 

Enzymes are easily inactivated in organic solvents, so the timing of solvent addition must be carefully controlled.

 

Microwave-Assisted Extraction

 

  • Microalgae powder is mixed with 95% ethanol and acetone (e.g., a 1:2 ratio);
  • Microwave treatment is performed (power 300–600 W) for less than 10 minutes.

 

Overheating may cause thermal degradation or isomerization of -carotene.

 

 

95.09% 5–6 hours
Aqueous Two-Phase Extraction 94.55% <30 minutes ★★★★
Ultrasound-Assisted Solvent Extraction >90% 3–5 hours ★★★★
80–85% 1–2 hours ★★★

 

 

  • Stability Control: -carotene is easily degraded by light, heat, and oxygen. The entire process must be performed in the dark and under nitrogen.
  • Comprehensive Utilization of Algal Residue: For example, the residue after -carotene extraction from Dunaliella contains polysaccharides (10%), which can be further isolated for anti-tumor active components.
  • Solvent residue: For food/pharmaceutical use, it must comply with GB 2760 or FDA standards, and supercritical or low-toxic two-phase aqueous systems are preferred.