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Beadlets Lutein Zeaxanthin Lycopene Microencapsulation — field notes from the carotenoid aisle If you’ve followed carotenoids the past few years, you’ve seen the shift: formulators want clean-label, vegetarian beadlets that disperse in cold water yet stand up to tableting pressure. To be honest, it was overdue. The uptick in ophthalmic and healthy-aging SKUs made it inevitable. This is where Beadlets Lutein Zeaxanthin Lycopene Microencapsulation gets interesting—free-flowing, gelatin-free spheres that behave nicely in the real world, not just in PowerPoint. What’s trending and why it matters Three trends collide here: cold-water dispersibility for better bioavailability, microencapsulation for oxidative stability, and vegetarian systems that ditch gelatin. In fact, many customers say they switched because “powders stopped clumping and tabs stopped chipping.” It sounds small. It isn’t. Technical snapshot Beadlets Lutein Zeaxanthin Lycopene Microencapsulation are spherical, free-flowing particles designed for capsules and tablets. The carrier system typically uses plant-based matrices with antioxidants, enabling good compressibility and sustained color integrity. Parameter Typical spec (≈) Method / Standard Lutein content 10–20% w/w HPLC, USP monograph/EP Zeaxanthin content 2–5% w/w HPLC, AOAC 2016.13 Lycopene content 5–10% w/w HPLC, USP/FCC Particle size 20–40 mesh, free-flowing USP Sieve Dispersibility T90 ≤ 30 s in 200 mL water (20°C) In-house, per AOAC guidance Heavy metals Pb ≤ 1 ppm; As ≤ 1 ppm; Cd ≤ 0.5 ppm; Hg ≤ 0.1 ppm ICP-MS, USP Shelf life 24 months, ≤25°C, ≤60% RH ICH Q1A(R2) Process flow (how it’s made) Materials: carotenoid oleoresins, plant-based carrier matrix, antioxidants, emulsifiers, purified water. Methods: pre-emulsification → high-shear homogenization → microencapsulation via spray-drying and fluid-bed layering → antioxidant fortification → classification → metal detection. Stability verified by accelerated testing (40°C/75% RH, 6 months; carotenoid retention typically ≥90%, real-world use may vary). Certifications: ISO 9001, FSSC 22000, Halal, Kosher (typical for this class; verify batch COA). Origin: Building 23B1, No.2 Yuanboyuan St., Zhengding Area of China (Hebei) Pilot Free Trade Zone. Application scenarios Direct compression tablets (high hardness, low friability) Hard-shell capsules and stick packs Cold-water beverage sachets and nutrition blends Vegetarian gummies and chewables (gelatin-free matrix helps) Vendor landscape (quick take) Vendor Certs Lead time Customization Stability/Dispersion Finutra (origin: Hebei, CN) ISO, FSSC, Halal, Kosher ≈ 2–4 weeks Ratios, mesh, carriers Robust; T90 ≈ 30 s Generic Trader A ISO (varies) ≈ 4–6 weeks Limited Inconsistent Contract Mfg B FSSC, GMP Project-based Extensive (MOQ ↑) Good, cost ↑ Customization options Adjust lutein:zeaxanthin:lycopene ratios, choose beadlet size (16–40 mesh), select carriers (e.g., modified starch/alginate), and request nitrogen-flushed, light-barrier packaging. Small digression: color targets can be tuned—handy for brand managers chasing a specific Pantone. Two quick case notes Tablet brand in the EU swapped in these beadlets; friability dropped from 1.0% to 0.3% and dissolution stayed clean. “No more orange dust on the line,” the ops lead joked. A beverage sachet maker reported zero clumping in pilot runs and kept the vegetarian claim intact. Standards and references: 1) USP elements by ICP-MS; 2) ICH Q1A(R2) stability; 3) AOAC carotenoid methods; 4) relevant USP/EP monographs for lutein/lycopene. USP General Chapter Elemental Impurities—Procedures. ICH Q1A(R2): Stability Testing of New Drug Substances and Products. AOAC Official Methods for Carotenoids (e.g., 2016.13). USP/FCC Monographs: Lutein, Lycopene; Ph. Eur. relevant monographs.
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Advanced molecular distillation and microencapsulation technology. Extremely bioavailable trace carotenoids Intuitively soluble.
Advanced molecular distillation and microencapsulation
technology. Extremely bioavailable 
trace carotenoids Intuitively soluble.
Liposomes are biocompatible, biodegradable,
and do not cause an immune response.
They also enhance drug solubility and distribution,
and can be modified for targeted release.
Liposomes are biocompatible, biodegradable, and do not cause an immune response. They also enhance drug solubility and distribution, and can be modified for targeted release.
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Building 23B1, No.2 Yuanboyuan St., Zhengding Area of China (Hebei) Pilot Free Trade Zone
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