Sodium hyaluronate

Sodium hyaluronate

Nazwa produktu Sodium Hyaluronate
Numer CAS 9067-32-7
Wygląd White to off-white powder
Dane techniczne 99% HPLC
Wzór cząsteczkowy (C14H20NO11Na)n
Masa cząsteczkowa Typically 0.8–2.0 MDa (variable)
Rozpuszczalność Soluble in water, insoluble in organic solvents
Opakowanie 1 kg, 5 kg, 10 kg

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Sodium hyaluronate Structure

Synonimy: Hyaluronic acid sodium salt, Sodium hyaluronate, HA sodium, Sodium hyaluronan, Hyaluronan sodium, Sodium salt of hyaluronic acid, CAS 9067-32-7

Sodium hyaluronate is the sodium salt of hyaluronic acid, a naturally occurring linear polysaccharide composed of repeating disaccharide units of D-glucuronic acid and N-acetyl-D-glucosamine. This polyanionic polymer is renowned for its exceptional water-binding capacity and viscoelastic properties, making it a key component in extracellular matrix and synovial fluid. Its biological functions are mediated through interactions with cell surface receptors such as CD44 and RHAMM, influencing cell proliferation, migration, and inflammation.

Commercially, sodium hyaluronate is produced via microbial fermentation using Streptococcus equi or Bacillus subtilis, followed by purification steps to achieve high purity. It is available in various molecular weight ranges, from low to high, to suit different applications. The product is typically standardized to ≥99% purity as determined by HPLC, ensuring consistent quality for pharmaceutical, cosmetic, and nutraceutical uses.

In the pharmaceutical industry, sodium hyaluronate is employed in ophthalmic surgeries, viscosupplementation for osteoarthritis, and wound healing. The cosmetic sector utilizes it as a moisturizer and anti-aging agent, while the food and supplement industry incorporates it for joint health. Its biocompatibility and biodegradability make it a preferred material for advanced drug delivery systems and tissue engineering.

Struktura chemiczna i właściwości

Sodium hyaluronate consists of alternating β-1,4-linked D-glucuronic acid and β-1,3-linked N-acetyl-D-glucosamine units. The sodium ions associate with the carboxyl groups of glucuronic acid, enhancing water solubility. The polymer exhibits high viscosity in solution, with rheological properties dependent on molecular weight and concentration. It is hygroscopic and should be stored in a cool, dry environment to prevent degradation.

Mechanizm działania

  • CD44 receptor binding: Sodium hyaluronate binds to CD44, a transmembrane glycoprotein, triggering intracellular signaling cascades that regulate cell adhesion, migration, and proliferation.
  • Hydration and lubrication: Its polyanionic nature attracts and retains water molecules, providing hydration and lubrication to tissues such as joints and eyes.
  • Anti-inflammatory effects: High molecular weight hyaluronan can inhibit pro-inflammatory cytokines and reduce macrophage activation, contributing to its therapeutic effects in osteoarthritis.
  • Scaffold for tissue repair: It forms a hydrated matrix that supports cell migration and tissue regeneration, making it valuable in wound healing and regenerative medicine.

Specyfikacje jakościowe

Parametr Specyfikacja
Oznaczenie (HPLC) ≥99,01 TP3T
Wygląd White to off-white powder
pH (1% solution) 6.0–8.0
Strata przy suszeniu ≤10.0%
Metale ciężkie ≤20 ppm
Wartości graniczne dla mikroorganizmów Total aerobic count ≤100 CFU/g

Dostawa i dokumentacja

  • Pojemność: 5 MT per month
  • Czas realizacji: 3–5 dni roboczych (towary dostępne w magazynie)
  • Dokumentacja: COA, MSDS, TDS available upon request
  • Opakowanie: 1 kg, 5 kg, 10 kg in double-lined polyethylene bags, stored in fiber drums

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