Lifecore-cDNA及合成纯化-试剂-生物在线
上海信裕生物科技有限公司
Lifecore

Lifecore

商家询价

产品名称: Lifecore

英文名称: Lifecore

产品编号: Lifecore

产品价格: 0

产品产地: Lifecore

品牌商标: Lifecore

更新时间: 2023-08-17T09:55:27

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上海信裕生物科技有限公司
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Lifecore

Lifecore  Pharmaceutical Grade Sodium Hyaluronate

Hyaluronan in Nature

Hyaluronan (also known as sodium hyaluronate or hyaluronic acid) is a polysaccharide composed of repeating disaccharide units of glucuronate and N-acetyl glucosamine (linked by ß 1-3 and ß 1-4 glycosidic bonds) and counter ions. Hyaluronan is a physiological substance that is widely distributed in the extracellular matrix of connective tissues in both animals and humans. It is found in high concentration in the aqueous humor of the eye, synovial fluid, skin, and umbilical cord.

Primary medical applications include: Ophthalmology, Orthopedics, Aesthetics, Tissue Engineering, and Veterinary Medicine

Lifecores Pharmaceutical Grade Sodium Hyaluronate

Lifecore’s sodium hyaluronate is produced by an efficient microbial fermentation and purified by a highly effective purification process. It is produced in large batches to promote consistency in supply and customer convenience. Pharmaceutical grade sodium hyaluronate is available as a powder in a broad range of molecular weights for use in various medical applications (150KDa – 1.8MDa). Sterile pharmaceutical grade sodium hyaluronate is available in select molecular weights – please inquire.

Why Choose Lifecore for Your Sodium Hyaluronate Needs?

Lifecore Biomedical offers quality, regulatory and technical support, including:

 

  • Certificate of Suitability (CEP) to the Sodium Hyaluronate Monograph of the European Pharmacopoeia
          - complies with the EU Pharmacopoeia monograph for NaHy
  • Compliance to the Japanese Pharmacopoeia
  • ISO 13485 Certified Quality System
  • ICH Q7 (Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients) compliance
  • CE Mark Certification on Lifecore’s Hyaluronan Based Products
  • Drug and Device Master Files
  • GMP Certification
  • 21 CFR 210, 211, 820, drug and device compliance