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Injectable Sodium Hyaluronate Medical Device Excipient

Bouliga injectable grade sodium hyaluronate acts as a high-quality raw material and excipient for pharmaceuticals and medical devices. With advanced purification ensuring ultra-low endotoxin levels, it is suitable for intra-articular injections, ophthalmic surgeries and cosmetic dermal fillers.
  • Injection grade Hyaluronic acid

  • Bouliga

  • 391390

Availability:

Injectable Sodium Hyaluronate Overview

Sodium hyaluronate is a glycosaminoglycan that occurs naturally in human connective tissues. It exhibits moisturizing, lubricating, viscoelastic and pseudoplastic properties. Injectable grade sodium hyaluronate undergoes additional purification steps compared to other grades, meeting the safety requirements for parenteral administration.

What Makes Injectable Grade Distinct

Injectable grade sodium hyaluronate has stricter limits on impurities, bacterial endotoxins and molecular weight distribution. These specifications ensure its safety when introduced directly into the human body through injection routes.

Injectable Sodium Hyaluronate Medical Device Excipient

Injectable Sodium Hyaluronate Technical Specifications

Item

Standard

Appearance

White Powder

Glucuronic Acid

≥45.0%

Sodium Hyaluronate

95.0%-105.0%

Absorbance

≤0.25 (A257nm), ≤0.15 (A280nm)

pH

6.0-7.5

Intrinsic Viscosity

1.6 m³/kg-2.5 m³/kg

Bacterial Endotoxins

<0.05 IU/mg

Injectable Sodium Hyaluronate Industrial Applications

Injectable grade sodium hyaluronate supports multiple medical and pharmaceutical applications.

Parenteral Preparations

It serves as an excipient in various parenteral formulations, providing viscosity control and stabilization for active pharmaceutical ingredients.

Intra-articular and Intraocular Preparations

This grade is used in intra-articular injections for joint lubrication and in intraocular preparations for ophthalmic surgeries. It helps maintain tissue structure and reduce friction during procedures.

Medical Cosmetic Applications

It functions as a raw material for intradermal cosmetic correctors, wrinkle fillers and medical cosmetic microsurgery products. It also supports the development of anti-adhesion products and damaged cartilage repair formulations.

Injectable Sodium Hyaluronate Production Process

Bouliga follows a standardized production process for injectable sodium hyaluronate:

  • Strain selection and cultivation

  • Fermentation to produce mucopolysaccharide

  • Multi-stage purification to remove impurities

  • Precipitation and dehydration

  • Three-in-one drying (filtering, dehydration and drying)

  • Sterile packaging and quality inspection

  • This process ensures consistent product quality across batches.

    Injectable Sodium Hyaluronate Medical Device Excipient

FAQ About Injectable Sodium Hyaluronate

What is the difference between injectable grade and cosmetic grade sodium hyaluronate?

Injectable grade has stricter impurity limits, lower bacterial endotoxin levels and more controlled molecular weight distribution. It meets the regulatory requirements for parenteral administration, while cosmetic grade is formulated for topical application only.

What packaging options are available for commercial procurement?

Bouliga offers customizable packaging options to meet different production needs. Contact our team for specific packaging requirements and minimum order quantities.

How is the quality of injectable sodium hyaluronate ensured?

Each batch undergoes comprehensive testing according to the specifications listed above. Quality control measures are implemented at every stage of the production process, from raw material selection to final packaging.

For inquiries about Bouliga injectable sodium hyaluronate for your commercial operations, contact Sunny at Tel/Whatsapp: +8615064743905. Our team provides technical support and product information to support your procurement decisions.

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Tel/Whatsapp:+8618765474836
Add:Room707, Building A, Xingguang SOHO, xiaoxue, Qufu City, Shandong Province, China
 
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