Cross-linked sodium hyaluronate biomembrane and preparation method thereof

A cross-linked hyaluronic acid and sodium hyaluronate technology, which is applied in the field of surgical wounds, can solve the problems of failing to meet industrialization requirements, low mechanical strength of sponges, and no practical application value, etc., and achieve long residence time and good tissue repair performance , the effect of uniform size

Active Publication Date: 2014-08-27
CHANGZHOU INST OF MATERIA MEDICA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the low mechanical strength of the sponge makes it inconvenient to use, has no practical application value, and does not meet the requirements of industrialization.

Method used

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  • Cross-linked sodium hyaluronate biomembrane and preparation method thereof
  • Cross-linked sodium hyaluronate biomembrane and preparation method thereof
  • Cross-linked sodium hyaluronate biomembrane and preparation method thereof

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Embodiment 1)

[0037] The reagents used in this example were all analytically pure.

[0038] The preparation method of the cross-linked sodium hyaluronate biofilm of the present embodiment comprises the following steps:

[0039] ①Add 500mL of a mixed solution consisting of 10 wt% to 20 wt% (15wt% in this example) sodium hydroxide aqueous solution and acetone to 20g of white sodium hyaluronate dry powder, or add 500mL of 15wt% Add 20g of white sodium hyaluronate dry powder to the mixed solution composed of sodium hydroxide aqueous solution and acetone; ); Stir the sodium hyaluronate to evenly disperse to obtain a sodium hyaluronate alkaline suspension, that is, the sodium hyaluronate is partially dissolved in a mixed solution composed of sodium hydroxide aqueous solution and acetone, and part of it exists in a solid form; Then add 11.1mL of cross-linking agent 1,4-butanediol diglycidyl ether (BDDE) to the sodium hyaluronate alkaline suspension, and mix well to obtain the reaction material, t...

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Abstract

The invention discloses a cross-linked sodium hyaluronate biomembrane and a preparation method thereof. The cross-linked sodium hyaluronate biomembrane is prepared by: conducting freeze drying on a prepared gel with a crosslinking degree up to 60%-80%, and then pressing the freeze-dried gel into a membrane. The preparation method of the gel includes: acquiring cross-linked sodium hyaluronate dry powder, then washing the collected sieved powder by dimethyl sulfoxide (DMSO); washing the DMSO washed powder by ethanol; then conducting vacuum drying to obtain cross-linked sodium hyaluronate powder; fully swelling the powder, performing purification for 6-10h at a room temperature of 15-35DEG C, then carrying out homogenization micronization treatment in a high-speed dispersion machine, and then collecting the uniform gel particles, thus obtaining the cross-linked sodium hyaluronate gel used for biomembrane preparation. The cross-linked sodium hyaluronate biomembrane prepared by the method provided by the invention has is pyrogen-free, sterile, free of residual crosslinking agent, and has low cytotoxicity. With long residence time in vivo, the biomembrane has good anti-adhesion effect, good biocompatibility and tissue repair performance.

Description

technical field [0001] The invention relates to a material used for surgical wounds, especially for preventing postoperative adhesions, in particular to a cross-linked sodium hyaluronate biofilm and a preparation method thereof. Background technique [0002] Clinically, there are high requirements for local hemostasis and postoperative anti-adhesion. Postoperative local bleeding and tissue adhesion may lead to serious clinical complications. Ideal hemostatic and anti-adhesion materials should have good biocompatibility, no obvious side effects, bioabsorbability, in vivo degradation rate synchronized with wound healing, rapid hemostasis, good tissue adhesion; and prevent postoperative adhesion effects Yes, it can promote the rapid healing of wounds and reduce mucosal damage. [0003] Among the anti-adhesion materials currently developed, the polylactic acid anti-adhesion film has low strength and poor flexibility. The maintenance time of collagen is short, mild inflammatory...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08J3/24C08J3/075C08L5/08C08K5/1515
Inventor 何浩明贾超孙小强戚春建何流漾郑昌虹钱陈杨双双王慧高坚杰
Owner CHANGZHOU INST OF MATERIA MEDICA
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