Hyaluronic acid gel for hyaluronic acid injection and use method of hyaluronic acid gel
A technology of hyaluronic acid and cross-linked hyaluronic acid, applied in the field of biomedicine, can solve the problems of short maintenance time of moisturizing effect, low toxicity of impurities, unsuitability, etc., achieve moisturizing effect, improve skin texture, and low strength Effect
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Embodiment 1
[0028] Example 1: Preparation of disulfide cross-linked hyaluronic acid gel
[0029] Hyaluronic acid thiolated derivatives were prepared from sodium hyaluronate with a molecular weight of 180KDa by the method reported by Shu et al. (Shu et al., Biomacromolecules 2002, 3:1304-1311), and the thiol content was 24 μmol / g and 38 μmol, respectively. / g and 57 μmol / g.
[0030] Dissolving the above-mentioned hyaluronic acid thiolated derivative to obtain 10ml aqueous solution, the contents are respectively 3, 4, 5.5, 6.5, 7, 8 and 10mg / mL; adjust the pH value of the solution to 7.4, transfer into 25ml sterile glass after sterilization filtration Container; airtight and stored at room temperature for 4 weeks, the solution loses fluidity and forms a disulfide cross-linked hydrogel.
Embodiment 2
[0031] Example 2: Evaluation of Injectable Properties of Disulfide Cross-Linked Hyaluronic Acid Gels
[0032] Adopt Derma (DeMarsha) 2nd generation water-light injection instrument, test the injectability of the gel prepared in Example 1 through conventional water-light injection needles (nine needles), and the test results are as follows:
[0033]
[0034] When the content of cross-linked hyaluronic acid is 3mg / mL and 4mg / mL, it usually has good injectability; while the content is ≥ 5.5mg / mL, it is difficult to inject through the water-light injector.
Embodiment 3
[0035] Example 3: Evaluation of injectable properties of disulfide-crosslinked hyaluronic acid gels after dilution
[0036] The gel prepared in Example 1 (the content of cross-linked hyaluronic acid was: 5.5 mg / mL, 6.5 mg / mL, 7 mg / mL, 8 mg / mL and 10 mg / mL; the thiol content of the thiolated derivative was 38 μmol / g) Physically mixed and diluted with normal saline at volume ratios of 1:1, 1:1.5 and 1:2. The dilution process was carried out in syringes connected with two-way joints, one of the syringes was filled with the gel prepared in Example 1 (1mL), and the other was filled with an appropriate volume of physiological saline (1mL, 1.5mL, 3mL), Push back and forth 60 to 80 times for physical dilution and mixing.
[0037] Adopt Derma (DeMartha) 2nd generation hydro-optical injection instrument to test the injectability of the diluted gel through conventional hydro-optical injection needles (nine needles). The test results are as follows:
[0038]
[0039] When diluted ...
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