Suspension of hyaluronic acid or salt thereof containing macromolecule hydrogel for injection and preparation method thereof
A technology of hyaluronic acid and macromolecular water, which is applied in the field of medicine, can solve the problems of restricting the use of people, and achieve the effects of easy control of product quality, long local action time, and easy injection
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Embodiment 1
[0030] Suspension consisting of BDDE-crosslinked SH gel particles and 1% SH solution. The preparation method is as follows:
[0031] Mix 10g SH (average molecular weight 700,000 Daltons) with 65ml 1% NaOH solution containing 0.5g BDDE, react at 50°C for 3h, and purify at 70°C with deionized water for 10h. Divide the gel into two parts evenly, squeeze one part to make the gel pass through a 60-mesh sieve (A), and squeeze the other part to make the gel pass through a 20-mesh sieve (B), collect the gel particles separately, add an equal volume of 2 times isotonic Concentration of PBS (every 1000ml contains NaH 2 PO 4 2H 2 O 90mg, Na 2 HPO 4 12H 2 O 1.12g, NaCl 17g), kept at 65°C for 4h, and filtered through a 200-mesh sieve to obtain two SH gels, 380ml of particles with an average particle size of about 250μm (A) and 375ml of particles with an average particle size of about 1200μm (B) .
[0032] Another 2.5g SH (average molecular weight 1.8 million Daltons) was dissolved ...
Embodiment 2
[0036] Suspension consisting of BDDE-crosslinked SH gel particles and 1% SH solution. The preparation method is as follows:
[0037] 10 g of SH (average molecular weight 1.2 million Daltons) was dissolved in 80 ml of 1% NaOH solution containing 0.5 g of BDDE. React at 50°C for 4 hours, purify with deionized water at 70°C for 10 hours, squeeze the gel through an 80-mesh sieve, collect the gel particles, add an equal volume of PBS with 2 times the isotonic concentration, incubate at 65°C for 4 hours, and centrifuge at 2000rpm for 15 minutes , and the gel precipitate was collected to obtain about 780 ml of SH gel particles with an average particle diameter of 150 μm.
[0038] Another 7.8 g of SH (average molecular weight: 1.2 million Daltons) was taken and dissolved in 780 ml of isotonic PBS to obtain an isotonic SH solution.
[0039] The gel particles obtained above are mixed with the SH solution, sterilized and packaged according to the method described in Example 1, and the ...
Embodiment 3
[0042] Suspension consisting of PLA microspheres and 1% SH solution. The preparation method is as follows:
[0043] Prepare PLA microspheres according to the literature [Hu Yiqiao et al., Chinese Journal of Pharmaceutical Sciences, 1999, 34(12): 822-826]: Take PLA (relative molecular weight 20KD), dissolve it in 3-5 times of dichloromethane, add 1 % Span-80 (Span-80) liquid paraffin solution (3 to 5 volumes of dichloromethane), stirred and emulsified (200 to 500 rpm) at 15°C to form a stable emulsion, evaporated the solvent at 15°C, and used Wash with water, ethanol and deionized water several times, filter, dry under reduced pressure and pass through a 150-mesh sieve to obtain PLA microspheres with an average particle size of 50-80 μm. After ethylene oxide sterilization, put them into isotonic PBS sterilized by moist heat beforehand. Equilibrate for 24h.
[0044] Take 0.6 g of SH (average molecular weight: 1.8 million Daltons) and dissolve it in 60 ml of isotonic PBS to obt...
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