Fine particle tissue filling material for injection and preparation method thereof
A technology of particulate tissue and filling material, applied in the field of medical biomaterials, can solve the problems of insufficient material source, limited material source, delayed allergic reaction, etc., and achieve the effect of easy storage and transportation, high biocompatibility, and promotion of injury healing.
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example 1
[0014] Step 1). Preparation of micronized acellular biologically derived material: Cut the pig skin with the fat layer removed into 1cm×2cm blocks, wash with phosphate buffer and freeze at -80°C for 40 minutes to keep the temperature inside and outside the pigskin After reaching the consistency, take it out and thaw it naturally at room temperature, and repeat the freezing and thawing 4 times so that the cells are completely broken and disintegrated; after washing with deionized water, soak it in 1M NaOH solution for 4 hours; then soak it in PBS until The pH value is about 7.2, soak it in 40 units / ml DNase solution for 1 hour, and then freeze-dry it to become decellularized pigskin; use a high-speed cutting machine to crush it into particles, and sieve it to a particle size of 100-300 μm The size is made into micronized decellularized pigskin material, the temperature is kept at 2-8°C throughout the operation, and finally sterilized by irradiation with cobalt 60.
[0015] Step...
example 2
[0019] Step 1). Preparation of micronized decellularized biologically derived materials: the small intestine submucosa (SIS) was obtained by mechanically scraping off the mucosal layer, muscle layer and serosa of the pig small intestine, cut into 1cm×1cm slices, and treated with phosphate After washing with the buffer solution, freeze at -80°C for 35 minutes to make the internal and external temperatures of the SIS consistent, then thaw naturally at room temperature, and repeat the freezing and thawing process twice to completely rupture and disintegrate the cells; wash with deionized water and place in 0.5 Soak in NaOH solution of M for 1 hour; then soak it with PBS solution until the pH value is about 7.0, put it in 50 units / ml DNase solution and soak it for half an hour, and then freeze-dry it to become the decellularized small intestinal submucosa material; Use a high-speed rotary pulverizer (German Fritsch company) to pulverize into particles (add liquid nitrogen to make i...
example 3
[0023] Step 1). Preparation of micronized acellular biologically derived material: Scrape off the mucosal layer, muscle layer and serosal layer of the porcine bladder mechanically to obtain the submucosa material, cut into 1cm×1cm slices, and wash with phosphate buffer saline After cleaning, freeze at -80°C for 30 minutes to make the internal and external temperatures of the material consistent, then thaw naturally at room temperature, and repeat the freezing and thawing process 3 times to completely rupture and disintegrate the cells; wash with deionized water and place in 0.5M Soak in NaOH solution for 2 hours; then soak in PBS solution until the pH value is about 7.1, put it in 40 units / ml DNase solution and soak for 40 minutes, and then freeze-dry to become the decellularized bladder submucosa material; Grinding into particles with a rotary pulverizer (adding liquid nitrogen to make them embrittled before crushing), sieving to a particle size of 100-200 μm, and preparing mi...
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