Bletilla striata polysaccharide iron complex, preparation method therefor and use thereof
US-2024374743-A1 · Nov 14, 2024 · US
US2019365801A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2019365801-A1 |
| Application number | US-201816477176-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 26, 2018 |
| Priority date | Jun 9, 2017 |
| Publication date | Dec 5, 2019 |
| Grant date | — |
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The present invention discloses an iron oxide/nanokaolin composite hemostatic agent and a preparation method thereof. The composite hemostatic agent is composed of nanokaolin and iron oxide, where the nanokaolin is used as a carrier, and the iron oxide is loaded on a surface of a nanokaolin flake. The composite hemostatic agent is obtained by a precipitation method. The composite hemostatic agent has the advantages of good hemostatic effect, rapid wound healing, no obvious cytotoxicity, no hemolysis, high biocompatibility, and the like.
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1 . An iron oxide/nanokaolin composite hemostatic agent, comprising an active ingredient of the composite hemostatic agent is a composite of a nanokaolin and an iron oxide. 2 . The iron oxide/nanokaolin composite hemostatic agent according to claim 1 , wherein the active ingredient is made by loading the iron oxide on a surface of the nanokaolin. 3 . The iron oxide/nanokaolin composite hemostatic agent according to claim 2 , wherein a mass percentage of the iron oxide is 15%-45%. 4 . The iron oxide/nanokaolin composite hemostatic agent according to claim 1 , wherein the iron oxide is iron oxyhydroxide, α-ferric oxide, γ-ferric oxide and/or ferroferric oxide. 5 . An iron oxide/nanokaolin composite hemostatic agent, comprising a composite of a nanokaolin and an iron oxide. 6 . The iron oxide/nanokaolin composite hemostatic agent according to claim 5 , wherein the iron oxide is loaded on a surface of the nanokaolin. 7 . The iron oxide/nanokaolin composite hemostatic agent according to claim 6 , wherein a mass percentage of the iron oxide is 15%-45%. 8 . The iron oxide/nanokaolin composite hemostatic agent according to claim 5 , wherein the iron oxide is iron oxyhydroxide, α-ferric oxide, γ-ferric oxide and/or ferroferric oxide. 9 . A preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 1 , comprising: a preparation of an iron oxyhydroxide/nanokaolin composite hemostatic agent comprises following steps of: A, mixing nanokaolin with a polymerized hydroxy iron ion solution, and reacting under a system pH value of 3-7 and a temperature of 50° C. to 70° C. to obtain the iron oxyhydroxide/nanokaolin composite hemostatic agent; or a preparation of an α-ferric oxide/nanokaolin composite hemostatic agent comprises following steps of: preparing the iron oxyhydroxide/nanokaolin composite hemostatic agent according to the step A; B, placing the iron oxyhydroxide/nanokaolin composite hemostatic agent in an air atmosphere, and calcining at a temperature of 500° C. to 550° C., to obtain the α-ferric oxide/nanokaolin composite hemostatic agent; or a preparation of a ferroferric oxide/nanokaolin composite hemostatic agent comprises following steps of: preparing the α-ferric oxide/nanokaolin composite hemostatic agent according to the steps A and B; C, placing the α-ferric oxide/nanokaolin composite hemostatic agent under a reducing atmosphere, and a calcination is carried out at a temperature of 400° C. to 450° C. to obtain the ferroferric oxide/nanokaolin composite hemostatic agent; or a preparation of a γ-ferric oxide/nanokaolin composite hemostatic agent comprises following steps of: preparing the ferroferric oxide/nanokaolin composite hemostatic agent according to the steps A, B and C; and D, placing the ferroferric oxide/nanokaolin composite hemostatic agent in an air atmosphere and calcining at a temperature of 200° C. to 250° C. to obtain the γ-ferric oxide/nanokaolin composite hemostatic agent. 10 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 9 , wherein the nanokaolin is obtained by intercalating and stripping a kaolin. 11 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 9 , wherein the polymerized hydroxy iron ion solution is prepared by following method of: adding a sodium hydroxide solution to a ferric chloride solution dropwise under a condition of 40° C. to 80° C., and then aging at room temperature for 12 h to 24 h to obtain the polymerized hydroxy iron ion solution. 12 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 9 , wherein a solid-liquid ratio of the nanokaolin to the polymerized hydroxy iron ion solution is (1-3)/50 g/mL, and a concentration of the polymerized hydroxy iron ion solution is 0.1-0.6 mol/L. 13 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 9 , wherein in the step A, a reaction time is 24-72 h. 14 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 9 , wherein in the step C, the calcination is performed in a hydrogen/argon mixed atmosphere with a hydrogen concentration of 5-12% by volume. 15 . A preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 5 , comprising: a preparation of an iron oxyhydroxide/nanokaolin composite hemostatic agent comprises following steps of: A, mixing nanokaolin with a polymerized hydroxy iron ion solution, and reacting under a system pH value of 3-7 and a temperature of 50° C. to 70° C. to obtain the iron oxyhydroxide/nanokaolin composite hemostatic agent; or a preparation of an α-ferric oxide/nanokaolin composite hemostatic agent comprises following steps of: preparing the iron oxyhydroxide/nanokaolin composite hemostatic agent according to the step A; B, placing the iron oxyhydroxide/nanokaolin composite hemostatic agent in an air atmosphere, and calcining at a temperature of 500° C. to 550° C., to obtain the α-ferric oxide/nanokaolin composite hemostatic agent; or a preparation of a ferroferric oxide/nanokaolin composite hemostatic agent comprises following steps of: preparing the α-ferric oxide/nanokaolin composite hemostatic agent according to the steps A and B; C, placing the α-ferric oxide/nanokaolin composite hemostatic agent under a reducing atmosphere, and a calcination is carried out at a temperature of 400° C. to 450° C. to obtain the ferroferric oxide/nanokaolin composite hemostatic agent; or a preparation of a γ-ferric oxide/nanokaolin composite hemostatic agent comprises following steps of: preparing the ferroferric oxide/nanokaolin composite hemostatic agent according to the steps A, B and C; and D, placing the ferroferric oxide/nanokaolin composite hemostatic agent in an air atmosphere and calcining at a temperature of 200° C. to 250° C. to obtain the γ-ferric oxide/nanokaolin composite hemostatic agent. 16 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 15 , wherein the nanokaolin is obtained by intercalating and stripping a kaolin. 17 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 15 , wherein the polymerized hydroxy iron ion solution is prepared by following method of: adding a sodium hydroxide solution to a ferric chloride solution dropwise under a condition of 40° C. to 80° C., and then aging at room temperature for 12 h to 24 h to obtain the polymerized hydroxy iron ion solution. 18 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 15 , wherein a solid-liquid ratio of the nanokaolin to the polymerized hydroxy iron ion solution is (1-3)/50 g/mL, and a concentration of the polymerized hydroxy iron ion solution is 0.1-0.6 mol/L. 19 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 15 , wherein in the step A, a reaction time is 24-72 h. 20 . The preparation method of the iron oxide/nanokaolin composite hemostatic agent according to claim 15 , wherein in the step C, the calcination is performed in a hydrogen/argon mixed atmosphere with a hydrogen concentration of 5-12% by volume.
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