Fibrinogen composition, method and wound articles
US-2021100929-A1 · Apr 8, 2021 · US
US2020038546A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2020038546-A1 |
| Application number | US-201716338803-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 4, 2017 |
| Priority date | Oct 5, 2016 |
| Publication date | Feb 6, 2020 |
| Grant date | — |
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Provided is a method of forming a fibrinogen hydrogel composition, the method including providing a fibrinogen hydrogel or precursor thereof, comprising fibrinogen hydrogel forming salt. The fibrinogen hydrogel forming salt concentration is greater than or equal to the threshold concentration to form a fibrinogen hydrogel. The method further includes denaturing the fibrinogen hydrogel such as by heating. The method optionally further includes combining the fibrinogen hydrogel with a carrier material. When present, the concentration of the carrier material typically ranges from 0.1 to about 50 wt.-%. The method further includes reducing the salt concentration below the threshold concentration to form a fibrinogen hydrogel.
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1 - 56 . (canceled) 57 . A method of forming a fibrinogen hydrogel composition comprising: providing a fibrinogen hydrogel or precursor thereof, comprising fibrinogen hydrogel forming salt at a concentration greater than or equal to the threshold concentration to form the fibrinogen hydrogel; denaturing the fibrinogen hydrogel; reducing the salt concentration below the threshold concentration to form the fibrinogen hydrogel before and/or after optionally combining the fibrinogen hydrogel with the carrier material. 58 . The method of claim 57 , wherein the fibrinogen hydrogel precursor comprises an aqueous solution comprising fibrinogen and the fibrinogen hydrogel forming salt. 59 . The method of claim 57 , wherein the fibrinogen hydrogel forming salt comprises sodium citrate optionally in combination with sodium chloride. 60 . The method of claim 57 , wherein the threshold hydrogel forming salt concentration of the aqueous solution is at least 0.45 wt.-%. 61 . The method of claim 57 , wherein the fibrinogen hydrogel composition further comprises a fibrinogen hydrogel plasticizer. 62 . The method of claim 61 wherein the plasticizer comprises a sugar alcohol, an alkane diol, or a combination thereof. 63 . The method of claim 57 , further comprising forming the fibrinogen hydrogel composition into a sheet, foam, or a plurality of pieces. 64 . The method of claim 57 , wherein the step of reducing the fibrinogen hydrogel forming salt concentration comprising rinsing the hydrogel with an aqueous solution. 65 . The method of claim 57 , further comprising dehydrating the fibrinogen hydrogel composition. 66 . The method of claim 57 , wherein the denaturing is accomplished by heating. 67 . The method of claim 65 , wherein the dehydrated denatured fibrinogen hydrogel composition has a salt concentration no greater than 20 wt.-%. 68 . The method of claim 57 , further comprising forming the fibrinogen hydrogel composition into a plurality of pieces. 69 . The method of claim 57 , further comprising combining the fibrinogen hydrogel with 0.1 to about 50 wt.-% of a carrier material. 70 . The method of claim 69 , wherein the carrier material comprises a water soluble polymer having a Fikentscher K-value of at least K-90. 71 . The method of claim 69 , wherein the carrier material comprises a polymer. 72 . The method of claim 71 , wherein the polymer comprises polymerized units of N-vinyl lactam polymer. 73 . The method of claim 69 , wherein the carrier material further comprises a swelling agent. 74 . The method of claim 73 , wherein the swelling agent also functions as a plasticizer for the fibrinogen hydrogel.
Fibrin; Fibrinogen · CPC title
Agents promoting blood coagulation, blood-clotting agents, embolising agents · CPC title
Hydrogels or hydrocolloids · CPC title
Proteins, polypeptides; Degradation products or derivatives thereof, e.g. albumin, collagen, fibrin, gelatin {(A61L15/225 takes precedence)} · CPC title
Fibrin; Fibrinogen · CPC title
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