US2004110686A1PendingUtilityA1
Methods and compositions for enhancing fibroblast migration
Priority: Feb 9, 1999Filed: Sep 19, 2003Published: Jun 10, 2004
Est. expiryFeb 9, 2019(expired)· nominal 20-yr term from priority
A61L 24/106A61K 38/363
41
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Claims
Abstract
Methods and compositions for enhancing fibroblast migration at a wound site are disclosed. The method includes contacting the wound site with fibrinogen that is prepared by a process which includes precipitating plasma with glycine. The compositions includes a lipid rich component and fibrinogen.
Claims
exact text as granted — not AI-modifiedWhat is claimed:
1 . A method for enhancing fibroblast migration at a wound site comprising:
contacting the wound site with a fibrinogen preparation, wherein the fibrinogen preparation includes a lipid rich component.
2 . A method according to claim 1 wherein the fibrinogen preparation further comprises fibrinogen prepared by a process which comprises precipitating plasma with glycine.
3 . A method according to claim 2 wherein the fibrinogen preparation further comprises a growth factor, an extracellular matrix material, or mixtures thereof.
4 . A method according to claim 2 wherein the precipitating is carried out by a process which comprises:
adding glycine to plasma to produce a precipitate and a supernatant;
dissolving the precipitate in a buffer to produce a solution; and
precipitating the solution by adding glycine to the solution.
5 . A method according to claim 2 wherein the fibrinogen in prepared by a process comprising:
precipitating plasma with glycine to produce a first precipitate and a first supernatant;
dissolving the first precipitate in a buffer to produce a first solution;
precipitating the first solution by adding glycine to the first solution to produce a second precipitate and a second supernatant;
dissolving the second precipitate in a buffer to produce a second solution; and
precipitating the second solution by adding ammonium sulfate to the second solution to produce a third precipitate and a third supernatant.
6 . A method according to claim 5 wherein the third supernatant comprises a lipid rich layer.
7 . A method according to claim 6 wherein the third supernatant is further treated to produce the lipid rich component.
8 . A method according to claim 7 wherein the third supernatant is precipitated to produce the lipid rich component.
9 . A composition comprising:
a lipid rich component and fibrinogen.
10 . A composition according to claim 9 wherein the fibrinogen has a purity of above 95%.
11 . A composition according to claim 9 wherein the fibrinogen has a purity of about 99%.
12 . A composition according to claim 9 wherein the fibrinogen is prepared by a process which comprises precipitating plasma with glycine.
13 . A composition according to claim 12 wherein the fibrinogen is prepared by a process which comprises:
precipitating plasma with glycine to produce a first precipitate and a first supernatant;
dissolving the first precipitate in a buffer to produce a first solution;
precipitating the first solution by adding glycine to the first solution to produce a second precipitate and a second supernatant;
dissolving the second precipitate in a buffer to produce a second solution; and
precipitating the second solution by adding ammonium sulfate to the second solution to produce a third precipitate and a third supernatant.
14 . A composition according to claim 9 wherein the lipid rich component is prepared by a process which comprises precipitating plasma with glycine.
15 . A composition according to claim 14 wherein the lipid rich component is prepared by a process which comprises:
precipitating plasma with glycine to produce a first precipitate and a first supernatant;
dissolving the first precipitate in a buffer to produce a first solution;
precipitating the first solution by adding glycine to the first solution to produce a second precipitate and a second supernatant;
dissolving the second precipitate in a buffer to produce a second solution;
precipitating the second solution by adding ammonium sulfate to the second solution to produce a third precipitate and a third supernatant; and
precipitating the third supernatant to produce the lipid rich component.Join the waitlist — get patent alerts
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