US2006167402A1PendingUtilityA1
Method and composition for inhibiting cardiovascular cell proliferation
Assignee: UNIV LELAND STANFORD JUNIORPriority: Jun 5, 1999Filed: Dec 20, 2005Published: Jul 27, 2006
Est. expiryJun 5, 2019(expired)· nominal 20-yr term from priority
Inventors:John CookeGarrison C. FathmanJonathan B. RothbardShiro UemuraRobert C. RobbinsMurray H. Kown
A61P 43/00A61L 33/128A61P 7/04A61K 38/16A61K 38/10A61P 9/14A61L 27/227A61K 38/03A61L 33/12A61L 27/34A61P 9/00A61K 38/08
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Claims
Abstract
Cardiovascular cell proliferation in a blood vessel subjected to trauma, such as angioplasty, vascular graft, anastomosis, or organ transplant, can be inhibited by contacting the vessel with a polymer consisting of from 6 to about 30 amino acid subunits, where at least 50% of the subunits are arginine, and the polymer contains at least six contiguous arginine subunits. Exemplary polymers for this purpose include arginine homopolymers 7 to 15 subunits in length.
Claims
exact text as granted — not AI-modified1 .- 28 . (canceled)
29 . A method for performing a vascular bypass procedure comprising:
contacting a bypass vessel with a polyarginine or salt thereof, and grafting said bypass vessel at a target site.
30 . The method of claim 29 wherein said vascular bypass procedure comprises an arterial-venous anastomosis.
31 . The method of claim 1 wherein said vascular bypass procedure comprises a coronary bypass.
32 . The method of claim 29 wherein said vascular bypass procedure comprises a non-coronary bypass procedure.
33 . The method of claim 4 wherein said vascular bypass procedure comprises a femoro-popliteal bypass.
34 . The method of claim 29 wherein said bypass vessel is autologous.
35 . The method of claim 29 wherein said bypass vessel is an allograft.
36 . The method of claim 29 wherein said bypass vessel is a xenograft.
37 . The method of claim 29 wherein said bypass vessel is about 3 to 12 inches in length.
38 . The method of claim 29 wherein said polyarginine is contacted with said bypass vessel ex vivo.
39 . The method of claim 29 wherein said polyarginine comprises at least 7 amino acid residue.
40 . The method of claim 29 wherein said polyarginine comprises 6 to 15 arginine residues.
41 . The method of claim 29 wherein said contacting step comprises contacting said bypass vessel with a polyarginine acetate salt.
42 . The method of claim 29 wherein said polyarginine is an arginine homopolymer.
43 . The method of claim 29 wherein said polyarginine is an arginine homopolymer of 9 residues.
44 . The method of claim 29 wherein said polyarginine is in a solution of less than 1 M of said polyarginine.
45 . The method of claim 1 wherein said polyarginine is in a solution of between about 0.01 μM and 100 μM of said polyarginine.
46 . The method of claim 29 wherein said contacting step comprises contacting said bypass vessel with said polyarginine for less than 30 minutes.Join the waitlist — get patent alerts
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