TY - JOUR
T1 - Comparison of methods for local delivery of tissue factor pathway inhibitor to balloon-injured arteries in rabbits
AU - Yang, Lu Ying
AU - St Pierre, James
AU - Scherrer, David E.
AU - Lasala, John M.
AU - Walsh, Robert G.s.
AU - Abendschein, Dana R.
PY - 1999
Y1 - 1999
N2 - Background. Prolonged intravenous infusions of recombinant tissue factor pathway inhibitor (rTFPI) have been shown to attenuate markedly neointimal formation and stenosis after balloon-induced injury to the carotid arteries in minipigs. Design. Because local delivery of rTFPI to the injury site would be clinically advantageous, we designed this study to compare the local delivery and retention of rTFPI in balloon-injured arteries using three catheter-based systems. Methods. Similar amounts (range 3-4.5 mg) of a mixture of 125I-labeled and unlabeled rTFPI were delivered by either passive diffusion at moderate pressure (5 x 105 Pa with the LocalMed InfusaSleeve, or 4 x 105 Pa with the SciMed Dispatch device), or facilitated diffusion combining lower pressure (2 x 105 Pa) and electrical current (3.5 mA/cm2; e-MED, iontophoresis) to balloon-injured carotid arteries in anesthetized rabbits. Results. Comparable amounts of rTFPI were retained on the injured vessels immediately after delivery (t = 0) with the LocalMed (628 ± 68 μg/g per cm2, n = 4), SciMed (522 ± 167 μg/g per cm2, n = 4), and e-MED (497 ± 142 μg/g per cm2, n = 4) catheters (NS). However, rTFPI was decreased by 37% after 24 h compared with t = 0 (P < 0.02) in the e-MED group, but was increased 1.5-fold (P = 0.02) and 1.3-fold in the SciMed and LocalMed groups, respectively, presumably because of redistribution of rTFPI from remote endothelial or perivascular sites. Retention of rTFPI was six to nine times higher for injured compared with non-injured arteries, and persisted for at least 48 h after delivery with the LocalMed catheter. Conclusions. Sustained, marked retention of rTFPI delivered locally at the site of balloon-induced arterial injury appears to result from catheter-based systems that use passive diffusion at moderate pressure.
AB - Background. Prolonged intravenous infusions of recombinant tissue factor pathway inhibitor (rTFPI) have been shown to attenuate markedly neointimal formation and stenosis after balloon-induced injury to the carotid arteries in minipigs. Design. Because local delivery of rTFPI to the injury site would be clinically advantageous, we designed this study to compare the local delivery and retention of rTFPI in balloon-injured arteries using three catheter-based systems. Methods. Similar amounts (range 3-4.5 mg) of a mixture of 125I-labeled and unlabeled rTFPI were delivered by either passive diffusion at moderate pressure (5 x 105 Pa with the LocalMed InfusaSleeve, or 4 x 105 Pa with the SciMed Dispatch device), or facilitated diffusion combining lower pressure (2 x 105 Pa) and electrical current (3.5 mA/cm2; e-MED, iontophoresis) to balloon-injured carotid arteries in anesthetized rabbits. Results. Comparable amounts of rTFPI were retained on the injured vessels immediately after delivery (t = 0) with the LocalMed (628 ± 68 μg/g per cm2, n = 4), SciMed (522 ± 167 μg/g per cm2, n = 4), and e-MED (497 ± 142 μg/g per cm2, n = 4) catheters (NS). However, rTFPI was decreased by 37% after 24 h compared with t = 0 (P < 0.02) in the e-MED group, but was increased 1.5-fold (P = 0.02) and 1.3-fold in the SciMed and LocalMed groups, respectively, presumably because of redistribution of rTFPI from remote endothelial or perivascular sites. Retention of rTFPI was six to nine times higher for injured compared with non-injured arteries, and persisted for at least 48 h after delivery with the LocalMed catheter. Conclusions. Sustained, marked retention of rTFPI delivered locally at the site of balloon-induced arterial injury appears to result from catheter-based systems that use passive diffusion at moderate pressure.
KW - Angioplasty
KW - Restenosis
KW - Tissue factor
UR - http://www.scopus.com/inward/record.url?scp=0032788199&partnerID=8YFLogxK
U2 - 10.1097/00019501-199907000-00009
DO - 10.1097/00019501-199907000-00009
M3 - Article
C2 - 10421973
AN - SCOPUS:0032788199
VL - 10
SP - 327
EP - 333
JO - Coronary Artery Disease
JF - Coronary Artery Disease
SN - 0954-6928
IS - 5
ER -