Title of article :
A New Intra-Arterial DeliveryPlatform for Pro-Arteriogenic Compounds to Stimulate Collateral Artery Growth Via Transforming Growth Factor-β1 Release Original Research Article
Author/Authors :
Sebastian Grundmann، نويسنده , , Niels van Royen، نويسنده , , Gerard Pasterkamp، نويسنده , , Nieves Gonzalez، نويسنده , , Edze J. Tijsma، نويسنده , , Jan J. Piek، نويسنده , , Imo E. Hoefer، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2007
Pages :
8
From page :
351
To page :
358
Abstract :
Objectives The purpose of this study was to develop a cytokine-eluting stent to stimulate collateral artery growth (arteriogenesis) in the peripheral circulation of the rabbit via local transforming growth factor (TGF)-β1 release. Background The stimulation of arteriogenesis with cytokines is a potential new treatment option for patients suffering from vascular occlusive diseases. However, the lack of a delivery platform for continuous intra-arterial application of pro-arteriogenic compounds has hampered the clinical implementation of this promising therapeutic strategy. Methods Different polymer coatings were tested regarding their suitability for cytokine release. Fifty-four rabbits underwent implantation of bare-metal stents (BMS), polymer-only coated stents (PDLLA), polymer-coated TGF-β1–eluting stents (TGF) in the iliac artery, or bolus infusion of TGF-β1 and subsequent femoral artery ligation. Collateral artery growth was assessed with fluorescent microspheres, angiography, and histological quantification of the proliferation marker Ki67. In-stent neointima formation was measured in histological sections of plastic-embedded stents. Results A TGF-β1–loaded coating based on poly(D,L-lactide) released up to 2.4 μg active TGF-β1 over a period of 24 h. Perfusion measurements revealed a significant increase in collateral conductance after TGF-β1 stent implantation compared with the control groups ([ml/min/100 mm Hg] BMS: 47.8 ± 2.5; PDLLA: 44.1 ± 3.9; TGF: 91.3 ± 32.6). Bolus infusion of TGF-β1 had no effect. Collateral arteries showed a higher proliferation activity in the TGF-treated group. At 7 days, no significant difference in in-stent neointima formation was observed. Conclusions We first describe the use of a cytokine-releasing stent to stimulate collateral artery growth. These results show that intra-arterial cytokine-releasing devices might serve as a novel platform for the delivery of compounds affecting biological processes downstream of the site of implantation.
Keywords :
BMS , vascular endothelial growth factor , VEGF , ELISA , Molecular weight , vascular smooth muscle cells , Fibroblast growth factor , MMA , PbS , PDLLA , Mw , VSMC , HE , HUVECs , FGF , bare-metal stent(s) , phosphate buffered saline , enzyme linked immunosorbent assay , hematoxyline and eosine , human umbilical endothelial cells , methyl-methacrylate , PBMA , poly(n-butyl methacrylate) , poly(D , L-lactide) , PEVA , poly(ethylene-co-vinyl acetate) , rhTGF-?1 , recombinant human transforming growth factor ?1
Journal title :
JACC (Journal of the American College of Cardiology)
Serial Year :
2007
Journal title :
JACC (Journal of the American College of Cardiology)
Record number :
472677
Link To Document :
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