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Kavanagh, CA,Gorelova, TA,Selezneva, II,Rochev, YA,Dawson, KA,Gallagher, WM,Gorelov, AV,Keenan, AK
2005
January
Journal Of Biomedical Materials Research Part A
Poly(N-isopropy acrylamide) copolymer films as vehicles for the sustained delivery of proteins to vascular endothelial cells
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thermoresponsive copolymers NiPAAm/Nt-BAAm FITC-labeled BSA VEGF(165) human aortic endothelial cells proliferation CORONARY-ARTERY DISEASE IN-STENT RESTENOSIS GROWTH-FACTOR N-ISOPROPYLACRYLAMIDE THERAPEUTIC ANGIOGENESIS BALLOON ANGIOPLASTY GENE-TRANSFER RELEASE IMPLANTATION HYPERPLASIA
72A
25
35
The aim of this study was to establish the capacity of thermoresponsive poly(N-isopropylacrylamide) copolymer films to deliver bioactive concentrations of vascular endothelial growth factor (VEGF,,,) to human aortic endothelial cells (HAEC) over an extended time period. Films were prepared using a 50:50 (w/w) mixture of noncrosslinkable and crosslinkable copolymers of the following monomer compositions (w/w): 85:15, N-isopropylacrylamide (NiPAAm):N-tert-butylacrylamide (NtBAAm); and 85: 13:2 NiPAAm:NtBAAm:acrylamidobenzophenone (ABzPh, crosslinking agent), respectively. After crosslinking by UV irradiation, the ability of films to incorporate a fluorescently labeled carrier protein (FITC-labeled BSA, 1 mg loaded per film), at 4degreesC, was first established. Incorporation into the matrix was confirmed by the observation that increasing film thickness from 5 to 10 mum increased release from collapsed films at 37degreesC (1.76 +/- 0.15 and 10.98 +/- 3.38 mug/mL, respectively, at 24 h postloading) and that this difference was maintained at 5 days postloading (1.81 +/- 0.25 and 13.8 +/- 2.3 mug/mL, respectively). Incorporation was also confirmed by visualization using confocal microscopy. When 10-mum films were loaded with a BSA solution (1 mg/mL) containing VEGF(165) (3 mug/mL), sustained release of VEGF(165) was observed (10.75 +/- 3.11 ng at 24 h; a total of 31.32 +/- 8.50 ng over 7 days). Furthermore, eluted VEGF(165). increased HAEC proliferation by 18.2% over control. The absence of cytotoxic species in medium released from the copolymer films was confirmed by the lack of effect of medium (incubated with copolymer films for 3 days) on HAEC viability. In conclusion this study has shown that NiPAAm:NtBAAm copolymers can be loaded with a therapeutic protein and can deliver bioactive concentrations to human vascular endothelial cells over an extended time period. (C) 2004 Wiley Periodicals, Inc.
DOI 10.1002/jbm.a.30192
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