Review Article

Vascular Tissue Engineering: Recent Advances in Small Diameter Blood Vessel Regeneration

Table 6

Studies of the scientific literature (2008–2013) on TEVGs fabricated with natural and synthetic polymers.

MaterialFabrication methodIDMechanical propertiesBiological in vitro resultsBiological in vivo resultsReference

Blend of PCL + elastin + collagen type I Electrospinning of 3 layers at different polymer ratios using a cylindrical rotating translating mandrel2 mmSRS = 91–189° gf, BP = 2387–>3000° mmHg;  = 2.83–0.77°%/100 mmHg, increase of PCL + decrease of elastin: increase of SRS and BP, decrease of [68]

Recombinant human tropoelastin (inner layer) + PCL (outer layer)Electrospinning using a rotating mandrel; cross-linking: glutaraldehyde vapors2.8 mm  kPa, BP ~ 1900* mmHg,   ~ 0.065* kPa−1, HP = minimal; similar to internal mammary artery:  ± 46 kPa, BP ~ 2267 ± 215 mmHg, ~ 0.09* kPa−1SEM and fluorescence microscope (3 days): HUVECs attached and proliferated; platelet attachment: reduced, compared to ePTFE and PCLModel: rabbit (1 month); maintenance of physical integrity; no evidence of dilatation, anastomotic dehiscence, or seroma; mechanical properties of implanted grafts remained similar to controls[26]

PGA + PLLA + collagen type ICollagen microsponge + woven tube made of core-sheath yarns (PLLA and PGA, resp.) fabricated by air-jet spinning4 mmAxial tensile testsbefore implantation: UTS ~ 30* MPa versus,    MPa;   after implantation: UTS ~ 5–9* MPa,   –100* MPa;   native carotid artery: UTS ~ 7.5* MPa,    MPaCell culture with NIH/3T3 or HUVEC (3 days); SEM analysis: higher cell number and better adhesion for grafts with collagenModel: dog (12 months); acellular grafts; 100% patency, no thrombosis or aneurysm; excellent tissue regeneration: complete endothelialization, SMCs, elastin, and collagen fibers; PGA fibers completely absorbed at 2 months, PLLA fibers unabsorbed at 12 months[69]

Blend of PCL + collagen type IElectrospinning using a rotating mandrel4.75 mmSRS = 3.0 ± 1.1 N, BP = 4915 ± 155 mmHg, = 5.6 ± 1.6%/100 mmHg; axial tensile tests: UTS = 4.0 ± 0.4 MPa,   = 2.7 ± 1.2 MPa,   = 140 ± 13%; maintenance of tensile properties in a perfusion bioreactor system under overphysiological conditions for 4 weeks; native porcine coronary artery: UTS ~ 2.5* MPa,    MPa,   %ECs and SMCs from bovine carotid artery; cytotoxicity via direct contact (7 days—MTS assay): no differences in cell viability compared to TCPs; cytocompatibility (7 days—MTS assay): EC and SMC adhesion and proliferation; cell culture on tubular grafts (48 h—SEM and histological analysis): SMCs formed multiple cell layers on the outer region, ECs formed a monolayer on the inner surface[45]

Blend of PCL + collagen type IElectrospinning using a rotating mandrel4.75 mmCircumferential tensile testsbefore implantation: UTS ~ 1.8* MPa;   after implantation: UTS ~ 0.8* MPa; comparable to native aorta: UTS ~ 1.2* MPaECs derived from endothelial progenitor cells isolated from live sheep; SMCs isolated from sheep artery explants; dynamic culture using a pulsatile bioreactor under physiologic conditions (9 days); SEM + histological analysis: ECs formed a confluent layer on the inner lumen, SMCs assumed a multilayered configuration on the exteriorPlatelet adhesion  in a live sheep model for 15 min: no adhesion for seeded grafts, abundant adhesion for unseeded grafts; model: rabbit (1 month); acellular grafts; no aneurysmal degeneration; majority of the grafts remained patent at 1 month; absence of inflammatory infiltrate[70]

PCL/PLA + collagen type IPCL/PLA electrospinning using a rotating mandrel + collagen coating after air plasma treatment1, 3 mmAxial tensile tests: UTS = 7.0 ± 0.4 MPa,   = 16.0 ± 7.1 MPa,   = 289 ± 55%; circumferential tensile tests: UTS = 3.9 ± 0.3 MPa,   = 16.6 ± 4.4 MPa,   = 292 ± 87%HCAECs rotationally seeded in the bioreactor for 4 h + static culture (10 days—SEM and histological analysis): HCAECs evenly distributed and well spread on the lumenModel: rabbit (7 weeks); acellular grafts without collagen coating; no blood leaking; graft structure integrity and patency; foreign body response: no cell infiltration[71]

PLDLA + fibrinPLDLA tubular warp knit structure + coating of fibrin gel with SMCs and fibroblasts~5 mmECs, SMCs, and fibroblasts isolated from ovine carotid arteries; ECs seeding in the inner layer using a rotating chamber; dynamic culture in a bioreactor under physiological pressure conditions for 21–28 days; histological analysis: a dense, homogenous distribution of cells throughout the scaffold thickness, extensive collagen Model: sheep (6 months); ID ~ 6 mm; cellular grafts (dynamic culture for 21–28 days); at 3 months 1 graft with a significant stenosis; other grafts: completely patent, no thrombus formation and aneurysm, infection, or calcification; remodeling: confluent endothelium, collagen and other ECM components, and elastin (not assembled in cohesive sheets);[43]
formation, and no evidence of calcification fibrin completely degraded after 1 month, sparse PLDLA material remained at 6 months

PCL/PLA: 70 : 30 copolymer of ε-caprolactone and L-lactide; PLDLA: 96 : 4 copolymer of L-lactide and D-lactide.
SRS: suture retention strength; BP: burst pressure; : compliance; °range of average values of grafts with 3 different media compositions; HP: hydraulic permeability; UTS: ultimate tensile strength; : elastic modulus; : strain at break; *values were graphically read.
HUVECs: human umbilical vein endothelial cells; HCAECs: human coronary artery endothelial cells; NIH/3T3: murine fibroblast cell line; TCPs: tissue culture plates.