Title of article :
Fabrication of cell penetration enhanced poly (l-lactic acid-co-ɛ-caprolactone)/silk vascular scaffolds utilizing air-impedance electrospinning
Author/Authors :
Yin، نويسنده , , Anlin and Li، نويسنده , , Jiukai and Bowlin، نويسنده , , Gary L. and Li، نويسنده , , Dawei and Rodriguez، نويسنده , , Isaac A. and Wang، نويسنده , , Jing and Wu، نويسنده , , Tong and EI-Hamshary، نويسنده , , Hany A. and Al-Deyab، نويسنده , , Salem S. and Mo، نويسنده , , Xiumei، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Abstract :
In the vascular prosthetic field, the prevailing thought is that for clinical, long-term success, especially bioresorbable grafts, cellular migration and penetration into the prosthetic structure is required to promote neointima formation and vascular wall development. In this study, we fabricated poly (l-lactic acid-co-ɛ-caprolactone) P(LLA-CL)/silk fibroin (SF) vascular scaffolds through electrospinning using both perforated mandrel subjected to various intraluminal air pressures (0–300 kPa), and solid mandrel. The scaffolds were evaluated the cellular infiltration in vitro and mechanical properties. Vascular scaffolds were seeded with smooth muscle cells (SMCs) to evaluate cellular infiltration at 1, 7, and 14 days. The results revealed that air-impedance scaffolds allowed significantly more cell infiltration as compared to the scaffolds fabricated with solid mandrel. Meanwhile, results showed that both mandrel model and applied air pressure determined the interfiber distance and the alignment of fibers in the enhanced porosity regions of the structure which influenced cell infiltration. Uniaxial tensile testing indicated that the air-impedance scaffolds have sufficient ultimate strength, suture retention strength, and burst pressure as well as compliance approximating a native artery. In conclusion, the air-impedance scaffolds improved cellular infiltration without compromising overall biomechanical properties. These results support the scaffoldʹs potential for vascular grafting and in situ regeneration.
Keywords :
vascular tissue engineering , Vascular prosthetic , Cell infiltration , electrospinning
Journal title :
Colloids and Surfaces B Biointerfaces
Journal title :
Colloids and Surfaces B Biointerfaces