Abstract

There has been substantial progress in tissue engineering of biological substitutes for medical applications. One of the major challenges in development of complex tissues is the difficulty of creating vascular networks for engineered constructs. The diameter of current artificial vascular channels is usually at millimeter or submillimeter level, while human capillaries are about 5 to 10 µm in diameter. In this paper, a novel core-sheath electrospinning process was adopted to fabricate nanoporous microtubes to mimic the structure of fenestrated capillary vessels. A mixture of polylactic acid (PLA) and polyethylene glycol (PEO) was used as the sheath solution and PEO was used as the core solution. The microtubes were observed under a scanning electron microscope and the images were analyzed by ImageJ. The diameter of the microtubes ranged from 1–8 microns. The diameter of the nanopores ranged from 100 to 800 nm. The statistical analysis showed that the microtube diameter was significantly influenced by the PEO ratio in the sheath solution, pump rate, and the viscosity gradient between the sheath and the core solution. The electrospun microtubes with nanoscale pores highly resemble human fenestrated capillaries. Therefore, the nanoporous microtubes have great potential to support vascularization in engineered tissues.

Highlights

  • Vascularization has been challenging for several decades in the tissue engineering field.The introduction of blood vessels into artificial tissues is one of the most critical steps toward viable organ transplant substitutes

  • When the mixture of polylactic acid (PLA) and polyethylene glycol (PEO) was used as the sheath material, a large portion of the dents became pores after the dissolution of PEO

  • Nanoporous microtubes were fabricated by core-sheath electrospinning to resemble capillary vessels

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Summary

Introduction

Vascularization has been challenging for several decades in the tissue engineering field. The introduction of blood vessels into artificial tissues is one of the most critical steps toward viable organ transplant substitutes. There are three different lining structures for capillary vessels: continuous, fenestrated, and sinusoidal [5,6]. The basement membrane layer and endothelial layer are closed in continuous capillaries, while the endothelial layer is porous in fenestrated and sinusoidal capillaries. The porous structure is believed to improve the efficiency of transportation of biological factors between inside and outside of the capillaries [7]. The incorporation of nanoporous microchannels into biomimetic scaffolds can significantly improve the viability of cultured cells inside scaffolds. There is a research gap to create biological substitutes for capillary vessels in relevant scale and nanoporous structures

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