4.7 Article

Vascular lumen simulation and highly-sensitive nitric oxide detection using three-dimensional gelatin chip coupled to TiC/C nanowire arrays microelectrode

期刊

LAB ON A CHIP
卷 12, 期 21, 页码 4249-4256

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2lc40148g

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资金

  1. National Natural Science Foundation of China [20975077, 31070995, 50902104, 21105077]
  2. Science Fund for Creative Research Groups [20921062]
  3. National Basic Research Program of China (973 Program) [2007CB714507]
  4. Program for New Century Excellent Talents in University [NCET-10-0611]
  5. Program for Changjiang Scholars and Innovative Research Team in University [IRT1030]
  6. Hong Kong Research Grants Council (RGC) [CityU 112510]
  7. City University of Hong Kong [7008009]

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Reproducing the physiological environment of blood vessels for the in vitro investigation of endothelial cell functions is very challenging. Here, we describe a vascular-like structure based on a three-dimensional (3D) gelatin chip with good compatibility and permeability which is also cost-effective and easy to produce. The controllable lumen diameter and wall thickness enable close mimicking of blood vessels in vitro. The 3D gelatin matrix between adjacent lumens is capable of generating soluble-factor gradients inside, and diffusion of molecules with different molecular weights through the matrix is studied. The cultured human umbilical vein endothelial cells proliferate on the gelatin lumen linings to form a vascular lumen. The hemodynamic behavior including adhesion, alignment of endothelial cells (ECs) under shear stress and pulsatile stretch is studied. Furthermore, a microelectrode comprising TiC/C nanowire arrays is fabricated to detect nitric oxide with sub-nM detection limits and NO generation from the cultured ECs is monitored in real time. This vascular model reproduces the surrounding parenchyma of endothelial cells and mimics the hemodynamics inside blood vessels very well, thereby enabling potential direct investigation of hemodynamics, angiogenesis, and tumor metastasis in vitro.

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