Bimodal Porous Scaffolds by Sequential Electrospinning of Poly(glycolic acid) with Sucrose Particles

Electrospinning is a method to produce fine, biopolymer mesh with a three-dimensional architecture that mimics native extra-cellular matrix. Due to the small fiber diameter created in this process, conventional electrospun scaffolds have pore sizes smaller than the diameter of most cells. These scaf...

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Main Authors: B. Wulkersdorfer, K. K. Kao, V. G. Agopian, A. Ahn, J. C. Dunn, B. M. Wu, M. Stelzner
Format: Article
Language:English
Published: Wiley 2010-01-01
Series:International Journal of Polymer Science
Online Access:http://dx.doi.org/10.1155/2010/436178
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author B. Wulkersdorfer
K. K. Kao
V. G. Agopian
A. Ahn
J. C. Dunn
B. M. Wu
M. Stelzner
author_facet B. Wulkersdorfer
K. K. Kao
V. G. Agopian
A. Ahn
J. C. Dunn
B. M. Wu
M. Stelzner
author_sort B. Wulkersdorfer
collection DOAJ
description Electrospinning is a method to produce fine, biopolymer mesh with a three-dimensional architecture that mimics native extra-cellular matrix. Due to the small fiber diameter created in this process, conventional electrospun scaffolds have pore sizes smaller than the diameter of most cells. These scaffolds have limited application in tissue engineering due to poor cell penetration. We developed a hybrid electrospinning/particulate leaching technique to create scaffolds with increased porosity and improved cellular ingrowth. Poly(glycolic acid) (PGA) and a sucrose-ethanol suspension were electrospun in equal, alternating sequences at intervals of one, two, and ten minutes each. The scaffolds revealed fiber mesh with micropores of 10 𝜇m and uniformly distributed sucrose particles. Particulate leaching of sucrose from the one- or two-minute scaffolds revealed honeycomb structures with interconnected macropores between 50 and 250 𝜇m. Sucrose leaching from the ten-minute scaffolds resulted in laminated structures with isolated macropores between 200 and 350 𝜇m. Macropore size was directly proportional to the duration of the sucrose spinning interval. After 24 hours of cell culture, conventionally spun scaffolds demonstrated no cellular penetration. Conversely, the PGA/sucrose scaffolds demonstrated deep cellular penetration. This hybrid technique represents a novel method of generating electrospun scaffolds with interconnected pores suitable for cellular ingrowth.
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institution Kabale University
issn 1687-9422
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publishDate 2010-01-01
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series International Journal of Polymer Science
spelling doaj-art-6887bbdcb639486481010f7b47f3ae752025-02-03T01:23:58ZengWileyInternational Journal of Polymer Science1687-94221687-94302010-01-01201010.1155/2010/436178436178Bimodal Porous Scaffolds by Sequential Electrospinning of Poly(glycolic acid) with Sucrose ParticlesB. Wulkersdorfer0K. K. Kao1V. G. Agopian2A. Ahn3J. C. Dunn4B. M. Wu5M. Stelzner6Department of Surgery, VA Greater Los Angeles Health Care System, Los Angeles, CA 90073, USADepartment of Surgery, VA Greater Los Angeles Health Care System, Los Angeles, CA 90073, USADepartment of Surgery, VA Greater Los Angeles Health Care System, Los Angeles, CA 90073, USADepartment of Surgery, VA Greater Los Angeles Health Care System, Los Angeles, CA 90073, USADepartment of Surgery, University of California at Los Angeles, Los Angeles, CA 90095, USADepartment of Surgery, University of California at Los Angeles, Los Angeles, CA 90095, USADepartment of Surgery, VA Greater Los Angeles Health Care System, Los Angeles, CA 90073, USAElectrospinning is a method to produce fine, biopolymer mesh with a three-dimensional architecture that mimics native extra-cellular matrix. Due to the small fiber diameter created in this process, conventional electrospun scaffolds have pore sizes smaller than the diameter of most cells. These scaffolds have limited application in tissue engineering due to poor cell penetration. We developed a hybrid electrospinning/particulate leaching technique to create scaffolds with increased porosity and improved cellular ingrowth. Poly(glycolic acid) (PGA) and a sucrose-ethanol suspension were electrospun in equal, alternating sequences at intervals of one, two, and ten minutes each. The scaffolds revealed fiber mesh with micropores of 10 𝜇m and uniformly distributed sucrose particles. Particulate leaching of sucrose from the one- or two-minute scaffolds revealed honeycomb structures with interconnected macropores between 50 and 250 𝜇m. Sucrose leaching from the ten-minute scaffolds resulted in laminated structures with isolated macropores between 200 and 350 𝜇m. Macropore size was directly proportional to the duration of the sucrose spinning interval. After 24 hours of cell culture, conventionally spun scaffolds demonstrated no cellular penetration. Conversely, the PGA/sucrose scaffolds demonstrated deep cellular penetration. This hybrid technique represents a novel method of generating electrospun scaffolds with interconnected pores suitable for cellular ingrowth.http://dx.doi.org/10.1155/2010/436178
spellingShingle B. Wulkersdorfer
K. K. Kao
V. G. Agopian
A. Ahn
J. C. Dunn
B. M. Wu
M. Stelzner
Bimodal Porous Scaffolds by Sequential Electrospinning of Poly(glycolic acid) with Sucrose Particles
International Journal of Polymer Science
title Bimodal Porous Scaffolds by Sequential Electrospinning of Poly(glycolic acid) with Sucrose Particles
title_full Bimodal Porous Scaffolds by Sequential Electrospinning of Poly(glycolic acid) with Sucrose Particles
title_fullStr Bimodal Porous Scaffolds by Sequential Electrospinning of Poly(glycolic acid) with Sucrose Particles
title_full_unstemmed Bimodal Porous Scaffolds by Sequential Electrospinning of Poly(glycolic acid) with Sucrose Particles
title_short Bimodal Porous Scaffolds by Sequential Electrospinning of Poly(glycolic acid) with Sucrose Particles
title_sort bimodal porous scaffolds by sequential electrospinning of poly glycolic acid with sucrose particles
url http://dx.doi.org/10.1155/2010/436178
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