The construction of three-dimensional micro-fluidic scaffolds of biodegradable polymers by solvent vapor based bonding of micro-molded layers

Won Hyoung Ryu, Sung Woo Min, Kyle E. Hammerick, Murty Vyakarnam, Ralph S. Greco, Fritz B. Prinz, Rainer J. Fasching

Research output: Contribution to journalArticle

57 Citations (Scopus)

Abstract

It is increasingly important to control cell growth into and within artificial scaffolds. Tissues such as skin, blood vessels, and cartilage have multi-layer structures with different cells in each layer. With the aid of micro-fabrication technology, a novel scaffolding method for biodegradable polymers such as polylactic acid (PLA), polyglycolic acid (PGA), and the copolymers poly(lactide-co-glycolide)(PLGA), was developed to construct three-dimensional multi-layer micro-fluidic tissue scaffolds. The method emphasizes micro-fluidic interconnections between layers within the scaffolds and maintenance of high-resolution geometries during the bonding process for the creation of multi-layered scaffolds. Micro-holes (10-100 μm), micro-channels, and micro-cavities were all created by micro-molding. Solvent-vapor based bonding of micro-molded layers preserved 20 μm sized structures. Sample scaffolds were constructed for purposes such as channel-directed cell growth and size-based cell sorting. Further extension of these techniques to create a micro-vascular network within or between layers is possible. Culturing of human coronary artery endothelial cells (HCAECs) on the sample scaffolds demonstrated the biocompatibility of the developed process and the strong influence of high-resolution micro-geometries on HCAEC growth.

Original languageEnglish
Pages (from-to)1174-1184
Number of pages11
JournalBiomaterials
Volume28
Issue number6
DOIs
Publication statusPublished - 2007 Feb 1

Fingerprint

Biodegradable polymers
Cell growth
Fluidics
Scaffolds
Polymers
Vapors
Endothelial cells
Scaffolds (biology)
Blood Vessels
Coronary Vessels
Endothelial Cells
Cell Enlargement
Tissue Scaffolds
Polyglactin 910
Acids
Geometry
Microfabrication
Blood vessels
Cartilage
Growth

All Science Journal Classification (ASJC) codes

  • Bioengineering
  • Ceramics and Composites
  • Biophysics
  • Biomaterials
  • Mechanics of Materials

Cite this

Ryu, Won Hyoung ; Min, Sung Woo ; Hammerick, Kyle E. ; Vyakarnam, Murty ; Greco, Ralph S. ; Prinz, Fritz B. ; Fasching, Rainer J. / The construction of three-dimensional micro-fluidic scaffolds of biodegradable polymers by solvent vapor based bonding of micro-molded layers. In: Biomaterials. 2007 ; Vol. 28, No. 6. pp. 1174-1184.
@article{56911fae0b8741f8919a76d4a4c577a5,
title = "The construction of three-dimensional micro-fluidic scaffolds of biodegradable polymers by solvent vapor based bonding of micro-molded layers",
abstract = "It is increasingly important to control cell growth into and within artificial scaffolds. Tissues such as skin, blood vessels, and cartilage have multi-layer structures with different cells in each layer. With the aid of micro-fabrication technology, a novel scaffolding method for biodegradable polymers such as polylactic acid (PLA), polyglycolic acid (PGA), and the copolymers poly(lactide-co-glycolide)(PLGA), was developed to construct three-dimensional multi-layer micro-fluidic tissue scaffolds. The method emphasizes micro-fluidic interconnections between layers within the scaffolds and maintenance of high-resolution geometries during the bonding process for the creation of multi-layered scaffolds. Micro-holes (10-100 μm), micro-channels, and micro-cavities were all created by micro-molding. Solvent-vapor based bonding of micro-molded layers preserved 20 μm sized structures. Sample scaffolds were constructed for purposes such as channel-directed cell growth and size-based cell sorting. Further extension of these techniques to create a micro-vascular network within or between layers is possible. Culturing of human coronary artery endothelial cells (HCAECs) on the sample scaffolds demonstrated the biocompatibility of the developed process and the strong influence of high-resolution micro-geometries on HCAEC growth.",
author = "Ryu, {Won Hyoung} and Min, {Sung Woo} and Hammerick, {Kyle E.} and Murty Vyakarnam and Greco, {Ralph S.} and Prinz, {Fritz B.} and Fasching, {Rainer J.}",
year = "2007",
month = "2",
day = "1",
doi = "10.1016/j.biomaterials.2006.11.002",
language = "English",
volume = "28",
pages = "1174--1184",
journal = "Biomaterials",
issn = "0142-9612",
publisher = "Elsevier BV",
number = "6",

}

The construction of three-dimensional micro-fluidic scaffolds of biodegradable polymers by solvent vapor based bonding of micro-molded layers. / Ryu, Won Hyoung; Min, Sung Woo; Hammerick, Kyle E.; Vyakarnam, Murty; Greco, Ralph S.; Prinz, Fritz B.; Fasching, Rainer J.

In: Biomaterials, Vol. 28, No. 6, 01.02.2007, p. 1174-1184.

Research output: Contribution to journalArticle

TY - JOUR

T1 - The construction of three-dimensional micro-fluidic scaffolds of biodegradable polymers by solvent vapor based bonding of micro-molded layers

AU - Ryu, Won Hyoung

AU - Min, Sung Woo

AU - Hammerick, Kyle E.

AU - Vyakarnam, Murty

AU - Greco, Ralph S.

AU - Prinz, Fritz B.

AU - Fasching, Rainer J.

PY - 2007/2/1

Y1 - 2007/2/1

N2 - It is increasingly important to control cell growth into and within artificial scaffolds. Tissues such as skin, blood vessels, and cartilage have multi-layer structures with different cells in each layer. With the aid of micro-fabrication technology, a novel scaffolding method for biodegradable polymers such as polylactic acid (PLA), polyglycolic acid (PGA), and the copolymers poly(lactide-co-glycolide)(PLGA), was developed to construct three-dimensional multi-layer micro-fluidic tissue scaffolds. The method emphasizes micro-fluidic interconnections between layers within the scaffolds and maintenance of high-resolution geometries during the bonding process for the creation of multi-layered scaffolds. Micro-holes (10-100 μm), micro-channels, and micro-cavities were all created by micro-molding. Solvent-vapor based bonding of micro-molded layers preserved 20 μm sized structures. Sample scaffolds were constructed for purposes such as channel-directed cell growth and size-based cell sorting. Further extension of these techniques to create a micro-vascular network within or between layers is possible. Culturing of human coronary artery endothelial cells (HCAECs) on the sample scaffolds demonstrated the biocompatibility of the developed process and the strong influence of high-resolution micro-geometries on HCAEC growth.

AB - It is increasingly important to control cell growth into and within artificial scaffolds. Tissues such as skin, blood vessels, and cartilage have multi-layer structures with different cells in each layer. With the aid of micro-fabrication technology, a novel scaffolding method for biodegradable polymers such as polylactic acid (PLA), polyglycolic acid (PGA), and the copolymers poly(lactide-co-glycolide)(PLGA), was developed to construct three-dimensional multi-layer micro-fluidic tissue scaffolds. The method emphasizes micro-fluidic interconnections between layers within the scaffolds and maintenance of high-resolution geometries during the bonding process for the creation of multi-layered scaffolds. Micro-holes (10-100 μm), micro-channels, and micro-cavities were all created by micro-molding. Solvent-vapor based bonding of micro-molded layers preserved 20 μm sized structures. Sample scaffolds were constructed for purposes such as channel-directed cell growth and size-based cell sorting. Further extension of these techniques to create a micro-vascular network within or between layers is possible. Culturing of human coronary artery endothelial cells (HCAECs) on the sample scaffolds demonstrated the biocompatibility of the developed process and the strong influence of high-resolution micro-geometries on HCAEC growth.

UR - http://www.scopus.com/inward/record.url?scp=33751410795&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=33751410795&partnerID=8YFLogxK

U2 - 10.1016/j.biomaterials.2006.11.002

DO - 10.1016/j.biomaterials.2006.11.002

M3 - Article

C2 - 17126395

AN - SCOPUS:33751410795

VL - 28

SP - 1174

EP - 1184

JO - Biomaterials

JF - Biomaterials

SN - 0142-9612

IS - 6

ER -