Growth factor delivery through electrospun nanofibers in scaffolds for tissue engineering applications

Tissue engineering scaffolds should ideally mimic the natural ECM in structure and function. Electrospun nanofibrous scaffolds are easily fabricated and possess a biomimetic nanostructure. Scaffolds can mimic ECM function by acting as a depot for sustained release of growth factors. bFGF, an importa...

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Veröffentlicht in:Journal of biomedical materials research. Part A 2010-06, Vol.93A (4), p.1539-1550
Hauptverfasser: Sahoo, Sambit, Ang, Lay Teng, Goh, James Cho-Hong, Toh, Siew-Lok
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container_issue 4
container_start_page 1539
container_title Journal of biomedical materials research. Part A
container_volume 93A
creator Sahoo, Sambit
Ang, Lay Teng
Goh, James Cho-Hong
Toh, Siew-Lok
description Tissue engineering scaffolds should ideally mimic the natural ECM in structure and function. Electrospun nanofibrous scaffolds are easily fabricated and possess a biomimetic nanostructure. Scaffolds can mimic ECM function by acting as a depot for sustained release of growth factors. bFGF, an important growth factor involved in tissue repair and mesenchymal stem cell proliferation and differentiation, is a suitable candidate for sustained delivery from scaffolds. In this study, we present two types of PLGA nanofibers incorporated with bFGF, fabricated using the facile technique of blending and electrospinning (Group I) and by the more complex technique of coaxial electrospinning (Group II). bFGF was randomly dispersed in Group I and distributed as a central core within Group II nanofibers; both scaffolds showed similar protein encapsulation efficiency and release over 1–2 weeks. Although both scaffold groups favored bone marrow stem cell attachment and subsequent proliferation, cells cultured on Group I scaffolds demonstrated increased collagen production and upregulated gene expression of specific ECM proteins, indicating fibroblastic differentiation. The study shows that the electrospinning technique could be used to prolong growth factor release from scaffolds and an appropriately sustained growth factor release profile in combination with a nanofibrous substrate could positively influence stem cell behavior and fate. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res 2010
doi_str_mv 10.1002/jbm.a.32645
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Although both scaffold groups favored bone marrow stem cell attachment and subsequent proliferation, cells cultured on Group I scaffolds demonstrated increased collagen production and upregulated gene expression of specific ECM proteins, indicating fibroblastic differentiation. The study shows that the electrospinning technique could be used to prolong growth factor release from scaffolds and an appropriately sustained growth factor release profile in combination with a nanofibrous substrate could positively influence stem cell behavior and fate. © 2009 Wiley Periodicals, Inc. 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Economical aspects ; Kinetics ; Medical sciences ; Microscopy, Electron, Scanning - methods ; Miscellaneous ; nanofibers ; Nanofibers - chemistry ; Nanotechnology - methods ; Rabbits ; Reverse Transcriptase Polymerase Chain Reaction ; Stem Cells - cytology ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Technology. Biomaterials. Equipments ; tissue engineering ; Tissue Engineering - methods</subject><ispartof>Journal of biomedical materials research. 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Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Tissue engineering scaffolds should ideally mimic the natural ECM in structure and function. Electrospun nanofibrous scaffolds are easily fabricated and possess a biomimetic nanostructure. Scaffolds can mimic ECM function by acting as a depot for sustained release of growth factors. bFGF, an important growth factor involved in tissue repair and mesenchymal stem cell proliferation and differentiation, is a suitable candidate for sustained delivery from scaffolds. In this study, we present two types of PLGA nanofibers incorporated with bFGF, fabricated using the facile technique of blending and electrospinning (Group I) and by the more complex technique of coaxial electrospinning (Group II). bFGF was randomly dispersed in Group I and distributed as a central core within Group II nanofibers; both scaffolds showed similar protein encapsulation efficiency and release over 1–2 weeks. Although both scaffold groups favored bone marrow stem cell attachment and subsequent proliferation, cells cultured on Group I scaffolds demonstrated increased collagen production and upregulated gene expression of specific ECM proteins, indicating fibroblastic differentiation. The study shows that the electrospinning technique could be used to prolong growth factor release from scaffolds and an appropriately sustained growth factor release profile in combination with a nanofibrous substrate could positively influence stem cell behavior and fate. © 2009 Wiley Periodicals, Inc. J Biomed Mater Res 2010</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>biomimetic scaffolds</subject><subject>Biomimetics</subject><subject>Biotechnology</subject><subject>Cell Proliferation</subject><subject>Collagen - chemistry</subject><subject>Electrochemistry - methods</subject><subject>electrospinning</subject><subject>Extracellular Matrix - metabolism</subject><subject>Fibroblast Growth Factor 2 - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>growth factors</subject><subject>Health. Pharmaceutical industry</subject><subject>Industrial applications and implications. Economical aspects</subject><subject>Kinetics</subject><subject>Medical sciences</subject><subject>Microscopy, Electron, Scanning - methods</subject><subject>Miscellaneous</subject><subject>nanofibers</subject><subject>Nanofibers - chemistry</subject><subject>Nanotechnology - methods</subject><subject>Rabbits</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Stem Cells - cytology</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Technology. Biomaterials. 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subjects Animals
Biological and medical sciences
biomimetic scaffolds
Biomimetics
Biotechnology
Cell Proliferation
Collagen - chemistry
Electrochemistry - methods
electrospinning
Extracellular Matrix - metabolism
Fibroblast Growth Factor 2 - chemistry
Fundamental and applied biological sciences. Psychology
growth factors
Health. Pharmaceutical industry
Industrial applications and implications. Economical aspects
Kinetics
Medical sciences
Microscopy, Electron, Scanning - methods
Miscellaneous
nanofibers
Nanofibers - chemistry
Nanotechnology - methods
Rabbits
Reverse Transcriptase Polymerase Chain Reaction
Stem Cells - cytology
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Technology. Biomaterials. Equipments
tissue engineering
Tissue Engineering - methods
title Growth factor delivery through electrospun nanofibers in scaffolds for tissue engineering applications
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