Abstract
Successful bone regeneration benefits from three-dimensional (3D) bioresorbable scaffolds that mimic the hierarchical architecture and mechanical characteristics of native tissue extracellular matrix (ECM). A scaffold platform that integrates unique material chemistry with nanotopography while mimicking the 3D hierarchical bone architecture and bone mechanics is reported. A biocompatible dipeptide polyphosphazene-polyester blend is electrospun to produce fibers in the diameter range of 50-500 nm to emulate dimensions of collagen fibrils present in the natural bone ECM. Various electrospinning and process parameters are optimized to produce blend nanofibers with good uniformity, appropriate mechanical strength, and suitable porosity. Biomimetic 3D scaffolds are created by orienting blend nanofiber matrices in a concentric manner with an open central cavity to replicate bone marrow cavity, as well as the lamellar structure of bone. This biomimicry results in scaffold stress-strain curve similar to that of native bone with a compressive modulus in the mid-range of values for human trabecular bone. Blend nanofiber matrices support adhesion and proliferation of osteoblasts and show an elevated phenotype expression compared to polyester nanofibers. Furthermore, the 3D structure encourages osteoblast infiltration and ECM secretion, bridging the gaps of scaffold concentric walls during in vitro culture. The results also highlight the importance of in situ ECM secretion by cells in maintaining scaffold mechanical properties following scaffold degradation with time. This study for the first time demonstrates the feasibility of developing a mechanically competent nanofiber matrix via a biomimetic strategy and the advantages of polyphosphazene blends in promoting osteoblast phenotype progression for bone regeneration. A new biomimetic scaffold design comprised of electrospun polymeric nanofibers combines unique material chemistry, hierarchical architecture, and mechanics suitable for load-bearing bone regeneration. Furthermore, the biomimicry-enabled scaffolds promote osteoblast migration, proliferation, phenotype progression, maturation, and mineralization while maintaining a uniform cell and extracellular matrix distribution. This nanofiber scaffold platform can also be adopted for regeneration of tissue interfaces such as bone-tendon.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2641-2651 |
| Number of pages | 11 |
| Journal | Advanced Functional Materials |
| Volume | 21 |
| Issue number | 14 |
| DOIs | |
| State | Published - Jul 22 2011 |
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All Science Journal Classification (ASJC) codes
- Chemistry(all)
- Materials Science(all)
- Condensed Matter Physics
Cite this
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Biomimetic structures : Biological implications of dipeptide-substituted polyphosphazene-polyester blend nanofiber matrices for load-bearing bone regeneration. / Deng, Meng; Kumbar, Sangamesh G.; Nair, Lakshmi S.; Weikel, Arlin L.; Allcock, Harry R.; Laurencin, Cato T.
In: Advanced Functional Materials, Vol. 21, No. 14, 22.07.2011, p. 2641-2651.Research output: Contribution to journal › Article
TY - JOUR
T1 - Biomimetic structures
T2 - Biological implications of dipeptide-substituted polyphosphazene-polyester blend nanofiber matrices for load-bearing bone regeneration
AU - Deng, Meng
AU - Kumbar, Sangamesh G.
AU - Nair, Lakshmi S.
AU - Weikel, Arlin L.
AU - Allcock, Harry R.
AU - Laurencin, Cato T.
PY - 2011/7/22
Y1 - 2011/7/22
N2 - Successful bone regeneration benefits from three-dimensional (3D) bioresorbable scaffolds that mimic the hierarchical architecture and mechanical characteristics of native tissue extracellular matrix (ECM). A scaffold platform that integrates unique material chemistry with nanotopography while mimicking the 3D hierarchical bone architecture and bone mechanics is reported. A biocompatible dipeptide polyphosphazene-polyester blend is electrospun to produce fibers in the diameter range of 50-500 nm to emulate dimensions of collagen fibrils present in the natural bone ECM. Various electrospinning and process parameters are optimized to produce blend nanofibers with good uniformity, appropriate mechanical strength, and suitable porosity. Biomimetic 3D scaffolds are created by orienting blend nanofiber matrices in a concentric manner with an open central cavity to replicate bone marrow cavity, as well as the lamellar structure of bone. This biomimicry results in scaffold stress-strain curve similar to that of native bone with a compressive modulus in the mid-range of values for human trabecular bone. Blend nanofiber matrices support adhesion and proliferation of osteoblasts and show an elevated phenotype expression compared to polyester nanofibers. Furthermore, the 3D structure encourages osteoblast infiltration and ECM secretion, bridging the gaps of scaffold concentric walls during in vitro culture. The results also highlight the importance of in situ ECM secretion by cells in maintaining scaffold mechanical properties following scaffold degradation with time. This study for the first time demonstrates the feasibility of developing a mechanically competent nanofiber matrix via a biomimetic strategy and the advantages of polyphosphazene blends in promoting osteoblast phenotype progression for bone regeneration. A new biomimetic scaffold design comprised of electrospun polymeric nanofibers combines unique material chemistry, hierarchical architecture, and mechanics suitable for load-bearing bone regeneration. Furthermore, the biomimicry-enabled scaffolds promote osteoblast migration, proliferation, phenotype progression, maturation, and mineralization while maintaining a uniform cell and extracellular matrix distribution. This nanofiber scaffold platform can also be adopted for regeneration of tissue interfaces such as bone-tendon.
AB - Successful bone regeneration benefits from three-dimensional (3D) bioresorbable scaffolds that mimic the hierarchical architecture and mechanical characteristics of native tissue extracellular matrix (ECM). A scaffold platform that integrates unique material chemistry with nanotopography while mimicking the 3D hierarchical bone architecture and bone mechanics is reported. A biocompatible dipeptide polyphosphazene-polyester blend is electrospun to produce fibers in the diameter range of 50-500 nm to emulate dimensions of collagen fibrils present in the natural bone ECM. Various electrospinning and process parameters are optimized to produce blend nanofibers with good uniformity, appropriate mechanical strength, and suitable porosity. Biomimetic 3D scaffolds are created by orienting blend nanofiber matrices in a concentric manner with an open central cavity to replicate bone marrow cavity, as well as the lamellar structure of bone. This biomimicry results in scaffold stress-strain curve similar to that of native bone with a compressive modulus in the mid-range of values for human trabecular bone. Blend nanofiber matrices support adhesion and proliferation of osteoblasts and show an elevated phenotype expression compared to polyester nanofibers. Furthermore, the 3D structure encourages osteoblast infiltration and ECM secretion, bridging the gaps of scaffold concentric walls during in vitro culture. The results also highlight the importance of in situ ECM secretion by cells in maintaining scaffold mechanical properties following scaffold degradation with time. This study for the first time demonstrates the feasibility of developing a mechanically competent nanofiber matrix via a biomimetic strategy and the advantages of polyphosphazene blends in promoting osteoblast phenotype progression for bone regeneration. A new biomimetic scaffold design comprised of electrospun polymeric nanofibers combines unique material chemistry, hierarchical architecture, and mechanics suitable for load-bearing bone regeneration. Furthermore, the biomimicry-enabled scaffolds promote osteoblast migration, proliferation, phenotype progression, maturation, and mineralization while maintaining a uniform cell and extracellular matrix distribution. This nanofiber scaffold platform can also be adopted for regeneration of tissue interfaces such as bone-tendon.
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U2 - 10.1002/adfm.201100275
DO - 10.1002/adfm.201100275
M3 - Article
VL - 21
SP - 2641
EP - 2651
JO - Advanced Functional Materials
JF - Advanced Functional Materials
SN - 1616-301X
IS - 14
ER -