Document Detail


Incorporation of a sequential BMP-2/BMP-7 delivery system into chitosan-based scaffolds for bone tissue engineering.
MedLine Citation:
PMID:  19361857     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The aim of this study was to develop a 3-D construct carrying an inherent sequential growth factor delivery system. Poly(lactic acid-co-glycolic acid) (PLGA) nanocapsules loaded with bone morphogenetic protein BMP-2 and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) nanocapsules loaded with BMP-7 made the early release of BMP-2 and longer term release of BMP-7 possible. 3-D fiber mesh scaffolds were prepared from chitosan and from chitosan-PEO by wet spinning. Chitosan of 4% concentration in 2% acetic acid (CHI4-HAc2) and chitosan (4%) and PEO (2%) in 5% acetic acid (CHI4-PEO2-HAc5) yielded scaffolds with smooth and rough fiber surfaces, respectively. These scaffolds were seeded with rat bone marrow mesenchymal stem cells (MSCs). When there were no nanoparticles the initial differentiation rate was higher on (CHI4-HAc2) scaffolds but by three weeks both the scaffolds had similar alkaline phosphatase (ALP) levels. The cell numbers were also comparable by the end of the third week. Incorporation of nanoparticles into the scaffolds was achieved by two different methods: incorporation within the scaffold fibers (NP-IN) and on the fibers (NP-ON). It was shown that incorporation on the CHI4-HAc2 fibers (NP-ON) prevented the burst release observed with the free nanoparticles, but this did not influence the total amount released in 25 days. However NP-IN for the same fibers revealed a much slower rate of release; ca. 70% released at the end of incubation period. The effect of single, simultaneous and sequential delivery of BMP-2 and BMP-7 from the CHI4-HAc2 scaffolds was studied in vitro using samples prepared with both incorporation methods. The effect of delivered agents was higher with the NP-ON samples. Delivery of BMP-2 alone suppressed cell proliferation while providing higher ALP activity compared to BMP-7. Simultaneous delivery was not particularly effective on cell numbers and ALP activity. The sequential delivery of BMP-2 and BMP-7, on the other hand, led to the highest ALP activity per cell (while suppressing proliferation) indicating the synergistic effect of using both growth factors holds promise for the production of tissue engineered bone.
Authors:
Pinar Yilgor; Kadriye Tuzlakoglu; Rui L Reis; Nesrin Hasirci; Vasif Hasirci
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2009-04-09
Journal Detail:
Title:  Biomaterials     Volume:  30     ISSN:  1878-5905     ISO Abbreviation:  Biomaterials     Publication Date:  2009 Jul 
Date Detail:
Created Date:  2009-05-25     Completed Date:  2009-07-24     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8100316     Medline TA:  Biomaterials     Country:  England    
Other Details:
Languages:  eng     Pagination:  3551-9     Citation Subset:  IM    
Affiliation:
METU, BIOMAT, Department of Biotechnology, 06531 Ankara, Turkey.
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MeSH Terms
Descriptor/Qualifier:
Animals
Biocompatible Materials / adverse effects,  chemistry*
Bone Morphogenetic Protein 2 / chemistry*
Bone Morphogenetic Protein 7 / chemistry*,  pharmacology
Cell Proliferation / drug effects
Cell Survival / drug effects
Cells, Cultured
Chitosan / chemistry*
Lactic Acid / chemistry,  pharmacology
Male
Mesenchymal Stem Cells / cytology,  drug effects,  ultrastructure
Microscopy, Electron, Scanning
Polyglycolic Acid / chemistry,  pharmacology
Rats
Rats, Sprague-Dawley
Tissue Engineering / methods*
X-Ray Microtomography
Chemical
Reg. No./Substance:
0/Biocompatible Materials; 0/Bone Morphogenetic Protein 2; 0/Bone Morphogenetic Protein 7; 0/polylactic acid-polyglycolic acid copolymer; 26009-03-0/Polyglycolic Acid; 50-21-5/Lactic Acid; 9012-76-4/Chitosan

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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