TY - JOUR
T1 - In vitro degradation of poly-L-D-lactic acid (PLDLA) pellets and powder used as synthetic alloplasts for bone grafting
AU - Coimbra, M. E.R.
AU - Elias, C. N.
AU - Coelho, P. G.
N1 - Funding Information:
Acknowledgments Thanks to Prof. Sidnei Paciornik, Image Digital Processing Laboratory, PUC-Rio, Rio de Janeiro, Brazil for processing the images and supplying the data for particle size distribution analysis, and to Major Cano, Department of Chemical Engineering, Military Institute of Engineering, Rio de Janeiro, Brazil for helping with the Thermal Analysis. This research was financially supported by CNPq (Brazil) grant 300216/94–7, 452834/03-1, 50016/052003 and 472449/2004-4, FAPERJ (Brazil) grant E-26/151.970/2004 and CAPES (Brazil). This research was also partly supported by the Department of Biomaterials and Biomimetics, New York University, College of Dentistry.
PY - 2008/10
Y1 - 2008/10
N2 - The objective of this study was to evaluate the in vitro degradation of pellet and powder forms of a poly-l-d-lactic acid material used to produce plates and screws for orthopedic, oral, and maxillofacial applications. Materials and methods: In order to produce the powder form the as-received pellets were milled in a cryogenic chamber. Particles size distribution (PSD) histograms were developed for both forms. The materials were then characterized by Scanning Electron Microscopy (SEM), Differential Scanning Calorimetry (DSC), and Thermogravimetric Analysis (TGA) before and after immersion in simulated body fluid for 30, 60, and 90 days. Results: SEM showed that for both forms material degradation started after 30 days of immersion in SBF and evolved until 90 days. Degradation started at the amorphous zones of the polymer and exposed of deeper crystalline layers. The pellet and powder samples PSD showed polydispersed patterns with mean diameters of 673.98 μm and 259.55 μm. Thermal onset degradation temperatures were 365.64°C and 360.30°C, and of 363.49°C and 359.83°C before immersion and after 90 days in SBF for the pellet and powder forms, respectively. The Tg's of the pellets and the powder were approximately 61.5°C and 66°C, and their respective endothermic peaks were observed at approximately 125°C and 120°C. The specific heat (c) was approximately 8.5 J/g and 6.2 J/g for the pellet and powder material, respectively. Conclusion: According to the results obtained, cryogenic milling resulted in particle plastic deformation, and alterations in glass transition temperature, melting temperature, and specific heat of the material.
AB - The objective of this study was to evaluate the in vitro degradation of pellet and powder forms of a poly-l-d-lactic acid material used to produce plates and screws for orthopedic, oral, and maxillofacial applications. Materials and methods: In order to produce the powder form the as-received pellets were milled in a cryogenic chamber. Particles size distribution (PSD) histograms were developed for both forms. The materials were then characterized by Scanning Electron Microscopy (SEM), Differential Scanning Calorimetry (DSC), and Thermogravimetric Analysis (TGA) before and after immersion in simulated body fluid for 30, 60, and 90 days. Results: SEM showed that for both forms material degradation started after 30 days of immersion in SBF and evolved until 90 days. Degradation started at the amorphous zones of the polymer and exposed of deeper crystalline layers. The pellet and powder samples PSD showed polydispersed patterns with mean diameters of 673.98 μm and 259.55 μm. Thermal onset degradation temperatures were 365.64°C and 360.30°C, and of 363.49°C and 359.83°C before immersion and after 90 days in SBF for the pellet and powder forms, respectively. The Tg's of the pellets and the powder were approximately 61.5°C and 66°C, and their respective endothermic peaks were observed at approximately 125°C and 120°C. The specific heat (c) was approximately 8.5 J/g and 6.2 J/g for the pellet and powder material, respectively. Conclusion: According to the results obtained, cryogenic milling resulted in particle plastic deformation, and alterations in glass transition temperature, melting temperature, and specific heat of the material.
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U2 - 10.1007/s10856-008-3425-2
DO - 10.1007/s10856-008-3425-2
M3 - Article
C2 - 18454304
AN - SCOPUS:50249086889
SN - 0957-4530
VL - 19
SP - 3227
EP - 3234
JO - Journal of Materials Science: Materials in Medicine
JF - Journal of Materials Science: Materials in Medicine
IS - 10
ER -