Influence of ultrasonic processing on the macromolecular properties of poly (D,L-lactide-co-glycolide) alone and in its biocomposite with hydroxyapatite
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作者:
Vukomanovic, Marija
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Serbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, SerbiaSerbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
Vukomanovic, Marija
[1
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Mitric, Miodrag
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Inst Nucl Sci Vinca, Belgrade, SerbiaSerbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
Mitric, Miodrag
[2
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Skapin, Sreco D.
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Jozef Stefan Inst, Ljubljana, SloveniaSerbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
Skapin, Sreco D.
[3
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Zagar, Ema
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Natl Inst Chem, Ljubljana, SloveniaSerbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
Zagar, Ema
[4
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Plavec, Janez
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Natl Inst Chem, Ljubljana, SloveniaSerbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
Plavec, Janez
[4
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Ignjatovic, Nenad
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Serbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, SerbiaSerbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
Ignjatovic, Nenad
[1
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Uskokovic, Dragan
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Serbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, SerbiaSerbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
Uskokovic, Dragan
[1
]
机构:
[1] Serbian Acad Arts & Sci, Inst Tech Sci, Belgrade 11000, Serbia
In this work poly(D,L-lactide-co-glycolide) (PLGA) and a poly(D,L-lactide-co-glycolide)/hydroxyapatite (PLGA/HAp) composite processed in an ultrasonic field at higher (25 degrees C) and lower (8 degrees C) temperatures were studied with respect to the molecular properties of the obtained materials. The processing of the PLGA and the PLGA/HAp composite in an ultrasonic field resulted in a change of molar mass averages of the polymer/polymeric part of these materials, while an amorphous structure and a 50:50 lactide-to-glycolide co-monomer ratio were preserved without the formation of crystalline oligomers. However, mobility of polymeric chains obtained after ultrasonic processing was lower indicating ordering the structure of polymeric chains as a result of processing. Additionally, it was observed that the mobility of the PLGA macromolecules was lower within the composite in comparison with the mobility of the chains within the PLGA alone in the case when both were obtained after ultrasonic processing. This was a consequence of the structure formation through the interactions between the PLGA and the HAp. Based on these results different degradation rate of PLGA in composite can be expected, which is important in the application of this material for the controlled drug delivery of medicaments. (C) 2010 Elsevier B.V. All rights reserved.