Resumen:
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Poly(L-lactic acid) Poly(e-caprolactone) blends (PLLA/PCL) porous membranes were prepared by freeze extraction (a modification of freeze drying) with ratios 100/0, 80/20, 60/40, 40/60, 20/80, 0/100 in weight. Degradation ...[+]
Poly(L-lactic acid) Poly(e-caprolactone) blends (PLLA/PCL) porous membranes were prepared by freeze extraction (a modification of freeze drying) with ratios 100/0, 80/20, 60/40, 40/60, 20/80, 0/100 in weight. Degradation of the membranes in phosphate buffer solution (PBS) up to 65 weeks was studied using weight loss measurements, high performance liquid chromatography (HPLC), differential scanning calorimetry (DSC), mechanical indentation, gel permeation chromatography (GPC), and scanning electron microscopy (SEM). Degradation rate as observed by weight loss and reduction of molecular weight and mechanical properties depended on the composition of the blends. In most blends the degradation was more prominent in the PLLA phase and was accompanied by consequent recrystallization that formed a crystalline phase with increased resistance to hydrolysis. Occurrence of such crystalline phases and degradation of intercrystalline domain led to formation of nearly monodisperse molecular weight populations.
Membranes with only 20% PCL presented favorable behavior compared to pure PLLA membranes as reflected in a lower degradation rate and a limited loss of the mechanical properties. At the same time, degradation rate of 80/20 membranes was enhanced with respect to pure PCL, and membranes were stiffer than PCL membranes at all degradation times. This composition could thus be useful for use in tissue engineering for bone or cartilage applications.
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Agradecimientos:
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Luis Andres Gaona wishes to thank "Programa de Doctorados Nacionales 2009" of COLCIENCIAS (Departamento Administrativo de Ciencia, Tecnologia e Innovacion Colombia) and COOPEN Project (Colombia, Costa Rica, Panama and ...[+]
Luis Andres Gaona wishes to thank "Programa de Doctorados Nacionales 2009" of COLCIENCIAS (Departamento Administrativo de Ciencia, Tecnologia e Innovacion Colombia) and COOPEN Project (Colombia, Costa Rica, Panama and European Network) for supporting his PhD studies. Myriam Lebourg acknowledges UPV for funding through project PAID 06-10, and CIBER-BBN for funding her postdoc research. CIBER-BBN is an initiative funded by the VI National R&D&i Plan 2008-2011, Iniciativa Ingenio 2010, Consolider Program, CIBER Actions and financed by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund. Jose Luis Gomez Ribelles acknowledges the support of the Spanish Ministry of Science and Innovation through MAT2010-21611-C03-01 (including the FEDER financial support) and funding in the Centro de Investigacion Principe Felipe in the field of Regenerative Medicine through the collaboration agreement from the Conselleria de Sanidad (Generalitat Valenciana), and the Instituto de Salud Carlos III (Ministry of Science and Innovation). The authors wish also to thank the Microscopy Service and Instituto de Tecnologia Quimica of Universidad Politecnica de Valencia for useful help and advices.
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