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1.
J Mater Sci Mater Med ; 20(1): 235-47, 2009 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18758917

RESUMEN

The present study describes the production of hyaluronan based porous microparticles by a semi-continuous gas anti-solvent (GAS) precipitation process to be used as a growth factor delivery system for in vivo treatment of ulcers. Operative process conditions, such as pressure, nozzle diameter and HYAFF11 solution concentrations, were adjusted to optimize particle production in terms of morphology and size. Scanning electron microscopy (SEM) and light scattering demonstrated that porous nano-structured particles with a size of 300 and 900 nm had a high specific surface suitable for absorption of growth factors from the aqueous environment within the polymeric matrix. Water acted as a plasticizer, enhancing growth factor absorption. Water contents within the HYAFF11 matrix were analyzed by differential scanning calorimetry (DSC). The absorption process was developed using fluorescence dyes and growth factors. Immunohistochemical analysis confirmed the high efficiency of absorption of growth factor and a mathematical model was generated to quantify and qualify the in vitro kinetics of growth factor release within the polymeric matrix. In vivo experiments were performed with the aim to optimize timed and focal release of PDGF to promote optimal tissue repair and regeneration of full-thickness wounds.


Asunto(s)
Materiales Biocompatibles/química , Sustancias de Crecimiento/administración & dosificación , Ácido Hialurónico/química , Nanopartículas/química , Nanopartículas/uso terapéutico , Úlcera Cutánea/terapia , Absorción , Animales , Masculino , Ensayo de Materiales , Microscopía Electrónica de Rastreo , Nanopartículas/ultraestructura , Nanotecnología/instrumentación , Factor de Crecimiento Derivado de Plaquetas/administración & dosificación , Ratas , Ratas Wistar , Úlcera Cutánea/tratamiento farmacológico , Úlcera Cutánea/patología , Andamios del Tejido , Factor de Crecimiento Transformador beta/administración & dosificación , Agua/química , Cicatrización de Heridas/efectos de los fármacos
2.
J Biomed Mater Res A ; 82(1): 213-21, 2007 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-17266017

RESUMEN

In this study we coated a new biocompatible, nanostructured titanium alloy, Ti13Nb13Zr, with a thin layer of hydroxyapatite nanocrystals and we investigated the response of human bone-marrow-derived mesenchymal cells. The coating was realized using a slightly supersaturated CaP solution, which provokes a fast deposition of nanocrystalline hydroxyapatite. A thin layer of deposition is appreciable on the etched Ti13Nb13Zr substrates after just 1.5 h soaking in the CaP solution, and it reaches a thickness of 1-2 mum after 3 h soaking. The coating seems thinner than that deposited on Ti6Al4V, which was examined for comparison, likely because of the different roughness profiles of the two etched alloys, and it is constituted of elongated HA nanocrystals, with a mean length of about 100 nm. Mesenchymal stem cells were seeded onto coated and uncoated Ti alloys and cultured for up to 35 days. Cell morphology, proliferation and differentiation were evaluated. The cells display good adhesion and proliferation on the uncoated substrates, whereas the presence of hydroxyapatite coating slightly reduces cell proliferation and induces differentiation of MSCs towards a phenotypic osteoblastic lineage, in agreement with the increase of the expression of osteopontin, osteonectin and collagen type I, evaluated by means of rt-PCR. Type I collagen expression is higher in Ti13Nb13Zr MSC culture compared to Ti6Al4V, standing for a more efficient extracellular matrix deposition.


Asunto(s)
Materiales Biocompatibles Revestidos/química , Durapatita/química , Células Madre Mesenquimatosas/citología , Nanopartículas/química , Titanio/química , Aleaciones/química , Secuencia de Bases , Células de la Médula Ósea/citología , Células de la Médula Ósea/metabolismo , Adhesión Celular , Técnicas de Cultivo de Célula/métodos , Diferenciación Celular , Proliferación Celular , Colágeno Tipo I/genética , Cartilla de ADN/genética , Expresión Génica , Humanos , Ensayo de Materiales , Células Madre Mesenquimatosas/metabolismo , Microscopía Electrónica de Rastreo , Osteoblastos/citología , Osteoblastos/metabolismo , Osteonectina/genética , Osteopontina/genética
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