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1.
Chirurg ; 73(8): 827-32, 2002 Aug.
Artículo en Alemán | MEDLINE | ID: mdl-12425160

RESUMEN

The technology of Orthogonal Polarization Spectral Imaging (OPSI), patented in the United States in 1999, has been heralded as an alternative to conventional intravital microscopy for several reasons, including ease of application and ability to perform continued observations. In the following examples, OPSI was applied to reconstructive plastic surgery. Two experimental and one clinical model are presented. Currently, the image quality does not allow a qualitative analysis of the microvasculature. The data analysis of images remains inconclusive. However, a technically modified version with improved image resolution and software could become a valuable experimental as well as clinical tool in the field of reconstructive plastic surgery in the future.


Asunto(s)
Microcirculación , Microscopía de Polarización , Microcirugia , Procedimientos de Cirugía Plástica , Colgajos Quirúrgicos , Animales , Predicción , Humanos , Isquemia , Masculino , Membrana Mucosa/cirugía , Músculo Esquelético/irrigación sanguínea , Neoplasias Faríngeas/cirugía , Faringe/cirugía , Ratas , Reperfusión , Investigación , Programas Informáticos , Porcinos , Grabación en Video
2.
J Biomed Mater Res ; 58(3): 313-8, 2001 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-11319747

RESUMEN

Fibrous capsule formation around implants can inhibit solute exchange between implantable devices and the circulation. Parylene-n coated polycarbonate disks surrounded with growth factor reduced Matrigel (MG) or several gelatin-based matrices were implanted intramuscularly into rats for 21 or 50 days. MG supplemented with vascular endothelial growth factor (VEGF) or basic fibroblast growth factor (bFGF) increased capsule microvascular density at 21 days (p < 0.05) when compared to bare parylene-coated polycarbonate disks (control). The increased microvascular density around VEGF- and bFGF-treated implants regressed by 50 days and was no longer significantly different from controls. The microvascular density induced by the gelatin-based matrices was not significantly different from controls at 21 days, but was increased at 50 days (p < 0.05), suggesting a slower, long-term effect. Disks treated with MG and gelatin-based matrices had thinner capsules at 21 days (p < 0.05). By 50 days, the capsule thicknesses around these implants were no longer statistically thinner than controls. The capsule thickness around implants treated with VEGF, bFGF, and essential gelatin-based matrix was thinner than controls at 50 days (p < 0.05). These results indicate that it is possible to increase functional microvascular density within fibrous capsules using angiogenic growth factors and gelatin-based matrices. However, this effect may be short-lived, requiring chronic administration of growth factors.


Asunto(s)
Materiales Biocompatibles/farmacología , Hidrogeles/farmacología , Prótesis e Implantes , Animales , Factores de Crecimiento Endotelial/farmacología , Factor 2 de Crecimiento de Fibroblastos/farmacología , Reacción a Cuerpo Extraño/patología , Linfocinas/farmacología , Masculino , Ensayo de Materiales , Microcirculación/efectos de los fármacos , Microcirculación/patología , Prótesis e Implantes/efectos adversos , Ratas , Ratas Sprague-Dawley , Factores de Tiempo , Factor A de Crecimiento Endotelial Vascular , Factores de Crecimiento Endotelial Vascular
3.
Biomaterials ; 17(8): 759-64, 1996 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-8730959

RESUMEN

Cell population motility and adhesion of rat skin fibroblasts were evaluated on aminophase glass modified with covalently-immobilized biologically active peptides, specifically, either arginine glycine-aspartic acid-serine (RGDS) or tyrosine-isoleucine-glycine-serine-arginine-glycine (YIGSRG). Fibroblast population motility was decreased and adhesion was increased on substrates modified with covalently immobilized RGDS peptide compared to substrates with the covalently immobilized non-adhesive peptides arginine-glycine-glutamic acid-serine and arginine-aspartic acid-glycine-serine. Fibroblast motility was not significantly changed on substrates modified with covalently-immobilized YIGSRG peptide; however, fibroblast adhesion was decreased on that substrate.


Asunto(s)
Fibroblastos/citología , Péptidos/farmacología , Aminas/química , Secuencia de Aminoácidos , Análisis de Varianza , Animales , Sitios de Unión , Adhesión Celular/efectos de los fármacos , Movimiento Celular/efectos de los fármacos , Fibroblastos/metabolismo , Vidrio/química , Datos de Secuencia Molecular , Péptidos/química , Péptidos/metabolismo , Prótesis e Implantes , Ratas , Albúmina Sérica Bovina/química , Piel/citología , Solubilidad , Propiedades de Superficie
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