Contents
Academic literature on the topic 'Matriz de colágeno de origen porcino'
Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles
Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Matriz de colágeno de origen porcino.'
Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.
You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.
Journal articles on the topic "Matriz de colágeno de origen porcino"
Gallón Nausa, Julian, and Diego Ernesto Castro Haiek. "Caracterización morfológica y Evaluación clínica de sustitutos óseos de origen porcino de la casa 3Biomat para su aplicación en lesiones óseas bimaxilares." Nova 15, no. 27 (August 10, 2017): 11. http://dx.doi.org/10.22490/24629448.1954.
Full textAlarcón, Marco Antonio, Karla Tatiana Diaz, and Milena Muñoz. "Recubrimiento de recesiones múltiples: Uso de matriz dérmica acelular vs. matriz de colágeno." Revista Estomatológica Herediana 26, no. 4 (March 16, 2017): 236. http://dx.doi.org/10.20453/reh.v26i4.3030.
Full textIsaac, Cesar, Francinni M. P. Rego, Pedro Ribeiro Soares de Ladeir, Silvana C. Altram, Renata C. de Oliveira, Johnny L. C. B. Aldunate, André O. Paggiaro, and Marcus Castro Ferreira. "Construção de substituto da pele composto por matriz de colágeno porcino povoada por fibroblastos dérmicos e queratinócitos humanos: avaliação histológica." Revista Brasileira de Cirurgia Plástica 27, no. 4 (December 2012): 503–8. http://dx.doi.org/10.1590/s1983-51752012000400004.
Full textCastejón S., Olivar, Oliver Castejón M., and Oliver Castejón M. "Microscopía electrónica de barrido de la transformación hidrópica de la vellosidad placentaria." Revista Peruana de Ginecología y Obstetricia 56, no. 1 (April 24, 2015): 44–49. http://dx.doi.org/10.31403/rpgo.v56i253.
Full textDissertations / Theses on the topic "Matriz de colágeno de origen porcino"
Castro, Rodríguez Yuri Alejandro. "Eficacia clínica de la matriz de colágeno de origen porcino versus el injerto conectivo subepitelial en el tratamiento de las recesiones gingivales Miller clase I y II." Bachelor's thesis, Universidad Nacional Mayor de San Marcos, 2015. https://hdl.handle.net/20.500.12672/4190.
Full textTesis
Gioia, Palavecino Claudio Francisco. "Ensayo clínico randomizado prospectivo experimental en humanos, del comportamiento de la matriz de colágeno de origen porcino (Mucoderm ®), usada sola o asociada a plasma rico en factores de crecimiento, en comparación con la técnica de injerto gingival libre." Doctoral thesis, Universidad de Murcia, 2016. http://hdl.handle.net/10803/371453.
Full text1. OBJECTIVES The aim of the present study was to evaluate weather the use of plasma rich in growth factors (PRGF) represents an improvement over the use of Mucoderm® alone, in patients with a limited amount of keratinized gingiva. 2. METHODS To develop this study, 21 patients were selected aged between 18 and 80 years who presented areas in which the presence of keratinized gingiva was less than 2 mm., existing bilateral involvement (maxillary or mandibular) and two teeth contiguous . In each individual patient hemimaxilla, free gingival graft was performed, using a collagen matrix of porcine origin (Mucoderm®) as graft material, in areas where there was a limited amount of keratinized gingiva. An area received the graft hydrated with saline solution and the other zone received the graft embedded in PRGF. The distribution of the regions and the type of treatment they would receive was randomly set. Pre- surgery and post-surgery (at 3 and 6 months) measures were taken in every patient. The following clinical parameters were recorded: amount and thickness of keratinized tissue and the presence and height of recessions. Statistical analysis was performed to determine the gain of keratinized gingiva using Mucoderm® as graft material, as well as differences between treated with PRGF and those with serum. 3. RESULTS When the band of keratinized gingiva was studied, we found that the average amount of keratinized gingiva in areas treated with saline solution was 1.19 mm. initially, of 2.35 mm. at 3 months and 2.43 mm . at 6 months . Mean in PRGF treated areas was: 1.22 mm . at the beginning , compared to 2.73 mm. at 3 months and 2.49 mm. at 6 months. When we evaluate the evolution of the average thickness of keratinized tissue, at baseline, areas treated with saline solution measured 0.88 mm., increasing to 1.05 mm. at 3 months and 6 months obtaining one mm. In areas treated with PRGF, the average thickness of keratinized gingiva at baseline was 0.88 mm., at 3 months was 1.05 mm. and at 6 months of a mm. Friedman test was applied to these two variables, and it determined a variation of measures over time. Wilcoxon Test determined that there was no statistically significant difference in the use of both products in terms of the band and thickness of keratinized tissue in the three measured times, except for the band of keratinized gingiva at three months, when the values of the group treated with PRGF were significantly higher. After analyzing the results obtained during the study, we were able to establish that Mucoderm® provides an improvement in the amount and thickness of keratinized gingiva and that the use of this matrix embedded in PRGF provides no additional profits to the results obtained when we used it alone, except at three -month, where there was significant differences, being the band of keratinized gingiva higher in areas treated with the graft hydrated in PRGF, although the result at the end of the study did not present significant differences between both groups.
Vilela, Antonella Sachsida Braga. "Matriz extracelular de pericardio fibroso porcino : estudo morfologico e bioquimico." [s.n.], 2006. http://repositorio.unicamp.br/jspui/handle/REPOSIP/316956.
Full textTese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia
Made available in DSpace on 2018-08-06T22:37:25Z (GMT). No. of bitstreams: 1 Vilela_AntonellaSachsidaBraga_D.pdf: 2767480 bytes, checksum: 9a51cd19ed225ec83edcd8d932e07114 (MD5) Previous issue date: 2006
Resumo: Tecido pericardial tem sido utilizado na confecção de biopróteses empregadas na reparação de diferentes lesões. Entretanto, calcificações e falência mecânica têm sido as principais causas de durabilidade limitada de biopróteses cardíacas fabricadas com pericárdio bovino. Nesse trabalho foi realizado um estudo do pericárdio fibroso porcino em sua estrutura microscópica e sua natureza bioquímica. A morfologia geral e a arquitetura das fibras colágenas e elásticas foram estudadas em tecido seccionado e também em montagens totais, corados por diferentes métodos histoquímicos e analisados em microscopia de luz convencional, de polarização, de fluorescência e confocal. O estudo bioquímico da matriz pericardial foram realizados de acordo com procedimentos bioquímicos pertinentes. O pericárdio mostrou-se um tecido altamente celularizado com características de tecido jovem. Os feixes colagênicos apresentaram-se arranjados em camadas multidirecionalmente orientadas, formando uma rede de trama fechada, com um número maior de fibras orientando-se obliquamente, partindo da região central inferior em direção súpero-lateral esquerda em relação ao coração. Uma discreta predominância de fibras colágenas no sentido base-ápice foi verificada na região anterior direita do pericárdio. A matriz extracelular apresentou-se pouco metacromática. Observaram-se finas fibrilas elásticas intimamente associadas às fibras colágenas, entrelaçadas em direções diversas ou paralelas entre si. Extração comparativa de componentes da matriz não revelou diferenças entre proteínas extraídas das regiões direita e esquerda e também entre material fresco e congelado. A análise em SDS-PAGE revelou dezesseis proteínas com valores de massa molecular aparente entre 11 e 109 kDa. Análises realizadas sugerem que o GAG encontrado possivelmente é o dermatam sulfato. Os dados obtidos podem subsidiar novos procedimentos direcionados à obtenção de biomembranas melhor preparadas e funcionalmente mais adequadas à construção de biopróteses.
Abstract: Pericardial tissue has been used to construct bioprostheses employed in the repair different kinds of injuries. However, calcification and mechanical failure have been the main causes of limited durability of cardiac bioprostheses constructed with bovine pericardium. In the course of this work a study has been conducted on the porcine fibrous pericardium and its microscopic structure and its biochemical nature. The general morphology and the architecture of the collagen and elastic fibers have been studied in sectioned tissue and also total assemblies, stained by diverse histochemical methods and analyzed by conventional light, polarizing light, fluorescence and confocal microscopy. Biochemical study of the pericardial matrix was conducted according to pertinent procedures. The pericardium was shown as a highly cellularized tissue with a vascular tree very ramified and collagen fibers arranged in multidirectionally oriented layers. A predominant direction was verified, with a larger number of fibers obliquely oriented, starting at the lower central region towards high-lateral-left relatively to the heart. A discreet predominance of collagen fibers is the base-apex direction was verified in the right-front region of the pericardium. Extracellular matrix with little metachromasy was observed, indicating small quantities of acid glycosaminoglycans. Fine elastic fibrils were observed, intimately associated to collagen fibers, interlaced in various directions or parallel to themselves. No differences were found between proteins extracted from the right or left regions and between fresh or frozen material. The quantities of extracted GAGs were too small to be detected by the method used. The SDS-PAGE showed proteins with values of apparent molecular mass between 11 and 109 kDa included two polydisperse bands around 71 and 85kDa. The ectrophoretic analysis showed that the found GAG is possibly dermatan sulfate.
Doutorado
Histologia
Doutor em Biologia Celular e Estrutural
Gasanz, Serrano Carlos. "Uso de una matriz de colágeno y elastina en la reparación de un defecto vesical con peritoneo parietal en modelo porcino." Doctoral thesis, Universitat Autònoma de Barcelona, 2018. http://hdl.handle.net/10803/666688.
Full textBladder reconstructive surgery consists in creating a substitute or an enlargement to the bladder. Currently, human intestine is the tissue used into clinical practice to make it possible although it has many relevant drawbacks. Human bladder engineering with other materials is merely anecdotic, and mostly in vitro and animal studies have been conducted. This thesis -supported by two articles- works towards the research of a material that could replace the intestine as the gold standard tissue for bladder reconstruction. The aim of the review article was to describe and classify the different biomaterials and explain the human clinical studies done so far. We concluded that if we had to choose an experimental method to perform a bladder reconstruction, current evidence suggests to opt for an acellular matrix or a synthetic polymer, and seed it with autologous urothelial cells, autologous smooth muscle cells and/or stem cells. The original article consisted of an experimental project conducted in a porcine model, in which we performed bladder augmentations using an autologous parietal peritoneum graft and determined whether the attachment or not of an acellular collagen–elastin matrix had better histologic and functional results. After six weeks, our data supports the benefit of an acellular collagen–elastin matrix to reinforce bladder regeneration in a porcine model of peritoneocystoplasty. Bladder reconstruction without using the intestine is still an enormous challenge nowadays despite of the improvements in providing new materials and cell cultures. In order to be able to set apart the intestine as the material to substitute the bladder, it is necessary to continue performing more studies, enroll more patients, increase the follow-up time and standardize the functional tests.