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生物人工“双瓣叶”中叶瓣组织形成的原位观察与增强

In situ observation and enhancement of leaflet tissue formation in bioprosthetic "biovalve".

作者信息

Funayama Marina, Takewa Yoshiaki, Oie Tomonori, Matsui Yuichi, Tatsumi Eisuke, Nakayama Yasuhide

机构信息

Division of Medical Engineering and Materials, National Cerebral and Cardiovascular Center Research Institute, 5-7-1 Fujishiro-dai, Suita, Osaka, 565-8565, Japan.

出版信息

J Artif Organs. 2015 Mar;18(1):40-7. doi: 10.1007/s10047-014-0793-x. Epub 2014 Nov 5.

Abstract

Biovalves, autologous tri-leaflet valved conduits, are formed in the subcutaneous spaces of animals. The valves are formed using molds encapsulated with autologous connective tissues. However, tissue migration into the small apertures in the molds for leaflet formation is generally slower than that for conduit formation around the molds. In this study, the formation of the leaflet tissues was directly and non-invasively observed using a wireless capsule endoscope. The molds were assembled from 6 parts, one of which was impregnated with the endoscope, and embedded into subcutaneous pouches in goats (n = 30). Tissue ingrowth into the apertures gradually occurred from the edges of the leaflet parts. Tissue formation was accompanied by capillary formation. At 63.1 ± 17.1 days after embedding, the apertures were completely replaced with autologous connective tissue, forming the leaflet tissues. Leaflet formation was enhanced by including fat tissue (46.7 ± 4.2 days) or blood (41.1 ± 6.9 days) in the apertures before embedding. The creation of slit openings, in conjunction with addition of blood to the apertures, further enhanced leaflet formation (37.0 ± 2.8 days). Since leaflet formation could be observed endoscopically, the appropriate embedding period for complete biovalve formation could be determined.

摘要

生物瓣膜,即自体三叶瓣带瓣管道,在动物皮下空间形成。瓣膜通过包裹自体结缔组织的模具形成。然而,组织迁移到用于小叶形成的模具小孔中的速度通常比围绕模具形成管道的速度慢。在本研究中,使用无线胶囊内窥镜直接且无创地观察小叶组织的形成。模具由6个部分组装而成,其中一个部分装有内窥镜,并植入山羊(n = 30)的皮下袋中。组织从小叶部分的边缘逐渐向内生长到小孔中。组织形成伴随着毛细血管形成。植入后63.1±17.1天,小孔完全被自体结缔组织取代,形成小叶组织。在植入前向小孔中加入脂肪组织(46.7±4.2天)或血液(41.1±6.9天)可增强小叶形成。与向小孔中添加血液相结合,创建狭缝开口进一步增强了小叶形成(37.0±2.8天)。由于可以通过内窥镜观察小叶形成,因此可以确定完整生物瓣膜形成的合适植入期。

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