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首页> 外文期刊>Macromolecular bioscience >Efficacy of Crosslinking on Tailoring In Vivo Biodegradability of Fibro-Porous Decellularized Extracellular Matrix and Restoration of Native Tissue Structure:A Quantitative Study using Stereology Methods
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Efficacy of Crosslinking on Tailoring In Vivo Biodegradability of Fibro-Porous Decellularized Extracellular Matrix and Restoration of Native Tissue Structure:A Quantitative Study using Stereology Methods

机译:交联对调节纤维状多孔脱细胞细胞外基质的体内生物降解能力和恢复天然组织结构的功效:使用立体学方法的定量研究

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摘要

Cholecyst-derived extracellular matrix (CEM) is a fibro-porous decellularized serosal layer of porcine gall-bladder. CEM loses 90% of its weight at 48h of in vitro collagenase digestion, but takes two months to be completely resorbed in vivo. Carbodiimide (EDC) crosslinking helps tailoring CEM's in vitro collagenase susceptibility. Here, the efficacy of EDC crosslinking on tailoring in vivo biodegradability of CEM is reported. CEM crosslinked with 0.0005 and 0.0033×10~3M of EDC/mg that lose 80% and 0% of their weight respectively to in vitro collagenase digestion, were present even after 180 days in vivo. Quantitative histopathology using stereology methods confirmed our qualitative observation that even a tiny degree of crosslinking can significantly prolong the rate of in vivo degradation and removal of CEM.
机译:胆囊来源的细胞外基质(CEM)是猪胆囊的纤维孔脱细胞浆膜层。在体外胶原酶消化48小时后,CEM失去了90%的重量,但要在体内完全吸收需要两个月的时间。碳二亚胺(EDC)交联有助于定制CEM的体外胶原酶敏感性。在此,报道了EDC交联对定制CEM的体内生物降解性的功效。甚至在体内180天后,仍存在以0.0005和0.0033×10〜3M EDC / mg交联的CEM,它们分别失去其重量的80%和0%至体外胶原酶消化。使用立体学方法进行的定量组织病理学证实了我们的定性观察,即使很小的交联度也可以显着延长体内降解和CEM去除的速度。

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