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Development of a rapid in vitro tissue deadhesion system using the thermoresponsive sol-gel transition of hydroxybutyl chitosan

机译:利用羟基丁糖丁糖热素溶胶转化的热溶胶 - 凝胶转变的快速体外组织止血系统的研制

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In regenerative medicine, it has become increasingly important to collect cultured tissues using non-invasive methods. Enzymatic deadhesion is normally used to collect cells, but this method cannot be used when trying to collect whole tissues in order to avoid damaging cell-cell interactions. In order to resolve this issue, a thermoresponsive culture dish with poly(N-isopropyl acrylamide) (PNIPAAm) has been employed. This system can change its hydrophobicity depending on temperature. Thus, tissues can attach above 37 degrees C and be detached below 20 degrees C. However, the PNIPAAm system has some issues related to cost and detachment time. In this study, we developed a novel thermoresponsive detachment system using a polysaccharide derivative. We chose hydroxy butyl chitosan (HBC) as the thermoresponsive polymer because of its high biocompatibility and rapid phase transition. We developed a novel method of HBC synthesis in conditions that were milder than previously reported. We used spin-coating to make a thin coating on two kinds of culture dishes with various concentrations of HBC solution. Seeded cells attached to the surface at less than 0.5 mg/ml HBC coating concentration, and they could be successfully detached by simply lowering the temperature of the suspension dishes without enzymatic treatment; the cells took only 5-20 min to detach. To evaluate this system, we measured three metrics related to cell culturing on culture dishes: initial attachment rate, detachment rate and tissue detachment time. The study revealed that tissues could be detached faster on the suspension dishes used in this study than on PNIPAAm grafted dishes when HBC was coated at 0.5 mg/ml. We successfully developed a novel tissue detachment system using HBC. These results suggest that smart polymers may be useful in regenerative medicine.
机译:在再生药中,使用非侵入性方法收集培养的组织变得越来越重要。通常用于收集细胞的酶止血,但是在尝试收集整个组织时不能使用该方法以避免损坏细胞细胞相互作用。为了解决这个问题,已经采用了具有聚(N-异丙基丙烯酰胺)(PNIPAAM)的热反应性培养皿。该系统可以根据温度改变其疏水性。因此,组织可以在37摄氏度上方附着并在20摄氏度以下分离。然而,PNIPAAM系统具有与成本和脱离时间相关的一些问题。在这项研究中,我们开发了一种使用多糖衍生物的新型热响应脱离系统。由于其高生物相容性和快速相转变,我们选择羟基丁基壳聚糖(HBC)作为热响应聚合物。我们在比以前报告的条件下开发了一种新的HBC合成方法。我们使用旋转涂层在两种培养皿中制作薄涂层,具有各种浓度的HBC溶液。在表面上附着在表面上的种子细胞小于0.5mg / ml HBc涂层浓度,并且可以通过简单地降低悬浮盘的温度而不会酶处理来成功地分离;细胞只花了5-20分钟才能分离。为了评估该系统,我们测量了与培养皿上的细胞培养有关的三项度量:初始附着速率,分离率和组织分离时间。该研究表明,当HBc涂覆在0.5mg / ml时,组织可以在本研究中使用的悬浮皿上脱离悬浮液。我们成功开发了一种使用HBC的新型组织分离系统。这些结果表明,智能聚合物可用于再生药物。

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