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用于细胞培养和诊断的微纳加工表面设计

Microfabricated surface designs for cell culture and diagnosis.

作者信息

Matsuda T, Chung D J

机构信息

Department of Bioengineering, National Cardiovascular Center Research Institute, Osaka, Japan.

出版信息

ASAIO J. 1994 Jul-Sep;40(3):M594-7. doi: 10.1097/00002480-199407000-00068.

Abstract

Grooved and holed surfaces with a well fabricated design may serve as microsubstrates for cell culture and microreactors for diagnosis. In this study, the authors prepared chemically treated, micrometer scale grooved and holed glass surfaces by combined surface modification and ultraviolet (UV) excimer laser ablation techniques, as follows. 1) Microcell-culture substrate: Amino group attached glass surfaces, prepared by the treatment with an aminopropylsilane, were condensed with a carboxylated radical initiator. Subsequently, polyacrylamide was grafted by surface initiated radical polymerization to create a very hydrophilic surface layer. Ultraviolet excimer laser beams (KrF: 248 nm) were irradiated through a microscope onto surfaces to create grooves or holes that were 10 and 50 microns in width or diameter, respectively. The depth, depending on the irradiation light strength, ranged from a few to several tenths of a micrometer. On endothelial cell (EC) seeding, ECs adhered and grew on the bottoms of the grooved or holed surface where glass was exposed on ablation. Little cell adhesion was observed on non ablated, grafted surfaces. Endothelial cells aligned along the groove, resulting in very narrow tube like tissue formation, whereas ECs tended to form a multilayered spherical aggregate in a hole. A single cell resided in a 10 microns square hole. 2) Microreactor for diagnosis: The glass surface, treated with a fluorinated silane, was ablated to create round holes. On addition of a few microliters of water, water could be quantitatively transferred into a hole because of the water repellent characteristics of non ablated, fluorinated glass. As a model of a microreactor, enzyme reactions to affect different levels of glucose were carried out in tiny holed surfaces.

摘要

设计精良的带凹槽和孔洞的表面可作为细胞培养的微基质和诊断用的微反应器。在本研究中,作者通过表面改性和紫外(UV)准分子激光烧蚀技术相结合,制备了经过化学处理的微米级带凹槽和孔洞的玻璃表面,具体如下。1)微细胞培养基质:用氨丙基硅烷处理制备的氨基连接玻璃表面,与羧化自由基引发剂缩合。随后,通过表面引发自由基聚合接枝聚丙烯酰胺,以形成非常亲水的表面层。紫外准分子激光束(KrF:248nm)通过显微镜照射到表面上,以形成宽度或直径分别为10和50微米的凹槽或孔洞。深度取决于照射光强度,范围从几微米到几十微米。在内皮细胞(EC)接种时,ECs粘附并生长在烧蚀后玻璃暴露的带凹槽或孔洞表面的底部。在未烧蚀的接枝表面上几乎没有观察到细胞粘附。内皮细胞沿着凹槽排列,形成非常狭窄的管状组织,而ECs倾向于在孔中形成多层球形聚集体。单个细胞存在于10微米见方的孔中。2)诊断用微反应器:用氟化硅烷处理的玻璃表面被烧蚀以形成圆孔。加入几微升水后,由于未烧蚀的氟化玻璃的疏水特性,水可以定量转移到孔中。作为微反应器的模型,在微小的带孔表面上进行了影响不同葡萄糖水平的酶反应。

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