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一种 3D 打印的流体装置,实现了集成功能。

A 3D printed fluidic device that enables integrated features.

机构信息

Department of Chemistry, Michigan State University, East Lansing, Michigan 48824, USA.

出版信息

Anal Chem. 2013 Jun 18;85(12):5622-6. doi: 10.1021/ac4009594. Epub 2013 May 29.

Abstract

Fluidic devices fabricated using conventional soft lithography are well suited as prototyping methods. Three-dimensional (3D) printing, commonly used for producing design prototypes in industry, allows for one step production of devices. 3D printers build a device layer by layer based on 3D computer models. Here, a reusable, high throughput, 3D printed fluidic device was created that enables flow and incorporates a membrane above a channel in order to study drug transport and affect cells. The device contains 8 parallel channels, 3 mm wide by 1.5 mm deep, connected to a syringe pump through standard, threaded fittings. The device was also printed to allow integration with commercially available membrane inserts whose bottoms are constructed of a porous polycarbonate membrane; this insert enables molecular transport to occur from the channel to above the well. When concentrations of various antibiotics (levofloxacin and linezolid) are pumped through the channels, approximately 18-21% of the drug migrates through the porous membrane, providing evidence that this device will be useful for studies where drug effects on cells are investigated. Finally, we show that mammalian cells cultured on this membrane can be affected by reagents flowing through the channels. Specifically, saponin was used to compromise cell membranes, and a fluorescent label was used to monitor the extent, resulting in a 4-fold increase in fluorescence for saponin treated cells.

摘要

使用传统软光刻技术制造的流体设备非常适合作为原型制作方法。三维(3D)打印技术常用于工业设计原型的生产,可以一步生产出设备。3D 打印机根据 3D 计算机模型逐层构建设备。在这里,创建了一种可重复使用、高通量、3D 打印的流体设备,该设备能够实现流动,并在通道上方集成了一个膜,以研究药物输送和影响细胞。该设备包含 8 个平行通道,宽 3 毫米,深 1.5 毫米,通过标准的螺纹配件与注射器泵连接。该设备还经过了打印处理,以允许与市售的膜插入件集成,其底部由多孔聚碳酸酯膜构成;该插入件可实现从通道到井上方的分子传输。当各种抗生素(左氧氟沙星和利奈唑胺)的浓度通过通道泵送时,约有 18-21%的药物通过多孔膜迁移,这表明该设备将非常适合研究药物对细胞的影响。最后,我们证明在该膜上培养的哺乳动物细胞可以受到流过通道的试剂的影响。具体来说,用皂素破坏细胞膜,并使用荧光标记物监测其程度,导致用皂素处理的细胞的荧光强度增加了 4 倍。

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