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A pneumatically-driven microfluidic system for size-tunable generation of uniform cell-encapsulating collagen microbeads with the ultrastructure similar to native collagen

机译:气动微流控系统,用于大小可调的均匀包裹细胞的胶原微珠,超微结构类似于天然胶原

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摘要

This study reports a microfluidic system for high throughput, uniform, and size-tunable generation of cell-containing collagen microbeads. The principle is based on two pneumatically-driven mechanisms to achieve multichannel mixture suspension transportation, and to actuate the spotting actions of micro-vibrators that continuously generate tiny collagen micro-droplets into a thin oil layer and then a sterile Pluronic~® F127 surfactant solution located below. The temporarily formed collagen microdroplets are then thermally gelatinized. By regulating the feeding rate of cells/collagen suspension, and the spotting frequency of micro-vibrator, the size of the collagen microbeads can be manipulated. One of the key technical features is its capability to generate uniform collagen microbeads (coefficient of variation: 5.4-8.6 %) with sizes ranging from 73.9 to 349.3 μm in diameter. This is currently difficult to achieve using the existing methods particularly the generation of cell-encapsulating collagen microbeads with diameter less than 100 μm. Another advantageous trait is that the ultrastructure of the generated collagen microbeads is similar to that found in native collagen. In this study, moreover, the use of the proposed device for the mi-croencapsulation of 3T3 cells in collagen microbeads has been successfully demonstrated showing that the encapsulated cells maintained high cell viability (96±2 %). Furthermore, a reasonable proliferative capability of the encapsulated cells was observed during 7 days culture. As a whole, the proposed device has opened up a new route to generate cell-containing collagen microbeads, which is found particularly meaningful for biomedical applications.
机译:这项研究报告了一种微流控系统,用于高通量,均匀且大小可调的含细胞胶原微珠生成。该原理基于两种气动机构,以实现多通道混合物悬浮液的输送,并激活微振​​动器的点滴作用,该微振动器连续产生微小的胶原蛋白微滴,形成薄的油层,然后形成无菌的Pluronic〜®F127表面活性剂溶液位于下方。然后将临时形成的胶原蛋白微滴热糊化。通过调节细胞/胶原蛋白悬浮液的进料速度和微振动器的点检频率,可以控制胶原微珠的大小。关键技术特征之一是它能够生成直径范围从73.9到349.3μm的均匀胶原微珠(变异系数:5.4-8.6%)。当前,使用现有方法尤其是直径小于100μm的细胞包封胶原蛋白微珠的产生难以实现。另一个有利特征是产生的胶原微珠的超微结构与天然胶原中的超微结构相似。此外,在这项研究中,已成功地证明了所提出的装置用于胶原微珠中3T3细胞的微croencapsulation,显示了封装的细胞保持了高细胞活力(96±2%)。此外,在7天的培养过程中观察到了包囊细胞的合理的增殖能力。总体而言,拟议中的装置开辟了一条新的途径来生产含细胞的胶原微珠,这对于生物医学应用特别有意义。

著录项

  • 来源
    《Biomedical Microdevices》 |2014年第3期|345-354|共10页
  • 作者单位

    Graduate Institute of Biochemical and Biomedical Engineering, Chang Gung University, Taoyuan, Taiwan;

    Department of Orthopaedic Surgery, Chang Gung Memorial Hospital, Linko, Taiwan;

    Graduate Institute of Biochemical and Biomedical Engineering, Chang Gung University, Taoyuan, Taiwan;

    Graduate Institute of Biochemical and Biomedical Engineering, Chang Gung University, Taoyuan, Taiwan;

    Graduate Institute of Biochemical and Biomedical Engineering, Chang Gung University, Taoyuan, Taiwan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Microfluidics; Collagen; Microbeads; Microencapsulation; Pneumatic vibrator;

    机译:微流体;胶原;微珠;微囊化;气动振动器;

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