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Design, fabrication and evaluation of a novel microfluidic based assay.

机译:一种基于微流的新型测定的设计,制造和评估。

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摘要

Microfabrication and microfluidic devices have been recognized as potential platforms for cell-based and drug screening studies. Human glioblastoma multiforme (hGBM) cells migrate inside the central nervous system (CNS) in narrow space constrictions and rarely metastasize through bloodstream. Hence, microfluidic devices consisting of narrow channels are considered as suitable models to study cell migration in vitro. Further the migratory capability of each individual cell could be easily obtained and quantified using such system.;This effort presents the design and development of an alternative microfluidic system that provides an integrated array of channels for screening multiple drugs simultaneously. This system is an altered version of traditional system, where a single unit is replaced with multiple units to achieve high-throughput multi-screening platform. The device is tailored to screen various types and doses of drugs simultaneously thus increasing its efficiency. This design has the advantage of using multiple types of drugs of varying concentrations to simultaneously study their effectiveness to inhibit cancer cell migration. Using this platform the migration characteristics of cancer cells in response to various anti-cancer drugs is investigated as part of this research effort. Also, the therapeutic potential of anti-cancer drugs were evaluated quantitatively, in comparison with standard cancer migration (scratch wound) assay.
机译:微加工和微流控设备已被认为是基于细胞和药物筛选研究的潜在平台。人多形胶质母细胞瘤(hGBM)细胞在狭窄的空间收缩区中枢神经系统(CNS)内迁移,很少通过血流转移。因此,由窄通道组成的微流体装置被认为是研究体外细胞迁移的合适模型。进一步地,使用这种系统可以容易地获得和定量每个细胞的迁移能力。这项工作提出了替代性微流体系统的设计和开发,该系统提供了用于同时筛选多种药物的整合通道阵列。该系统是传统系统的改进版本,其中单个单元替换为多个单元,以实现高通量多筛选平台。该设备经过定制,可同时筛选各种类型和剂量的药物,从而提高了效率。这种设计的优点是可以使用多种浓度不同的药物来同时研究其抑制癌细胞迁移的有效性。作为该研究工作的一部分,使用该平台研究了癌细胞对各种抗癌药物的响应迁移特性。此外,与标准的癌症迁移(划痕伤口)分析相比,定量评估了抗癌药物的治疗潜力。

著录项

  • 作者

    Dhavala, Sai Sirisha.;

  • 作者单位

    The University of Texas at Arlington.;

  • 授予单位 The University of Texas at Arlington.;
  • 学科 Engineering Biomedical.
  • 学位 M.S.
  • 年度 2013
  • 页码 80 p.
  • 总页数 80
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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