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Metallic foil-assisted laser cell printing.金属箔辅助激光细胞打印
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Biofabrication. 2010 Sep;2(3):032001. doi: 10.1088/1758-5082/2/3/032001. Epub 2010 Jul 12.
8
Paper-based ELISA.基于纸的酶联免疫吸附测定
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Diagnostics for the developing world: microfluidic paper-based analytical devices.发展中国家的诊断技术:微流控纸基分析器件。
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10
Quantification of the activity of biomolecules in microarrays obtained by direct laser transfer.通过直接激光转移获得的微阵列中生物分子活性的定量分析。
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基于激光诱导向前转移的纸质比色酶联免疫吸附测定。

Paper-based colorimetric enzyme linked immunosorbent assay fabricated by laser induced forward transfer.

机构信息

Optoelectronics Research Centre, University of Southampton, Highfield, Southampton SO17 1BJ, United Kingdom.

Clinical and Experimental Science, Faculty of Medicine and Institute for Life Sciences, University of Southampton and NIHR Wellcome Trust Clinical Research Facility and Respiratory Biomedical Research Unit, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.

出版信息

Biomicrofluidics. 2014 May 19;8(3):036502. doi: 10.1063/1.4878696. eCollection 2014 May.

DOI:10.1063/1.4878696
PMID:24926392
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4032417/
Abstract

We report the Laser Induced Forward Transfer (LIFT) of antibodies from a liquid donor film onto paper receivers for application as point-of-care diagnostic sensors. To minimise the loss of functionality of the active biomolecules during transfer, a dynamic release layer was employed to shield the biomaterial from direct exposure to the pulsed laser source. Cellulose paper was chosen as the ideal receiver because of its inherent bio-compatibility, liquid transport properties, wide availability and low cost, all of which make it an efficient and suitable platform for point-of-care diagnostic sensors. Both enzyme-tagged and untagged IgG antibodies were LIFT-printed and their functionality was confirmed via a colorimetric enzyme-linked immunosorbent assay. Localisation of the printed antibodies was exhibited, which can allow the creation of complex 2-d patterns such as QR codes or letters for use in a final working device. Finally, a calibration curve was determined that related the intensity of the colour obtained to the concentration of active antibodies to enable quantitative assessment of the device performance. The motivation for this work was to implement a laser-based procedure for manufacturing low-cost, point-of-care diagnostic devices on paper.

摘要

我们报告了从液体供体薄膜向纸接收器进行激光诱导正向转移(LIFT),以将抗体用作即时诊断传感器。为了在转移过程中最小化活性生物分子的功能损失,采用了动态释放层将生物材料屏蔽在脉冲激光源之外。由于纤维素纸具有固有的生物相容性、液体传输性能、广泛的可用性和低成本,因此它是即时诊断传感器的高效且合适的平台。酶标记和未标记的 IgG 抗体都通过 LIFT 进行打印,并通过比色酶联免疫吸附测定法确认其功能。显示了打印抗体的定位,这可以允许创建复杂的 2D 图案,如 QR 码或字母,用于最终的工作设备。最后,确定了校准曲线,该曲线将获得的颜色强度与活性抗体的浓度相关联,从而能够对设备性能进行定量评估。这项工作的动机是在纸上实施基于激光的低成本即时诊断设备制造程序。