Rapid Multiplexed Detection on Lateral-Flow Devices Using a Laser Direct-Write Technique

被引:18
作者
He, Peijun J. W. [1 ]
Katis, Ioannis N. [1 ]
Eason, Robert W. [1 ]
Sones, Collin L. [1 ]
机构
[1] Univ Southampton, Optoelect Res Ctr, Southampton SO17 1BJ, Hants, England
来源
BIOSENSORS-BASEL | 2018年 / 8卷 / 04期
基金
英国工程与自然科学研究理事会;
关键词
lateral-flow device; multiplexed detection; laser direct-write; biosensors; inflammation detection; VISUAL DETECTION; VIRAL AMPLICONS; PAPER; POINT; ASSAY;
D O I
10.3390/bios8040097
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Paper-based lateral flow devices (LFDs) are regarded as ideal low-cost diagnostic solutions for point-of-care (POC) scenarios that allow rapid detection of a single analyte within a fluidic sample, and have been in common use for a decade. In recent years, there has been an increasing need for rapid and simultaneous detection of multiple analytes present within a single sample and to facilitate this, we report here a novel solution-detection using a multi-path LFD created via the precise partitioning of the single flow-path of a standard LFD using our previously reported laser direct-write (LDW) technique. The multiple flow-paths allow the simultaneous detection of the different analytes individually within each of the parallel channels without any cross-reactivity. The appearance of coloured test lines in individual channels indicates the presence of the different analytes within a sample. We successfully present the use of a LDW-patterned multi-path LFD for multiplexed detection of a biomarker panel comprising C-reactive protein (CRP) and Serum amyloid A-1 (SAA1), used for the diagnosis of bacterial infections. Overall, we demonstrate the use of our LDW technique in the creation of a novel LFD that enables multiplexed detection of two inflammation markers within a single LFD providing a detection protocol that is comparatively more efficient than the standard sequential multiplexing procedure.
引用
收藏
页数:11
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