Early sepsis diagnosis via protein and miRNA biomarkers using a novel point-of-care photonic biosensor

被引:65
作者
Fabri-Faja, Nuria [1 ,2 ]
Calvo-Lozano, Olalla [1 ,2 ]
Dey, Priyanka [1 ,2 ]
Terborg, Roland A. [3 ]
Estevez, M-Carmen [1 ,2 ]
Belushkin, Alexander [4 ]
Yesilkoy, Filiz [4 ]
Duempelmann, Luc [3 ]
Altug, Hatice [4 ]
Pruneri, Valerio [3 ,5 ]
Lechuga, Laura M. [1 ,2 ]
机构
[1] CSIC, Catalan Inst Nanosci & Nanotechnol ICN2, Nanobiosensors & Bioanalyt Applicat Grp, CIBER BBN, Campus UAB, Bellaterra 08193, Barcelona, Spain
[2] BIST, Campus UAB, Bellaterra 08193, Barcelona, Spain
[3] Barcelona Inst Sci & Technol, ICFO Inst Ciencies Foton, Castelldefels 08860, Barcelona, Spain
[4] Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1015 Lausanne, Switzerland
[5] ICREA, Barcelona 08010, Spain
基金
欧盟地平线“2020”;
关键词
Point-of-care; Label-free multiplexed biosensing; Nanoplasmonics; Sepsis; Protein and miRNA biomarkers; Microarray; MICRORNAS; ANTIBODY;
D O I
10.1016/j.aca.2019.05.038
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
y Sepsis is a condition characterized by a severe stage of blood-infection often leading to tissue damage, organ failure and finally death. Fast diagnosis and identification of the sepsis stage (sepsis, severe sepsis or septic shock) is critical for the patient's evolution and could help in defining the most adequate treatment in order to reduce its mortality. The combined detection of several biomarkers in a timely, specific and simultaneous way could ensure a more accurate diagnosis. We have designed a new optical point-of-care (POC) device based on a phase-sensitive interferometric biosensor with a label-free microarray configuration for potential high-throughput evaluation of specific sepsis biomarkers. The sensor chip, which relies on the use of metallic nanostructures, provides versatility in terms of biofunctionalization, allowing the efficient immobilization of different kind of receptors such as antibodies or oligonucleotides. We have focused on two structurally different types of biomarkers: proteins, including C-reactive protein (CRP) and Interleukin 6 (IL6), and miRNAs, using miRNA-16 as an example. Limits of Detection (LoD) of 18 mu g mL(-1), 88 mu g mL(-1) and 1 mM (6 mu g mL(-1)) have been respectively obtained for CRP, IL6 and miRNA-16 in individual assays, with high accuracy and reproducibility. The multiplexing capabilities have also been assessed with the simultaneous analysis of both protein biomarkers. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:232 / 242
页数:11
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