Low-cost, facile droplet modification of screen-printed arrays for internally validated electrochemical detection of serum procalcitonin

被引:15
|
作者
de Oliveira, Paulo Roberto [1 ,2 ]
Crapnell, Robert D. [1 ]
Ferrari, Alejandro Garcia -Miranda [1 ]
Wuamprakhon, Phatsawit [1 ,3 ]
Hurst, Nicholas J. [1 ]
Dempsey-Hibbert, Nina C. [1 ]
Sawangphruk, Montree [3 ]
Janegitz, Bruno Campos [2 ]
Banks, Craig E. [1 ]
机构
[1] Manchester Metropolitan Univ, Fac Sci & Engn, Chester St, Manchester M1 5GD, England
[2] Univ Fed Sao Carlos, Lab Sensors Nanomed & Nanostruct Mat, BR-13600970 Araras, Brazil
[3] Vidyasirimedhi Inst Sci & Technol, Ctr Excellence Energy Storage Technol CEST, Sch Energy Sci & Engn, Dept Chem & Biomol Engn, Rayong 21210, Thailand
来源
BIOSENSORS & BIOELECTRONICS | 2023年 / 228卷
基金
巴西圣保罗研究基金会;
关键词
Electrochemistry; Screen-printed electrodes (SPE); Biosensor; Procalcitonin (PCT); Sepsis; Screen-printed arrays; SEPSIS; ELECTRODES; BIOMARKERS; DIAGNOSIS; THERAPY; FOOD;
D O I
10.1016/j.bios.2023.115220
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This manuscript presents the design and facile production of screen-printed arrays (SPAs) for the internally validated determination of raised levels of serum procalcitonin (PCT). The screen-printing methodology pro-duced SPAs with six individual working electrodes that exhibit an inter-array reproducibility of 3.64% and 5.51% for the electrochemically active surface area and heterogenous electrochemical rate constant respectively. The SPAs were modified with antibodies specific for the detection of PCT through a facile methodology, where each stage simply uses droplets incubated on the surface, allowing for their mass-production. This platform was used for the detection of PCT, achieving a linear dynamic range between 1 and 10 ng mL-1 with a sensor sensitivity of 1.35 x 10-10 NIC%/ng mL-1. The SPA produced an intra-and inter-day %RSD of 4.00 and 5.05%, with a material cost of 1.14 pound. Internally validated human serum results (3 sample measurements, 3 control) for raised levels of PCT (>2 ng mL-1) were obtained, with no interference effects seen from CRP and IL-6. This SPA platform has the potential to offer clinicians vital information to rapidly begin treatment for "query sepsis" patients while awaiting results from more lengthy remote laboratory testing methods. Analytical ranges tested make this an ideal approach for rapid testing in specific patient populations (such as neonates or critically ill patients) in which PCT ranges are inherently wider. Due to the facile modification methods, we predict this could be used for various analytes on a single array, or the array increased further to maintain the internal validation of the system.
引用
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页数:9
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