A magnetic nanoparticle-based microfluidic device fabricated using a 3D-printed mould for separation of Escherichia coli from blood

被引:6
|
作者
Joskowiak, Agnieszka [1 ,2 ,3 ]
Nogueira, Catarina L. [3 ,4 ,5 ]
Costa, Susana P. [1 ,2 ,3 ,4 ,5 ]
Cunha, Alexandra P. [1 ,2 ,3 ]
Freitas, Paulo P. [3 ,4 ,5 ]
Carvalho, Carla M. [3 ]
机构
[1] Univ Minho, Ctr Biol Engn, Campus Gualtar, P-4710057 Braga, Portugal
[2] LABBELS Associate Lab, Braga, Portugal
[3] Int Iberian Nanotechnol Lab, Av Mestre Jose Veiga S-N, P-4715330 Braga, Portugal
[4] Inst Engn Sistemas & Comp Microsistemas & Nanotecn, Rua Alves Redol 9, P-1000029 Lisbon, Portugal
[5] IN Inst Nanosci & Nanotechnolnol, Rua Alves Redol 9, P-1000029 Lisbon, Portugal
关键词
Microfluidic; 3D-printed; Magnetic nanoparticles; Escherichia coli; Bacteriophage receptor binding protein (RBP); Blood; STREAM INFECTIONS; DIAGNOSIS; SYSTEMS; SEPSIS;
D O I
10.1007/s00604-023-05924-7
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Herein, A microfluidic device is described, produced with a 3D-printed master mould that rapidly separates and concentrates Escherichia coli directly from whole blood samples, enabling a reduction in the turnaround time of bloodstream infections (BSIs) diagnosis. Moreover, it promotes the cleansing of the blood samples whose complexity frequently hampers bacterial detection. The device comprises a serpentine mixing channel with two inlets, one for blood samples (spiked with bacteria) and the other for magnetic nanoparticles (MNPs) functionalized with a (bacterio)phage receptor-binding protein (RBP) with high specificity for E. coli. After the magnetic labelling of bacteria throughout the serpentine, the microchannel ends with a trapping reservoir where bacteria-MNPs conjugates are concentrated using a permanent magnet. The optimized sample preparation device successfully recovered E. coli (on average, 66%) from tenfold diluted blood spiked within a wide range of bacterial load (10(2) CFU to 10(7) CFU mL(-1)). The non-specific trapping, tested with Staphylococcus aureus, was at a negligible level of 12%. The assay was performed in 30 min directly from diluted blood thus presenting an advantage over the conventional enrichment in blood cultures (BCs). The device is simple and cheap to fabricate and can be tailored for multiple bacterial separation from complex clinical samples by using RBPs targeting different species. Moreover, the possibility to integrate a biosensing element to detect bacteria on-site can provide a reliable, fast, and cost-effective point-of-care device.
引用
收藏
页数:9
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