Online SERS Quantification of Staphylococcus aureus and the Application to Diagnostics in Human Fluids

被引:54
作者
Catala, Carme [1 ,2 ,3 ]
Mir-Simon, Bernat [3 ,4 ]
Feng, Xiaotong [1 ,2 ,3 ]
Cardozo, Celia [5 ,6 ]
Pazos-Perez, Nicolas [1 ,2 ,3 ]
Pazos, Elena [1 ,2 ]
Gomez-de Pedro, Sara [3 ]
Guerrini, Luca [3 ]
Soriano, Alex [5 ,6 ]
Vila, Jordi [7 ,8 ]
Marco, Francec [7 ,8 ]
Garcia-Rico, Eduardo [9 ]
Alvarez-Puebla, Ramon A. [1 ,2 ,10 ]
机构
[1] Univ Rovira & Virgili, Carrer Marcel Li Domingo S-N, E-43007 Tarragona, Spain
[2] Ctr Tecnol Quim Cataluna, Carrer Marcel Li Domingo S-N, Tarragona 43007, Spain
[3] Medcom Adv SA, Av Roma, Barcelona 08840, Spain
[4] Univ Autonoma Barcelona, Dept Surg, UD Vall dHebron Sch Med, Barcelona, Spain
[5] Univ Barcelona, Dept Infect Dis, Hosp Clin & Sch Med, E-08036 Barcelona, Spain
[6] Univ Barcelona, Inst Invest Biomed August Pi i Sunyer IDIBAPS, E-08036 Barcelona, Spain
[7] Univ Barcelona, Hosp Clin & Sch Med, Dept Clin Microbiol, E-08036 Barcelona, Spain
[8] Univ Barcelona, Hosp Clin, Barcelona Ctr Int Hlth Res CRESIB, ISGlobal, E-08036 Barcelona, Spain
[9] Hosp Univ Hm Madrid Torrelodones, Dept Clin Oncol, Madrid 28250, Spain
[10] ICREA, Passeig Lluis Co 23, Barcelona 08010, Spain
关键词
ENHANCED RAMAN-SPECTROSCOPY; BACTERIA; APTAMERS; TAGS; IDENTIFICATION; NANOPROBES; CHALLENGES; SCATTERING;
D O I
10.1002/admt.201600163
中图分类号
T [工业技术];
学科分类号
120111 [工业工程];
摘要
Staphylococcus aureus is a common cause of serious infections. One of the main drawbacks in its treatment is the time required for a positive diagnosis, over 24 h, as most methods are still based in bacterial culture. Herein, a microfluidic optical device for the rapid and ultrasensitive quantification of S. aureus in real human fluids is designed. In this approach, the surface-enhanced Raman scattering (SERS)-encoded particles, functionalized with either an antibody or an aptamer, form a dense collection of electromagnetic hot spots on the surface of S. aureus. This allows for an exponentially increase of the SERS signal when particles accumulate on the microorganism as compared to their free condition in bulk solution. Quantification is achieved by passing the sample through a microfluidic device with a collection window where a laser interrogates and classifies each of the induced bacteria-nanoparticle aggregates in real time. Further, the advantages of using aptamers versus antibodies as biorecognition elements are extensively investigated.
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页数:9
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