Integrated lab-on-a-chip: a combined sample preparation and PCR system as an ultrafast analytical tool for pathogen detection

2011 ◽  
Author(s):  
Holger Becker ◽  
Nadine Hlawatsch ◽  
Richard Klemm ◽  
Claudia Gärtner
Author(s):  
Mandy L. Y. Sin ◽  
Pak Kin Wong

AC electrokinetics is a promising approach for sample preparation and reaction enhancement in lab-on-a-chip devices. However, relative little has been done on the electrokinetic manipulation of physiological fluids and buffers with similar properties, such as conductivity. Herein, electrokinetic manipulation of fluids with a wide range of conductivities has been studied as a function of voltage and frequency. AC electrothermal flow is determined to dominate the fluid motion when the applied frequency of the AC potential is above 100 kHz. Interestingly, experimental data deviate from theoretical prediction for fluids with high conductivities (> 1 Sm−1). The deviation can be understood by voltage modulated electrochemical reactions and should be accounted for when manipulating clinical materials with high conductivities. The study will provide useful in sights in designing lab-on-a-chip devices for manipulating clinical samples in the future.


Author(s):  
Mylena Lemes Cunha ◽  
Stella Schuster da Silva ◽  
Mateus Cassaboni Stracke ◽  
Dalila Luciola Zanette ◽  
Mateus Nóbrega Aoki ◽  
...  

2019 ◽  
Vol 288 ◽  
pp. 171-179 ◽  
Author(s):  
K. Tsougeni ◽  
A.S. Kastania ◽  
G.D. Kaprou ◽  
Michael Eck ◽  
Gerhard Jobst ◽  
...  

2011 ◽  
Vol 77 (7) ◽  
pp. 2531-2533 ◽  
Author(s):  
Peter Rossmanith ◽  
Patrick Mester ◽  
Karin Frühwirth ◽  
Sabine Fuchs ◽  
Martin Wagner

ABSTRACTIn this study, we present the concept of internal sample process controls (ISPCs) to monitor the efficiency of an analytical chain using sample preparation and quantitative PCR (qPCR). A recombinantListeria monocytogenesΔprfA(targeted deletion) strain containing a competitive artificial single-copy genomic target was applied to naturally contaminated samples to demonstrate its analytical suitability as an ISPC.


Author(s):  
M. T. Taylor ◽  
P. Belgrader ◽  
R. Joshi ◽  
G. A. Kintz ◽  
M. A. Northrup

Lab on a Chip ◽  
2015 ◽  
Vol 15 (18) ◽  
pp. 3749-3759 ◽  
Author(s):  
G. Czilwik ◽  
T. Messinger ◽  
O. Strohmeier ◽  
S. Wadle ◽  
F. von Stetten ◽  
...  

Integrated PCR LabDisk and portable LabDisk-Player.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Fei Zhao ◽  
Eun Yeong Lee ◽  
Geun Su Noh ◽  
Jaehyup Shin ◽  
Huifang Liu ◽  
...  

Abstract Here, we describe a simple, universal protocol for use in nucleic acid testing-based pathogen diagnostics, which requires only hand-powered sample preparation, including the processes of pathogen enrichment and nucleic acid isolation. The protocol uses low-cost amine-functionalized diatomaceous earth with a 1-μm Teflon filter as a reaction matrix in both stages of the process, using homobifunctional imidoesters. Using a simple syringe as a pump, the capture efficiency for a large sample volume (<50 mL) was enhanced by up to 98.3%, and the detection limit was 1 CFU/mL, 100-fold better than that of common commercial nucleic acid isolation kit. This protocol can also be combined with commercialized 96-well filter plates for robust sample preparation. Our proposed system is robust, simple, low-cost, universal, and rapid (taking <20 min), and it works regardless of the ambient environment and sample pretreatment, requiring no electricity or instruments. Its benefits include the simplicity of producing its components and its ease of operation, and it can be readily integrated with other assays for point-of-care diagnostics.


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