Literature DB >> 23471315

An enclosed in-gel PCR amplification cassette with multi-target, multi-sample detection for platform molecular diagnostics.

Dammika P Manage1, Jana Lauzon, Alexey Atrazev, Ravi Chavali, Roshini A Samuel, Brandon Chan, Y C Morrissey, Walter Gordy, Ann L Edwards, Kyle Larison, Stephanie K Yanow, Jason P Acker, George Zahariadis, Linda M Pilarski.   

Abstract

This work describes a self-contained, simple, disposable, and inexpensive gel capillary cassette for DNA amplification in near point of care settings. The cassette avoids the need for pumps or valves during raw sample delivery or polymerase chain reaction (PCR) amplification steps. The cassette contains capillary reaction units that can be stored at room temperature for up to 3 months. The current cassette configuration format simultaneously tests up to 16 patients for two or more targets, accommodates different sample types on the same cassette, has integrated positive and negative controls and allows flexibility for multiple geometries. PCR reagents in the cassette are desiccated to allow storage at room temperature with rehydration by raw sample at the time of testing. The sample is introduced to the cassette via a transfer pipette simply by capillary force. DNA amplification was carried out in a portable prototype instrument for PCR thermal cycling with fluorescence detection of amplified products by melt curve analysis (MCA). To demonstrate performance, raw genital swabs and urine were introduced to the same cassette to simultaneously detect four sexually transmitted infections. Herpes Simplex Viruses (HSV-1 and HSV-2) were detected from raw genital swabs. Ureaplasma urealyticum (UU) and Mycoplasma homonis (MH) were detected from raw urine. Results for multiple patients were obtained in as little as 50 min. This platform allows multiparameter clinical testing with a pre-assembled cassette that requires only the introduction of raw sample. Modification of the prototype device to accommodate larger cassettes will ultimately provide high throughput simultaneous testing of even larger numbers of samples for many different targets, as is required for some clinical applications. Combinations of wax and/or polymer cassettes holding capillary reaction units are feasible. The components of the cassette are suited to mass production and robotic assembly to produce a readily manufactured disposable reaction cassette that can be configured for disease-specific testing panels. Rapid testing with a disposable reaction cassette on an inexpensive instrument will enable on the spot evaluation of patients in the clinic for faster medical decision-making and more informed therapeutic choices.

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Year:  2013        PMID: 23471315     DOI: 10.1039/c3lc41419a

Source DB:  PubMed          Journal:  Lab Chip        ISSN: 1473-0189            Impact factor:   6.799


  8 in total

1.  Biomolecule storage on non-modified thermoplastic microfluidic chip by ink-jet printing of ionogels.

Authors:  M Tijero; R Díez-Ahedo; F Benito-Lopez; L Basabe-Desmonts; V Castro-López; A Valero
Journal:  Biomicrofluidics       Date:  2015-08-26       Impact factor: 2.800

2.  Probe-free real-time reverse transcription polymerase chain reaction assays for the detection and typing of porcine reproductive and respiratory syndrome virus in Canada.

Authors:  Michael Eschbaumer; Wansi May Li; Kerstin Wernike; Frank Marshall; Markus Czub
Journal:  Can J Vet Res       Date:  2015-07       Impact factor: 1.310

3.  Reagent integration and controlled release for multiplexed nucleic acid testing in disposable thermoplastic 2D microwell arrays.

Authors:  S Padmanabhan; A Sposito; M Yeh; M Everitt; I White; D L DeVoe
Journal:  Biomicrofluidics       Date:  2021-01-15       Impact factor: 2.800

4.  Detection of pathogenic Escherichia coli on potentially contaminated beef carcasses using cassette PCR and conventional PCR.

Authors:  Dammika P Manage; Jana Lauzon; Christina M Jones; Patrick J Ward; Linda M Pilarski; Patrick M Pilarski; Lynn M McMullen
Journal:  BMC Microbiol       Date:  2019-07-30       Impact factor: 3.605

Review 5.  Advances in Directly Amplifying Nucleic Acids from Complex Samples.

Authors:  Faye M Walker; Kuangwen Hsieh
Journal:  Biosensors (Basel)       Date:  2019-09-30

6.  Alberta Provincial Pediatric EnTeric Infection TEam (APPETITE): epidemiology, emerging organisms, and economics.

Authors:  Stephen B Freedman; Bonita E Lee; Marie Louie; Xiao-Li Pang; Samina Ali; Andy Chuck; Linda Chui; Gillian R Currie; James Dickinson; Steven J Drews; Mohamed Eltorki; Tim Graham; Xi Jiang; David W Johnson; James Kellner; Martin Lavoie; Judy MacDonald; Shannon MacDonald; Lawrence W Svenson; James Talbot; Phillip Tarr; Raymond Tellier; Otto G Vanderkooi
Journal:  BMC Pediatr       Date:  2015-07-31       Impact factor: 2.125

7.  A lab-on-chip for malaria diagnosis and surveillance.

Authors:  Brian J Taylor; Anita Howell; Kimberly A Martin; Dammika P Manage; Walter Gordy; Stephanie D Campbell; Samantha Lam; Albert Jin; Spencer D Polley; Roshini A Samuel; Alexey Atrazhev; Alex J Stickel; Josephine Birungi; Anthony K Mbonye; Linda M Pilarski; Jason P Acker; Stephanie K Yanow
Journal:  Malar J       Date:  2014-05-09       Impact factor: 2.979

8.  Monitoring food pathogens: Novel instrumentation for cassette PCR testing.

Authors:  Darin Hunt; Curtis Figley; Dammika P Manage; Jana Lauzon; Rachel Figley; Linda M Pilarski; Lynn M McMullen; Patrick M Pilarski
Journal:  PLoS One       Date:  2018-05-10       Impact factor: 3.240

  8 in total

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