Literature DB >> 33090158

High-throughput roll-to-roll production of polymer biochips for multiplexed DNA detection in point-of-care diagnostics.

Pelin Toren1, Martin Smolka1, Anja Haase1, Ursula Palfinger1, Dieter Nees1, Stephan Ruttloff1, Ladislav Kuna1, Cindy Schaude1, Sandra Jauk1, Markus Rumpler2, Bettina Hierschlager3, Ingo Katzmayr3, Max Sonnleitner3, Manuel W Thesen4, Mirko Lohse4, Martin Horn5, Wilfried Weigel5, Matija Strbac6, Goran Bijelic6, Suhith Hemanth7, Nastasia Okulova7, Jan Kafka7, Stefan Kostler1, Barbara Stadlober1, Jan Hesse1.   

Abstract

Roll-to-roll UV nanoimprint lithography has superior advantages for high-throughput manufacturing of micro- or nano-structures on flexible polymer foils with various geometries and configurations. Our pilot line provides large-scale structure imprinting for cost-effective polymer biochips (4500 biochips/hour), enabling rapid and multiplexed detections. A complete high-volume process chain of the technology for producing structures like μ-sized, triangular optical out-couplers or capillary channels (width: from 1 μm to 2 mm, height: from 200 nm up to 100 μm) to obtain biochips (width: 25 mm, length: 75 mm, height: 100 μm to 1.5 mm) was described. The imprinting process was performed with custom-developed resins on polymer foils with resin thicknesses ranging between 125-190 μm. The produced chips were tested in a commercial point-of-care diagnostic system for multiplexed DNA analysis of methicillin resistant Staphylococcus aureus (e.g., mecA, mecC gene detections). Specific target DNA capturing was based on hybridisation between surface bound DNA probes and biotinylated targets from the sample. The immobilised biotinylated targets subsequently bind streptavidin-horseradish peroxidase conjugates, which in turn generate light upon incubation with a chemiluminescent substrate. To enhance the light out-coupling thus to improve the system performance, optical structures were integrated into the design. The limits-of-detection of mecA (25 bp) for chips with and without structures were calculated as 0.06 and 0.07 μM, respectively. Further, foil-based chips with fluidic channels were DNA functionalised in our roll-to-roll micro-array spotter following the imprinting. This straightforward approach of sequential imprinting and multiplexed DNA functionalisation on a single foil was also realised for the first time. The corresponding foil-based chips were able to detect mecA gene DNA sequences down to a 0.25 μM concentration.

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Year:  2020        PMID: 33090158     DOI: 10.1039/d0lc00751j

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


  3 in total

1.  Low-entry-barrier point-of-care testing of anti-SARS-CoV-2 IgG in the population of Upper Austria from December 2020 until April 2021-a feasible surveillance strategy for post-pandemic monitoring?

Authors:  Christian Doppler; Michael Feischl; Clara Ganhör; Spela Puh; Marina Müller; Michaela Kotnik; Teresa Mimler; Max Sonnleitner; David Bernhard; Christian Wechselberger
Journal:  Anal Bioanal Chem       Date:  2022-02-28       Impact factor: 4.142

Review 2.  Fabrication Methods for Microfluidic Devices: An Overview.

Authors:  Simon M Scott; Zulfiqur Ali
Journal:  Micromachines (Basel)       Date:  2021-03-18       Impact factor: 2.891

Review 3.  Recent Developments in Phenotypic and Molecular Diagnostic Methods for Antimicrobial Resistance Detection in Staphylococcus aureus: A Narrative Review.

Authors:  Andrea Sanchini
Journal:  Diagnostics (Basel)       Date:  2022-01-15
  3 in total

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