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  • Royal Society of Chemistry (RSC)  (3)
  • Gijs, Martin A. M.  (3)
  • Biodiversity Research  (3)
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  • Royal Society of Chemistry (RSC)  (3)
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  • Biodiversity Research  (3)
  • 1
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2023
    In:  Lab on a Chip Vol. 23, No. 8 ( 2023), p. 2141-2141
    In: Lab on a Chip, Royal Society of Chemistry (RSC), Vol. 23, No. 8 ( 2023), p. 2141-2141
    Abstract: Correction for ‘Bubble-enhanced ultrasonic microfluidic chip for rapid DNA fragmentation’ by Lin Sun et al. , Lab Chip , 2022, 22 , 560–572, https://doi.org/10.1039/D1LC00933H.
    Type of Medium: Online Resource
    ISSN: 1473-0197 , 1473-0189
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2056646-3
    SSG: 12
    Location Call Number Limitation Availability
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  • 2
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Lab on a Chip Vol. 22, No. 3 ( 2022), p. 560-572
    In: Lab on a Chip, Royal Society of Chemistry (RSC), Vol. 22, No. 3 ( 2022), p. 560-572
    Abstract: DNA fragmentation is an essential process in developing genetic sequencing strategies, genetic research, as well as for the diagnosis of diseases with a genetic signature like cancer. Efficient on-chip DNA fragmentation protocols would be beneficial to process integration and open new opportunities for microfluidics in genetic applications. Here we present an acoustic microfluidic chip comprising an array of ultrasound-actuated microbubbles located at dedicated positions adjacent to a channel containing the DNA sample solution. The efficiency of the on-chip DNA fragmentation process arises mainly from tensile forces generated by acoustic streaming near the oscillating bubble interfaces, as well as a synergistic effect of streaming stress and ultrasonic cavitation. Acoustic microstreaming and the pressure distribution in the DNA channel were assessed by finite element simulation. We characterized the bubble-enhanced effect by measuring gene fragment size distributions with respect to different ultrasound parameters. For optimized on-chip conditions, purified lambda (λ) DNA (48.5 kbp) could be disrupted to fragments with an average size of 2 kbp after 30 s and down to 300 bp after 90 s. Mouse genomic DNA (1.4 kbp) fragmentation size decreased to 500 bp in 30 s and reduced further to 250 bp in 90 s. Bubble-induced fragmentation was more than 3 times faster than without bubbles. On-chip performance and process yield were found to be comparable to a sophisticated high-end commercial system. In this view, our new bubble-enhanced microfluidic approach is a promising tool for current and next generation sequencing platforms with high efficiency and good capacity. Moreover, the availability of an efficient on-chip DNA fragmentation process opens perspectives for implementing full molecular protocols on a single microfluidic platform.
    Type of Medium: Online Resource
    ISSN: 1473-0197 , 1473-0189
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2056646-3
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    Royal Society of Chemistry (RSC) ; 2022
    In:  Lab on a Chip Vol. 22, No. 21 ( 2022), p. 4224-4237
    In: Lab on a Chip, Royal Society of Chemistry (RSC), Vol. 22, No. 21 ( 2022), p. 4224-4237
    Abstract: Next-generation sequencing (NGS) is an essential technology for DNA identification in genomic research. DNA fragmentation is a critical step for NGS and doing this on-chip is of great interest for future integrated genomic solutions. Here we demonstrate fast acoustofluidic DNA fragmentation via ultrasound-actuated elastic polydimethylsiloxane (PDMS) microstructures that induce acoustic streaming and associated shear forces when placed in the field of an ultrasonic transducer. Indeed, acoustic streaming locally generates high tensile stresses that can mechanically stretch and break DNA molecule chains. The improvement in efficiency of the on-chip DNA fragmentation is due to the synergistic effect of these tensile stresses and ultrasonic cavitation phenomena. We tested these microstructure-induced effects in a DNA-containing microfluidic channel both experimentally and by simulation. The DNA fragmentation process was evaluated by measuring the change in the DNA fragment size over time. The chip works well with both long and short DNA chains; in particular, purified lambda (λ) DNA was cut from 48.5 kbp to 3 kbp in one minute with selected microstructures and further down to 300 bp within two and a half minutes. The fragment size of mouse genomic DNA was reduced from 1.4 kbp to 400 bp in one minute and then to 200 bp in two and a half minutes. The DNA fragmentation efficiency of the chip equipped with the PDMS microstructures was twice that of the chip without the microstructures. Exhaustive comparison shows that the on-chip fragmentation performance reaches the level of high-end professional standards. Recently, DNA fragmentation was shown to be enhanced using vibrating air microbubbles when the chip was placed in an acoustic field. We think the microbubble-free microstructure-based device we present is easier to operate and more reliable, as it avoids microbubble preparation and maintenance, while showing high DNA fragmentation performance.
    Type of Medium: Online Resource
    ISSN: 1473-0197 , 1473-0189
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2056646-3
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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