Centrifugally driven microfluidic disc for detection of chromosomal translocations

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Centrifugally driven microfluidic disc for detection of chromosomal translocations. / Brøgger, Anna Line; Kwasny, Dorota; Bosco, Filippo; Silahtaroglu, Asli; Tümer, Zeynep; Boisen, Anja; Svendsen, Winnie Edith.

I: Lab On a Chip, Bind 12, Nr. 22, 21.11.2012, s. 4628-4634.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Brøgger, AL, Kwasny, D, Bosco, F, Silahtaroglu, A, Tümer, Z, Boisen, A & Svendsen, WE 2012, 'Centrifugally driven microfluidic disc for detection of chromosomal translocations', Lab On a Chip, bind 12, nr. 22, s. 4628-4634. https://doi.org/10.1039/c2lc40554g

APA

Brøgger, A. L., Kwasny, D., Bosco, F., Silahtaroglu, A., Tümer, Z., Boisen, A., & Svendsen, W. E. (2012). Centrifugally driven microfluidic disc for detection of chromosomal translocations. Lab On a Chip, 12(22), 4628-4634. https://doi.org/10.1039/c2lc40554g

Vancouver

Brøgger AL, Kwasny D, Bosco F, Silahtaroglu A, Tümer Z, Boisen A o.a. Centrifugally driven microfluidic disc for detection of chromosomal translocations. Lab On a Chip. 2012 nov. 21;12(22):4628-4634. https://doi.org/10.1039/c2lc40554g

Author

Brøgger, Anna Line ; Kwasny, Dorota ; Bosco, Filippo ; Silahtaroglu, Asli ; Tümer, Zeynep ; Boisen, Anja ; Svendsen, Winnie Edith. / Centrifugally driven microfluidic disc for detection of chromosomal translocations. I: Lab On a Chip. 2012 ; Bind 12, Nr. 22. s. 4628-4634.

Bibtex

@article{697934f700b34c31a73ed2af5d6d190f,
title = "Centrifugally driven microfluidic disc for detection of chromosomal translocations",
abstract = "Chromosome translocations are a common cause of congenital disorders and cancer. Current detection methods require use of expensive and highly specialized techniques to identify the chromosome regions involved in a translocation. There is a need for rapid yet specific detection for diagnosis and prognosis of patients. In this work we demonstrate a novel, centrifugally-driven microfluidic system for controlled manipulation of oligonucleotides and subsequent detection of chromosomal translocations. The device is fabricated in the form of a disc with capillary burst microvalves employed to control the fluid flow. The microvalves in series are designed to enable fluid movement from the center towards the periphery of the disc to handle DNA sequences representing translocation between chromosome 3 and 9. The translocation detection is performed in two hybridization steps in separate sorting and detection chambers. The burst frequencies of the two capillary burst microvalves are separated by 180 rpm enabling precise control of hybridization in each of the chambers. The DNA probes targeting a translocation are immobilized directly on PMMA by a UV-activated procedure, which is compatible with the disc fabrication method. The device performance was validated by successful specific hybridization of the translocation derivatives in the sorting and detection chambers.",
author = "Br{\o}gger, {Anna Line} and Dorota Kwasny and Filippo Bosco and Asli Silahtaroglu and Zeynep T{\"u}mer and Anja Boisen and Svendsen, {Winnie Edith}",
year = "2012",
month = nov,
day = "21",
doi = "10.1039/c2lc40554g",
language = "English",
volume = "12",
pages = "4628--4634",
journal = "Lab on a Chip",
issn = "1473-0197",
publisher = "Royal Society of Chemistry",
number = "22",

}

RIS

TY - JOUR

T1 - Centrifugally driven microfluidic disc for detection of chromosomal translocations

AU - Brøgger, Anna Line

AU - Kwasny, Dorota

AU - Bosco, Filippo

AU - Silahtaroglu, Asli

AU - Tümer, Zeynep

AU - Boisen, Anja

AU - Svendsen, Winnie Edith

PY - 2012/11/21

Y1 - 2012/11/21

N2 - Chromosome translocations are a common cause of congenital disorders and cancer. Current detection methods require use of expensive and highly specialized techniques to identify the chromosome regions involved in a translocation. There is a need for rapid yet specific detection for diagnosis and prognosis of patients. In this work we demonstrate a novel, centrifugally-driven microfluidic system for controlled manipulation of oligonucleotides and subsequent detection of chromosomal translocations. The device is fabricated in the form of a disc with capillary burst microvalves employed to control the fluid flow. The microvalves in series are designed to enable fluid movement from the center towards the periphery of the disc to handle DNA sequences representing translocation between chromosome 3 and 9. The translocation detection is performed in two hybridization steps in separate sorting and detection chambers. The burst frequencies of the two capillary burst microvalves are separated by 180 rpm enabling precise control of hybridization in each of the chambers. The DNA probes targeting a translocation are immobilized directly on PMMA by a UV-activated procedure, which is compatible with the disc fabrication method. The device performance was validated by successful specific hybridization of the translocation derivatives in the sorting and detection chambers.

AB - Chromosome translocations are a common cause of congenital disorders and cancer. Current detection methods require use of expensive and highly specialized techniques to identify the chromosome regions involved in a translocation. There is a need for rapid yet specific detection for diagnosis and prognosis of patients. In this work we demonstrate a novel, centrifugally-driven microfluidic system for controlled manipulation of oligonucleotides and subsequent detection of chromosomal translocations. The device is fabricated in the form of a disc with capillary burst microvalves employed to control the fluid flow. The microvalves in series are designed to enable fluid movement from the center towards the periphery of the disc to handle DNA sequences representing translocation between chromosome 3 and 9. The translocation detection is performed in two hybridization steps in separate sorting and detection chambers. The burst frequencies of the two capillary burst microvalves are separated by 180 rpm enabling precise control of hybridization in each of the chambers. The DNA probes targeting a translocation are immobilized directly on PMMA by a UV-activated procedure, which is compatible with the disc fabrication method. The device performance was validated by successful specific hybridization of the translocation derivatives in the sorting and detection chambers.

U2 - 10.1039/c2lc40554g

DO - 10.1039/c2lc40554g

M3 - Journal article

C2 - 22911443

VL - 12

SP - 4628

EP - 4634

JO - Lab on a Chip

JF - Lab on a Chip

SN - 1473-0197

IS - 22

ER -

ID: 40840799