Device Fabrication and Fluorescent Labeling of Preterm Birth Biomarkers for Microchip Electrophoresis.

Cyclic olefin copolymer Hot embossing Laser induced fluorescence Microfluidics Photolithography Point-of-care diagnostics Rapid analysis

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2019
Historique:
entrez: 9 3 2019
pubmed: 9 3 2019
medline: 8 8 2019
Statut: ppublish

Résumé

An unmet need exists for a clinical diagnostic to determine preterm birth (PTB) risk. Such an assessment is possible with high sensitivity and specificity using a panel of nine biomarkers. An integrated microfluidic analysis system for these biomarkers is being developed which includes microchip electrophoresis (μCE) separation. A t-shaped microchip device can be used to test the μCE portion of this integrated system to find appropriate separation conditions. These t-shaped microchips can be fabricated using photolithographically patterned Si templates and hot embossing. PTB biomarkers can be fluorescently labeled using an amine-reactive dye prior to μCE. The μCE conditions established using this t-shaped device should be useful in developing a complete integrated microfluidic system for PTB risk assessment.

Identifiants

pubmed: 30847791
doi: 10.1007/978-1-4939-9213-3_12
doi:

Substances chimiques

Biomarkers 0
Fluorescent Dyes 0
Silicon Z4152N8IUI

Types de publication

Journal Article

Langues

eng

Pagination

175-184

Références

World Health Organization (2012) Born too soon: the global action report on preterm birth. WHO, Geneva
March of Dimes (2013) Prematurity campaign: 2013 progress report. March of Dimes Foundation, White Plains
Esplin MS, Merrell K, Goldenberg R et al (2011) Proteomic identification of serum peptides predicting subsequent spontaneous preterm birth. Am J Obstet Gynecol 204:391e1–391e8
doi: 10.1016/j.ajog.2010.09.021
Sonker M, Knob R, Sahore V, Woolley AT (2017) Integrated electrokinetically driven microfluidic devices with pH-mediated solid-phase extraction coupled to microchip electrophoresis for preterm birth biomarkers. Electrophoresis 38:1743–1754
doi: 10.1002/elps.201700054
Sahore V, Sonker M, Nielsen AV, Knob R, Kumar S, Woolley AT (2018) Automated microfluidic devices integrating solid-phase extraction, fluorescent labeling, and microchip electrophoresis for preterm birth biomarker analysis. Anal Bioanal Chem 410:933–941
doi: 10.1007/s00216-017-0548-7
Sonker M, Parker EK, Nielsen AV, Sahore V, Woolley AT (2018) Electrokinetically operated microfluidic devices for integrated immunoaffinity monolith extraction and electrophoretic separation of preterm birth biomarkers. Analyst 143:224–231
doi: 10.1039/C7AN01357D
Nielsen AV, Nielsen JB, Knob R, Sahore V, Woolley AT (2018) Separation of a panel of preterm birth biomarkers using microchip electrophoresis. Electrophoresis 39:2300–2307
Beauchamp MJ, Nordin GP, Woolley AT (2017) Moving from millifluidic to truly microfluidic sub-100-μm cross-section 3D printed devices. Anal Bioanal Chem 409:4311–4319
doi: 10.1007/s00216-017-0398-3
Gong H, Bickham BP, Woolley AT, Nordin GP (2017) Custom 3D printer and resin for 18 μm × 20 μm microfluidic flow channels. Lab Chip 17:2899–2909
doi: 10.1039/C7LC00644F

Auteurs

Anna V Nielsen (AV)

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, USA.

Adam T Woolley (AT)

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, USA. atw@byu.edu.

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Classifications MeSH