3D printed microfluidic devices for integrated solid-phase extraction and microchip electrophoresis of preterm birth biomarkers.

3D printing Microchip electrophoresis Microfluidics Preterm birth biomarkers Sample preparation Solid-phase extraction

Journal

Analytica chimica acta
ISSN: 1873-4324
Titre abrégé: Anal Chim Acta
Pays: Netherlands
ID NLM: 0370534

Informations de publication

Date de publication:
01 Apr 2024
Historique:
received: 05 12 2023
revised: 31 01 2024
accepted: 04 02 2024
medline: 25 2 2024
pubmed: 25 2 2024
entrez: 24 2 2024
Statut: ppublish

Résumé

Preterm birth (PTB) is a leading cause of neonatal mortality, such that the need for a rapid and accurate assessment for PTB risk is critical. Here, we developed a 3D printed microfluidic system that integrated solid-phase extraction (SPE) and microchip electrophoresis (μCE) of PTB biomarkers, enabling the combination of biomarker enrichment and labeling with μCE separation and fluorescence detection. Reversed-phase SPE monoliths were photopolymerized in 3D printed devices. Microvalves in the device directed sample between the SPE monolith and the injection cross-channel in the serpentine μCE channel. Successful on-chip preconcentration, labeling and μCE separation of four PTB-related polypeptides were demonstrated in these integrated microfluidic devices. We further show the ability of these devices to handle complex sample matrices through the successful analysis of labeled PTB biomarkers spiked into maternal blood serum. The detection limit was 7 nM for the PTB biomarker, corticotropin releasing factor, in 3D printed SPE-μCE integrated devices. This work represents the first successful demonstration of integration of SPE and μCE separation of disease-linked biomarkers in 3D printed microfluidic devices. These studies open up promising possibilities for rapid bioanalysis of medically relevant analytes.

Sections du résumé

BACKGROUND BACKGROUND
Preterm birth (PTB) is a leading cause of neonatal mortality, such that the need for a rapid and accurate assessment for PTB risk is critical. Here, we developed a 3D printed microfluidic system that integrated solid-phase extraction (SPE) and microchip electrophoresis (μCE) of PTB biomarkers, enabling the combination of biomarker enrichment and labeling with μCE separation and fluorescence detection.
RESULTS RESULTS
Reversed-phase SPE monoliths were photopolymerized in 3D printed devices. Microvalves in the device directed sample between the SPE monolith and the injection cross-channel in the serpentine μCE channel. Successful on-chip preconcentration, labeling and μCE separation of four PTB-related polypeptides were demonstrated in these integrated microfluidic devices. We further show the ability of these devices to handle complex sample matrices through the successful analysis of labeled PTB biomarkers spiked into maternal blood serum. The detection limit was 7 nM for the PTB biomarker, corticotropin releasing factor, in 3D printed SPE-μCE integrated devices.
SIGNIFICANCE CONCLUSIONS
This work represents the first successful demonstration of integration of SPE and μCE separation of disease-linked biomarkers in 3D printed microfluidic devices. These studies open up promising possibilities for rapid bioanalysis of medically relevant analytes.

Identifiants

pubmed: 38401930
pii: S0003-2670(24)00139-9
doi: 10.1016/j.aca.2024.342338
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

342338

Informations de copyright

Copyright © 2024 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: GPN and ATW own shares in Acrea3D, a company that is commercializing 3D printers. The other authors have no conflicts to declare.

Auteurs

Joule E Esene (JE)

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, 84602, USA.

Addalyn J Burningham (AJ)

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, 84602, USA.

Anum Tahir (A)

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, 84602, USA.

Gregory P Nordin (GP)

Department of Electrical and Computer Engineering, Brigham Young University, Provo, UT, 84602, USA.

Adam T Woolley (AT)

Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT, 84602, USA. Electronic address: atw@byu.edu.

Classifications MeSH