Show simple item record

dc.contributor.authorSummers, A.J.
dc.contributor.authorDevadhasan, J.P.
dc.contributor.authorGu, J.
dc.contributor.authorMontgomery, D.C.
dc.contributor.authorFischer, B.
dc.contributor.authorGates-Hollingsworth, M.A.
dc.contributor.authorPflughoeft, K.J.
dc.contributor.authorVo-Dinh, T.
dc.contributor.authorAucoin, D.P.
dc.contributor.authorZenhausern, F.
dc.date.accessioned2022-10-24T23:48:32Z
dc.date.available2022-10-24T23:48:32Z
dc.date.issued2022
dc.identifier.citationSummers, A. J., Devadhasan, J. P., Gu, J., Montgomery, D. C., Fischer, B., Gates-Hollingsworth, M. A., Pflughoeft, K. J., Vo-Dinh, T., Aucoin, D. P., & Zenhausern, F. (2022). Optimization of an Antibody Microarray Printing Process Using a Designed Experiment. ACS Omega.
dc.identifier.issn2470-1343
dc.identifier.doi10.1021/acsomega.2c03595
dc.identifier.urihttp://hdl.handle.net/10150/666448
dc.description.abstractAntibody microarrays have proven useful in immunoassay-based point-of-care diagnostics for infectious diseases. Noncontact piezoelectric inkjet printing has advantages to print antibody microarrays on nitrocellulose substrates for this application due to its compatibility with sensitive solutions and substrates, simple droplet control, and potential for high-capacity printing. However, there remain real-world challenges in printing such microarrays, which motivated this study. The effects of three concentrations of capture antibody (cAb) reagents and nozzle hydrostatic pressures were chosen to investigate three responses: the number of printed membrane disks, dispensing performance, and microarray quality. Printing conditions were found to be most ideal with 5 mg/mL cAb and a nozzle hydrostatic pressure near zero, which produced 130 membrane disks in a single print versus the 10 membrane disks per print before optimization. These results serve to inform efficient printing of antibody microarrays on nitrocellulose membranes for rapid immunoassay-based detection of infectious diseases and beyond. © 2022 The Authors. Published by American Chemical Society.
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.rightsCopyright © 2022 The Authors. Published by American Chemical Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License.
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.titleOptimization of an Antibody Microarray Printing Process Using a Designed Experiment
dc.typeArticle
dc.typetext
dc.contributor.departmentCenter for Applied NanoBioscience and Medicine, College of Medicine, University of Arizona
dc.contributor.departmentDepartment of Basic Medical Sciences, University of Arizona, College of Medicine
dc.contributor.departmentDepartment of Biomedical Engineering, University of Arizona, College of Engineering
dc.identifier.journalACS Omega
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal published version
dc.source.journaltitleACS Omega
refterms.dateFOA2022-10-24T23:48:32Z


Files in this item

Thumbnail
Name:
acsomega.2c03595.pdf
Size:
7.755Mb
Format:
PDF
Description:
Final Published Version

This item appears in the following Collection(s)

Show simple item record

Copyright © 2022 The Authors. Published by American Chemical Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License.
Except where otherwise noted, this item's license is described as Copyright © 2022 The Authors. Published by American Chemical Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License.