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Optimization of an Antibody Microarray Printing Process Using a Designed Experiment.
Summers, Alexander J; Devadhasan, Jasmine P; Gu, Jian; Montgomery, Douglas C; Fischer, Brittany; Gates-Hollingsworth, Marcellene A; Pflughoeft, Kathryn J; Vo-Dinh, Tuan; AuCoin, David P; Zenhausern, Frederic.
Afiliación
  • Summers AJ; Center for Applied NanoBioscience and Medicine, College of Medicine, University of Arizona, Phoenix, Arizona 85004, United States.
  • Devadhasan JP; Center for Applied NanoBioscience and Medicine, College of Medicine, University of Arizona, Phoenix, Arizona 85004, United States.
  • Gu J; Center for Applied NanoBioscience and Medicine, College of Medicine, University of Arizona, Phoenix, Arizona 85004, United States.
  • Montgomery DC; Department of Basic Medical Sciences, The University of Arizona, College of Medicine, 475 N 5th Street, Phoenix, Arizona 85004, United States.
  • Fischer B; School of Computing and Augmented Intelligence, Arizona State University, Tempe, Arizona 85287-1004, United States.
  • Gates-Hollingsworth MA; School of Computing and Augmented Intelligence, Arizona State University, Tempe, Arizona 85287-1004, United States.
  • Pflughoeft KJ; Department of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada 89557-0705, United States.
  • Vo-Dinh T; Department of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada 89557-0705, United States.
  • AuCoin DP; Fitzpatrick Institute for Photonics, Departments of Biomedical Engineering and Chemistry, Duke University, Durham, North Carolina 27708-0281, United States.
  • Zenhausern F; Department of Microbiology and Immunology, University of Nevada School of Medicine, Reno, Nevada 89557-0705, United States.
ACS Omega ; 7(36): 32262-32271, 2022 Sep 13.
Article en En | MEDLINE | ID: mdl-36120062
ABSTRACT
Antibody 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.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: ACS Omega Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: ACS Omega Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos