Electrostatic capture of viruses on cationic biopolymer membranes for intra-oral disease sampling

Sunil Kumar Boda, Nora Willkomm, Maria S. Barrera, Louis Mansky, Conrado Aparicio

Research output: Contribution to journalArticlepeer-review

Abstract

Naso- and oropharyngeal swabs are the Center for Disease Control and Prevention (CDC) -recommended disease sampling methods for respiratory viruses. The short swabbing time for sampling by these methods may lead to variability in test results. Further, these methods are mildly invasive and can cause discomfort, tearing or gag reflexes in tested individuals. If longer sampling time is coupled with lesser patient discomfort, test reliability and patient compliance can be improved. Towards this end, we developed cationic biopolymer membranes for the electrostatic capturing of viruses in the oral cavity. Here, chemically (EDC-NHS) crosslinked uncharged chitosan (CS) nanofiber membranes were conferred either with negative surface charge by anionic poly-aspartic acid (pAsp) coating or positive charge by cationic poly-L-lysine (PLL). Consistent with our preliminary findings of dynamic light scattering (DLS) size measurements showing large agglomerates of anionic virus-like particles (VLPs) and cationic PLL in solution, a 75% increase in VLP adsorption by PLL coated CS membranes was recorded by enzyme linked immunosorbent assay (ELISA), in comparison to untreated controls. It is envisaged that the electrostatic concentration of respiratory viruses on cationic membranes can be superior alternatives to traditional swabbing in the oral cavity.

Original languageEnglish (US)
Article number113602
JournalColloids and Surfaces B: Biointerfaces
Volume232
DOIs
StatePublished - Dec 2023

Bibliographical note

Publisher Copyright:
© 2023 Elsevier B.V.

Keywords

  • Cationic biopolymer membranes
  • Disease sampling
  • Dynamic light scattering (DLS)
  • Electrostatic capture of viruses
  • Enzyme linked immunosorbent assay (ELISA)
  • Virus-like particles (VLPs)

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