Bioengineering PhD candidate working on point of care and wearable sensors for applications in oral health and broader healthcare domains.

University of Bologna

Chemical Engineering BA '18, University of Bologna

Georgia Institute of Technology

Materials Science and Engineering Master's Degree '20, Georgia Institute of Technology

Bioengineering PhD Candidate @ Polytechnic of Milan

Biomedical Engineering

Media Technology

Physiology

Astronomy And Astrophysics

Atomic And Molecular Physics, And Optics

Electrochemistry

Infectious Diseases

Oral Surgery

Bioengineering

Electrical And Electronic Engineering

Materials Chemistry

Cognitive Neuroscience

Demography

Pediatrics, Perinatology And Child Health

Cellular And Molecular Neuroscience

Information Systems

Statistical And Nonlinear Physics

Ecology, Evolution, Behavior And Systematics

Molecular Biology

Health, Toxicology And Mutagenesis

General Health Professions

Renewable Energy, Sustainability And The Environment

Rehabilitation

Pharmaceutical Science

Polymers And Plastics

Cultural Studies

Health Informatics

Transportation

Pulmonary And Respiratory Medicine

Biosensing

I am developing a sensor that will be used for diagnostic purposes to detect target analytes in biofluids and I've come across several protocols for the testing phase.Some authors dissolve the target analyte in 1x PBS, while others do that in 10x PBS. Since reports are not consistent, I was wondering if there were any tangible differences in using 1x vs 10x PBS solutions to detect my target analyte.If so, I'd like an advice on what I should use, considering the following conditions:- Target analyte: Ascorbic acid- Expected target biofluid: Saliva

What's the difference between using 1x PBS and 10x PBS for analytical applications?

What's the difference between using 1x PBS and 10x PBS for analytical applications?

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