Uncertainty quantification in modeling of microfluidic T-sensor based diffusion immunoassay.

Biomicrofluidics

Department of Mechanical Engineering, Indian Institute of Technology Delhi, New Delhi 110016, India.

Published: January 2016

AI Article Synopsis

  • Comparing experimental data with model predictions is crucial for accurately measuring properties like diffusion coefficients and species concentrations using a T-sensor.
  • Uncertainty in model predictions arises from uncertain values of parameters such as diffusion constants and flow speeds, which can significantly impact the results.
  • Utilizing polynomial chaos expansions for uncertainty quantification reveals that the diffusivity of the fluorescent probe antigen contributes most to the overall uncertainty, and indicates that measuring centerline fluorescence intensity improves detection reliability compared to using the first derivative of fluorescence intensity.

Article Abstract

Comparison of experimental data with modeling predictions is essential for making quantitative measurements of species properties, such as diffusion coefficients and species concentrations using a T-sensor. To make valid comparisons between experimental data and model predictions, it is necessary to account for uncertainty in model predictions due to uncertain values of model parameters. We present an analysis of uncertainty induced in model predictions of a T-sensor based competitive diffusion immunoassay due to uncertainty in diffusion constants, binding reaction rate constants, and inlet flow speed. We use a non-intrusive stochastic uncertainty quantification method employing polynomial chaos expansions to represent the dependence of uncertain species concentrations on the uncertainty in model parameters. Our simulations show that the uncertainties in model parameters lead to significant spatially varying uncertainty in predicted concentration. In particular, the diffusivity of fluorescently labeled probe antigen dominates the overall uncertainty. The predicted uncertainty in fluorescence intensity is minimum near the centerline of T-sensor and relatively high in the regions with gradients in fluorescence intensity. We show that using centerline fluorescence intensity instead of first derivative of fluorescence intensity as the system response for measuring sample antigen concentration in T-sensor based competitive diffusion immunoassay leads to lower uncertainty and higher detection sensitivity.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4714986PMC
http://dx.doi.org/10.1063/1.4940040DOI Listing

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