Quantification and profiling of urine cells by integrated cytocentrifugation and infrared spectroscopy.

Autors de IIS La Fe

• Guillermo Quintas Soriano

  Autor

• Julia Kuligowski

  Autor

Autors aliens a IIS La Fe

• Navarro-Esteve, Victor
• Felderer, Birgit
• Wood, Bayden R
• Perez-Guaita, David

Grups d'Investigació

• Perinatología

  

  Leader

  Máximo Vento Torres

Abstract

The presence of cells in urine and in particular White Blood Cells (WBCs) is often associated with Urinary Tract Infections (UTIs) and other diseases. Non-invasive screening of WBCs requires the development of cost-effective point of care diagnostic tools. Infrared (IR) spectroscopy has the potential to identify and quantify cells in urine. However, the quantification of cells by compact IR spectrophotometers can be hindered by the presence of highly concentrated interfering biomolecules. The use of separation procedures can assist in identifying and quantifying cells but reduces the point of care capabilities of the technology. In this study, we propose coupling cytocentrifugation with transflection IR spectroscopy for the isolation and quantification of cells in urine. Urine samples were spiked with monocytes and T-lymphocytes, cyto-centrifuged onto low-e slides and measured in transflection mode. An optional cell clean-up step, either performed before (by resuspending in PBS) or after the cytocentrifugation (by soaking the slide in water), was evaluated. In a first experiment using monocytes, IR band areas were linear (R2=0.98) in the 8*103-2*105cellsmL-1 range, thus demonstrating the detection of cells at pathological numbers (pyuria, i.e., >104 WBCs mL-1). Secondly, to mimic real samples with varying cell types, urine samples containing both monocytes and T-lymphocytes were analysed to determine their concentration simultaneously. Partial Least Squares (PLS) regression enabled the simultaneous quantification of two types of different cells, yielding prediction errors of 2*104cellsmL-1 for monocytes and 4*104cellsmL-1 for T-lymphocytes. The results suggest that the technique has the potential to be implemented as a fast, simple, versatile, and cost-effective method for quantifying and profiling cells in urine.