Abstract

Abstract. Fluorescent dyed polystyrene latex spheres (PSLs) are commonly used for characterization and calibration of instruments detecting fluorescence signals from particles suspended in the air and other fluids. Instruments like the Ultraviolet Aerodynamic Particle Sizer (UV-APS) and the Waveband Integrated Bioaerosol Sensor (WIBS) are widely used for bioaerosol research, but these instruments present significant technical and physical challenges requiring careful characterization with standard particles. Many other research communities use flow cytometry and other instruments that interrogate fluorescence from individual particles, and these also frequently rely on fluorescent PSLs as standards. Nevertheless, information about physical properties of commercially available PSLs provided by each manufacturer is generally proprietary and rarely available, making their use in fluorescence validation and calibration very difficult. This technical note presents an overview of steady-state fluorescence properties of fluorescent and non-fluorescent PSLs, as well as of polystyrene-divinylbenzene (PS-DVB) particles, by using on- and offline spectroscopic techniques. We show that the “fluorescence landscape” of PSLs is more complex than the information typically provided by manufacturers may imply, especially revealing multimodal emission patterns. Furthermore, non-fluorescent PSLs also exhibit defined patterns of fluorescent emission originating from a mixture of polystyrene and detergents, which becomes a crucial point for fluorescence threshold calibrations and qualitative comparison between instruments. By comparing PSLs of different sizes, but doped with the same dye, changes in emission spectra from bulk solutions are not immediately obvious. On a single-particle scale, however, fluorescence intensity values increase with increasing particle size. No significant effect in the fluorescence signatures was detectable by comparing PSLs in dry vs. wet states, indicating that solvent water may only play a minor role as a fluorescence quencher. Because information provided by manufacturers of commercially available PSLs is generally very limited, we provide the steady-state excitation–emission matrices (EEMs) of PSLs as open-access data within the Supplement. Detergent and solvent effects are also discussed in order to provide information not available elsewhere to researchers in the bioaerosol and other research communities. These data are not meant to serve as a fundamental library of PSL properties because of the variability of fluorescent properties between batches and as a function of particle aging and agglomeration. The data presented, however, provide a summary of spectral features which are consistent across these widely used fluorescent standards. Using these concepts, further checks will likely be required by individual researchers using specific lots of standards.

Highlights

  • Available microspheres are widely used as tools in numerous scientific research disciplines (e.g., DNA hybridization probes, as tracers for blood flow and neuronal pathways), diagnostics, and size calibrations (e.g., Härmä et al, 2000; Hiesinger et al, 2001; Katz and Iarovici, 1990; Luchtel et al, 1998; Schwartz et al, 1998; Spiro et al, 2000)

  • As a further general feature, all fluorescent polystyrene latex spheres (PSLs) samples measured within this study reveal a multimodal fluorescence signal, in which main and minor modes occur in the same emission band, but being spectrally separated due to different excitation wavelengths

  • This study presents an overview of relevant physical properties of fluorescent and non-fluorescent PSLs utilizing onand offline techniques

Read more

Summary

Introduction

Available microspheres are widely used as tools in numerous scientific research disciplines (e.g., DNA hybridization probes, as tracers for blood flow and neuronal pathways), diagnostics (e.g., immunoassays), and size calibrations (e.g., flow cytometry and microscope calibration) (e.g., Härmä et al, 2000; Hiesinger et al, 2001; Katz and Iarovici, 1990; Luchtel et al, 1998; Schwartz et al, 1998; Spiro et al, 2000). The main principle common to these techniques is the detection of intrinsic fluorescence from fluorophores such as amino acids, coenzymes, vitamins, and pigments that ubiquitously occur in aerosols of biological origin (e.g., Hill et al, 2009; Li et al, 1991; Pan et al, 2010; Pöhlker et al, 2012, 2013) These PBAP represent a diverse and dynamic subset of airborne particles, consisting of whole organisms like bacteria, viruses, archaea, algae, fungi, and related reproductive units (e.g., pollen, bacterial and fungal spores), as well as decaying biomass and fragments from plants or insects (e.g., Deepak and Vali, 1991; Després et al, 2012; Jaenicke, 2005; Madelin, 1994; Pöschl, 2005). These results will provide researchers fundamental information regarding fluorescent PSLs as key calibrant particles on which they can base their instrument operation, enabling results based on a more coherent set of fluorescent properties

Materials and methods
Fluorescence spectroscopy on PSLs in aqueous suspension
Fluorescence spectroscopy on PSLs in dry state
Additional measurements and PSL preparation
Fluorescence microscopy on selected PSL samples
Online PSL analysis using the WIBS-4A
Fluorescence signatures of PSLs in suspension
Fluorescence emission variations after PSL preparation
Fluorescence microscopy of PSLs
PSL measurements with the WIBS-4A
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call