Evaluation of methods for aerosolising polystyrene latex nanoparticles and assessment of their toxicity
(2025) In Journal of Aerosol Science 188.- Abstract
Aerosolised Polystyrene Latex (PSL) nanoparticles are, due to their well-defined size, spherical shape, and inert surface, useful in many experimental applications, including studies of particle deposition in the human lung. Aerosolising nanoparticles entails added challenges, and nanoparticles can potentially be more hazardous than otherwise equivalent microparticles. The objective of this work was to evaluate methods for aerosolising PSL nanoparticles and assess their toxicity. We investigated a Collison-type generator, a TSI Electrospray, and the recent Kanomax NanoAerosol Generator (NAG). We also examined the cyto- and genotoxicity of nano-PSL to human bronchial epithelial cells (BEAS-2B) in serum-free conditions and to... (More)
Aerosolised Polystyrene Latex (PSL) nanoparticles are, due to their well-defined size, spherical shape, and inert surface, useful in many experimental applications, including studies of particle deposition in the human lung. Aerosolising nanoparticles entails added challenges, and nanoparticles can potentially be more hazardous than otherwise equivalent microparticles. The objective of this work was to evaluate methods for aerosolising PSL nanoparticles and assess their toxicity. We investigated a Collison-type generator, a TSI Electrospray, and the recent Kanomax NanoAerosol Generator (NAG). We also examined the cyto- and genotoxicity of nano-PSL to human bronchial epithelial cells (BEAS-2B) in serum-free conditions and to monocyte-derived macrophages (THP-1) in both serum-free and serum-enriched conditions. When comparing the generators, we found that the NAG produced an aerosol with greater separation between the PSL and residual particles than the Collison and was the most stable generator tested. The electrospray generated an aerosol without any overlap between the residual and the PSL modes but was also the most unpredictable, making it less suited for areas where ease of use and high repeatability are needed. We found that the Collison is generally unsuitable to generate nano-sized aerosol. The lowest observed effect level for cytotoxicity in BEAS-2B was 25, 50 and 50 μg/mL for 30, 50 and 100 nm PSL, respectively. For serum-free THP-1 macrophages, it was 50 μg/mL for 30 nm PSL and 150 μg/mL for 50 and 100 nm PSL. THP-1 macrophages displayed no cytotoxicity in serum-enriched culture. None of the tested particles were genotoxic in the alkaline comet assay. Overall, the NAG exceeded the Collison and electrospray in stability but produced a more polydisperse aerosol than the electrospray. PSL particles induced dose- and size-dependent cytotoxicity in BEAS-2B and in THP-1 cells with the smallest particles (30 nm) being the most toxic. However, the concentration is several orders of magnitude higher than typical concentrations for experimental applications.
(Less)
- author
- Öhrneman, Hugo
LU
; McCarrick, Sarah
; Gliga, Anda
LU
; Wollmer, Per
LU
; Broberg, Karin
and Löndahl, Jakob
LU
- organization
-
- LTH Profile Area: Aerosols
- LTH Profile Area: Engineering Health
- Ergonomics and Aerosol Technology
- NanoLund: Centre for Nanoscience
- LTH Profile Area: Nanoscience and Semiconductor Technology
- LU Profile Area: Light and Materials
- Clinical Microbiology, Malmö (research group)
- Clinical Physiology and Nuclear Medicine, Malmö (research group)
- MERGE: ModElling the Regional and Global Earth system
- Metalund
- Infect@LU
- publishing date
- 2025-08
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Aerosol Science
- volume
- 188
- article number
- 106607
- publisher
- Elsevier
- external identifiers
-
- scopus:105005207610
- ISSN
- 0021-8502
- DOI
- 10.1016/j.jaerosci.2025.106607
- language
- English
- LU publication?
- yes
- id
- 96a04328-17db-42e8-a391-ee9424ea41b6
- date added to LUP
- 2025-07-18 08:45:17
- date last changed
- 2025-07-18 08:46:39
@article{96a04328-17db-42e8-a391-ee9424ea41b6, abstract = {{<p>Aerosolised Polystyrene Latex (PSL) nanoparticles are, due to their well-defined size, spherical shape, and inert surface, useful in many experimental applications, including studies of particle deposition in the human lung. Aerosolising nanoparticles entails added challenges, and nanoparticles can potentially be more hazardous than otherwise equivalent microparticles. The objective of this work was to evaluate methods for aerosolising PSL nanoparticles and assess their toxicity. We investigated a Collison-type generator, a TSI Electrospray, and the recent Kanomax NanoAerosol Generator (NAG). We also examined the cyto- and genotoxicity of nano-PSL to human bronchial epithelial cells (BEAS-2B) in serum-free conditions and to monocyte-derived macrophages (THP-1) in both serum-free and serum-enriched conditions. When comparing the generators, we found that the NAG produced an aerosol with greater separation between the PSL and residual particles than the Collison and was the most stable generator tested. The electrospray generated an aerosol without any overlap between the residual and the PSL modes but was also the most unpredictable, making it less suited for areas where ease of use and high repeatability are needed. We found that the Collison is generally unsuitable to generate nano-sized aerosol. The lowest observed effect level for cytotoxicity in BEAS-2B was 25, 50 and 50 μg/mL for 30, 50 and 100 nm PSL, respectively. For serum-free THP-1 macrophages, it was 50 μg/mL for 30 nm PSL and 150 μg/mL for 50 and 100 nm PSL. THP-1 macrophages displayed no cytotoxicity in serum-enriched culture. None of the tested particles were genotoxic in the alkaline comet assay. Overall, the NAG exceeded the Collison and electrospray in stability but produced a more polydisperse aerosol than the electrospray. PSL particles induced dose- and size-dependent cytotoxicity in BEAS-2B and in THP-1 cells with the smallest particles (30 nm) being the most toxic. However, the concentration is several orders of magnitude higher than typical concentrations for experimental applications.</p>}}, author = {{Öhrneman, Hugo and McCarrick, Sarah and Gliga, Anda and Wollmer, Per and Broberg, Karin and Löndahl, Jakob}}, issn = {{0021-8502}}, language = {{eng}}, publisher = {{Elsevier}}, series = {{Journal of Aerosol Science}}, title = {{Evaluation of methods for aerosolising polystyrene latex nanoparticles and assessment of their toxicity}}, url = {{http://dx.doi.org/10.1016/j.jaerosci.2025.106607}}, doi = {{10.1016/j.jaerosci.2025.106607}}, volume = {{188}}, year = {{2025}}, }