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Atomic Absorption Spectroscopy (AAS) atomizes samples through flame atomization or electrothermal atomization. Flame atomization typically involves a nebulizer and spray chamber assembly to combine the sample with a fuel–oxidant mixture, creating a fine aerosol mist that enters a burner. Typically, the fuel and oxidant are combined in an approximately stoichiometric ratio. However, for atoms that are easily oxidized, a fuel-rich mixture may be more advantageous. Only about 5% of the...
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Effervescent Atomizer as Novel Cell Spray Technology to Decrease the Gas-to-Liquid Ratio.

Anja Lena Thiebes1,2, Sarah Klein1,2, Jonas Zingsheim1,3

  • 1Department of Biohybrid & Medical Textiles (BioTex), AME-Institute of Applied Medical Engineering, Helmholtz Institute Aachen, RWTH Aachen University, Forckenbeckstraße 55, 52074 Aachen, Germany.

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|November 11, 2022
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Summary
This summary is machine-generated.

A novel effervescent atomizer effectively sprays cells for therapy and tissue engineering, using less air. This method preserves cell viability and differentiation potential, marking a breakthrough in cell processing.

Keywords:
adipose-derived stromal cells (ASCs)cell aerosolizationcell atomizationsurvivaltri-lineage differentiationtwin-fluid atomizer

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Area of Science:

  • Biomedical Engineering
  • Cell Therapy
  • Tissue Engineering

Background:

  • Cell spraying is a key technique in cell therapy and tissue engineering.
  • Traditional twin-fluid atomizers require high gas velocities, potentially harming cells.
  • Reducing air requirements is crucial for optimizing cell aerosolization.

Purpose of the Study:

  • To design and evaluate a custom effervescent atomizer for cell spraying.
  • To assess the impact of effervescent aerosolization on human adipose-derived mesenchymal stromal cells.
  • To determine the suitability of this new method for cell-based applications.

Main Methods:

  • Development of a custom effervescent atomizer based on the effervescent principle.
  • Evaluation of spray characteristics, including droplet size (15.4–33.5 µm).
  • Assessment of cell viability, metabolic activity, apoptosis, necrosis, and tri-lineage differentiation post-aerosolization.

Main Results:

  • The effervescent atomizer produced droplets in the 15.4–33.5 µm range.
  • Cell survival exceeded 90% at low gas-to-liquid ratios, decreasing to ~50% at higher ratios.
  • No significant impact on metabolic activity or tri-lineage differentiation was observed; necrosis increased with higher ratios.

Conclusions:

  • Effervescent aerosolization is suitable for cell applications, requiring less air than traditional methods.
  • This study demonstrates the first use of an effervescent atomizer for cell processing.
  • The method shows promise for preserving cell function and viability in therapeutic applications.