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Inhalation Toxicology
International Forum for Respiratory Research
Volume 30, 2018 - Issue 4-5
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Research Article

Physicochemical studies of direct interactions between lung surfactant and components of electronic cigarettes liquid mixtures

, , , &
Pages 159-168 | Received 05 Jan 2018, Accepted 16 May 2018, Published online: 22 Jun 2018

Figures & data

Table 1. Nominal deposited dose per session (NDDS) and the corresponding mixture concentrations in the pulmonary fluid for different propylene glycol/vegetable glycerin (PG/VG) ratios in the inhaled aerosolized e-liquid.

Figure 1. Definition of the mean surface tension (mean ST) and the surface tension amplitude (ST amplitude) in the experimental γ-A relationship (hysteresis loop).

Figure 1. Definition of the mean surface tension (mean ST) and the surface tension amplitude (ST amplitude) in the experimental γ-A relationship (hysteresis loop).

Figure 2. Mean surface tension of lung surfactant (LS) in the presence of e-liquid mixture of various compositions and concentrations (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz). Dashed lines show the control range (pure LS).

Figure 2. Mean surface tension of lung surfactant (LS) in the presence of e-liquid mixture of various compositions and concentrations (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz). Dashed lines show the control range (pure LS).

Figure 3. Amplitude of surface tension variations (amplitude ST) in the lung surfactant (LS) in the presence of e-liquid mixture of various compositions and concentrations (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz). Dashed lines show the control range (pure LS).

Figure 3. Amplitude of surface tension variations (amplitude ST) in the lung surfactant (LS) in the presence of e-liquid mixture of various compositions and concentrations (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz). Dashed lines show the control range (pure LS).

Figure 4. Surface dilatational elasticity of the lung surfactant (LS) liquid interface in the presence of e-liquid mixtures of various compositions and concentrations (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz). Dashed lines show the control range (pure LS).

Figure 4. Surface dilatational elasticity of the lung surfactant (LS) liquid interface in the presence of e-liquid mixtures of various compositions and concentrations (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz). Dashed lines show the control range (pure LS).

Figure 5. Surface dilatational viscosity of the lung surfactant (LS) liquid interface in the presence of e-liquid mixtures of various compositions and concentrations (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz). Dashed lines show the parameter range as in .

Figure 5. Surface dilatational viscosity of the lung surfactant (LS) liquid interface in the presence of e-liquid mixtures of various compositions and concentrations (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz). Dashed lines show the parameter range as in Figures 2–4.

Figure 6. Total deviation (TDP) based on the combined deviations of three numerical parameters according to Equation (3) for e-liquids with different compositions and concentrations in the lung surfactant (LS) solution (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz).

Figure 6. Total deviation (TDP) based on the combined deviations of three numerical parameters according to Equation (3) for e-liquids with different compositions and concentrations in the lung surfactant (LS) solution (NDDS – estimated nominal deposition dose per session). Data for the normal rate of breathing (0.25 Hz).

Figure 7. Schematic illustration of the local boost of humectants concentration in the pulmonary liquid after deposition and spreading of a single inhaled e-liquid droplet.

Figure 7. Schematic illustration of the local boost of humectants concentration in the pulmonary liquid after deposition and spreading of a single inhaled e-liquid droplet.

Figure 8. Proposed mechanism for lung surfactant (LS) – aerosol former (e-liquid) interactions.

Figure 8. Proposed mechanism for lung surfactant (LS) – aerosol former (e-liquid) interactions.
Supplemental material

Supplemental Material

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