Fig. 2From: Establishment of a rat ovarian peritoneal metastasis model to study pressurized intraperitoneal aerosol chemotherapy (PIPAC)PSD curves of nebulized saline showing the distribution density (left curves) and cumulative distribution (right curves). Mean droplet diameters were measured (n = 3 for each confirmation) in a range of 0.5 to 900 μm. The error bars show one time the standard deviation. a Volume-weighted PSD curves showing the influence of maximal upstream injection pressure on D(v,0.5). 20 mL of saline was nebulized in open space at a fixed flow rate of 0.5 mL/s and a maximal upstream injection pressure of 20 bar (blue graph), 10 bar (red graph) or 5 bar (black graph). b Volume-weighted PSD curves illustrating the influence of flow rate on D(v,0.5). 20 mL of saline was nebulized in open space at a fixed maximal upstream injection pressure of 20 bar and a flow rate of 0.5 mL/s (blue graph) or 0.8 mL/s (red graph). c Volume-weighted PSD curves demonstrating the influence of the volume of the peritoneal cavity on D(v,0.5). To simulate a nebulization in a rat’s abdominal cavity, 20 mL of saline was nebulized in a plastic box (V = 100 mL) with a flow rate of 0.8 mL/s and a maximal upstream injection pressure of 20 bar (red graph). 200 mL of saline was nebulized in a plastic box (V = 5 L) with a flow rate of 0.5 mL/s and a maximal upstream injection pressure of 20 bar (blue graph) as a comparison with the nebulization in human. The plastic boxes were bilaterally pierced to transvers laser light and a third perforation was made at the top of the boxes to insert the nebulizerBack to article page