Title :
Oxygen diffusion in the pulmonary capillaries
Author :
Frank, Andreas O. ; Chuong, C. J Charles
Author_Institution :
Biomed. Eng. Prog., Texas Univ., Arlington, TX, USA
Abstract :
We determined the overall pulmonary diffusing capacity (DL ), membrane diffusing capacity (DM), and red cell (RBC) diffusing capacity (DE) for oxygen (O2,) using a finite element model representing the sheet flow characteristics of the pulmonary capillaries. The results showed that the membrane contributing the major resistance (1/DM), with the RBC resistance (1/DE) had increasing significance as O2 saturation rises during RBC transit, from 7% at the capillary inlet to 30% towards the exit. DM and DL increased with increasing hematocrit (Hct) but gradually approached a plateau at higher Hcts (Hct>35%). Axisymmetric model results were similar to the 2D model but significantly overestimated DM and DL (~2.2 times), due to an exaggerated air-tissue surface area available for gas transport associated with the axisymmetric geometry. The 2D model geometry correlated reasonably well with the experimental data and better represents the oxygen uptake at the pulmonary capillary bed
Keywords :
biodiffusion; biomembrane transport; blood; finite element analysis; haemorheology; lung; oxygen; physiological models; 2D model geometry; O2; O2 saturation; RBC transit; air-tissue surface area; axisymmetric geometry; axisymmetric model; finite element model; gas transport; hematocrit; membrane diffusing capacity; oxygen diffusion; oxygen uptake; pulmonary capillaries; pulmonary capillary bed; pulmonary diffusing capacity; red cell diffusing capacity; sheet flow characteristics; Biomembranes; Delta modulation; Finite element methods; Geometry; Immune system; Lungs; Oxygen; Plasmas; Shape; Solid modeling;
Conference_Titel :
Biomedical Engineering Conference, 1997., Proceedings of the 1997 Sixteenth Southern
Conference_Location :
Biloxi, MS
Print_ISBN :
0-7803-3869-3
DOI :
10.1109/SBEC.1997.583311