TY - JOUR
T1 - Influence of cell shape and aggregate formation on the optical properties of flowing whole blood
AU - Shankar, Annika M.K.
AU - Swartling, Johannes
AU - Andersson-Engels, Stefan
PY - 2003/3/1
Y1 - 2003/3/1
N2 - We studied the influence of shape and secondary, or intercellular, organization on the absorption and scattering properties of red blood cells to determine whether these properties are of any practical significance for optical evaluation of whole blood and its constituents. A series of measurements of transmittance and reflectance of light from bovine blood in a flow cuvette was conducted with a 650–900-nm integrating sphere at shear rates of 0–1600 s–1, from which the influence of cell orientation, elongation, and aggregate formation on the absorption (μα) and the reduced scattering (μs) coefficients could be quantified. Aggregation was accompanied by a decrease of 4% in μαcompared with the value in randomly oriented single cells. Increasing the degree of cell alignment and elongation as a result of increasing shear rate reduced μsby 6% and μαby 3%, evaluated at a shear rate of 1600 s–1. Comparison with T-matrix computations for oblate- and prolate-shaped cells with corresponding elongation and orientation indicates that the optical properties of whole blood are determined by those of its individual cells, though influenced by a collective scattering factor that depends on the cell-to-cell organization. We demonstrate that cell morphological changes must be taken into consideration when one is conducting whole blood spectroscopy.
AB - We studied the influence of shape and secondary, or intercellular, organization on the absorption and scattering properties of red blood cells to determine whether these properties are of any practical significance for optical evaluation of whole blood and its constituents. A series of measurements of transmittance and reflectance of light from bovine blood in a flow cuvette was conducted with a 650–900-nm integrating sphere at shear rates of 0–1600 s–1, from which the influence of cell orientation, elongation, and aggregate formation on the absorption (μα) and the reduced scattering (μs) coefficients could be quantified. Aggregation was accompanied by a decrease of 4% in μαcompared with the value in randomly oriented single cells. Increasing the degree of cell alignment and elongation as a result of increasing shear rate reduced μsby 6% and μαby 3%, evaluated at a shear rate of 1600 s–1. Comparison with T-matrix computations for oblate- and prolate-shaped cells with corresponding elongation and orientation indicates that the optical properties of whole blood are determined by those of its individual cells, though influenced by a collective scattering factor that depends on the cell-to-cell organization. We demonstrate that cell morphological changes must be taken into consideration when one is conducting whole blood spectroscopy.
UR - https://www.scopus.com/pages/publications/0037363747
U2 - 10.1364/AO.42.001384
DO - 10.1364/AO.42.001384
M3 - Article
C2 - 12638895
AN - SCOPUS:0037363747
SN - 1559-128X
VL - 42
SP - 1384
EP - 1394
JO - Applied Optics
JF - Applied Optics
IS - 7
ER -