TY - JOUR
T1 - Metabolism of hemoglobin-vesicles (artificial oxygen carriers) and their influence on organ functions in a rat model
AU - Sakai, Hiromi
AU - Horinouchi, Hirohisa
AU - Masada, Yohei
AU - Takeoka, Shinji
AU - Ikeda, Eiji
AU - Takaori, Masuhiko
AU - Kobayashi, Koichi
AU - Tsuchida, Eishun
N1 - Funding Information:
The authors gratefully acknowledge Dr. N. Hirose (Department of Gerontology, School of Medicine, Keio University) for the discussion on the results. This work was supported in part by Health Sciences Research Grants (H15-Research on Pharmaceutical and Medical Safety, Artificial Blood Project, -011, -016), the Ministry of Health, Labor and Welfare, Japan, Grants in Aid for Scientific Research from the Japan Society for the Promotion of Science (B12480268), and 21 COE “Practical Nano-Chemistry” from MEXT, Japan.
PY - 2004/8
Y1 - 2004/8
N2 - Phospholipid vesicles encapsulating Hb (Hb-vesicles: HbV) have been developed for use as artificial O2 carriers (250nmφ). As one of the safety evaluations, we analyzed the influence of HbV on the organ functions by laboratory tests of plasma on a total of 29 analytes. The HbV suspension ([Hb]=10g/dl) was intravenously infused into male Wistar rats (20ml/kg; whole blood = 56ml/kg). The blood was withdrawn at 8h, and 1, 2, 3, and 7 days after infusion, and the plasma was ultracentrifuged to remove HbV in order to avoid its interference effect on the analytes. Enzyme concentrations, AST, ALT, ALP, and LAP showed significant, but minor changes, and did not show a sign of a deteriorative damage to the liver that was one of the main organs for the HbV entrapment and the succeeding metabolism. The amylase and lipase activities showed reversible changes, however, there was no morphological changes in pancreas. Plasma bilirubin and iron did not increase in spite of the fact that a large amount of Hb was metabolized in the macrophages. Cholesterols, phospholipids, and β-lipoprotein transiently increased showing the maximum at 1 or 2 days, and returned to the control level at 7 days. They should be derived from the membrane components of HbV that are liberated from macrophages entrapping HbV. Together with the previous report of the prompt metabolism of HbV in the reticuloendothelial system by histopathological examination, it can be concluded that HbV infusion transiently modified the values of the analytes without any irreversible damage to the corresponding organs at the bolus infusion rate of 20ml/kg.
AB - Phospholipid vesicles encapsulating Hb (Hb-vesicles: HbV) have been developed for use as artificial O2 carriers (250nmφ). As one of the safety evaluations, we analyzed the influence of HbV on the organ functions by laboratory tests of plasma on a total of 29 analytes. The HbV suspension ([Hb]=10g/dl) was intravenously infused into male Wistar rats (20ml/kg; whole blood = 56ml/kg). The blood was withdrawn at 8h, and 1, 2, 3, and 7 days after infusion, and the plasma was ultracentrifuged to remove HbV in order to avoid its interference effect on the analytes. Enzyme concentrations, AST, ALT, ALP, and LAP showed significant, but minor changes, and did not show a sign of a deteriorative damage to the liver that was one of the main organs for the HbV entrapment and the succeeding metabolism. The amylase and lipase activities showed reversible changes, however, there was no morphological changes in pancreas. Plasma bilirubin and iron did not increase in spite of the fact that a large amount of Hb was metabolized in the macrophages. Cholesterols, phospholipids, and β-lipoprotein transiently increased showing the maximum at 1 or 2 days, and returned to the control level at 7 days. They should be derived from the membrane components of HbV that are liberated from macrophages entrapping HbV. Together with the previous report of the prompt metabolism of HbV in the reticuloendothelial system by histopathological examination, it can be concluded that HbV infusion transiently modified the values of the analytes without any irreversible damage to the corresponding organs at the bolus infusion rate of 20ml/kg.
KW - Biomimetic material
KW - Blood
KW - Drug delivery
KW - In vivo test
KW - Liposome
KW - Nanoparticle
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U2 - 10.1016/j.biomaterials.2003.11.005
DO - 10.1016/j.biomaterials.2003.11.005
M3 - Article
C2 - 15046922
AN - SCOPUS:1642408475
SN - 0142-9612
VL - 25
SP - 4317
EP - 4325
JO - Biomaterials
JF - Biomaterials
IS - 18
ER -