Effects of Pegylated Hamster Red Blood Cells on Microcirculation

REFERENCES

• Intaglietta M. Microcirculatory basis for the design of artificial blood. Microcir 1999; 6: 247–258
   PubMed Web of Science ®Google Scholar
• Cheung A. T. W., Duong To P. L., Chan D. M., Ramanujam S., Barbosa M. A. Comparison of treatment modalities for hemorrhagic shock. Artificial Cells, Blood Substitutes, and Biotechnology 2007; 35: 173–190
   PubMed Web of Science ®Google Scholar
• Klein H. G. Oxygen carriers and transfusion medicine. Art Cell Blood Substit Immobil Biotech 1995; 22: 123–135
   Google Scholar
• Klein H. G. The prospects of red-cell substitutes (Editorial). N Engl J Med 2000; 342: 838–843
   Web of Science ®Google Scholar
• Tsai A. G. Influence of cell-free Hb on local tissue perfusion and oxygenation in acute anemia after isovolemic hemodilution. Transfus Med 2001; 41: 1290–1298
   Web of Science ®Google Scholar
• Olson J. S., Foley E. W., Rogge C., Tsai A. L., Doyle M. P., Lemon D. D. NO scavenging and the hypertensive effect of hemoglobin-based blood substitutes. Free Radic Biol Med 2004; 36: 685–697
   PubMed Web of Science ®Google Scholar
• Garratty G., Telen M. J., Petz L. D. Red cell antigens as functional molecules and obstacles to transfusion. Hematology Am Soc Hematol Educ Program 2002; 1: 445–462
   Google Scholar
• Garratty G. Progress in modulating the RBC membrane to produce transfusable universal/stealth donor RBCs. Transfusion Medicine Reviews 2004; 18: 245–256
   PubMed Web of Science ®Google Scholar
• Albertsson P. A. Partition of Cell Particles and Macromolecules. Wiley, New York 1986
   Google Scholar
• Abbott N. L., Blankschtein D., Hatton T. A. Protein partitioning in two-phase aqueous polymer systems. Decoupling of effects of protein concentration, salt type, and polymer molecular weight. Macromolecules 1991; 24: 4334–4348
   Web of Science ®Google Scholar
• McPherson A. Crystallization of Biological Macromolecules. Cold Spring Harbor Lab. Press, Plainview, NY 1999
   Google Scholar
• Veronese F. M. Peptide and protein PEGylation: a review of problem and solutions. Biomaterials 2001; 22: 405–417
   PubMed Web of Science ®Google Scholar
• Jeong S. T., Byun S. M. Decreased agglutinability of methoxy-polyethylene glycol attached red blood cells: significance as a blood substitute. Art Cells Blood Subst Immob Biotech 1996; 24: 503–511
   PubMed Web of Science ®Google Scholar
• Hortin G. L., Lok H. T., Huang S. T. Progress toward preparation of universal donor red cells. Art Cells Blood Subst Immob Biotech 1997; 25: 487–491
   PubMed Web of Science ®Google Scholar
• Scott M. D., Murad K. L., Koumpouras F., Talbot M., Eaton J. W. Chemical camouflage of antigenic determinants: stealth erythrocytes. Proc Natl Acad Sci USA 1997; 94: 7566–7571
   PubMed Web of Science ®Google Scholar
• Armstrong J. K., Meiselman H. J., Fisher T. C. Covalent binding of poly(ethylene glycol) (PEG) to the surface of red blood cells inhibits aggregation and reduces low-shear viscosity. Am J Hematol 1997; 56: 26–28
   PubMed Web of Science ®Google Scholar
• Fisher T. C., Armstrong J. K., US Patent 6312685, 2001
   Google Scholar
• Bradley A. J., Murad K. L., Regan K. L., Scott M. D. Biophysical consequences of linker chemistry and polymer size on stealth erythrocytes: Size does matter. Biochim Biophys Acta 2002; 1561: 147–158
   PubMed Web of Science ®Google Scholar
• Mathur S., Clark B., Castro G., Zhou X. M., Bowers S., Stassinopoulos A. Efficient full unit Pegylation of human red blood cells (RBC) using linear methoxy-capped polyethylene glycol (mPEG). Blood 2003; 102: 556A
   Web of Science ®Google Scholar
• Nacharaju P., Manjula B. N., Acharya S. A. Thiolation mediated pegylation platform to generate functional universal red blood cells. Artif Cells Blood Substit Immobil Biotechnol 2007; 35: 107–118
   PubMed Web of Science ®Google Scholar
• Colantuoni A., Bertuglia S., Intaglietta M. Quantitation of rhythmic diameter changes in arterial microcirculation. Am J Physiol 1984; 246: H508–H517
   PubMed Web of Science ®Google Scholar
• Endrich B., Asaishi K., Götz A., Messmer K. Technical report: A new chamber technique for microvascular studies in unanaesthetized hamsters. Res Exp Med 1980; 177: 125–134
   PubMedGoogle Scholar
• NIH Consensus Conference. Perioperative red cell transfusion. JAMA 1988; 260: 2700
   PubMed Web of Science ®Google Scholar
• Murad K. L., Mahany K. L., Brugnara C., Kuypers F. A., Eaton J. W., Scott M. D. Structural and functional consequences of antigenic modulation of red blood cells with methoxypoly(ethylene glycol). Blood 1999; 93: 2121–2127
   PubMed Web of Science ®Google Scholar
• Tsai A. G., Vandegriff K. D., Intaglietta M., Winslow R. M. Targeted O2 delivery by low-P50 hemoglobin: a new basis for O2 therapeutics. Am J Physiol 2003; 285: H1411–H1419
   PubMed Web of Science ®Google Scholar
• Cabrales P., Kanika N. D., Manjula B. N., Tsai A. G., Acharya S. A., Intaglietta M. Microvascular PO2 during extreme hemodilution with hemoglobin site specifically PEGylated at Cys-93(beta) in hamster window chamber. Am J Physiol 2004; 287: H1609–H1617
   Google Scholar
• Ogada Y. Characteristics and function of human hemoglobin vesicles as an oxygen carrier. Polymers for Advanced Technologies 2000; 11: 205–209
   Web of Science ®Google Scholar
• Fahraeus R. The suspension stability of blood. Physiol Rev 1929; 9: 241–274
   Google Scholar
• Chien S., Jan K.-M. Ultrastructural basis of the mechanism of rouleaux formation. Microvasc Res 1973; 5: 155–166
   PubMed Web of Science ®Google Scholar