Biocompatibility: bioengineering aspects.

Bioengineers have contributed to biocompatibility research. Many materials have been designed, synthesized and characterized by use of various analytical instruments. The blood compatibility of materials has been studied by focusing on the blood-material interfacial reactions. Although much information has been accumulated regarding such local reactions, understanding of biocompatibility is still limited. A more global approach to study is needed. A new approach to understanding biocompatibility is proposed and discussed. Three points are stressed: interaction within body's defense system and its effect on blood-material reactions; induction of a systemic reaction by a local reaction, which then affects the blood-material interaction; the time sequence of such interactions between local and systemic reactions. To establish a logical approach to study biocompatibility is most important at this moment for the future progress in biocompatibility research.

[1]  D. Chenoweth Complement activation during hemodialysis: clinical observations, proposed mechanisms, and theoretical implications. , 1984, Artificial organs.

[2]  Tony E. Hugh Structure and function of the anaphylatoxins , 1984, Springer Seminars in Immunopathology.

[3]  A. Cheung,et al.  Anaphylatoxin formation during hemodialysis: effects of different dialyzer membranes. , 1983, Kidney international.

[4]  D. Ogston The physiology of hemostasis , 1983 .

[5]  D. Chenoweth,et al.  Induction of interleukin 1 secretion and enhancement of humoral immunity by binding of human C5a to macrophage surface C5a receptors , 1982, The Journal of experimental medicine.

[6]  R. Hakim Biocompatibility of Dialysis Membranes , 1982 .

[7]  J. Chesebro,et al.  Platelet Deposition In Extracardiac Conduits In Humans: A Noninvasive Quantification , 1981, Thrombosis and Haemostasis.

[8]  V. Pollak,et al.  Multiple use of dialyzers: safety and efficacy. , 1981, Kidney international.

[9]  E. Blackstone,et al.  Complement activation during cardiopulmonary bypass: evidence for generation of C3a and C5a anaphylatoxins. , 1981, The New England journal of medicine.

[10]  P. Henson,et al.  The release of a platelet-activating factor by stimulated rabbit neutrophils. , 1979, Journal of immunology.

[11]  S. Cooper,et al.  Transient in vivo protein adsorption onto polymeric biomaterials. , 1979, Journal of biomedical materials research.

[12]  J. White,et al.  Complement (C5-a)-induced granulocyte aggregation in vitro. A possible mechanism of complement-mediated leukostasis and leukopenia. , 1977, The Journal of clinical investigation.

[13]  A. Dalmasso,et al.  Hemodialysis leukopenia. Pulmonary vascular leukostasis resulting from complement activation by dialyzer cellophane membranes. , 1977, The Journal of clinical investigation.

[14]  R S Kronenberg,et al.  Complement and leukocyte-mediated pulmonary dysfunction in hemodialysis. , 1977, The New England journal of medicine.

[15]  J. Margolis,et al.  Activation of plasma by contact with glass: evidence for a common reaction which releases plasma kinin and initiates coagulation , 1958, The Journal of physiology.

[16]  H. Hartung,et al.  Synthesis of complement by macrophages and modulation of their functions through complement activation , 2005, Springer Seminars in Immunopathology.

[17]  D. Fair,et al.  Relationships among the complement, kinin, coagulation, and fibrinolytic systems , 2004, Springer Seminars in Immunopathology.

[18]  S. Hanson Blood-material interactions , 1998 .

[19]  T. Nakamura,et al.  The blood interface with segmented polyurethanes: "multilayered protein passivation mechanism". , 1984, Transactions - American Society for Artificial Internal Organs.

[20]  P S Malchesky,et al.  Biocompatibility of membrane plasma separation. , 1984, Transactions - American Society for Artificial Internal Organs.

[21]  S. Cooper,et al.  Physicochemical characterization and in vivo blood tolerability of cast and extruded Biomer. , 1983, Journal of biomedical materials research.

[22]  R Kiraly,et al.  Polyester fibril flocked surface for blood pumps. , 1983, Transactions - American Society for Artificial Internal Organs.

[23]  J. Andrade,et al.  Calcification of nontextured implantable blood pumps. , 1981, Transactions - American Society for Artificial Internal Organs.

[24]  T. Agishi,et al.  Malignant tumours in dialysis patients: a nationwide survey. , 1981, Proceedings of the European Dialysis and Transplant Association. European Dialysis and Transplant Association.

[25]  Panel conference. Is atherosclerosis accelerated by dialysis - fact - fiction? , 1981, Transactions - American Society for Artificial Internal Organs.

[26]  P. Ward,et al.  C5 chemotactic fragment induces leukocyte production of tissue factor activity: a link between complement and coagulation. , 1979, The Journal of clinical investigation.

[27]  H. Harasaki,et al.  Powdered metal surface for blood pump. , 1979, Transactions - American Society for Artificial Internal Organs.

[28]  S. D. Bruck The behavior of three different types of materials in vitro and in the dynamic physiological environment: review and analyses of critical parameters. , 1979, The International journal of artificial organs.

[29]  H. Harasaki,et al.  Endothelialization in blood pumps. , 1978, Transactions - American Society for Artificial Internal Organs.

[30]  E. Grabowski,et al.  PLATELET ADHESION TO FOREIGN SURFACES UNDER CONTROLLED CONDITIONS OF WHOLE BLOOD FLOW: HUMAN VS RABBIT, DOG, CALF, SHEEP, PIG, MACAQUE, AND BABOON , 1977, Transactions - American Society for Artificial Internal Organs.

[31]  P. Henson The adherence of leucocytes and platelets induced by fixed IgG antibody or complement. , 1969, Immunology.

[32]  S. Niewiarowski,et al.  Rôle du Facteur Contact (Facteur Hageman) dans la Fibrinolyse , 1959, Thrombosis and Haemostasis.