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Assessment of hemocompatibility of materials with arterial blood flow by platelet functional tests

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Hemocompatibility test of medical materials aims to detect adverse interaction between artificial surface and blood, which can activate or destruct blood components. In arterial flow conditions, due to a high shear stress, platelet is the cell critical for the hemocompatibility compliance. A classical instrumentation for the dynamic test of hemocompatibility involves a flow chamber with a contact surface between blood stream and tested plate. In the current study we investigated a simplified model of the whole blood shear stress, based on a cone and plate rotational viscometer. Several indices of platelet activation were analyzed, including platelet- and granulocyte-platelet aggregates, platelet activation markers and platelet-derived microparticles. This model allowed to estimate platelet destruction, however no adhesion could be measured directly. In following tests of several polymer and metallic layer coated materials, the test revealed comparable performance to more laborious hemocompatibility experiments. We suggest, that thrombogenic potential of platelet-derived microparticles, which can be accurately measured in blood plasma, offers very useful estimate of hemocompatibility. Moreover, this parameter has already been validated in clinics and could be used for monitoring of implanted cardiovascular materials.
Rocznik
Strony
317--322
Opis fizyczny
Bibliogr. 13 poz., rys.
Twórcy
autor
autor
autor
  • Department of Medicine, Jagiellonian University Medical College, 8 Skawińska St., 31-066 Cracow, Poland, nfsanak@cyf-kr.edu.pl
Bibliografia
  • [1] U.T. Seyfert, V. Biehl, and J. Schenk, “In vitro hemocompatibility testing of biomaterials according to the ISO 10993-4”, Biomol. Eng. 19 (2–6), 91–96 (2002).
  • [2] M. Otto, C.L. Klein, H. Koehler, M. Wagner, O. Roehrig, and C.J. Kirkpatrick, “Dymanic blood cell contact with biomaterials: validation of a flow chamber system according to international standards”, J. Mater. Sci. Mater. Med. 8 (3), 119–129 (1997).
  • [3] U. Streller, C. Sperling, J. Huebner, R. Ranke, and C. Werner, “Design and evaluation of novel blood incubation systems for in vitro hemocompatibility assessment of planar solid surfaces”, J. Biomed. Mater. Res. B Appl. Biomater. 66B (1), 379–390 (2003).
  • [4] R.D. Schaub, M.V. Kameneva, H.S. Borovetz, and W.R. Wagner, “Assessing acute platelet adhesion on opaque metallic and polymeric biomaterials with fiber otpic microscopy”, J. Biomed. Mater. Res. 49 (4), 460–468 (2000).
  • [5] S. Sbrana, F. Della Pina, A. Rizza, M. Buffa, R. De Filippis, J. Gianetti, and A. Clerico, “Relationships between optical aggregometry (type born) and flow cytometry in evaluating ADPinduced platelet activation”, Cytometry B Clin. Cytom. 74 (1), 30-39 (2008).
  • [6] S. Nomura, A. Shouzu, K. Tamoto, Y. Togane, S. Goto, S. Uchiyama, and Y. Ikeda, “Assessment of an ELISA kit for platelet-derived microparticles by joint research at many institutes in Japan”, J. Atheroscler. Thromb. JOI JST.JSTAGE/jat/26432 (2009), published online.
  • [7] P. Harrison, “Progress in the assessment of platelet function” Br. J. Hematol 111 (3), 733–744 (2000).
  • [8] B. Shenkman, N. Savion, R. Dardik, I. Tamarin, and D. Varon, “Testing of platelet deposition on polystyrene surface under plow conditions by the cone and plate(let) analyser: role of platelet activation, fibrinogen and von Willebrand factor”, Thromb. Res. 99 (4), 353–362 (2000).
  • [9] C.H. Gemmel, “Activation of platelets by in vitro whole blood contact with materials: increases in microparticle procoagulant activity, and soluble P-selectin blood levels”, J. Biomater. Sci. Polym. Ed. 12 (8), 933–934 (2001).
  • [10] D. Varon, I. Lashevski, B. Brenner, R. Beyar, N. Lanir, I. Tamarin, and N. Savion, “Cone and plate(let) analyzer: monitoring glycoprotein IIb/IIIa antagonists and von Willebrand disease replacement therapy by testing platelet deposition under flow conditions”, Am. Heart J. 135 (5 Pt 2 Su), S187–193 (1998).
  • [11] S. Nomura, Y. Ozaki, and Y. Ikeda, “Function and role of microparticles in various clinical settings”, Thromb. Res. 123 (1), 8–23 (2008).
  • [12] A. Blann, E. Shantsila, and A. Shantsila, “Microparticles and arterial disease”, Semin. Thromb. Hemost. 35 (5), 488–496 (2009).
  • [13] C.H. Gemmel, S.M. Ramirez, E.L. Yeo, and M.V. Sefton, “Platelet activation in whole blood by artificial surfaces: identification of platelet-derived microparticles and activated platelet binding to leukocytes as material-induced activation events”, J. Lab. Clin. Med. 125 (2), 276–287 (1995).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BPG8-0020-0029
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