Thromb Haemost 1983; 50(04): 814-820
DOI: 10.1055/s-0038-1665319
Original Article
Schattauer GmbH Stuttgart

Non-Thrombogenicity of Clean Glass Revealed by Native Whole Blood Assay in Bead Columns

J A Bergeron
*   The General Electric Corporate Research and Development, Schenectady, N. Y., U.S.A.
,
J M DiNovo
**   The Center for Laboratories and Research, New York State Department of Health, Albany, N.Y., U.S.A.
,
A F Razzano
*   The General Electric Corporate Research and Development, Schenectady, N. Y., U.S.A.
,
W J Dodds
**   The Center for Laboratories and Research, New York State Department of Health, Albany, N.Y., U.S.A.
› Author Affiliations
Further Information

Publication History

Received 27 January 1983

Accepted 16 September 1983

Publication Date:
18 July 2018 (online)

Summary

The previously described native whole blood assay for materials in solution or suspension has been adapted to materials in a bead column configuration. These experiments showed that the glass itself accounts for little or none of the high blood-reactivity observed with conventional glass bead columns. Columns composed solely of soft glass that was “cleaned” by heat treatment (500-595° C 18 hr, electric oven) were benign toward flowing native whole blood for all variables measured (platelet count and platelet-free plasma [C14]-serotonin content, platelet factor 3 and factor XII activities, and recalcification time) with the standard contact protocol. In addition, the effluent successfully maintained perfusion of the isolated kidney, a measure of the ability of platelets to support vascular integrity. Prolonged (30 min) normothermic contact with titrated whole blood increased the subsequent reactivity of initially clean glass toward whole blood albeit to a level much less than that of conventional glass bead columns.

 
  • References

  • 1 National heart, lung, and blood institute working group report. Guidelines for blood-materials interactions. NIH No 80-2185 1980
  • 2 National heart, lung, and blood institute working group report. Guidelines for physico-chemical characterization of biomaterials. NIH No 80-2186 1980
  • 3 Dodds WJ, DiNovo JM, Bergeron JA. A native whole blood assay for blood-materials interaction. Thromb Haemostas 1981; 45: 12-17
  • 4 Salzman EW. Measurement of platelet adhesiveness. A simple in vitro technique demonstrating an abnormality in von Willebrand disease J Lab Clin Med 1963; 62: 724-735
  • 5 Bowie EJ W, Owen CA. Platelet retention and other adhesion- aggregation phenomena. In: Platelet function testing. Day HJ, Holmsen H, Zucker MB. (eds) NIH 78-1084 pp 160-173 1980
  • 6 Zucker MB. Mechanism of platelet retention in glass bead columns, ibid. 174-180
  • 7 Salzman EW. Discussion, ibid. 199
  • 8 Bowie EJ W, Owen CA. Test of platelet function. Vox Sang 1981; 40 (suppl) (Suppl. 01) 36-47
  • 9 Lindon JN, Rodvein R, Brier D, Greenberg R, Merrill E, Salzman EW. In vitro assessment of interaction of blood with model surfaces. J Lab Clin Med 1978; 92: 904-914
  • 10 Brier-Russell D, Salzman EW, Lindon J, Handin R, Merrill EW, Dincer AK, Wu J-S. In vitro assessment of interaction of blood with model surfaces: acrylates and methacrylates. J Colloid Interface Sci 1981; 81: 311-318
  • 11 DaCosta US, Brier-Russell D, Salzman EW, Merrill EW. ESCA studies of polyurethanes: Blood platelet activation in relation to surface composition. J Colloid Interface Sci 1981; 80: 445-452
  • 12 Robertson CR, Chang HN. Platelet retention in columns packed with glass beads. Ann Biomed Eng 1974; 2: 361-391
  • 13 Friedberg NM, Zucker MB. ADP as the cause of reversible inhibition of platelet retention in glass bead columns. J Lab Clin Med 1972; 80: 603-612
  • 14 Salzman EW, Lindon J, Brier D, Merrill EW. Surface induced platelet adhesion, aggregation and release. Ann NY Acad Sri 1977; 283: 114-127
  • 15 Zucker MB, McPherson J. Reactions of platelets near surfaces in vitro Lessons from the platelet retention test. Ann NY Acad Sri 1977; 283: 127-137
  • 16 Dodds WJ, Ramond SL, Pert JH. Isolated kidney perfusion: A model for testing platelet function. Proc Soc Exper Biol Med 1973; 144: 189-194
  • 17 Raymond SL, Pert JH, Dodds WJ. Evaluation of platelet cryopreservation techniques by isolated kidney perfusion. Transfusion 1975; 15: 219-225
  • 18 Brown Jr JF, Bergeron JA, Fromageot HP M, Groves JN, Slusarczuk GM, Dodds WJ. Studies of elastin as a biomaterial. NIH No l-HV-4-2981; NTIS PB 272 829/AS 1977
  • 19 Groves JN, Sears AR. Alternating streaming current measurements. J Colloid Interface Sci 1975; 53: 83-89
  • 20 Sears AR, Groves JN. The use of oscillating laminar flow streaming potential measurement to define the zeta potential of a capillary surface. J Colloid Interface Sci 1978; 65: 479-482
  • 21 Snedecor GW. Statistical methods. Down State College Press; Iowa: 1946. p 43
  • 22 Hahn GJ, Shapiro SS. Statistical models in engineering. John Wiley and Sons; New York: 1967. p 294
  • 23 Wright BW, Lee ML, Graham SW, Phillips LV, Hercules OM. Glass surface analytical studies in the preparation of open tubular columns for gas chromatography. J Chromatogr 1980; 199: 355-369
  • 24 Baier RE, Depalma VA, Furuse A, Gott VL, Kamlott GW, Lucas T, Sawyer PN, Srnivasan S, Slanczewski B. Thromboresistance of glass after glow discharge treatment in argon. J Biomed Mat Res 1975; 9: 547-560
  • 25 Baier RE, Akers C, Perlmutter S, Gott VL, O’Riordan J. Interfacial biophysics of materials in contact with blood. NIH No l-HB-3-2954- 2; NTIS PB 277 928 NS 1976
  • 26 Cuypers PA, Hermens WT, Hemker HC. Ellipsometric study of protein film on chromium. Ann NY Acad Sci 1977; 283: 77-86
  • 27 Brash JL, Uniyal S, Samak Q. Exchange of albumin absorbed on polymer surfaces. Trans Am Soc Art Int Organs 1974; 20: 69-76