Thromb Haemost 1970; 23(01): 182-188
DOI: 10.1055/s-0038-1654132
Originalarbeiten – Original Articles – Travaux Originaux
Schattauer GmbH

A Method for Automatic Recording of the Osmotic Fragility of Blood Platelets

J Zahavi
1   University Department of Medicine “B”, Ichilov Municipal Hospital, Tel Aviv, Section of Biological Ultrastructure, The Weizmann Institute of Science, Rehovot, and Dept. of Immunology, The Hebrew University Hadassah Medical School, Jerusalem, Israel
,
D Danon
1   University Department of Medicine “B”, Ichilov Municipal Hospital, Tel Aviv, Section of Biological Ultrastructure, The Weizmann Institute of Science, Rehovot, and Dept. of Immunology, The Hebrew University Hadassah Medical School, Jerusalem, Israel
,
F Dreyfuss
1   University Department of Medicine “B”, Ichilov Municipal Hospital, Tel Aviv, Section of Biological Ultrastructure, The Weizmann Institute of Science, Rehovot, and Dept. of Immunology, The Hebrew University Hadassah Medical School, Jerusalem, Israel
,
D Nelken
1   University Department of Medicine “B”, Ichilov Municipal Hospital, Tel Aviv, Section of Biological Ultrastructure, The Weizmann Institute of Science, Rehovot, and Dept. of Immunology, The Hebrew University Hadassah Medical School, Jerusalem, Israel
› Author Affiliations
Further Information

Publication History

Publication Date:
27 June 2018 (online)

Summary

A method for automatically recording the osmotic fragility of blood platelets, using a Fragiligraph, was developed. Platelet specimens taken from 20 healthy males and 9 females were examined. The mean rate of platelet change and the extent of increase in light transmission (LT) of washed platelets suspended in veronal, Tris, or phosphate buffered saline and dialyzed against water and 0.1% sodium chloride solutions, were analyzed. The recorded curves showed a slow phase lasting 2–74 sec, followed by a phase representing a rapid rate of platelet change in which gradually swelling of the platelets occurred concomitantly with an increase in the LT. This was followed by a third phase of plateau formation. The mean rate of platelet swelling was temperature-dependent, having twice the value at 37° C as at 15° C; the extent (% increase in LT) did not vary with temperature.