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20 red cell concentrates (buffy-coat not removed), 5 pools of 5 and 5 pools of 10 standards plateles concentrates, as well as 5 single donor platelet concentrates obtained through Haemonetics V50-1 cytoplasmapheresis procedure, were filtered, within 48 hours after donation, using RC 100 and PL 100 blood filters developed by Pall Company. Using the RC 100 filter on red cell concentrates, the rate of leukocyte removal exceeded 99% of the initial values. The residual leukocyte count per unit was 5.8 +/- 3.4 10(6). Leukocytes in red cell concentrates filtered after a previous one on the same filter numbered 18.6 +/- 8.9 10(6). The rate of platelet removal exceeded 97% of the initial amount. Red cell loss was 6 +/- 9% or 4 +/- 3% of a single or a subsequent unit were filtered respectively. Using the PL 100 filter on platelet concentrates, the rate of leukocyte removal exceeded 88% of the initial values. Residual leukocyte counts were 1.4 +/- 0.4 10(6), 6.2 +/- 3.8 10(6) and 1.4 +/- 0.8 10(6) respectively in 6-unit pools, 10-unit pools and machine prepared platelet concentrates. The average platelet loss was 15%. There was no evidence of alteration in the qualitative parameters of red cells or platelets. The filters were easy to handle and the time needed for the whole filtration process was remarkably short.

The trypsin-polybren-citrate (TPC) technique is based on Lalezari's method and has been developed in the Groupamatic equipment to allow the screening of irregular allo-antibodies which are not detectable on this machine by the present routine techniques. TPC screening has two main advantages: it gives more reliable results for Rh, Kell, Lewis and P antibodies than bromelin-methyl-cellulose, and it permits the screening of Duffy and Kidd antibodies, However, although the TPC technique contributes to an improved quality of the automated screening of blood donor samples, it should not be used as the only method when recipient samples are concerned.

Oxygen affinity of haemoglobin is modulated by several parameters such as the allosteric effector 2-3 DPG for most mammalians. Inositol hexaphosphate (I.H.P.) exerts the same effect on haemoglobin. A previously developed new methodology for the entrapment of drugs into erythrocytes has been adapted to I.H.P.; it is based on a reversible osmotic shock. I.H.P. loaded red blood cells have characteristics very similar to those of native cells. The decrease in oxygen affinity is related to the dose of encapsulated I.H.P. In piglets, transfusion of such cells has led to an increase of oxygen extraction from haemoglobin. Normal anesthetized animals regulate their oxygen consumption by reduction of cardiac output.