The Preparation of Frozen Red Blood Cells and Deglycerolization of Frozen RBCs with Haemonetics V50plus.
- Author:
Tae Hee HAN
1
;
In Ki PAIK
Author Information
1. Department of Laboratory Medicine, Inje University Sanggye Paik Hospital, Seoul, Korea. kscosby@sanggyepaik.ac.kr
- Publication Type:Original Article
- Keywords:
Cryopreservation;
Deglycerolization;
Frozen RBC
- MeSH:
2,3-Diphosphoglycerate;
Adenosine Triphosphate;
Cryopreservation;
Erythrocytes*;
Glycerol;
Hemolysis;
Osmolar Concentration;
Plasma;
Potassium
- From:Korean Journal of Blood Transfusion
2002;13(2):149-155
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: The method utilizing high concentration glycerol is a common way to make frozen red bool cells (RBCs) for extended period, but it requires special deglycerolization equipment for washing after thawing. For economics reason, we could not have a cell washer for wahing the frozen RBCs, so attempted to use Haemonetics V50plus that we have had. METHODS: Twelve fresh packed RBCs were cryopreserved with 40% glycerol method. After 3 months, the RBCs were thawed and washed with Haemonetics V50plus. For the evaluation of the procedure, RBC reovery rate, osmolarity, 30 min saline stability (SS), % hemolysis, ATP, 2,3-DPG, LDH, potassium, and plasma hemoglobin were tested at 24hrs after washing. RESULTS: The RBC recovery rate was 82.1 +/- 4.5% (75.8-89.2) and two units of Frozen RBCs were under 80%. The Hb ATP and Hb 2,3-DPG of RBCs were 5.2 +/- 0.6 micro mol/g Hb (3.9-6.0) and 13.0 +/- 2.1 micro mol/g Hb (8.8-15.1). The supernatant osmalrity, potassium, plasma Hb and LDH were 352 +/- 7mosmol/kg H2O (342~367), 0.8 +/- 0.2 mmol/L (0.5~1.2), 0.8 +/- 0.3 mg/dL (0.4~1.1), 352 +/- 7 U/L (342~367). The 30min SS was 98.9 +/- 0.8. CONCLUSION: We could successfully freeze, thaw, and wash the frozen RBCs with Haemonetics V50 plus.
