BACKGROUND: Photochemical methods can effectively inactivate extracellular
Viruses and bacteria found in blood components. Treatment of plasma with me
thylene blue (MB), a phenothiazine dye, and visible light inactivates envel
oped Viruses including HIV-1. The effects of MB-treated plasma on cellular
components stored in vitro have not been well characterized.
STUDY DESIGN AND METHODS: MB-treated plasma (83 mu g MB/250 mL plasma) was
added to single-donor platelets, stored AS-1 red cells (RBCs), irradiated R
BCs, and frozen-deglycerolized RBCs. In vitro platelet assays performed aft
er 1 and 5 days of storage in MB-treated plasma included pH, pO(2), pCO(2),
HCO3, platelet number, lactate dehydrogenase, glucose, osmotic recovery, a
nd CD62 expression. RBC components were examined at specific intervals for
leakage of potassium, plasma hemoglobin level, and percentage of hemolysis.
Direct antiglobulin tests, osmotic fragilities, and RBC antigen stability
tests were also performed on RBCs stored in MB-treated plasma. Components s
tored with autologous plasma or nontreated allogeneic plasma served as cont
rols.
RESULTS: Similar storage-induced changes in pH, glucose, and platelet numbe
rs, as well as increases in lactate dehydrogenase, CD62 expression, and lac
tate were seen in single-donor platelets stored with MB-treated and control
plasma. Platelet morphology scores and osmotic recoveries were not altered
. Plasma hemoglobin and potassium and percentage of hemolysis increased equ
ally in the Various RBC components stored with MB-treated or nontreated pla
sma. Osmotic fragility and RBC antigen stability were not appreciably alter
ed by MB-treated plasma.
CONCLUSION: Plasma treated by MB photoinactivation can be used for in vitro
resuspension and storage of platelets or RBCs, because of the lack of infl
uence of MB-treated plasma on a variety of in vitro platelet and RBC assays
.