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. 2023 Jul 20;4:100122. doi: 10.1016/j.jvssci.2023.100122

Table I.

Composition of storage buffers

Opti-MEM Krebs-HEPES WI Krebs-PSS
K lactobionate, mmol/L - - 100 -
KH2PO4, mmol/L - 1.03 25 2
MgSO4, mmol/L 0.8 1.2 5 1.2
NaHCO3, mmol/L 26 25 - 25
EDTA, mmol/L - - - 0.026
Raffinose, mmol/L - - 30 -
Adenosine, mmol/L - - 5 -
Glutathione, mmol/L - - 3 -
Allopurinol, mmol/L - - 1 -
Hydroxyl starch, g/L - - 50 -
HEPES, mmol/L - 20 - -
Glucose, mmol/L 5.5 5.6 - 11
Na, mmol/L - 145 25 144
K, mmol/L - 5 120 4.7
Cl, mmol/L - 108.7 - 127.7
Ca, mmol/L - 1.8 or 2.5 - 2.5
Osmolality, mOsm/L 280-320 320
pH 7.1-7.4 7.4 7.4 7.4
Notes Proprietary Insulin, steroid, antibiotics

EDTA, Ethylenediaminetetraacetic acid; HEPES, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid; MEM, minimal essential medium; PSS, physiological salt solution.

Arterial storage was tested in physiologic solutions including Opti-MEM at 4 °C and 37 °C, Krebs-HEPES with 1.8 mmol/L calcium and 2.5 mmol/L calcium, and compared Wisconsin buffer. Arterial function was tested in physiologic salt solution (Krebs-PSS).