Application volume
Thaw, and mix the HL-60 and Raji cell stock suspensions. Dispense 90-µL aliquots into individual incubation tubes. Add 3 µL of the
Test solution to each incubation tube, and mix on a vortex mixer for 5 seconds. Incubate for 30 minutes with gentle rocking at 37 ± 2
.
Procedure
Mix each incubation tube on a vortex mixer. Immediately remove, and apply 10 µL of sample to the origin of the
Adsorbent ATLC strip (2 cm from bottom). Allow the sample to adsorb onto the strip, and immediately develop the strip by ascending chromatography (see
Thin-Layer Chromatography under
Chromatography 621) until the solvent front has moved about 7.5 cm from the origin. Remove the strips, and allow to air-dry. Cut both strips 4 cm above the origin. Separately measure and record the background-corrected radioactivity found on the top and bottom sections of each strip, using a suitable radiation detector. Immunoreactive technetium
99mTc fanolesomab, bound to the HL-60 cells, remains at the origin, while nonbound forms of
99mTc migrate away from the origin. Nonspecific binding is measured using the Raji negative control cells. Calculate the specific immunoreactive binding by the formula:
[100AB(HL-60) /(AB(HL-60) + AT(HL-60))] [100AB(Raji) /(AB(Raji) + AT(Raji))]
in which
AB(HL-60) and
AB(Raji) are the radioactivity of the HL-60 positive control cells and Raji negative control cells, respectively, measured on the bottom section of each strip; and
AT(HL-60) and
AT(Raji) are the radioactivity of the HL-60 positive control cells and Raji negative control cells measured on the top section of each strip. A minimum specific immunoreactive binding of 40% is required for the CD15-positive HL-60 cells.