Not really. The study below indicates that aliquots were only brought to temperature and not kept at 37°.
"Here, we report that LDX hydrolytic activity resides in human red blood cell lysate and cytosolic extract but not in the membrane fraction."
"Duplicate 1.98 mL samples of blood or fractionated blood were equilibrated to 37°C for 5 minutes before addition of 20 μL of stock LDX to produce a final LDX concentration of 1 μg/mL. At 0, 15, 30, 60, 120, and 240 minutes after addition of LDX..."
Notice they did not keep the blood samples at 37°, simply brought to temp for 5 min.
Lisdexamfetamine dimesylate (LDX) is approved as a once-daily treatment for attention-deficit/hyperactivity disorder in children, adolescents, and adults in some countries. LDX is a prodrug comprising d-amphetamine covalently linked to l-lysine via ...
www.ncbi.nlm.nih.gov
But letting it sit there for 4 hours is necessary for it to get (most of) the d-amphetamine out.
If you read the paper, you'll see that you can actually mix it into human blood, let it sit there for 4 or 5 hours and then it will be pretty much all d-amphetamine.
It's sort of gross, I mean that's really going beyond the pale.