Related Experiment Video
Updated: Aug 11, 2026

Determination of Protein-ligand Interactions Using Differential Scanning Fluorimetry
Published on: September 13, 2014
[Effect of temperature on plasma concentration of FK506]
1Department of Urology, Gunma University School of Medicine.
Because the affinity of FK506 for red blood cells is strong, plasma FK506 levels vary depending upon the temperature at which plasma is separated from whole blood. This study was undertaken to investigate the effects on plasma FK506 of blood temperature at the time of separation and of its rewarming at 37 degrees C, using A) blood samples from rats administered with FK506 at 1 mg/kg for 7 days, and B) human blood samples added with FK506 at 1.0, 3.2 and 10 ng/ml in vitro. 1) Plasma FK506 levels of samples from rats were not affected by storage time, but samples separated at 20 degrees C were significantly lower in FK506 levels than those separated at 37 degrees C. Plasma FK506 level after rewarming blood at 37 degrees C was not significantly different from that of blood stored at 37 degrees C. 2) FK506 levels in human plasma, separated at 30 degrees C and 20 degrees C were 51% and 33%, respectively, of the corresponding value for plasma separated at 37 degrees C. But the level of plasma separated at 0 degrees C was 56%, which was higher than that at 20 degrees C. 3) Rewarming of human blood at 37 degrees C for 5 minutes allowed the plasma FK506 level to return to the initial level. FK506 levels of plasma separated without regard to temperature are less reliable and reproducible.(ABSTRACT TRUNCATED AT 250 WORDS)
Because the affinity of FK506 for red blood cells is strong, plasma FK506 levels vary depending upon the temperature at which plasma is separated from whole blood. This study was undertaken to investigate the effects on plasma FK506 of blood temperature at the time of separation and of its rewarming at 37 degrees C, using A) blood samples from rats administered with FK506 at 1 mg/kg for 7 days, and B) human blood samples added with FK506 at 1.0, 3.2 and 10 ng/ml in vitro. 1) Plasma FK506 levels of samples from rats were not affected by storage time, but samples separated at 20 degrees C were significantly lower in FK506 levels than those separated at 37 degrees C. Plasma FK506 level after rewarming blood at 37 degrees C was not significantly different from that of blood stored at 37 degrees C. 2) FK506 levels in human plasma, separated at 30 degrees C and 20 degrees C were 51% and 33%, respectively, of the corresponding value for plasma separated at 37 degrees C. But the level of plasma separated at 0 degrees C was 56%, which was higher than that at 20 degrees C. 3) Rewarming of human blood at 37 degrees C for 5 minutes allowed the plasma FK506 level to return to the initial level. FK506 levels of plasma separated without regard to temperature are less reliable and reproducible.(ABSTRACT TRUNCATED AT 250 WORDS)
Related Concept Videos
Effects of Temperature on Free Energy
Atomic Spectroscopy: Effects of Temperature
At thermal equilibrium, the relative populations of excited and ground state atoms can be estimated using the Maxwell–Boltzmann distribution. For example, an increase in temperature from...
Drug Concentration Versus Time Correlation
Two pivotal parameters are the minimum effective concentration (MEC) and the minimum toxic concentration (MTC). The MEC is the lowest drug...
Factors Affecting Protein-Drug Binding: Protein-Related Factors
The physicochemical properties of a drug play a significant role in its ability to bind to proteins. Lipophilic drugs, which dissolve in fats, oils, and lipids, can be bound by...
Factors Affecting Protein-Drug Binding: Patient-Related Factors
Age stands as a key determinant in protein-drug binding. Neonates, characterized by low albumin content, experience heightened concentrations of unbound drugs such as phenytoin and...
Determination of Multiple Dosing Parameters: Steady-State, Minimum and Maximum Concentrations

