Monir Shalbafan - Department of chemistry, Imam Khomeini International University, Qazvin, Iran
Gholamreza Rezaei Behbehani - Department of chemistry, Imam Khomeini International University, Qazvin, Iran
Hosein Ghasemzadeh - Department of chemistry, Imam Khomeini International University, Qazvin, Iran

Human serum albumin (HSA) is one of the main endogenous vehicles for biodistribution of molecules by blood plasma. Association constants and thermodynamic parameters for the interaction of HSA with doxorubicin were studied by docking. Docking study suggests that doxorubicin is able to interact with HSA by means of hydrogen bond with one arginine residue, whereas the hydroxyl group is inserted in a hydrophobic pocket. The estimated of Gibbs free energies (ΔG°) is equal to -9.1 kcal/mol for the best model. The negative values of ΔG° indicate a spontaneous process. The association constant value (Ka ≈ 8×103 L.mol−1) is favorable for its efficient biodistribution by blood plasma. 

Human Serum Albumin, doxorubicin, Docking, thermodynamic parameters