应用紫外-可见光谱法和荧光光谱法并以中性红(NR)作光谱探针研究了Sm(Ⅲ)HP配合物与DNA的作用机制。研究表明,血卟啉(HP)与Sm(i11)的配合比nSm(Ⅲ):nHP=1:1,Sm(Ⅲ)HP配合物与DNA的结合比nSm(Ⅲ)HP:nDNA=1:1,Sm(Ⅲ)HP配合物与DNA的结合常数K30℃^θ=1.67×10^4L/mol。该过程为熵所驱动,其△r巩。为4.86×10^4J/mol,△rSm^θ为195.61J/(mol·K),30℃时△rGm^θ为-1.06×10^4J/mol。Scatchard法和探针法研究表明,Sm(Ⅲ)HP与DNA之间的结合方式主要是沟区作用。
Using neutral red (NR) as a probe, functionary mechanism between Sm ( Ⅲ ) HP and DNA was studied by UV-vis and fluorescence spectroscopy. The results indicated that the binding ratio of nsm(Ⅲ) : nHP is 1 : 1, nsm(Ⅲ)HP: nDNA =1 : 1, and the binding constant of Sm ( Ⅲ ) HP complex with Herring Sperm DNA was K30℃^θ = 1.67 × 10^4 L/mol. Thermodynamic parameters of enthalpy (△rHm^θ), entropy (△rSm^θ) , and Gibbs free energy (△rGm^θ) were calculated to be 4. 86 × 104 J/mol, 195.61 J/ ( mol · K) and - 1.06 × 104 J/mol, respectively. The results suggested that the process of interaction of Sm ( Ⅲ ) HP complex and Herring Sperm DNA was driven by entropy. The results of scatchard and probe methods suggested that the primary interaction mode between Sm ( Ⅲ ) HP and DNA was groove binding.