Department of Chemistry, University of Sistan and Baluchestan, Zahedan, Iran.
Luminescence. 2024 Sep;39(9):e4869. doi: 10.1002/bio.4869.
In the present study, the drug delivery by albumin protein and antiproliferetaive activity of new transition metal complex i.e., [Pd (phen)(SSA)] (where phen and SSA represent 1, 10 phenanthroline and sulfosalicylic acid, respectively) was investigated. DFT (density functional theory) calculations were conducted at B3LYP level with 6-311G(d,p)/aug-ccpVTZ-PP basis set for the purpose of geometry optimization, frontier molecular orbital (FMO) analysis, molecular electrostatic potential (MEP), and natural bond orbital (NBO) analysis. Experimental tests were conducted to preliminarily assess the lipophilicity and antitumor activity of the metal complex, resulting in promising findings. In-silico prediction was accomplished to assess its toxicity and bioavailability. To evaluate the binding of the newly formed complex with DNA (which results in halting the cell cycle) or serum albumin protein (drug transporter to the tissues), in-silico molecular modeling was employed. Experimental results (spectroscopic and non-spectroscopic) showed that the new compound interacts with each biomolecule via hydrogen bond and van der Waals interactions. Molecular docking demonstrated the binding of this complex to the DNA groove and site I of BSA occurs mainly through hydrogen bonds. Molecular dynamics simulation confirmed the interactions between [Pd (phen)(SSA)] with DNA or BSA through stable hydrogen bonds.
在本研究中,研究了白蛋白蛋白的药物传递和新的过渡金属配合物的抗增殖活性,即[Pd(phen)(SSA)](其中 phen 和 SSA 分别代表 1,10-菲咯啉和磺基水杨酸)。为了进行几何优化、前沿分子轨道(FMO)分析、分子静电势(MEP)和自然键轨道(NBO)分析,在 B3LYP 水平上使用 6-311G(d,p)/aug-ccpVTZ-PP 基组进行了密度泛函理论(DFT)计算。进行了实验测试,初步评估了金属配合物的亲脂性和抗肿瘤活性,结果令人鼓舞。通过计算预测评估了其毒性和生物利用度。为了评估新形成的配合物与 DNA(导致细胞周期停滞)或血清白蛋白蛋白(药物转运蛋白到组织)的结合,进行了计算机分子建模。实验结果(光谱和非光谱)表明,新化合物通过氢键和范德华相互作用与每种生物分子相互作用。分子对接表明,该配合物主要通过氢键与 DNA 沟槽和 BSA 的 I 位点结合。分子动力学模拟通过稳定的氢键证实了[Pd(phen)(SSA)]与 DNA 或 BSA 之间的相互作用。