Molecular simulation of Cu, Ag, and Au-decorated Molybdenum doped graphene nanoflakes as biosensor for carmustine, an anticancer drug

被引:10
|
作者
Chima, Chioma M. [1 ,2 ]
Louis, Hitler [1 ,2 ,3 ]
Charlie, Destiny [1 ,2 ]
Imojara, Ann [1 ]
Benjamin, Innocent [1 ]
Uzowuru, Emmanuel E. [1 ,4 ]
Adeyinka, Adedapo S. [5 ]
机构
[1] Univ Calabar, Computat & Biosimulat Res Grp, Calabar, Nigeria
[2] Univ Calabar, Dept Pure & Appl Chem, Calabar, Nigeria
[3] Chettinad Hosp & Res Inst, Chettinad Acad Res & Educ, Fac Allied Hlth Sci, Kelambakkam 603103, Tamil Nadu, India
[4] Fed Univ Technol Owerri, Dept Phys, Owerri, Nigeria
[5] Univ Johannesburg, Dept Chem Sci, Johannesburg, South Africa
关键词
Carmustine; Sensor; Adsorption; and DFT; REVEALING NONCOVALENT INTERACTIONS; QUANTUM-THEORY; ADSORPTION; DELIVERY; DFT; THERMODYNAMICS; ATOMS; QTAIM;
D O I
10.1016/j.mssp.2023.107669
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
This study delves into the fascinating realm of molybdenum-doped graphene (Mo@GP) complexes, featuring captivating adsorption sites for oxygen (O) and chlorine (Cl), adorned with the mesmerizing presence of silver (Ag), gold (Au), and copper (Cu). These alluring metal-doped compounds have been proposed as potential biosensor materials, with a particular focus on their prowess in the adsorption of carmustine (cmt). Employing the formidable density functional theory (DFT) at the B3LYP-GD3BJ/def2-SVP computational approach. Enveloped by the intrigue of two distinct adsorption sites-O and Cl-we stumbled upon a remarkable revelation. Among the contenders, Cl_cmt@Ag_Mo@GP emerged triumphant with the lowest energy gap at the Cl site of carmustine adsorption, an astonishingly meager value of 0.082 eV. Following closely behind, Cl_cmt@Au_Mo@GP boasted a respectable energy gap of 0.852 eV. However, Cl_cmt@Cu_Mo@GP and Cl_cmt@Mo@GP took the stage with their grandiose energy gaps, exhibiting values of 1.128 eV and 1.843 eV, respectively. Substantially, the captivating saga unfolds, presenting the distribution of adsorption energies as follows: Cl_cmt@Mo@GP > O_cmt@Mo@GP > Cl_cmt@Au_Mo@GP > Cl_cmt@Cu_Mo@GP > O_cmt@Cu_Mo@GP > Cl_cmt@Ag_Mo@GP. In a captivating interplay of energies, the system Ag_Mo@GP unveils its preferences: the O site reigns supreme with an Eads of -0.59 eV, while the Cl site humbly follows with an Eads of -0.03. Meanwhile, within the realm of the Au_Mo@GP system, the Chlorine site claims dominance, boasting an Eads of -1.30eV, while the Oxygen site asserts its presence with an Eads of -0.21 eV. As for the Cu_Mo@GP system, the Chlorine site emerges as the epitome of favorability, commanding an Eads of -0.83 eV, while the Oxygen site modestly exhibits an Eads of -0.29 eV. Through meticulous exploration, the results unequivocally demonstrate the remarkable qualities of the investigated complexes, positioning them as promising nanomaterials for the realm of drug delivery.
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页数:14
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