共 45 条
Studying Adsorption and Cellular Toxicity of Boron Nitride Nanostructure versus Melphalan Anti-ovaria n Cancer Drug
被引:19
作者:
Fu, Min
[1
]
Tayebee, Reza
[2
]
Saberi, Satar
[3
]
Nourbakhsh, Narjes
[2
]
Esmaeili, Effat
[4
]
Maleki, Behrooz
[2
]
Vatanpour, Hamid R.
[3
]
机构:
[1] Weifang Peoples Hosp, Dept Pharm Intravenous Admixture Serv, Weifang City, Shandong, Peoples R China
[2] Hakim Sabzevari Univ, Sch Sci, Dept Chem, Sabzevar 9617976487, Iran
[3] Farhangian Univ, Dept Basic Sci, Tehran, Iran
[4] Payame Noor Univ PNU, Dept Chem, Tehran 193954697, Iran
关键词:
Melphalan;
adsorption;
DFT method;
boron nitride fullerene;
anti-ovarian cancer drug;
WASTE-WATER;
METHYLENE-BLUE;
REMOVAL;
KINETICS;
IRON;
DYE;
TECHNOLOGIES;
BIOSORPTION;
NANOTUBES;
MOLECULES;
D O I:
10.2174/1566524021666210111104428
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Background: Inclusion of anticancer drugs into biocompatible nanoparticulate carriers decreases the general toxicity and improves the efficacy of clinical treatments due to the reduction of soluble circulating free drugs. Methods: In addition, removal of emerging drug contaminants from wastewaters is a necessity that should be seriously attended. Boron nitride (BN) is a choice in drug delivery because of its many surprising properties. Here, boron nitride nanoparticles are prepared, characterized by Fourier-transform infrared spectroscopy (FT-IR) and x-ray diffraction (XRD) and used in the delivery of melphalan anti-cancer drug. Results: Then, density functional theory (DFT) calculations are carried out to study the adsorption of this drug on the surface of pure boron nitride fullerene via familiar hybrid functionals B3LYP and B3PW91. In addition, the polarizable continuum model (PCM) calculations show that BN is stable in water. Conclusion: Finally, the in vitro cellular toxicity and viability of BN nanoparticles was examined on ES-2 cancer cells. The inhibitory dose IC50 of the material confirmed acceptable cytotoxicity and nanoparticles affected the average growth of the ES-2 cancer cells.
引用
收藏
页码:698 / 705
页数:8
相关论文