Comparative cytotoxic response of nickel ferrite nanoparticles in human liver HepG2 and breast MFC-7 cancer cells

Chemosphere

Volumn 135, Issue , 2015, Pages 278-288

  Ahamed, Maqusood ^a   Akhtar, Mohd Javed ^a   Alhadlaq, Hisham A ^a   Khan, M A Majeed ^a   Alrokayan, Salman A ^a  

^a KING SAUD UNIVERSITY   (Saudi Arabia)

Author keywords

Cytotoxicity; Human breast cells; Human health; Human liver cells; Nickel ferrite nanoparticles; Oxidative stress

Indexed keywords

AMINO ACIDS; CELL CULTURE; CYTOTOXICITY; DISEASES; DRUG DELIVERY; GENES; MAGNETIC RESONANCE IMAGING; MITOCHONDRIA; NANOMAGNETICS; NANOPARTICLES; NICKEL; OXIDATIVE STRESS; TOXICITY;

HUMAN BREAST; HUMAN HEALTH; HUMAN LIVER CELLS; LACTATE DEHYDROGENASE ASSAYS; MITOCHONDRIAL MEMBRANE POTENTIAL; NICKEL FERRITE NANOPARTICLE; REACTIVE OXYGEN SPECIES; TUMOR SUPPRESSOR GENES;

FERRITE;

ACETYLCYSTEINE; ANTINEOPLASTIC AGENT; CASPASE 3; CASPASE 9; FERRITE; GLUTATHIONE; MESSENGER RNA; NANOPARTICLE; NICKEL; NICKEL FERRITE NANOPARTICLE; PROTEIN BAX; PROTEIN P53; REACTIVE OXYGEN METABOLITE; UNCLASSIFIED DRUG; FERRIC ION; METAL NANOPARTICLE; NEUTRAL RED; NICKEL FERRITE;

CANCER; ENZYME ACTIVITY; GENE EXPRESSION; GERM CELL; HEALTH RISK; NANOTECHNOLOGY; NICKEL; OXIDATION; RNA; TOXICITY TEST;

ANTINEOPLASTIC ACTIVITY; ARTICLE; BREAST CANCER; CELL VIABILITY; COMPARATIVE STUDY; CONTROLLED STUDY; CYTOTOXICITY; DRUG ACTIVITY; HUMAN; INVESTIGATIVE PROCEDURES; LIPID PEROXIDATION; LIVER CANCER; MITOCHONDRIAL MEMBRANE POTENTIAL; OXIDATIVE STRESS; PROTEIN DEPLETION; QUANTITATIVE ANALYSIS; REAL TIME POLYMERASE CHAIN REACTION; ROENTGEN SPECTROSCOPY; TRANSMISSION ELECTRON MICROSCOPY; X RAY DIFFRACTION; ZETA POTENTIAL; APOPTOSIS; HEPG2 CELL LINE; LIVER; MCF 7 CELL LINE; METABOLISM;

APOPTOSIS; CASPASE 3; CASPASE 9; FERRIC COMPOUNDS; GLUTATHIONE; HEP G2 CELLS; HUMANS; LIPID PEROXIDATION; LIVER; MCF-7 CELLS; MEMBRANE POTENTIAL, MITOCHONDRIAL; METAL NANOPARTICLES; NEUTRAL RED; NICKEL; OXIDATIVE STRESS; REACTIVE OXYGEN SPECIES;

EID: 84930426207     PISSN: 00456535     EISSN: 18791298     Source Type: Journal    
DOI: 10.1016/j.chemosphere.2015.03.079     Document Type: Article

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