2017
DOI: 10.1007/s10948-017-4094-5
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Preparation and Characterization of Magnetite–Chitosan Nanoparticles and Evaluation of Their Cytotoxicity Effects on MCF7 and Fibroblast Cells

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Cited by 30 publications
(15 citation statements)
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“…The band that corresponds only to Tween 80 is presented at 1741 cm −1 , which indicates a C=O stretching vibration. The bands that correspond only to the chitosan are the vibratory stretching mode of C-N observed at 1468 cm −1 and the bending mode of N-H at 1508 cm −1 [ 33 , 34 , 35 , 36 , 37 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The band that corresponds only to Tween 80 is presented at 1741 cm −1 , which indicates a C=O stretching vibration. The bands that correspond only to the chitosan are the vibratory stretching mode of C-N observed at 1468 cm −1 and the bending mode of N-H at 1508 cm −1 [ 33 , 34 , 35 , 36 , 37 ].…”
Section: Resultsmentioning
confidence: 99%
“…The results obtained by measuring the viability of 3T3L1 cells after exposure with magnetite nanoparticles and M-CS/Tween 80 microspheres at concentrations of 1–10,000 µg/mL were compared by those obtained by Lotfi et al In their study, they used concentrations of 10, 25, 50, 75, and 100 µg/mL of magnetite nanoparticles coated with chitosan for 24 h in MCF7 cells and fibroblasts. They obtained 78% cell viability for bare magnetite nanoparticles and a cell viability of 80% for magnetite coated with chitosan in the MCF7 cell line [ 35 ]. Viabilities obtained by our research group at concentrations of 100 µg/mL at the first 24 h are 87% for magnetite nanoparticles and 93% for M-CS/Tween 80 microspheres.…”
Section: Resultsmentioning
confidence: 99%
“…bands assigned, in dash lines, to chitosan biopolymer at 3440 cm −1 (νO-H and νΝ-Η from the amine group) (1), 1630 cm −1 (δΝ-Η) (2), 1407 cm −1 (νC-Ν) (3) and in the region of 1024 cm −1 (νC-Ο-C) (4) [50][51][52][53]. In addition, Fig.…”
Section: Fourier Transform Infrared (Ftir) Spectroscopymentioning
confidence: 95%
“…This leads to faster and more efficient removal and rebinding of the template molecules with improved binding kinetics, which saves time and the cost of analysis. Therefore, strategies to obtain core–shell structures have been developed in recent years to introduce a myriad of cores in addition to common core materials. , Biomass-derived FCDs are trending materials due to their biocompatibility and low toxicity for utilization in optoelectronics, fluorescent sensing, and bioimaging applications. , The photoluminescent properties of FCDs can be tuned by functionalization with organic–inorganic modifiers such as amino functionalities, poly­(ethylenimine), Ag and Ni doping, and biological molecules. , Among inorganic–organic linkers, alkoxysilanes are excellent linkers to introduce desirable moieties on the surface of FCDs. , Therefore, TPA is grafted on the surface of FCDs within the 3D network of mesoporous silica via the Schiff base condensation and the sol–gel process using 3-aminopropyltriethoxysilane as a linker using modified methods. The mesopores on the surface of FCDs provide channels for the mobilization of the analyte to interact with the tripodal pockets. This interaction leads to the quenching of the contributory fluorescent signal produced due to the FCDs and TPA.…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, strategies to obtain core−shell structures have been developed in recent years to introduce a myriad of cores in addition to common core materials. 21,22 Biomass-derived FCDs are trending materials due to their biocompatibility and low toxicity for utilization in optoelectronics, fluorescent sensing, and bioimaging applications. 23,24 The photoluminescent properties of FCDs can be tuned by functionalization with organic−inorganic modifiers such as amino functionalities, poly(ethylenimine), Ag and Ni doping, and biological molecules.…”
Section: Introductionmentioning
confidence: 99%