Fabrication of a novel cellulose acetate imprinted membrane assisted with chitosan-wrapped multi-walled carbon nanotubes for selective separation of salicylic acid from industrial wastewater

2015 ◽  
Vol 132 (42) ◽  
pp. n/a-n/a ◽  
Author(s):  
Minjia Meng ◽  
Zhihui He ◽  
Li Yan ◽  
Yongsheng Yan ◽  
Fengquan Sun ◽  
...  
2021 ◽  
Author(s):  
Reza Alisani ◽  
Navid Rakhshani ◽  
maryam Abolhallaj ◽  
Foojan Motevallid ◽  
Parvaneh Ghaderi-shekhi Abadi ◽  
...  

Abstract The cellulose acetate (CA)/poly (ε-caprolactone diol)/poly (tetramethylene ether) glycol-polyurethane (PCL-Diol/PTMG-PU)/multi-walled carbon nanotubes (MWCNTs) composite nanofibers were prepared via two-nozzle electrospinning on both counter sides of the collector. The performance of synthesized composite nanofibers was investigated as an environmental application and anticancer delivery system for the adsorption/release of doxorubicin (DOX). The synergic effect of MWCNTs and DOX incorporated into the nanofibers was investigated against LNCaP prostate cancer cells. The status of MWCNTs and DOX in composite nanofibers was demonstrated by SEM, FTIR and UV-Vis determinations. The adsorption tests using nanofibrous adsorbent toward DOX sorption was evaluated under various DOX initial concentrations (100-2000 mgL-1 ), adsorption times (5-120 minutes), and pH values (pH:2-9). Due to the fitting of isotherm and kinetic data with Redlich-Peterson and pseudo-second order models, both chemisorption and surface adsorption of DOX molecules mechanisms have been predicted. The drug release from both nanofibers and MWCNTs-loaded nanofibers was compared. The better drug sustained release profiles verified in the presence of composite nanofibers. LNCaP prostate cancer and L929 normal cells were treated to investigate the cytotoxicity and compatibility of synthesized composite nanofibers. The apoptosis/necrosis of hybrid nanofibers and MWCNTs loaded-nanofibers was investigated. The obtained results demonstrated the synergic effects of MWCNTs and DOX loaded-nanofibers on the LNCaP prostate cancer cells death.


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