Title of article
Synthesis and Characterization of Targeted Magnetic Bentonite Nanohybrid for Enhanced Drug Delivery: A Promising Approach for Cancer Therapy
Author/Authors
Asadi Tokmedash ، Mohammad School of Chemical Engineering, College of Engineering - University of Tehran , Salehi ، Zeinab School of Chemical Engineering, College of Engineering - University of Tehran , Rezaeitavabe ، Fatemeh Department of Civil Engineering - Ohio University , Mousavi ، Maede School of Chemical Engineering, College of Engineering - University of Tehran
From page
935
To page
945
Abstract
The use of smart materials to deliver anticancer drugs to tumors has been considerably increased in cancer therapy. In this work, a novel pH-responsive system for drug delivery is proposed that employs magnetite nanoparticles and bentonite loaded with doxorubicin (DOX), a known anticancer drug, to investigate its loading capacity and release. This magnetic bentonite nanohybrid is first synthesized using a single-step method. The structural and spectral properties of the nano-assemblies are analyzed employing a variety of analytical methods including Fourier Transform InfraRed (FT-IR) spectroscopy, Scanning and Transmission Electron Microscopy (SEM and TEM, respectively), X-Ray Diffraction (XRD), and Vibrating Sample Magnetometer (VSM). The drug-loading capacity, entrapment, and yield are compared with different ratios of 1:1, 1:2, and 1:4 of the drug: nanohybrid to choose the best ratio. Moreover, a pH-sensitive release is measured at pH 7.4 and 5.5 with a total release of 57% and 80% after 72 h, respectively. Considering all these findings, the magnetic bentonite shows significant promise as a potential candidate for drug delivery applications targeting cancer cells.
Keywords
magnetic bentonite nanohybrid , doxorubicin , Drug Delivery , Magnetite nanoparticles
Journal title
Iranian Journal of Chemistry and Chemical Engineering (IJCCE)
Journal title
Iranian Journal of Chemistry and Chemical Engineering (IJCCE)
Record number
2768276
Link To Document