Title of article :
BSA nanoparticles loaded with IONPs for biomedical applications: fabrication optimization, physicochemical characterization and biocompatibility evaluation
Author/Authors :
Najafi Anamaghi, Parvin Protein Research Centre - Shahid Beheshti University, G. C. Velenjak, Tehran, Iran , Kouchakzadeh, Hasan Protein Research Centre - Shahid Beheshti University, G. C. Velenjak, Tehran, Iran
Abstract :
Objective(s): Cancer diagnosis in its early stages of progress, can enhance the efficiency of treatment utilizing
conventional therapy methods. Non-biocompatibility of iron oxide nanoparticles (IONPs) has made a big
challenge against their usage as a contrast agent. Efficient coverage by biomolecules such as albumin can be
a solution to overcome this problem. Herein, albumin-coated IONPs were prepared and the process was
optimized using the response surface methodology (RSM) to achieve optimum loading of IONPs in albumin
nanoparticles.
Materials and Methods: IONPs were incorporated into bovine serum albumin nanoparticles (BSA NPs)
matrix, to yield IONPs-BSA NPs. The resulting nanoparticles were characterized physicochemically by
scanning electron microscopy (SEM), dynamic light scattering (DLS), inductively coupled plasma optical
emission spectrometry (ICP-OES), Fourier transform infrared spectroscopy (FTIR) and vibrating sample
magnetometer (VSM). The stability test was conducted over 6 months.
Results: Under optimum conditions of 2.28 mg for iron weight and pH 9.21, loading of 7.76% was obtained
for the spherical IONPs-BSA NPs with the size of 177±12 nm, PDI of 0.222±0.07 and zeta-potential of
-36.4±2.3 mV. These findings revealed that more than 90% and 60% of the particles retained their size over
four and six months of storage at 4 °C, respectively. In addition, non-cytotoxicity and hemocompatibility of
IONPs-BSA NPs were verified in vitro thereby offering them as a biocompatible contrast agent for cancer
diagnosis
Keywords :
Bovine serum albumin nanoparticles , Iron oxide nanoparticles , Optimum production , Response surface methodology (RSM)
Journal title :
Astroparticle Physics