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. 2020 Jan 7;13(2):266. doi: 10.3390/ma13020266

Table 2.

Benefits and limitations of the MNP synthesis methods.

MNP Synthesis Methods Advantages Disadvantages References
Mechanical attrition Simple; inexpensive equipment; adequate for scale-up. Contamination from the materials in the media and/or atmosphere; difficulty to consolidate the powder core without coarsening the crystalline structure. [35,36]
Thermal quenching Up-scalable process; favorable composition control. Elevated temperatures required; large size distribution; lack of homogeneity in microstructure. [37]
Pyrolysis Reduced reaction times; high purity. High-pressure and temperature conditions; gas as adsorbent and carrier; large size distribution; aggregation phenomena. [36,38]
Co-precipitation Simple execution; adequate for the synthesis of complex metal oxide NPs; high reproducibility; inexpensive method. Requires a nanoparticle separation step, for obtaining uniform size distribution; quasi-spherical NPs; risk of oxidation and aggregation phenomena. [36,39]
Thermal decomposition Size control; narrow size distribution; crystallinity; Easy scale-up process. Dilatory process; uses organic solvents; requires further steps to obtain water-soluble MNPs. [40]
Hydrothermal Fine particles; no required organic solvents; no required post-treatment; Environmentally benign. Long reaction times. [36]
Microemulsification Simple method; adequate for in vitro and in vivo applications; controllable size and MNP morphology. Low scalability; reduced quantity of MNPs synthesized; difficult removal of surfactant. [41]
Polyol-based Uniform MNPs; size and shape control; simple and reproducible process. May require high temperature and pressure environment for higher magnetization values. [42]
Sol-gel Controlled particle size and shape; production of oxide MNP by gel calcination; adequate for hybrid MNPs. Requires thermal treatment at elevated temperatures; incomplete removal of matrix components from MNP surface. [35]
Electrochemical Ambient temperature environment; narrow size distribution; high purity; adequate for maghemite NPs. Complicated and long process. [40,43]
Biosynthesis High crystallinity; prominent T2 relaxation reduction and contrast. Reduced control in MNP specifications; mixture of cubic, octahedral and dodecahedral MNPs; low scalability potential. [37,40]