Magnetic particles are widely used as signal labels in a variety of biological sensing applications, such as molecular detection and related strategies that rely on ligand-receptor binding. In this review, we explore the fundamental concepts involved in designing magnetic particles for biosensing applications and the techniques used to detect them. First, we briefly describe the magnetic properties that are important for bio-sensing applications and highlight the associated key parameters (such as the starting materials, size, functionalization methods, and bio-conjugation strategies). Subsequently, we focus on magnetic sensing applications that utilize several types of magnetic detection techniques: spintronic sensors, nuclear magnetic resonance (NMR) sensors, superconducting quantum interference devices (SQUIDs), sensors based on the atomic magnetometer (AM), and others. From the studies reported, we note that the size of the MPs is one of the most important factors in choosing a sensing technique.

MSM-AFM images of Fe ₃ O ₄ nanoparticles arranged on glass: individual nanoparticles that are invisible in topography frames can be mapped using MSM-AFM.

MicroRNA (miRNA) has emerged as a promising alternative therapeutic treatment for cancer, but its delivery has been hindered by low cellular uptake and degradation during circulation. In this review, we discuss the various methods of delivering miRNA, including viral and non-viral delivery systems such as liposomes and nanoparticles. We also examine the use of nanoparticles for miRNA-based diagnostics. We focus specifically on non-viral delivery systems utilizing coinage metals in the form of nanoparticles and the use of self-assembled monolayers (SAMs) as a method of surface modification. We review the use of SAMs for the conjugation and delivery of small noncoding ribonucleic acid (ncRNA), particularly SAMs derived from positively charged adsorbates to generate charged surfaces that can interact electrostatically with negatively charged miRNA. We also discuss the effects of the cellular uptake of gold and other plasmonic nanoparticles, as well as the challenges associated with the degradation of oligonucleotides. Our review highlights the potential of SAM-based systems as versatile and robust tools for delivering miRNA and other RNAs in vitro and in vivo and the need for further research to address the challenges associated with miRNA delivery and diagnostics.

This study examines the effect of annealing on 135 nm Fe₃O₄ nanospheres and establishes a direct correlation among particle shape, crystallite size, and magnetic properties. Polycrystalline nanospheres and highly crystalline nanocubes with an equivalent diameter/body diagonal of 135 nm were synthesized via solvothermal and thermal decomposition methods, respectively. Scanning electron microscopy (SEM) revealed that the nanospheres developed smoother surfaces and gradually transformed toward a cubic morphology upon annealing, with increasing temperature and duration. Vibrating sample magnetometry (VSM) measurements showed that both saturation magnetization and coercivity increased with annealing as the particles evolved toward cube-like morphology and larger crystallite size, indicating that the magnetic properties of Fe₃O₄ nanoparticles are strongly dependent on crystallite size and shape. Nanospheres annealed between 500 and 850 °C exhibited increases in both crystallite size and saturation magnetization; however, coercivity decreased at 850 °C, where the crystallite size was maximal. Annealing at 700 °C for 12 h resulted in enhanced crystallite size and improved magnetic properties. Prolonged annealing at 700 °C (24 h) yielded the largest crystallite size but led to a significant reduction in saturation magnetization. This study demonstrates a clear correlation between magnetic properties, crystallinity, and morphology in nanoparticles beyond the superparamagnetic size regime (e.g., 135 nm). It further provides a strategy for tuning structural parameters that govern magnetic behavior and establishes an alternative, more facile route to obtain Fe₃O₄ nanospheres with crystallite sizes and magnetic properties comparable to nanocubes obtained via direct synthesis.