Magnetic drug targeting (MDT) and magnetic-based drug/cargo delivery are emerging treatment methods which attracting the attention of many researchers for curing different cancers and artery diseases such as atherosclerosis. Herein, computational studies are accomplished by utilizing magnetic approaches for cancer and artery atherosclerosis drug delivery, including nanomagnetic drug delivery and magnetic-based drug/cargo delivery. For the first time, the four-layer structural model of the artery tissue and its porosity parameters are modeled in this study which enables the interaction of particles with the tissue walls in blood flow. The effects of parameters, including magnetic field strength (MFS), magnet size, particle size, the initial position of particles, and the relative magnetic permeability of particles, on the efficacy of MDT through the artery walls are characterized. The magnetic particle penetration into artery layers and fibrous cap (the covering layer over the inflamed part of the artery) is further simulated. The MDT in healthy and diseased arteries demonstrates that some of the particles stuck in these tissues due to the collision of particles or blood flow deviation in the vicinity of the inflamed part of the artery. Therefore the geometry of artery and porosity of its layers should be considered to show the real interaction of particles with the artery walls. Also, the results show that increasing the particles/drug/cargo size and MFS leads to more particles/drug/cargo retention within the tissue. The present work provides insights into the decisive factors in arterial MDT with an obvious impact on locoregional cancer treatment, tissue engineering, and regenerative medicine.
Over the past decade, the growing interest in targeted lung cancer therapy has guided researchers toward the cutting edge of controlled drug delivery, particularly magnetic particle targeting. Targeting of tissues by magnetic particles has tackled several limitations of traditional drug delivery methods for both cancer detection (e.g., using magnetic resonance imaging) and therapy. Delivery of magnetic particles offers the key advantage of high efficiency in the local deposition of drugs in the target tissue with the least harmful effect on other healthy tissues. This review first overviews clinical aspects of lung morphology and pathogenesis as well as clinical features of lung cancer. It is followed by reviewing the advances in using magnetic particles for diagnosis and therapy of lung cancers: (i) a combination of magnetic particle targeting with MRI imaging for diagnosis and screening of lung cancers, (ii) magnetic drug targeting (MDT) through either intravenous injection and pulmonary delivery for lung cancer therapy, and (iii) computational simulations that models new and effective approaches for magnetic particle drug delivery to the lung, all supporting improved lung cancer treatment. The review further discusses future opportunities to improve the clinical performance of MDT for diagnosis and treatment of lung cancer and highlights clinical therapy application of the MDT as a new horizon to cure with minimal side effects a wide variety of lung diseases and possibly other acute respiratory syndromes (COVID-19, MERS, and SARS).
Primary bronchial cancer accounts for almost 20% of all cancer death worldwide. One of the emerging techniques with tremendous power for lung cancer therapy is magnetic aerosol drug targeting (MADT). The use of a permanent magnet for effective drug delivery in a desired location throughout the lung requires extensive optimization, but it has not been addressed yet. In the present study, the possibility of using a permanent magnet for trapping the particles on a lung tumor is evaluated numerically in the Weibel's model from G0 to G3. The effect of different parameters is considered on the efficiency of particle deposition in a tumor located on a distant position of the lung bronchi and bronchioles. Also, the effective position of the magnetic source, tumor size, and location are the objectives for particle deposition. The results show that a limited particle deposition occurs on the lung branches in passive targeting. However, the incorporation of a permanent magnet next to the tumor enhanced the particle deposition fraction on G2 to up to 49% for the particles of 7 mm diameter. Optimizing the magnet size could also improve the particle deposition fraction by 68%. It was also shown that the utilization of MADT is essential for effective drug delivery to the tumors located on the lower wall of airway branches given the dominance of the air velocity and resultant drag force in this region. The results demonstrated the high competence and necessity of MADT as a noninvasive drug delivery method for lung cancer therapy. ARTICLE HISTORY
Induced charge electrokinetics (ICEK) has recently expanded its range of applications in biomedical engineering due to its high potential for being used in particle/cell manipulation platforms, micromixers, micropumps, and microvalves. In these devices, the generated microvortices around conducting hurdles/electrodes are used in order to achieve the desired operations. In the present study, the influences of non-uniform electric field on the generated microvortices around a conducting cylinder are analyzed in a micromixer. The electric field non-uniformities are produced either by pin-plate electrodes or by geometrical configuration. Results show that inhomogeneous electric fields lead to reduction of the induced zeta potential (IZP) and the microvortices velocity around the cylinder in the majority of the studied cases. However, imposing two electric fields with appropriate directions or positioning the cylinder in a suitable location enhances the IZP reductions. In this study, such electric fields are utilized in the ICEK micromixer for investigation of their effects on the mixing efficiency. Based on our findings, it is demonstrated that the generated electric field by two electrodes with angle of 30° increases the mixing efficiency from 69.07% to 96.89%. The present study provides new insights into the effects of non-uniform electric field on the IZP over a conducting hurdle and the generated microvortices in ICEK flows with an application in lab-on-a-chip (LOC) devices such as micromixers, microvalves, micropumps, and particle/cell separators.
Applying an external electric field over a polarizable electrode or object within microchannels can induce an electric double layer (EDL) around channel walls and create induced-charge electrokinetics (ICEK) within channels. The primary consequence of the induced charge is the generation of micro-vortices around the polarizable electrode or object, presenting great potential for various microfluidic applications. This review presents the advances in theoretical, numerical and experimental studies on the physics and applications of ICEK within microfluidics. In particular, the characteristics and performance of ICEK-based microfluidic components in active micromixers, micropumps, and microvalves are critically reviewed, followed by discussing the applications of ICEK in electrophoresis and particle/cell manipulation within microfluidics. Furthermore, the opportunities and challenges of ICEK-based microfluidic devices are highlighted. This work facilitates recognizing deliverable ICEK-based microfluidic technologies with unprecedented functionality for the next generation of biomedical applications with predictable manufacturability and functionality.
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