arXiv subjects

E. P. Furlani

Publications and source records attributed to E. P. Furlani.

6 recordsLinked to original sources

arXiv2008

Free-space Excitation of Resonant Cavities formed from Cloaking Metamaterial

We propose a new class of resonant electromagnetic structures, and study their response to free-space illumination. The structures consist of partial cylindrical shells that have cloaking material properties proposed by Pendry et al. These metamaterial shells have apertures that allow the propagation of incident irradiation into an interior resonant cavity. We use full wave time-harmonic analysis to study the field distribution inside the cavity, and show that an analogue of Whispering Gallery Modes (WGMs) can be efficiently excited via free-space illumination.

physics.optics↗

arXiv2007

Continuous Magnetophoretic Separation of Blood Cells from Plasma at the Microscale

We present a method for the direct and continuous separation of red and white blood cells from plasma at the microscale. The method is implemented in a microfluidic system with magnetic functionality. The fluidic structure within the microsystem consists of an inlet and a single microfluidic channel with multiple outlets. The magnetic functionality is provided by an array of integrated soft-magnetic elements that are embedded transverse and adjacent to the microchannel. The elements are magnetized using an external field, and once magnetized they produce a magnetic force on blood cells as they flow through the microchannel. In whole blood, white blood cells (WBCs) behave as diamagnetic microparticles, while red blood cells (RBCs) exhibit diamagnetic or paramagnetic behavior depending on the oxygenation of their hemoglobin. We study the motion of blood cells through the microchannel using a mathematical model that takes into account the magnetic, fluidic and gravitational forces on the cells. We use the model to study blood cell separation, and our analysis indicates that the microsystem is capable of separating WBC-rich plasma, deoxygenated RBC-rich plasma and cell-depleted plasma into respective outlets.

physics.bio-ph↗

arXiv2006

Analysis of Particle Transport in a Magnetophoretic Microsystem

An analytical analysis is presented of the transport and capture of magnetic micro/nano-particles in a magnetophoretic microsystem that consists of an array of integrated soft-magnetic elements embedded beneath a microfluidic channel. The elements, which are polarized by a bias field, produce a nonuniform field distribution that gives rise to a force on magnetic particles within the microchannel. The equations governing particle motion are derived using analytical expressions for the dominant magnetic and fluidic forces. The magnetic force is obtained using an analytical expression for the field distribution in the microchannel combined with a linear magnetization model for the magnetic response of particles. The theory takes into account particle size and material properties, the bias field, the dimensions of the microchannel, the fluid properties, and the flow velocity. The equations of motion are solved to study particle transport and capture. The analysis indicates that the particles exhibit an oscillatory motion as they traverse the microsystem, and that a high capture efficiency can be obtained in practice.

physics.bio-ph↗

arXiv2006

A Model for Predicting Magnetic Targeting of Multifunctional Particles in the Microvasculature

A mathematical model is presented for predicting magnetic targeting of multifunctional carrier particles that are designed to deliver therapeutic agents to malignant tissue in vivo. These particles consist of a nonmagnetic core material that contains embedded magnetic nanoparticles and therapeutic agents such as photodynamic sensitizers. For in vivo therapy, the particles are injected into the vascular system upstream from malignant tissue, and captured at the tumor using an applied magnetic field. The applied field couples to the magnetic nanoparticles inside the carrier particle and produces a force that attracts the particle to the tumor. In noninvasive therapy the applied field is produced by a permanent magnet positioned outside the body. In this paper a mathematical model is developed for predicting noninvasive magnetic targeting of therapeutic carrier particles in the microvasculature. The model takes into account the dominant magnetic and fluidic forces on the particles and leads to an analytical expression for predicting their trajectory. An analytical expression is also derived for predicting the volume fraction of embedded magnetic nanoparticles required to ensure capture of the carrier particle at the tumor. The model enables rapid parametric analysis of magnetic targeting as a function of key variables including the size of the carrier particle, the properties and volume fraction of the embedded magnetic nanoparticles, the properties of the magnet, the microvessel, the hematocrit of the blood and its flow rate.

physics.bio-ph↗

arXiv2006

A Model for Predicting Magnetic Particle Capture in a Microfluidic Bioseparator

A model is presented for predicting the capture of magnetic micro/nano-particles in a bioseparation microsystem. This bioseparator consists of an array of conductive elements embedded beneath a rectangular microfluidic channel. The magnetic particles are introduced into the microchannel in solution, and are attracted and held by the magnetic force produced by the energized elements. Analytical expressions are obtained for the dominant magnetic and fluidic forces on the particles as they move through the microchannel. These expressions are included in the equations of motion, which are solved numerically to predict particle trajectories and capture time. This model is well-suited for parametric analysis of particle capture taking into account variations in particle size, material properties, applied current, microchannel dimensions, fluid properties, and flow velocity.

physics.bio-ph↗

arXiv2006

Magnetophoretic separation of blood cells at the microscale

We present a method and model for the direct and continuous separation of red and white blood cells in plasma. The method is implemented at the microscale using a microfluidic system that consists of an array of integrated soft-magnetic elements embedded beneath a microfluidic channel. The microsystem is passive, and is activated via application of a bias field that magnetizes the elements. Once magnetized, the elements produce a nonuniform magnetic field distribution in the microchannel, which gives rise to a force on blood cells as they pass through the microsystem. In whole blood, white blood cells behave as diamagnetic microparticles while red blood cells exhibit diamagnetic or paramagnetic behavior depending on the oxygenation of their hemoglobin. We develop a mathematical model for predicting the motion of blood cells in the microsystem that takes into account the dominant magnetic, fluidic and buoyant forces on the cells. We use the model to study red/white blood cell transport, and our analysis indicates that the microsystem is capable of rapid and efficient red/white blood cell separation.

physics.bio-ph↗