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1.
Biomed Microdevices ; 21(4): 101, 2019 11 23.
Article in English | MEDLINE | ID: mdl-31760501

ABSTRACT

E-cadherin is a cell-cell adhesion protein that plays a prominent role in cancer invasion. Inactivation of E-cadherin in breast cancer can arise from gene promoter hypermethylation or genetic mutation. Depending on their E-cadherin status, breast cancer cells adopt different morphologies with distinct invasion modes. The tumor microenvironment (TME) can also affect the cell morphology and invasion mode. In this paper, we used a previously developed microfluidic system to quantify the three-dimensional invasion of breast cancer cells with different E-cadherin status, namely MCF-7, CAMA-1 and MDA-MB-231 with wild type, mutated and promoter hypermethylated E-cadherin, respectively. The cells migrated into a stable and reproducible microfibrous polycaprolactone mesh in the chip under a programmed stable chemotactic gradient. We observed that the MDA-MB-231 cells invaded the most, as single cells. MCF-7 cells collectively invaded into the matrix more than CAMA-1 cells, maintaining their E-cadherin expression. The CAMA-1 cells exhibited multicellular multifocal infiltration into the matrix. These results are consistent with what is seen in vivo in the cancer biology literature. In addition, comparison between complete serum and serum gradient conditions showed that the MDA-MB-231 cells invaded more under the serum gradient after one day, however this behavior was inverted after 3 days. The results showcase that the microfluidic system can be used to quantitatively assess the invasion behavior of cancer cells with different E-cadherin expression, for a longer period than conventional invasion models. In the future, it can be used to quantitatively investigate effects of matrix structure and cell treatments on cancer invasion.


Subject(s)
Breast Neoplasms/pathology , Cadherins/metabolism , Cytological Techniques/instrumentation , Lab-On-A-Chip Devices , Cell Line, Tumor , Gene Expression Regulation, Neoplastic , Humans , Neoplasm Invasiveness
2.
Biomed Microdevices ; 19(4): 92, 2017 Oct 17.
Article in English | MEDLINE | ID: mdl-29038872

ABSTRACT

A major challenge in studying tumor cell invasion into its surrounding tissue is to identify the contribution of individual factors in the tumor microenvironment (TME) to the process. One of the important elements of the TME is the fibrous extracellular matrix (ECM) which is known to influence cancer cell invasion, but exactly how remains unclear. Therefore, there is a need for new models to unravel mechanisms behind the tumor-ECM interaction. In this article, we present a new microfabrication method, called selective curing, to integrate ECM-mimicking layers between two microfluidic channels. This method enables us to study the effect of 3D matrices with controlled architecture, beyond the conventionally used hydrogels, on cancer invasion in a controlled environment. As a proof of principle, we have integrated two electrospun Polycaprolactone (PCL) matrices with different fiber diameters in one chip. We then studied the 3D migration of MDA-MB-231 breast cancer cells into the matrices under the influence of a chemotactic gradient. The results show that neither the invasion distance nor the general cell morphology is affected significantly by the difference in fiber size of these matrices. The cells however do produce longer and more protrusions in the matrix with smaller fiber size. This microfluidic system enables us to study the influence of other factors in the TME on cancer development as well as other biological applications as it provides a controlled compartmentalized environment compatible with cell culturing.


Subject(s)
Biomimetics , Extracellular Matrix/chemistry , Lab-On-A-Chip Devices , Cell Line, Tumor , Humans , Hydrogels/chemistry , Microchip Analytical Procedures , Microtechnology , Models, Theoretical , Neoplasm Invasiveness , Tumor Microenvironment
3.
Article in English | MEDLINE | ID: mdl-24827250

ABSTRACT

Magnetic particles are widely used in biological research and bioanalytical applications. As the corresponding tools are progressively being miniaturized and integrated, the understanding of particle dynamics and the control of particles down to the level of single particles become important. Here, we describe a numerical model to simulate the dynamic behavior of ensembles of magnetic particles, taking account of magnetic interparticle interactions, interactions with the liquid medium and solid surfaces, as well as thermal diffusive motion of the particles. The model is verified using experimental data of magnetic field-induced disaggregation of magnetic particle clusters near a physical surface, wherein the magnetic field properties, particle size, cluster size, and cluster geometry were varied. Furthermore, the model clarifies how the cluster configuration, cluster alignment, magnitude of the field gradient, and the field repetition rate play a role in the particle disaggregation process. The simulation model will be very useful for further in silico studies on magnetic particle dynamics in biotechnological tools.


Subject(s)
Colloids/chemistry , Magnetite Nanoparticles/chemistry , Magnetite Nanoparticles/ultrastructure , Models, Chemical , Computer Simulation , Diffusion , Particle Size , Surface Properties
4.
Phys Rev E Stat Nonlin Soft Matter Phys ; 86(4 Pt 1): 041503, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23214587

ABSTRACT

A simple and fast numerical method is developed capable of accurately determining the 3D rotational dynamics of a magnetic particle chain in an infinite fluid domain. The focus is to control the alternating breakup and reformation of the bead chain which we believe is essential to achieve effective fluid mixing at small scales. The numerical scheme makes use of magnetic dipole moments and extended forms of the Oseen-Burgers tensor to account for both the magnetic and hydrodynamic interactions between the particles. It is shown that the inclusion of hydrodynamic interaction between the particles is crucial to obtain a good description of the particle dynamics. Only a small error of deviation is observed when benchmarking the numerical scheme against a more computationally intensive method, the direct simulation method. The numerical results are compared with experiments and the simulated rotational dynamics correspond well with those obtained from video-microscopy experiments qualitatively and quantitatively. In addition, a dimensionless number (R(T)) is derived as the sole control parameter for the rotational bead chain dynamics. Numerically and experimentally, R(T)≈ 1 is the boundary between rigid "rod" and dynamic "breaking and reformation" behaviors.


Subject(s)
Biophysics/methods , Magnetics , Algorithms , Computer Simulation , Equipment Design , Hydrodynamics , Imaging, Three-Dimensional , Microscopy, Video/methods , Models, Statistical , Models, Theoretical , Motion , Particle Size , Reproducibility of Results , Stress, Mechanical , Temperature , Torque , Viscosity
5.
Biomicrofluidics ; 6(1): 14106-1410614, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22662092

ABSTRACT

Using a magneto-mechanical solid-fluid numerical model for permanently magnetic artificial cilia, we show that the metachronal motion of symmetrically beating cilia establishes a net pressure gradient in the direction of the metachronal wave, which creates a unidirectional flow. The flow generated is characterised as a function of the cilia spacing, the length of the metachronal wave, and a dimensionless parameter that characterises the relative importance of the viscous forces over the elastic forces in the cilia.

6.
Langmuir ; 28(20): 7921-37, 2012 May 22.
Article in English | MEDLINE | ID: mdl-22416971

ABSTRACT

Natural cilia are hairlike microtubule-based structures that are able to move fluid on the micrometer scale using asymmetric motion. In this article, we follow a biomimetic approach to design artificial cilia lining the inner surfaces of microfluidic channels with the goal of propelling fluid. The artificial cilia consist of polymer films filled with superparamagnetic nanoparticles, which can mimic the motion of natural cilia when subjected to a rotating magnetic field. To obtain the magnetic field and associated magnetization local to the cilia, we solve the Maxwell equations, from which the magnetic body moments and forces can be deduced. To obtain the ciliary motion, we solve the dynamic equations of motion, which are then fully coupled to the Navier-Stokes equations that describe the fluid flow around the cilia, thus taking full account of fluid inertial forces. The dimensionless parameters that govern the deformation behavior of the cilia and the associated fluid flow are arrived at using the principle of virtual work. The physical response of the cilia and the fluid flow for different combinations of elastic, fluid viscous, and inertia forces are identified.


Subject(s)
Biomimetics , Cilia , Hydrodynamics , Magnetic Phenomena , Microfluidic Analytical Techniques , Elasticity , Models, Theoretical
7.
Biomicrofluidics ; 5(3): 34108-3410815, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21918678

ABSTRACT

Bio-inspired designs can provide an answer to engineering problems such as swimming strategies at the micron or nano-scale. Scientists are now designing artificial micro-swimmers that can mimic flagella-powered swimming of micro-organisms. In an application such as lab-on-a-chip in which micro-object manipulation in small flow geometries could be achieved by micro-swimmers, control of the swimming direction becomes an important aspect for retrieval and control of the micro-swimmer. A bio-inspired approach for swimming direction reversal (a flagellum bearing mastigonemes) can be used to design such a system and is being explored in the present work. We analyze the system using a computational framework in which the equations of solid mechanics and fluid dynamics are solved simultaneously. The fluid dynamics of Stokes flow is represented by a 2D Stokeslets approach while the solid mechanics behavior is realized using Euler-Bernoulli beam elements. The working principle of a flagellum bearing mastigonemes can be broken up into two parts: (1) the contribution of the base flagellum and (2) the contribution of mastigonemes, which act like cilia. These contributions are counteractive, and the net motion (velocity and direction) is a superposition of the two. In the present work, we also perform a dimensional analysis to understand the underlying physics associated with the system parameters such as the height of the mastigonemes, the number of mastigonemes, the flagellar wave length and amplitude, the flagellum length, and mastigonemes rigidity. Our results provide fundamental physical insight on the swimming of a flagellum with mastigonemes, and it provides guidelines for the design of artificial flagellar systems.

8.
Lab Chip ; 11(12): 2002-10, 2011 Jun 21.
Article in English | MEDLINE | ID: mdl-21331419

ABSTRACT

In this paper we quantitatively analyse the performance of magnetically-driven artificial cilia for lab-on-a-chip applications. The artificial cilia are fabricated using thin polymer films with embedded magnetic nano-particles and their deformation is studied under different external magnetic fields and flows. A coupled magneto-mechanical solid-fluid model that accurately captures the interaction between the magnetic field, cilia and fluid is used to simulate the cilia motion. The elastic and magnetic properties of the cilia are obtained by fitting the results of the computational model to the experimental data. The performance of the artificial cilia with a non-uniform cross-section is characterised using the numerical model for two channel configurations that are of practical importance: an open-loop and a closed-loop channel. We predict that the flow and pressure head generated by the artificial cilia can be as high as 18 microlitres per minute and 3 mm of water, respectively. We also study the effect of metachronal waves on the flow generated and show that the fluid propelled increases drastically compared to synchronously beating cilia, and is unidirectional. This increase is significant even when the phase difference between adjacent cilia is small. The obtained results provide guidelines for the optimal design of magnetically-driven artificial cilia for microfluidic propulsion.


Subject(s)
Cilia/chemistry , Magnetics , Microfluidic Analytical Techniques/instrumentation , Computer Simulation , Viscosity
9.
Phys Rev E Stat Nonlin Soft Matter Phys ; 82(2 Pt 2): 027302, 2010 Aug.
Article in English | MEDLINE | ID: mdl-20866944

ABSTRACT

In this Brief Report we investigate biomimetic fluid propulsion due to an array of periodically beating artificial cilia. A generic model system is defined in which the effects of inertial fluid forces and the spatial, temporal, and orientational asymmetries of the ciliary motion can be individually controlled. We demonstrate that the so-far unexplored orientational asymmetry plays an important role in generating flow and that the flow increases sharply with Reynolds number and eventually becomes unidirectional. We introduce the concept of configurational symmetry that unifies the spatial, temporal, and orientational symmetries. The breaking of configurational symmetry leads to fluid propulsion in microfluidic channels.


Subject(s)
Biomimetics/methods , Cilia/physiology , Hydrodynamics , Microfluidics , Models, Biological
10.
Phys Rev E Stat Nonlin Soft Matter Phys ; 79(4 Pt 2): 046304, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19518330

ABSTRACT

In this work we mimic the efficient propulsion mechanism of natural cilia by magnetically actuating thin films in a cyclic but non-reciprocating manner. By simultaneously solving the elastodynamic, magnetostatic, and fluid mechanics equations, we show that the amount of fluid propelled is proportional to the area swept by the cilia. By using the intricate interplay between film magnetization and applied field we are able to generate a pronounced asymmetry and associated flow. We delineate the functional response of the system in terms of three dimensionless parameters that capture the relative contribution of elastic, inertial, viscous, and magnetic forces.

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