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1.
Biomicrofluidics ; 17(5): 051503, 2023 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-37781135

RESUMO

Biomicrofluidics, a subdomain of microfluidics, has been inspired by several ideas from nature. However, while the basic inspiration for the same may be drawn from the living world, the translation of all relevant essential functionalities to an artificially engineered framework does not remain trivial. Here, we review the recent progress in bio-inspired microfluidic systems via harnessing the integration of experimental and simulation tools delving into the interface of engineering and biology. Development of "on-chip" technologies as well as their multifarious applications is subsequently discussed, accompanying the relevant advancements in materials and fabrication technology. Pointers toward new directions in research, including an amalgamated fusion of data-driven modeling (such as artificial intelligence and machine learning) and physics-based paradigm, to come up with a human physiological replica on a synthetic bio-chip with due accounting of personalized features, are suggested. These are likely to facilitate physiologically replicating disease modeling on an artificially engineered biochip as well as advance drug development and screening in an expedited route with the minimization of animal and human trials.

2.
Phys Rev E ; 104(1-2): 015108, 2021 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-34412219

RESUMO

The shape of a microchannel during flow through it is instrumental to understanding the physics that govern various phenomena ranging from rheological measurements of fluids to separation of particles and cells. Two commonly used approaches for obtaining a desired channel shape (for a given application) are (i) fabricating the microchannel in the requisite shape and (ii) actuating the microchannel walls during flow to obtain the requisite shape. However, these approaches are not always viable. We propose an alternative, passive approach to a priori tune the elastohydrodynamics in a microsystem toward achieving a predetermined (but not prefabricated) flow geometry when the microchannel is subjected to flow. That is, we use the interaction between a soft solid layer, the viscous flow beneath it, and the shaped rigid wall above it to tune the fluid domain's shape. Specifically, we study a parallel-wall microchannel whose top wall is a slender soft coating of arbitrary thickness attached to a rigid platform. We derive a nonlinear differential equation for the soft coating's fluid-solid interface, which we use to infer how to achieve specific conduit shapes during flow. Using this theory, we demonstrate the tuning of four categories of microchannel geometries, which establishes, via a proof-of-concept, the viability of our modeling framework. We also explore slip length patterning on the rigid bottom wall of the microchannel, a common technique in microfluidics, as an additional "handle" for microchannel shape control. However, we show that this effect is much weaker in practice.

3.
Soft Matter ; 16(24): 5777-5786, 2020 Jun 24.
Artigo em Inglês | MEDLINE | ID: mdl-32531014

RESUMO

Axial gradients in wall elasticity may have significant implications in the deformation and flow characteristics of a narrow fluidic conduit, bearing far-reaching consequences in physiology and bio-engineering. Here, we present a theoretical and experimental framework for fluid-structure interactions in microfluidic channels with axial gradients in wall elasticity, in an effort to arrive at a potential conceptual foundation for in vitro study of mirovascular physiology. Towards this, we bring out the static deformation and steady flow characteristics of a circular microchannel made of polydimethylsiloxane (PDMS) bulk, considering imposed gradients in the substrate elasticity. In particular, we study two kinds of elasticity variations - a uniformly soft (or hard) channel with a central strip that is hard (or soft), and, increasing elasticity along the length of the channel. The former kind yields a centrally constricted (or expanded) deformed profile in response to the flow. The latter kind leads to increasingly bulged channel radius from inlet to outlet in response to flow. We also formulate an analytical model capturing the essential physics of the underlying elastohydrodynamic interactions. The theoretical predictions match favourably with the experimental observations and are also in line with reported results on stenosis in mice. The present framework, thus, holds the potential for acting as a fundamental design basis towards developing in vitro models for micro-circulation, capable of capturing exclusive artefacts of healthy and diseased conditions.


Assuntos
Elasticidade , Microfluídica , Modelos Biológicos , Fenômenos Biofísicos , Dimetilpolisiloxanos , Microcirculação
4.
Electrophoresis ; 40(5): 616-624, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-30474869

RESUMO

Segregation of phases in the vicinity of hydrophobic surfaces may turn out to be immensely consequential towards altering the coupling of electrostatics and hydrodynamics over interfacial scales. Here, we review the fundamental advances towards bringing out the various facets of electrokinetic transport over hydrophobic interfaces. We lay significant emphasis on the developments in understanding the slippery electrohydrodynamics over such interfaces, by appealing to the considerations across various spatio-temporal scales as unveiled by molecular dynamics as well as mesoscopic modelling paradigms (such as phase field and lattice Boltzmann). We envisage that despite significant advancements being achieved towards relating the macroscopic slip-length with the underlying molecular or mesoscopic phenomena, future efforts could be directed towards developing more robust statistically based models that may connect rarefied gas dynamics in the segregated phase with bulk electrokinetic transport and possible giant augmentations in the consequent fluid flow.


Assuntos
Eletro-Osmose , Hidrodinâmica , Interações Hidrofóbicas e Hidrofílicas , Eletricidade Estática , Cinética , Simulação de Dinâmica Molecular
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