The particular bacterium under investigation here (S. pasteurii) is unique in its ability, under the right conditions, to induce the hydrolysis of urea (ureolysis) in naturally occurring environments through secretion of an enzyme urease. This process of ureolysis, through a chain of chemical reactions, leads to the formation of calcium carbonate precipitates. This is known as Microbiologically Induced Calcite Precipitation (MICP). The proper culture protocols for MICP are detailed here. Finally, visualization experiments under different modes of microscopy were performed to understand various aspects of the precipitation process. Techniques like optical microscopy, Scanning Electron Microscopy (SEM) and XRay Photo-electron Spectroscopy (XPS) were employed to chemically characterize the end-product. Further, the ability of these precipitates to clog pores inside a natural porous medium was demonstrated through a qualitative experiment where sponge bars were used to mimic a porenetwork with a range of length scales. A sponge bar dipped in the culture medium containing the bacterial cells hardens due to the clogging of its pores resulting from the continuous process of chemical precipitation. This hardened sponge bar exhibits superior strength when compared to a control sponge bar which becomes compressed and squeezed under the action of an applied external load, while the hardened bar is able to support the same weight with little deformation. Video LinkThe video component of this article can be found at

The work investigates fouling in a microfluidic membrane mimic (MMM) filtration system for foulants such as polystyrene particles and large polymeric molecules. Our MMM device consists of a staggered arrangement of pillars which enables real-time visualization and analysis of pore-scale phenomena. Different fouling scenarios are investigated by conducting constant-pressure experiments. Fouling experiments are performed with three different types of foulants: polystyrene particle solution (colloidal fouling), polyacrylamide polymer solution (organic fouling) and a mixture of these two solutions (combined fouling). Four major categories of microscopic fouling are observed: cake filtration (upstream), pore blocking (inside the pores), colloidal aggregation (downstream) and colloidal streamer fouling (downstream). Our microfluidic experiments show that downstream colloidal aggregation and streamer fouling have a significant effect on overall membrane fouling which were not studied before.

IMEAC is an integrated microfluidic electrochemical assay for cervical cancer detection at point of-care testing.

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In this work, we report the phenomenon of formation of particle aggregates in the form of thin slender strings when a polyacrylamide (PAM) solution, laden with polystyrene (PS) beads is introduced into a microfluidic device containing an array of micropillars. PAM and a dilute solution of PS beads are introduced into the microfluidic channel through two separate inlets and localized particle aggregation is found to occur under certain flow regimes. The particle aggregates initially have a string-like morphology and are tethered at their ends to the micropillar walls, while the structure remains suspended in the fluid medium. Such a morphology inspired us to name these structures streamers. The flow regimes under which streamer formation is observed are quantified through state diagrams. We discuss the streamer formation time-scales and also show that streamer formation is likely the result of the flocculation of PS beads. Streamer formation has implications in investigating particle-laden complex flows through porous media.

Biomarker detection in whole blood enables understanding of the cause, progression, relapse, or outcome of treatment of a disease. Conventional biomarker detection techniques such as enzyme-linked immunosorbent assay, polymerase chain...

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