Abstract:
The present invention comprises methods of contact printing of patterned, self-assembling monolayers of alkanethiolates, carboxylic acids, hydroxamic acids, and phosphonic acids on metallized thermoplastic films, the compositions produced thereby, and the use of these compositions. Patterned self-assembling monolayers allow for the controlled placement of fluids thereon which contain a chemically reactive, indicator functionality. The optical sensing devices produced thereby when the film is exposed to an analyte and light, can produce optical diffraction patterns which differ depending on the reaction of the self-assembling monolayer with the analyte of interest. The light can be in the visible spectrum, and be either reflected from the film, or transmitted through it, and the analyte can be any compound reacting with the fluid on the self-assembling monolayer. The present invention also provides a flexible support for a self-assembling monolayer on gold or another suitable metal.
Abstract:
A technique for creating patterns of material deposited on a surface involves forming a self-assembled monolayer in a pattern on the surface and depositing, via chemical vapor deposition or via sol-gel processing, a material on the surface in a pattern complementary to the self-assembled monolayer pattern. The material can be a metal, metal oxide, or the like. The surface can be contoured, including trenches or holes, the trenches or holes remaining free of self-assembled monolayer while the remainder of the surface is coated. When exposed to deposition conditions, metal or metal oxide is deposited in the trenches or holes, and remaining portions of the article surface remain free of deposition. The technique finds particular use in creation of conductive metal pathways selectively within holes passing from one side of a substrate to another.
Abstract:
6-Deoxy-D-fructose and 6-deoxy-L-sorbose, useful starting materials for the synthesis of 4-hydroxy-2,5dimethyl-2,3-dihydrofuran-3-one, are obtained from fructose-1,6-diphosphate by a reaction with lactaldehyde, in the presence of an enzymatic system composed of aldolase and triose phosphate isomerase (TPI) in an aqueous medium at pH 7.0, followed by the hydrolysis of the monophosphate salt thus obtained. The same deoxy-sugars are obtained by the reaction between 1,3-dihydroxyacetone phosphate and lactaldehyde in the presence of the same enzymatic system composed of aldolase and TPI. The aforementioned deoxy-sugars are also prepared by the reaction of 1,3-dihydroxy-acetone with lactaldehyde in the presence of an anionic exchange resin.
Abstract:
A polyphosphate material is disclosed. The polyphosphate material can include a plurality of polyphosphate chains. The polyphosphate chains can have a backbone that include oxygen-phosphate bonds. Two or more cations can be included. Further, the polyphosphate material can be amorphous. The two or more cations can be monovalent cations, divalent cations, trivalent cations, tetravalent cations, and combinations thereof. The two or more cations can be lithium, sodium, potassium, rubidium, cesium, francium, ammonium, beryllium, magnesium, calcium, strontium, barium, radium, zinc, titanium, iron (Fe2+), chromium (Cr2+), manganese (Mn2+), cobalt (Co2+), nickel (Ni2+), copper (Cu2+), cadmium, tin (Sn2+), mercury (Hg2+), lead (Pb2+), aluminum, boron, gallium, iron (Fe+3), chromium (Cr+3), cobalt (Co+3), gold (Au+3), antimony (Sb+3), nickel (Ni+3), bismuth (Bi+3), manganese (Mn+3), zirconium, silicon, and combinations of thereof. The two or more cations can be monovalent cations. The two or more cations can be sodium and potassium or potassium and lithium.
Abstract:
Embodiments of the invention provide cellophane based microplates and microfluidic devices. Under one aspect, a microplate includes a plate; and an array of wells formed in the plate, wherein the plate comprises cellophane. Under another aspect, a microfluidic device includes at least one sheet of cellophane; a second sheet of material sealed to the sheet of cellophane; a channel formed between the at least one sheet of cellophane and the second sheet; and at least a first liquid inlet in communication with the channel.
Abstract:
A three-dimensional microfluidic device is described, including: a plurality of porous, hydrophilic cellulosic layers each comprising one or more hydrophilic regions and/or hydrophilic channels embedded in the porous, hydrophilic cellulosic layer; wherein the hydrophilic channel is fluidically connected to the hydrophilic region; the hydrophilic regions comprise a sample deposition zone, one or more assay zones in fluidic communication with the sample deposition zone; and a buffer deposition zone; and the assay zone comprises one or more reagents embedded therein selected from the group consisting of antigens and antibodies; and a valve layer comprising a valve switchable from a first position where the buffer zone and the assay zone are not in fluidic communication, to a second position where the buffer zone and the assay zone are in fluidic communication.
Abstract:
The present invention relates to methods, compositions and kits related to a novel in vitro assay for a high-capacity and high-throughput method for measuring the ability of cancer cells to migrate in a three-dimensional cellular assay. The three-dimensional cellular invasion assay provides a method for determining and quantitating the metastatic potential and invasive capacity of a cancer cell. Other aspects of the invention further relate to the use of the in vitro assay to screen for agents and compounds capable of inhibiting intravasation, and thereby modulating the metastatic potential of cancer cells. The methods, compositions and three-dimensional assay provide a highly sensitive assay system capable of mimicking the in vivo cellular and molecular interactions required for successful completion of intravasation.
Abstract:
A soft robotic device includes a flexible body having a width, a length and a thickness, wherein the thickness is at least 1 mm, the flexible body having at least one channel disposed within the flexible body, the channel defined by upper, lower and side walls, wherein at least one wall is strain limiting; and a pressurizing inlet in fluid communication with the at least one channel, the at least one channel positioned and arranged such that the wall opposite the strain limiting wall preferentially expands when the soft robotic device is pressurized through the inlet.
Abstract:
The present invention generally relates to amplification of biological entities, for example, for phage display. In one aspect, members of a library of biological entities are encapsulated in separate compartments (e.g., in separate microfluidic droplets) and amplified. As a specific example, by putting members of a phage display library into microfluidic droplets such that no droplet contains more than one member of the library, the library can be amplified without any substantial changes in growth rates or population distributions, or other artifacts created due to differences in growth rates or amplification between different members of the library. In some cases, the volume of the compartments can be used to control the copy number of a biological entity during amplification. In certain cases, biological entities with different amplification rates can be amplified independently of each other. In some embodiments, the ratio of a rapidly amplifying biological entity to a slowly amplifying biological entity can be controlled. This can be advantageous, for example, in preserving diversity within a library by preventing rapidly amplifying biological entities from outcompeting slowly amplifying biological entities. For example, certain methods and systems of the invention can be useful in situations where preferential amplification of library members can present a problem.
Abstract:
The present invention generally relates to amplification of biological entities, for example, for phage display. In one aspect, members of a library of biological entities are encapsulated in separate compartments (e.g., in separate microfluidic droplets) and amplified. As a specific example, by putting members of a phage display library into microfluidic droplets such that no droplet contains more than one member of the library, the library can be amplified without any substantial changes in growth rates or population distributions, or other artifacts created due to differences in growth rates or amplification between different members of the library. In some cases, the volume of the compartments can be used to control the copy number of a biological entity during amplification. In certain cases, biological entities with different amplification rates can be amplified independently of each other. In some embodiments, the ratio of a rapidly amplifying biological entity to a slowly amplifying biological entity can be controlled. This can be advantageous, for example, in preserving diversity within a library by preventing rapidly amplifying biological entities from outcompeting slowly amplifying biological entities. For example, certain methods and systems of the invention can be useful in situations where preferential amplification of library members can present a problem.