572 results about "Biological substances" patented technology

An electrical impedance probe is provided that includes a surgical needle. In an exemplary embodiment, the probe is a two-part trocar needle designed to acquire impedance measurements at its tip. The impedance measurements are representative of the local properties of a biological substance at the needle tip. Thus, the probe may be used to confirm needle insertion into a desired anatomical target or to identify the nature of the cells surrounding the tip of the needle. In urology, this sensor is used for confirming the needle insertion into the urinary tract, for localizing renal cell carcinoma, and prostate cancer.

An apparatus and method for identifying and/or quantifying a charged biological substance in a conductive liquid medium.

The invention is directed to a ready-to-use modular cleanroom and facility, in particular for the production of drugs and biological substances, which is equipped with pre-approved manufacturing equipment cores. The modular cleanroom is implemented in the interior space of a container, such as a standard shipping container, and includes at least one bioreactor station. The modular facility can be installed on-site from pre-approved cleanroom modules without further regulatory approval. The cleanroom and facility comply with FDA-approved good manufacturing practices (GMP) and good laboratory practices (GLP).

This invention is based on size and mass separation of suspended particles, including biological matter, which are made to flow in a spiral channel. On the spiral sections, the inward directed transverse pressure field from fluid shear competes with the outward directed centrifugal force to allow for separation of particles. At high velocity, centrifugal force dominates and particles move outward. At low velocities, transverse pressure dominates and the particles move inward. The magnitudes of the two opposing forces depend on flow velocity, particle size, radius of curvature of the spiral section, channel dimensions, and viscosity of the fluid. At the end of the spiral channel, a parallel array of outlets collects separated particles. For any particle size, the required channel dimension is determined by estimating the transit time to reach the side-wall. This time is a function of flow velocity, channel width, viscosity, and radius of curvature. Larger particles may reach the channel wall earlier than the smaller particles which need more time to reach the side wall. Thus a spiral channel may be envisioned by placing multiple outlets along the channel. This technique is inherently scalable over a large size range from sub-millimeter down to 1 μm.

This invention provides novel methods for the formation of biocompatible membranes around biological materials using photopolymerization of water soluble molecules. The membranes can be used as a covering to encapsulate biological materials or biomedical devices, as a “glue” to cause more than one biological substance to adhere together, or as carriers for biologically active species. Several methods for forming these membranes are provided. Each of these methods utilizes a polymerization system containing water-soluble macromers, species, which are at once polymers and macromolecules capable of further polymerization. The macromers are polymerized using a photoinitiator (such as a dye), optionally a cocatalyst, optionally an accelerator, and radiation in the form of visible or long wavelength UV light. The reaction occurs either by suspension polymerization or by interfacial polymerization. The polymer membrane can be formed directly on the surface of the biological material, or it can be formed on material, which is already encapsulated.

Airborne particles are impacted on a collection surface, analyzed, and then the collection surface is regenerated. Thus, the same collection surface can be used in numerous cycles. The analysis can be focused on one or more properties of interest, such as the concentration of airborne biologicals. Sensors based on regenerative collection surfaces may be incorporated in many networks for applications such as building automation.

A process and apparatus for purifying one or more target substances from a source liquid, employing one or more cross-flow filter elements, and one or more types of chromatography resins, in combination, to provide purification with advantageous yield, product purity, and cost- and time-efficiency.

A process and system for electrical extraction of intracellular matter from biological matter, and intracellular matter products formed thereby, based on preparing a mixture of biological matter featuring cells, and an electro-conductive liquid, and electrifying the mixture by transmitting controlled cycles of pulses and pauses of electrical current into the mixture by using electrodes, whereby the pulses of electrical current pierce holes into or perforate the cell membranes of the cells, enabling the release of intracellular matter for collecting and separating into target intracellular matter extract and solid waste. Pauses included in each cycle of transmitting pulses of electrical current enable firm control of electrical extraction processing conditions, including extent of extraction, temperature effects, and pressure effects, during the electrical extraction process. Electrical extraction of the present invention is applicable to a wide variety of biological matter originating from human, animal, and plant entities. Intracellular matter extracts so obtained include highly concentrated liquid fertilizer, valuable elements, nutrients, oils, and fats, which are used for manufacturing a diversity of end products of the agricultural, pharmaceutical, cosmetic, and food industries.

A biological/chemical detector is disclosed that is capable of manipulating liquids, such as reagent droplets, without relying on microchannels. In a first embodiment, fluid flow is passed through the detector, thus causing particles wholly or partially containing an illustrative chemical compound or biological species to be collected on the tips of nanostructures in the detector. A droplet of liquid is moved across the tips of the nanostructures, thus absorbing the particles into the liquid. The droplet is caused to penetrate the nanostructures in a desired location, thus causing the chemical compound or biological species in said liquid droplet to come into contact with, for example, a reagent. In another embodiment, a fluid flow is passed through the nanostructured surfaces of the detector such that the chemical compound and/or biological species are deposited between the nanoposts of a desired pixel. A droplet of liquid is moved across the surface to that desired pixel and is caused to penetrate the nanostructures of the pixel, thus contacting a reagent.

The invention pertains to the new material technical field, and relates to a method for preparing a carbonaceous solid acid catalyst and biodiesel by taking pure natural biological substances as raw materials. The method is characterized by: taking the pure natural and renewable biological substances as the raw materials; adopting the technical route and method of low-temperature carbonization firstly, oxidation secondly and sulfonation then according to the constituent and structural characteristics to prepare the bio-carbonaceous solid acid catalyst; and adopting a continuous rectification-water separating esterification reaction technology to produce the biodiesel by carrying out the catalytic esterification reaction of a free fatty acid or waste oil and short chain alcohol. The raw materials adopted by the invention are rich in resources, low in price, pure natural and renewable, which pertains to waste utilization; the preparation technology is simple with moderate and controllable reaction conditions; the catalyst has the advantages of high activity, good stability, easy recycling and no corrosion to equipment, which is an really environment-friendly catalyst, thus being applicable to the large scale industrial production of the biodiesel. The method can also be applied to a plurality of organic reactions such as alkylation, hydrolysis and hydration, etc.

A calculation system is constituted by: one light source apparatus configured to irradiate illuminating light; a wavelength selection unit configured to select light of at least two specific wavelength regions included in the illuminating light; an image sensor configured to receive light from biological tissue, which is a subject, and output pixel signals corresponding to the received light; and a signal processing unit configured to perform predetermined signal processing on the pixel signals output from the image sensor. In this configuration, the signal processing unit calculates an index indicating a concentration of a predetermined biological substance included in the biological tissue, based on the pixel signals output from the image sensor according to the light of the at least two specific wavelength regions.

The invention belongs to the technical field of microalga biology, and particularly relates to a microalga strain with high CO2 tolerance and high fixation rate and a breeding method thereof. The microalga is named Chlorella sp.Y-1, and is collected into Common Microorganism Center of China General Microbiological Culture Collection Committee; and collection number is CGMCC No.5429. The invention has the following characteristics: the initial strain is separated from natural environment; after high-CO2-concentration enrichment culture, gene cloning, induced mutation breeding and other operations, the carbon content of the target strain is increased to 56.981%, the optimal fixation concentration is up to 20% (v/v), the fixation rate is up to 5.762g/(L.d), and the maximum tolerance concentration is 100% (v/v); and the target strain has high adaptability to a series of physical and chemical culture conditions, has high culture transfer stability, and high better overall properties than the like research findings at present. The invention aims to solve the bottleneck problem in high concentration CO2 biological fixation technology, cultures an efficient organism capable of efficiently fixing high concentration CO2, implements effective fixation of CO2 in high concentration flue gas and other complex environments, and meanwhile, generates beneficial biological substances.

A process and apparatus for purifying one or more target substances from a source liquid, employing one or more cross-flow filter elements, and one or more types of chromatography resins, in combination, to provide purification with advantageous yield, product purity, and cost-and time-efficiency.

A portable system and method for measuring the concentration of multiple chemical or biological substances where an onsite analysis of such substances is needed. The new and original handheld sensor system uses a disposable optical test element and a spectroscopic detector that measures the test element response to specific analytes through a change in light absorbance, luminescence, and other forms of light-based response. In this way, reflection light intensities indicative of the test element response can be used to measure the concentration of the target analytes. The sensor system is also capable of being interfaced to an information processing unit or computer so that analytical data can be manipulated or stored electronically.

A device for figuring objects by means of material erosion of the surface thereof, comprising a pulsed laser beam and a deflection device through which the laser beam is directed at the object surface and via which the object surface is guided. The invention is suitable for figuring natural optical lenses made from a biological substance or artificial optical lenses. The inventive device is provided with an optical device to modify the distribution of the radiation intensity inside the laser beam cross section. The radiation intensity, once the laser beam has passed through the optical device, has a bell-shaped or Gaussian-like distribution in at least one cross sectional direction through the laser beam.

For certain mixed mode resins having anionic character, a ligand is joined to a solid support via a linkage that includes a mercapto-, ether- or amino-containing moiety. A suitable ligand comprises an aromatic group, a heteroaromatic group, or a heterocyclic group, optionally fused, that is sulfate-, sulfonate-, phosphonate- or phosphate-substituted and that is linked to such a moiety. These resins possess an anionic character under conditions prescribed for their use. Separation of a biological substance, such as a peptide or protein, can be accomplished with a resin of this type via a change in the pH of eluants, thereby effecting adsorption and desorption.

A chemically functionalized cantilever system has a cantilever coated on one side thereof with a reagent or biological species which binds to an analyte. The system is of particular value when the analyte is a toxic chemical biological warfare agent or an explosive.

Methods, compositions and a two-chamber apparatus are provided for use in the separation of a biological substances type from a complex liquid mixture utilizing buoyant microbubble compositions.

A specimen cup (100) has slide-in cassette (102) hermetically sealed in a chamber (104), with a outer partition being transparent. The cassette comprised chemical test strips (106) used to provide testing of drugs of abuse or other chemical or biological substances. The cassette is designed to draw urine up from the front bottom of the cup, thereby reduces the amount of urine required to perform the test. Further the cassette is designed to form isolated test channels through the use of strategically placed vertical and horizontal bars which are hermetically sealed. The cup further comprises a spill prevention flap or float (108) and an optionally enlarged sample collection portion (110) for its operation. The windows of the test cassette are covered with transparent fluid-resistant plate to prevent urine from accidentally spill onto the strips.

The present invention is directed to devices and methods in which one or more miniature synthetic jet actuators are integrated with a chemical fluidic sensor (ChemFET) to effect inhalation and exhalation of ambient gas samples and induce small scale mixing at the surface of the sensor. The fluidically integrated jet transports ambient gas or liquid into the jet/sensor assembly through integrated gas or liquid channels, impinges the sample gas or liquid on the sensing element, and finally ejects the sample gas or liquid back into the ambient gas or liquid. The response of the sensor in the presence of the active jet is compared to its response when the jet is inactive. The jet actuator directs entrained ambient gas or liquid toward the active surface of the sensor, and the impingement of sample gas or liquid onto the surface of the sensor results in faster response time. Other embodiments are also claimed and described.

A chemical analyzing apparatus accommodates therein a structure for retaining a sample and reagents. A detecting mechanism detects the sample after reaction with a reagent. After or during extraction of a biological substance from the sample in the structure, a temperature of a fluid in a space around the structure is controlled to a value which is suitable for enzyme.

An integrated chromatography-immunoassay system for integrated chromatography-immunoassay system includes a chromatographic unit that receives labeled nano-structured probes comprising nano particles and antibodies attached to the nano particles, and a test membrane comprising coating antigens. The chromatographic unit allows the labeled nano-structured probes to diffuse there through and into the test membrane, wherein the antibodies on the nano particles are bound to the coating antigens. A laser device emits a laser light to illuminate the labeled nano-structured probes having the antibodies bound to the coating antigens on the test membrane. A spectral analyzer obtains a Raman spectrum from light scattered from the labeled nano-structured probes having the antibodies bound to the coating antigens on the test membrane, and to identify a spectral signature in the Raman spectrum associated with the antibody-antigen pair, which enables detection and identification of the antibody.

A metallic stent that, when it is contacted with an input alternating current electromagnetic field and a static magnetic field that contacts biological matter located within the stent, an output signal is produced that that has a fixed phase relationship with the input signal and that has a magnitude that is at least about 0.01 times as great as the magnitude of the input signal.