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112results about "Fluid transfer labware" patented technology

Disposable polymer-structured filtering kit

The disposable polymer-structured filtering kit includes a disposable, polymer-structured filtering funnel with a stem having a distal tip. A flow discharge end is formed at the distal tip. Preferably, a polymer fritted filter disc is positioned in the funnel, providing filtering for liquids passing therethrough. The kit preferably also includes a glass vacuum take-off adapter having a port for connecting to a vacuum source for providing negative pressure. The adapter securely and snuggly receives the funnel and maintains position of the distal tip thereof with the flow discharge end below the port, thus preventing contaminants from entering the adapter. A reusable, glass round bottle flask or a disposable vial receives the adapter and the stem of the funnel. The funnel and fritted disc are formed from disposable materials, thus removing the necessity of cleaning them following use. The adapter is reusable, since no contaminants come in contact therewith during filtering.
Owner:CHEMRUS

Method for preventing contamination of an inner surface of a hollow glass body by alkali compounds and glass container, especially for medicinal purposes

In order to avoid deposition of evaporating alkali compounds on an inner surface of a hollow glass body during thermal processing to form a glass container from the hollow glass body, an overpressure is provided in the hollow glass body during the thermal processing. Either rinsing the hollow glass body with a gas, such as air, or at least partially closing the glass body at one end so that sufficiently rapid pressure equilibration is avoided, can provide this overpressure. The glass containers made by these methods are especially suited for food or pharmaceuticals because they have a reduced alkali release from their inner surfaces, for example at most about 2.0 mg / l sodium oxide.
Owner:SCHOTT AG

Methods and systems for calibration of a positional orientation between a sample container and nozzle tip

Disclosed are methods to aid in a calibration of a vertical orientation of a nozzle tip to a sample container in a processing or testing system. The method includes positioning the nozzle over a calibration target at a home height location (HM), moving the nozzle downward a distance (D) until contact with the calibration target is sensed, positioning the nozzle over the sample rack and moving the nozzle downward until contact with a registration location is sensed, imaging the sample rack and calibration target to determine a height (H) between the registration location and calibration target, and calculating a translation ratio (TR) between the height (H) measured in pixel space and the distance (D) measured in machine space. The translation ratio (TR) may be used to drive the nozzle tip to a predetermined depth. A robot calibration system is disclosed, as are other aspects.
Owner:SIEMENS HEALTHCARE DIAGNOSTICS INC

Pierceable cap

ActiveUS20140011292A1Preventing specimen backsplashInhibit transferCapsClosure using stoppersThin membraneEngineering
A pierceable cap 11 may be used for containing sample specimens. The pierceable cap 11 may prevent escape of sample specimens before transfer with a transfer device 43. The pierceable cap 11 may fit over a vessel 21. An access port in the shell of the pierceable cap 11 may allow passage of a transfer device 43 through the pierceable cap 11. At least one frangible layer 215, 216 may be configured with cross slits 506 in a particular cross slit geometry. The cross slits 506 may contain an openable portion 644 or be covered by a thin membrane 645. The shell 610 and frangible layer (s) 215, 216 may be integrated into a one piece cap 601, or be separate components 634. The membrane on which the cross slits 506 are placed can be flat or contoured to guide the transfer device 43 to the cross slits 506.
Owner:BECTON DICKINSON & CO

Biological sample reaction box

The invention relates to the technical field of biological sample detection, in particular to a biological sample reaction box. A reagent storage part and a push rod capable of moving relative to the reagent storage part are packaged in the reaction box; the reagent storage part is provided with at least one reagent accommodating cavity, and the reagent accommodating cavity is sealed by a sealing element; the push rod is connected with the sealing element, and the push rod is used for being matched with external equipment mutually so that the sealing element is separated from the reagent storage part. The reagent storage part and the push rod are both packaged inside the biological sample reaction box; during reaction, the biological sample reaction box is matched with a detection box only, the biological sample reaction box is inserted in the external equipment through one-step operation, and quick release of reagents in the reagent storage part can be realized.
Owner:ACON BIOTECH (HANGZHOU) CO LTD

Specimen Collection Container Having a Transitional Fill-Volume Indicator Indicating Extraction Method

A specimen collection container having a transitional fill-volume indicator is disclosed. The specimen collection container includes an open top end, a closed bottom end, and a sidewall extending therebetween defining an interior. The specimen collection container includes a transitional fill-volume indicator adjacent the sidewall, such that the container defines a first volumetric interior defined by the sidewall between the closed bottom end and the transitional indicator. The specimen collection container also defines a second volumetric interior defined by the sidewall between the closed bottom end and a portion of the sidewall disposed above the transitional indicator. The first volumetric interior is adapted to allow extraction of a specimen therefrom by a first extraction process, and the second volumetric interior is adapted to allow extraction of a specimen therefrom by either the first extraction process or a second extraction process, the second extraction process being different than the first extraction process.
Owner:BECTON DICKINSON & CO

Equivalent continuous dropping liquid-transferring gun

InactiveCN105618169ARealize continuous equivalent outputEasy to useFluid transfer labwareBurettes/pipettesPiston rodIndustrial engineering
The invention discloses an equivalent continuous dropping liquid-transferring gun. The liquid-transferring gun comprises an outer casing, an outer sleeve and a piston assembly, wherein the piston assembly comprises a piston rod and a piston arranged on the lower side of the piston rod; a spring reset mechanism sleeves the rod body of the piston rod; the liquid-transferring gun further comprises an inner sleeve; the inner sleeve is fixedly arranged in a cavity formed by the outer casing and the outer sleeve; the piston assembly is arranged in the inner sleeve in a penetrating manner; a tooth groove is formed in the outer side wall of the inner sleeve in the axial direction of the inner sleeve; a plurality of one-way ratchets distributed in the axial direction of the inner sleeve in sequence are arranged in the tooth groove; the intervals of the adjacent one-way ratchets are the same; the liquid-transferring gun is also provided with a quantifying buckle; the upper end of the quantifying buckle sleeves a rod body of the piston rod; a tooth hook raised inwards and matched with the one-way ratchets in the tooth groove is arranged at the lower end of the quantifying buckle. The liquid-transferring gun has the advantages that liquid sucked in one time can be divided into a plurality of equivalent liquid drops, the liquid drops are output continuously, the use is convenient and fast, the time is saved, and the efficiency is improved. The gun is simple to maintain, and the production and use costs are relatively low.
Owner:ANHUI AGRICULTURAL UNIVERSITY

Dialysis like therapeutic (DLT) device

A dialysis like therapeutic (DLT) device is provided. The DLT device includes at least one source channel connected at least one collection channels by one or more transfer channels. Fluid contacting surface of the channels can be an anti-fouling surface such as slippery liquid-infused porous surface (SLIPS). Fluids can be flown at high flow rates through the channels. The target components of the source fluid can be magnetic or bound to magnetic particles using an affinity molecule. A source fluid containing magnetically bound target components can be pumped through the source channel of the microfluidic device. A magnetic field gradient can be applied to the source fluid in the source channel causing the magnetically bound target components to migrate through the transfer channel into the collection channel. The collection channel can include a collection fluid to flush the target components out of the collection channel. The target components can be subsequently analyzed for detection and diagnosis. The source channel and the collection channels of the microfluidic device are analogous to the splenic arterioles and venules, respectively; the transfer channels mimic the vascular sinusoids of the spleen where opsonized particles are retained. Thus, the device acts as a dialysis like therapeutic device by combining fluidics and magnetics.
Owner:PRESIDENT & FELLOWS OF HARVARD COLLEGE +1

Pierceable cap

ActiveUS9545632B2Preventing specimen backsplashInhibit transferClosuresFluid transfer labwareThin membraneEngineering
A pierceable cap 11 may be used for containing sample specimens. The pierceable cap 11 may prevent escape of sample specimens before transfer with a transfer device 43. The pierceable cap 11 may fit over a vessel 21. An access port in the shell of the pierceable cap 11 may allow passage of a transfer device 43 through the pierceable cap 11. At least one frangible layer 215, 216 may be configured with cross slits 506 in a particular cross slit geometry. The cross slits 506 may contain an openable portion 644 or be covered by a thin membrane 645. The shell 610 and frangible layer (s) 215, 216 may be integrated into a one piece cap 601, or be separate components 634. The membrane on which the cross slits 506 are placed can be flat or contoured to guide the transfer device 43 to the cross slits 506.
Owner:BECTON DICKINSON & CO

Platelet rich plasma and bone marrow aspirate cell separation and removal methods and devices

Compositions and methods for separating a sample of whole blood or bone marrow aspirate into a fraction rich in at least one of platelets and pluripotent cells are provided. A sample of whole blood can be centrifuged in a collection tube comprising a separator substance formulated to settle between the PRP fraction and the at least one other fraction. Preferably, centrifugation is completed without substantial activation of platelets. Optionally, the separator substance could be hardened to form a solid barrier that allows removal of all or substantially all of the platelets in the PRP fraction without remixing of the PRP fraction with the at least one other fraction. Transfer devices and methods are also provided in which a sterile sample can be transferred from a separation / preparation container (e.g., vacutainer) to a consumer or other container (e.g., dropper) while maintaining sterility of the sample.
Owner:RGT UNIV OF CALIFORNIA +1

Cell microinjection system with force feedback

A novel piezo-driven cell injection system with force feedback overcomes the unsatisfied force interaction between the pipette needle and embryos in conventional position control. By integrating semiconductor strain-gage sensors for detecting the cell penetration force and the micropipette relative position in real time, the developed cell microinjection system features high operation speed, confident success rate, and high survival rate. The effectiveness of the developed cell injection system is experimentally verified by penetrating zebrafish embryos. The injection of 100 embryos are conducted with separate position control and force control. Results indicate that the force control enables a survival rate of 86%, which is higher than the survival rate of 82% produced by the position control in the same control environment. The experimental results quantitatively demonstrate the superiority of force control over conventional position control for the first time.
Owner:UNIVERSITY OF MACAU

Droplet tweezers and droplet control method

The invention discloses a pair of droplet tweezers and a droplet control method. The pair of droplet tweezers comprises two tweezer arms, and two hydrophobic plates which are respectively fixed at thehead ends of the two forceps arms; the two hydrophobic plates are arranged at an angle; and the two hydrophobic plates can relatively translate, and the angle between the two hydrophobic plates is adjustable. According to the droplet tweezers, the direction and the value of capillary force borne by droplets can be changed through structural changes of the hydrophobic non-parallel plates, upward movement and downward movement of droplets can be achieved, and therefore capture / release of droplets is achieved. The method is different from other droplet capturing / releasing methods; the force forcapturing / releasing the droplets comes from the structural characteristics of the non-parallel plates, the droplet tweezers show wide applicability and biocompatibility for hydrophobic properties of different bottom faces, and can become a powerful platform in the aspects of microfluid systems, liquid drop conveying, biological analysis, micro-reaction containers and the like.
Owner:SUZHOU UNIV

Laboratory test tube rack and associated devices, systems and methods of use

The disclosed devices, systems and methods related to the use of a test tube rack to assist with withdrawal of a needle from a container. The rack has a plurality of notches on a top shelf and corresponding openings on a second shelf that allow for the movement of a container stored therein between positions so as to prevent needle sticks and allow for one-handed operation.
Owner:UNIV OF IOWA RES FOUND

Microfluidic syringe filter head and use method thereof

The invention discloses a microfluidic syringe filter head and a use method thereof. The filter head uses a microfluidic technology to concentrate and enrich micro-particles or cells, wherein a spirally extending micro-flow channel and a Y-shaped forked flow channel communicated with the micro-flow channel are formed inside the filter head; micro-particles of sample liquid are subjected to dragging force in a flowing direction, and are also subjected to inertial lifting force and Dean dragging force perpendicular to a main flowing direction in the micro-flow channel; under coupling action of the two transverse forces, the micro-particles may be gradually focused to a wall surface on one side close to a spiral center to form a regular arrangement bundle and flow out along a branch inside the Y-shaped forked flow channel so as to collect the concentrated sample liquid. The micro-flow channel and the Y-shaped forked flow channel in the invention are arranged on the same plane so as to effectively reduce a volume occupied by the flow channels and benefit to miniaturization of the filter head; the filter head is simple in use method and suitable for use in the field and low-hardware configuration laboratory environments.
Owner:SOUTHEAST UNIV

Auto-pipetting apparatus and method

An auto-pipetting apparatus includes a dispensing head with at least one pipetting tip mandrel having an elongated stud body with an insertion end. The at least one pipetting tip mandrel mates with a pipetting tip. A first adjustable seal, disposed on the elongated stud body, and a second adjustable seal, disposed on the elongated stud body, seal the pipetting tip mated to the at least one pipetting tip mandrel. The first adjustable seal defines a snub surface. The snub surface effects a substantially continuous circumferential contact seal with radially impinging contact between the pipetting tip and the at least one pipetting tip mandrel. The second adjustable seal is adjustable between a disengaged position and an engaged position and effects a releasable grip and another substantially continuous circumferential contact seal between the pipetting tip and the at least one pipetting tip mandrel around the pipetting tip.
Owner:HIGHRES BIOSOLUTIONS INC

Disposable integrated polymeric vacuum filtration funnel

This invention discloses a disposable integrated polymeric vacuum filtration funnel. The integrated polymeric vacuum filtration funnel comprises a filtration funnel body having a filter frit disposed inside at the bottom, an outlet stem connected with an outlet at the outer bottom of the filtration funnel body; the outlet stem is integrated with the filtration funnel body; the filter frit is sealed to the inner bottom and the inner side surface of the filtration funnel body; the integrated polymeric vacuum filtration funnel comprises a sealing joint disposed underneath the outer bottom of the filtration funnel body, the sealing joint having a side-arm for vacuum connection and a standard adaptor to connect the receiving receptacle; the outlet stem protrudes from the standard adaptor; the filter frit, filtration funnel body, and sealing joint are integrated as one device. The invention can effectively reduce or eliminate the loss of the filtrate and filter cake, avoid contamination, easy to use, and cost-effective.
Owner:CHI HAITAO +2

Cell adhesion inhibitor

Provided is a cell adhesion inhibitor which exhibits low cytotoxicity and an excellent cell adhesion prevention effect; a tool and an apparatus each having a surface modified through application of the cell adhesion inhibitor thereto; a method for producing each of the surface-modified tool and apparatus; a biomedical structure and a production method therefor; and a microchannel device and a production method therefor.The invention provides a cell adhesion inhibitor comprising, as an active ingredient, a polymer comprising a repeating unit having a sulfinyl group in a side chain thereof.
Owner:JSR CORPORATIOON

Microfluidic sample treatment equipment

The invention discloses microfluidic sample treatment equipment, which can achieve the automatic treatment of microfluidic samples, and comprises: a tray device for accommodating a reagent and a chipclamp provided with a microfluidic chip; a mechanical arm, wherein the mechanical arm has a gun head for loading the chip clamp, and a gas flow channel communicated to the inner cavity of the chip clamp is arranged in the gun head; a negative pressure liquid suction device for providing air pressure for the gas flow channel of the gun head; a lifting device for driving the gun head to lift so as to load the chip clamp or make the chip clamp be inserted into or separated from the reagent; and a translation device for driving the gun head to move to a position above the chip clamp or move to a position above the reagent, wherein the tray device is located below the mechanical arm, and the mechanical arm is arranged on the translation device and connected to the lifting device.
Owner:HEMOSMART MEDICAL TECH LTD

Disposable polymer-structured filtering kit

The disposable polymer-structured filtering kit (100) includes a disposable, polymer-structured filtering funnel (110) with a stem (115) having a distal tip (116). Preferably, a polymer fritted filter disc (119) is positioned in the funnel (110), providing filtering for liquids passing therethrough. The kit (100) preferably also includes a glass vacuum take-off adapter (112) having a port (120) for connecting to a vacuum source for providing negative pressure. The adapter (112) securely and snuggly receives the funnel (110) and maintains position of the distal tip (116) thereof with a flow discharge end thereof positioned below the port (120), thus preventing contaminants from entering the adapter (112). A reusable, glass round bottle flask (114) or a disposable vial (214) receives the adapter (112) and the stem (115) of the funnel (110). The funnel (110) and fritted disc (119) are formed from disposable materials, thus removing the necessity of cleaning them in following use. The glass vacuum take-off adapter is not soiled after use, and can be used repeatedly without cleaning.
Owner:蔡健健 +1

Fluid transfer device, system and method

A fluid transfer device includes a syringe barrel having a chamber, a first plunger slidably movable inside the chamber, and a second plunger slidably movable inside the chamber. The distal end portion of the first plunger is engageable with the proximal end portion of the second plunger such that when the distal end portion of the first plunger and the proximal end portion of the second plunger are engaged, the second plunger is movable by the first plunger. A check valve may be incorporated into the distal end portion of the second plunger to allow a fluid to pass therethrough in a direction towards the proximal end portion of the second plunger and prevent a fluid to pass therethrough in a reverse direction. A fluid transfer assembly and a sampling method are also described.
Owner:MILLIPORE CORP

Fluid extractor for closed body fluid retention devices

The invention relates to the field of medical appliances, particularly a collecting device for collecting the body fluid. The fluid extractor for closed body fluid retention devices comprises an annular side wall and a channel assembly, wherein the annular side wall forms a channel; the channel assembly is arranged in the channel and positioned on the lower part of the channel; the channel assembly and annular side wall form a split fit; the channel assembly is provided with a through hole; the upper part of the channel is used for collecting the fluid; and the lower part of the channel is matched and connected with the channel assembly. The fluid extractor is capable of lowering the cost and enhancing the production efficiency; and when the excess fluid is poured out of the fluid extractor, the fluid in the test tube can be prevented from being poured out from the diversion channel or exhaust channel.
Owner:WUXI KAISHUN MEDICAL DEVICE MFG CO LTD

Method for rapid and precise manipulation of a tiny volume of liquid droplets

An apparatus and method are provided for rapid and precise manipulation and transfer of tiny liquid droplets. by dynamically introducing microstructures with relatively high surface energy to a non-wettable surface, which surface has in-situ switchable adhesion to liquid droplets. By penetrating microstructures on the background surface, the chemical property of the surface is locally modified. Capillary bridges will form between microstructures and liquid droplets which lead to high adhesive forces. When the microstructures are retracted, the capillary bridges either pinch-off or recede, which drastically reduces the adhesion. With proper chemical modification, the surface can either manipulate a liquid droplet in air or in an immiscible carrier liquid. Tiny droplets with volumes down to nanoliter scale can be prepared and dispensed by using the surface.
Owner:THE UNIVERSITY OF HONG KONG

Compact extractor/separator apparatus for solid/liquid/gel sample

The invention provides for the steam of a solvent to reach the space of an extractor following two possible routes thus exposing the sample to a continuous flow of fresh solvent, causing the extractant fluid to be fed through the sample by its upper and lower ends, which increases the extraction radius and as result a high percentage of the extracted component is obtained, reducing substantially the amount of solvent used and therefore reducing the processing time.
Owner:CHAVEZ GIL TULIO

Disposable polymer-structured filtering kit

ActiveUS8978897B2Preventing contaminants from entering the adapterReduce necessityPreparing sample for investigationFluid transfer labwareEngineeringBottle
The disposable polymer-structured filtering kit includes a disposable, polymer-structured filtering funnel with a stem having a distal tip. A flow discharge end is formed at the distal tip. Preferably, a polymer fritted filter disc is positioned in the funnel, providing filtering for liquids passing therethrough. The kit preferably also includes a glass vacuum take-off adapter having a port for connecting to a vacuum source for providing negative pressure. The adapter securely and snuggly receives the funnel and maintains position of the distal tip thereof with the flow discharge end below the port, thus preventing contaminants from entering the adapter. A reusable, glass round bottle flask or a disposable vial receives the adapter and the stem of the funnel. The funnel and fritted disc are formed from disposable materials, thus removing the necessity of cleaning them following use. The adapter is reusable, since no contaminants come in contact therewith during filtering.
Owner:CHEMRUS

Laboratory device for handling liquids

The invention relates to a laboratory device for handling liquids comprising a unit for handling liquids and an operating and / or display unit, wherein a device module comprises the unit for handling liquids, an operating and / or display module physically separate from the device module completely or partially comprises the operating and / or display unit, and means are provided for wirelessly communicating between the device module and the operating and / or display module.
Owner:EPPENDIRF AG

Lossless droplet transfer device and method and droplet micro-reaction method

The invention discloses a lossless transfer device for droplets. The device comprises a power generation part and a clamping part, the power generation part comprises a movable friction material and at least two fixed friction materials, the clamping part comprises a supporting mechanism, a left dielectric wetting clamping plate and a right dielectric wetting clamping plate, the left dielectric wetting clamping plate and the right dielectric wetting clamping plate are installed on the supporting mechanism, the movable friction materials are connected with the left dielectric wetting clamping plate, and the at least two fixed friction materials are connected with the right dielectric wetting clamping plate. The invention also discloses a lossless droplet transfer method and a droplet micro-reaction method. The device is more portable; by using a crank connecting rod mechanism, the left dielectric wetting clamping plate moves in the horizontal direction, and the device can adapt to liquid drops of different sizes conveniently; the accuracy of horizontal movement of the left clamping plate is ensured; a bolt and a spring are arranged, so that the left dielectric wetting clamping platecan horizontally move leftwards or rightwards conveniently; and the movement of droplets can be controlled, and the driving and fusion of the droplets are realized.
Owner:SUZHOU UNIV

Liquid reagent transferring and mixing apparatus

A liquid reagent transferring and mixing apparatus relates to the field of experimental instruments. The apparatus comprises a liquid taking device and a mixing device; the liquid taking device comprises a support, a mounting seat is arranged at the upper end of the support, the mounting seat is horizontally provided with at least two first gears, a second gear is arranged between the adjacent first gears, a fixed rod is arranged at the middle part of every second gear, the middle part of every first gear is in threaded connection with a lead screw, the lower end of every lead screw is fixedlyconnected to the inner ring of a bearing, the lower end of the outer ring of every bearing is fixedly connected with a piston, and a syringe sleeves the outer side of every piston; and the lower endof every syringe is connected to the mixing device through a conduit. The brand new liquid taking device and the novel mixing device are designed to meet requirements of transferring and mixing of a volatile liquid; and the apparatus has the advantages of simple structure, convenience in operation, and great promotion and practical values.
Owner:北京普利智诚生物技术有限公司

Analytical aids with hydrophilic coating containing nanoparticles with silica structure and methods of producing and using the same

Disclosed herein are analytical aids having a surface coated at least partially with a hydrophilic coating, where the hydrophilic coating includes nanoparticles with silica structure and an average particle size in a range from about 1 nm to about 500 nm. Also disclosed are methods of producing the analytical aids, as well as using the analytical aids in, for example, a sampling device containing the at least partially coated analytical aid.
Owner:ROCHE DIABETES CARE INC
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