CA2702367A1 - Flow focusing method and system for forming concentrated volumes of microbeads, and microbeads formed further thereto - Google Patents
Flow focusing method and system for forming concentrated volumes of microbeads, and microbeads formed further thereto Download PDFInfo
- Publication number
- CA2702367A1 CA2702367A1 CA2702367A CA2702367A CA2702367A1 CA 2702367 A1 CA2702367 A1 CA 2702367A1 CA 2702367 A CA2702367 A CA 2702367A CA 2702367 A CA2702367 A CA 2702367A CA 2702367 A1 CA2702367 A1 CA 2702367A1
- Authority
- CA
- Canada
- Prior art keywords
- focusing
- stream
- microbeads
- operatively
- fluid
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/70—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving virus or bacteriophage
- C12Q1/701—Specific hybridization probes
- C12Q1/706—Specific hybridization probes for hepatitis
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/04—Making microcapsules or microballoons by physical processes, e.g. drying, spraying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/45—Magnetic mixers; Mixers with magnetically driven stirrers
- B01F33/453—Magnetic mixers; Mixers with magnetically driven stirrers using supported or suspended stirring elements
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/45—Magnetic mixers; Mixers with magnetically driven stirrers
- B01F33/453—Magnetic mixers; Mixers with magnetically driven stirrers using supported or suspended stirring elements
- B01F33/4534—Magnetic mixers; Mixers with magnetically driven stirrers using supported or suspended stirring elements using a rod for supporting the stirring element, e.g. stirrer sliding on a rod or mounted on a rod sliding in a tube
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/255—Flow control means, e.g. valves
- B29C48/2552—Flow control means, e.g. valves provided in the feeding, melting, plasticising or pumping zone, e.g. screw, barrel, gear-pump or ram
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/12—Powdering or granulating
- C08J3/14—Powdering or granulating by precipitation from solutions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/205—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase
- C08J3/21—Compounding polymers with additives, e.g. colouring in the presence of a continuous liquid phase the polymer being premixed with a liquid phase
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/70—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving virus or bacteriophage
- C12Q1/701—Specific hybridization probes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F23/00—Mixing according to the phases to be mixed, e.g. dispersing or emulsifying
- B01F23/40—Mixing liquids with liquids; Emulsifying
- B01F23/41—Emulsifying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/30—Micromixers
- B01F33/301—Micromixers using specific means for arranging the streams to be mixed, e.g. channel geometries or dispositions
- B01F33/3011—Micromixers using specific means for arranging the streams to be mixed, e.g. channel geometries or dispositions using a sheathing stream of a fluid surrounding a central stream of a different fluid, e.g. for reducing the cross-section of the central stream or to produce droplets from the central stream
Abstract
In a method and system for forming concentrated volumes of microbeads, a polymer solution and/or suspension includes a polymer dissolved and/or dispersed in a medium. Streams of a focusing fluid and of the polymer solution and/or suspension flow towards a fluid bath, and into intersection with one another, so &s to focus the polymer solution and/or suspension. The polymer solution and/or suspension stream forms microbeads in the fluid bath. Some of the focusing fluid is drawn from the fluid bath, so as to concentrate the microbeads in die fluid bath. The system includes a flow focusing apparatus and a liquid-containing cell. The focusing apparatus includes polymer and focusing nozzles. The cell contains the fluid bath and has an outlet port, through which the focusing fluid is drawn from the fluid bath.
Claims (73)
1. A method of forming one or more concentrated volumes of microbeads, the method comprising the steps of:
(a) flowing a focused stream of a polymer solution and/or suspension towards a fluid bath, with the polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium;
(b) flowing a focusing stream of a focusing fluid towards the fluid bath, and into intersection with the focused stream;
(b.1) after step (b), maintaining the fluid bath under stirring;
(c) flowing the focusing stream and the focused stream from intersection with one another, so as to form the microbeads in the fluid bath, and allowing the microbeads to solidify; and (d) flowing a volume of the focusing fluid from the fluid bath, so as to concentrate the microbeads in the fluid bath.
(a) flowing a focused stream of a polymer solution and/or suspension towards a fluid bath, with the polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium;
(b) flowing a focusing stream of a focusing fluid towards the fluid bath, and into intersection with the focused stream;
(b.1) after step (b), maintaining the fluid bath under stirring;
(c) flowing the focusing stream and the focused stream from intersection with one another, so as to form the microbeads in the fluid bath, and allowing the microbeads to solidify; and (d) flowing a volume of the focusing fluid from the fluid bath, so as to concentrate the microbeads in the fluid bath.
2. The method according to claim 1, wherein in step (d), the fluid bath is controlled so as to be maintained at a substantially constant liquid level.
3. The method according to claim 2, wherein the substantially constant liquid level is maintained by balancing respective flow rates for the focused stream in step (a), the focusing stream in step (b), and the focusing fluid in step (d).
4. The method according to claim 1, wherein in step (d), the volume of the focusing fluid flows through one or more filters.
5. The method according to claim 4, wherein in step (d), the filters retain the microbeads in the fluid bath.
6. The method according to claim 4, wherein in step (d), the filters retain a substantially monodisperse set of the microbeads in the fluid bath.
7. The method according to any one of claims 4 and 5, wherein in step (d), the filters divide the microbeads into one or more collections of microbeads, with each of the collections including a respectively monodisperse set of the microbeads.
8. The method according to claim 1, wherein at least one of steps (a) and (b) is performed within an interior chamber of a flow focusing body.
9. The method according to claim 8, wherein steps (a) and (b) are both performed within the interior chamber of the flow focusing body, with an outlet portion of the flow focusing body being located below a liquid level of the fluid bath, and wherein in step (c), the focusing stream and the focused stream flow out from the outlet portion of the flow focusing body.
10. The method according to claim 9, wherein in step (b), the focused stream is focused by the focusing fluid, and wherein in step (c), the focusing stream and the focused stream flow out from the outlet portion as a single flow stream.
11. The method according to claim 10, wherein in step (c), the focusing stream substantially surrounds the focused stream in the single flow stream.
12. The method according to claim 1, further comprising a preliminary step, before step (a), of providing the fluid bath within a sealed liquid-containing cell.
13. The method according to claim 12, wherein at least one of steps (a) through (c) is performed within the liquid-containing cell.
14. The method according to any one of claims 12 and 13, wherein in the preliminary step, the liquid-containing cell additionally contains a volume of a gas at a predetermined pressure.
15. The method according to claim 14, wherein in the preliminary step, a gas pressure source pressurizes the gas, via an inlet valve, in the sealed liquid-containing cell.
16. The method according to any one of claims 14 to 15, further comprising step (c.1), after the preliminary step, of releasing a portion of the gas or the fluid bath, via a pressure safety valve, when the pressure exceeds a predetermined maximum safety pressure for the sealed liquid-containing cell.
17. The method according to any one of claims 14 to 16, wherein the gas comprises an inert gas.
18. The method according to any one of claims 14 to 17, wherein the pressure of the gas in the preliminary step is predetermined, in balance with respective flow rates for the focused stream in step (a) and the focusing stream in step (b), to maintain the fluid bath at a substantially constant liquid level.
19. The method according to any one of claims 1 to 18, wherein in step (U), a stirring bar maintains the fluid bath under stirring, and wherein the stirring bar comprises an electric stirring bar or a magnetic stirring bar.
20. The method according to any one of claims 1 to 19, further comprising step (d.1), after step (d), of recovering solidified microbeads from the fluid bath.
21. A method of forming one or more concentrated volumes of microbeads, the method comprising the steps of:
(a) flowing a focused stream of a polymer solution and/or suspension towards a fluid bath, with the polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium;
(b) flowing a focusing stream of a focusing fluid towards the fluid bath, and into intersection with the focused stream;
(c) flowing the focusing stream and the focused stream from intersection with one another, so as to form the microbeads in the fluid bath;
(d) flowing a volume of the focusing fluid from the fluid bath, so as to concentrate the microbeads in the fluid bath; and (e) recycling at least part of the volume of the focusing fluid, flowing from the fluid bath in step (d), as at least part of the focusing stream flowing into intersection with the focused stream in step (b).
(a) flowing a focused stream of a polymer solution and/or suspension towards a fluid bath, with the polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium;
(b) flowing a focusing stream of a focusing fluid towards the fluid bath, and into intersection with the focused stream;
(c) flowing the focusing stream and the focused stream from intersection with one another, so as to form the microbeads in the fluid bath;
(d) flowing a volume of the focusing fluid from the fluid bath, so as to concentrate the microbeads in the fluid bath; and (e) recycling at least part of the volume of the focusing fluid, flowing from the fluid bath in step (d), as at least part of the focusing stream flowing into intersection with the focused stream in step (b).
22. The method according to any one of claims 1 to 21, wherein in step (a), the medium comprises an organic solvent.
23. The method according to claim 22, wherein the organic solvent comprises chloroform or dichloromethane.
24. The method according to any one of claims 1 to 23, wherein in step (a), the polymer is substantially hydrophobic.
25. The method according to any one of claims 1 to 24, wherein in step (a), the polymer comprises a polystyrene powder or a derivative thereof.
26. The method according to any one of claims 1 to 25, wherein in step (b), the focusing fluid comprises water.
27. The method according to any one of claims 1 to 26, wherein in step (a), the polymer solution further comprises particles dissolved and/or dispersed in the medium, and wherein in step (c), each of the microbeads binds an identifiable set of the particles.
28. The method according to claim 27, wherein in step (a), the particles comprise fluorophores.
29. The method according to claim 27, wherein in step (a), the particles comprise nanoparticles.
30. The method according to claim 29, wherein the nanoparticles comprise semiconductor nanoparticles, magnetic nanoparticles, metallic conductor nanoparticles, metal oxide nanoparticles, fluorescent nanoparticles, or phosphorescent nanoparticles.
31. The method according to claim 27, wherein in step (a), the particles comprise quantum dots.
32. The method according to claim 27, wherein in step (a), the particles comprise a combination of quantum dots and magnetic nanoparticles.
33. The method according to any one of claims 1 to 32, wherein in step (a), the polymer solution and/or suspension has a concentration of about 0.04 by weight-weight percentage (4 wt%).
34. A concentrated volume of microbeads formed according to the method in any one of claims 1 to 33.
35. A concentrated volume of microbeads according to claim 34, wherein one or more of the microbeads in the concentrated volume comprises one or more functional groups at a surface thereof, with the functional groups being adapted to operatively bind with biorecognition molecules.
36. A concentrated volume of microbeads according to claim 35, wherein one or more of the microbeads in the concentrated volume, operatively bound with the biorecognition molecules, is adapted for use as a probe in a multiplexed diagnostic test for detection of one or more diseases.
37. A concentrated volume of microbeads according to claim 36, wherein the diseases include malaria, HIV, Hepatitis B, Hepatitis C, Dengue virus, or avian flu (H5N1).
38. A concentrated volume of microbeads according to claim 35, wherein one or more of the microbeads in the concentrated volume, operatively bound with the biorecognition molecules, is adapted for use as a probe in a multiplexed diagnostic test for detection of one or more genetic expression factors.
39. A system for forming one or more concentrated volumes of microbeads, the system comprising:
(a) a fluid bath, a focusing fluid, and a polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium;
(b) a flow focusing apparatus comprising:
(i) a polymer nozzle operatively delivering a focused stream of the polymer solution and/or suspension; and -26a-(ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution;
with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath; and (c) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; wherein the liquid-containing cell further comprises a stirring bar operatively maintaining the fluid bath under stirring, and wherein the fluid bath operatively allows the microbeads to solidify.
(a) a fluid bath, a focusing fluid, and a polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium;
(b) a flow focusing apparatus comprising:
(i) a polymer nozzle operatively delivering a focused stream of the polymer solution and/or suspension; and -26a-(ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution;
with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath; and (c) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; wherein the liquid-containing cell further comprises a stirring bar operatively maintaining the fluid bath under stirring, and wherein the fluid bath operatively allows the microbeads to solidify.
40. The system according to claim 39, wherein operative flow rates for (i) the focused stream through the polymer nozzle, (ii) the focusing stream through the focusing nozzle, and (iii) the focusing fluid through the outlet port, respectively, are predetermined in dependent relation upon one another, so as to maintain the fluid bath at a substantially constant liquid level.
41. The system according to claim 39, wherein the liquid-containing cell comprises one or more filters on the outlet port, with the volume of the focusing fluid being operatively delivered, through the filters, out from the fluid bath.
42. The system according to claim 41, wherein the filters operatively retain the microbeads in the fluid bath.
43. The system according to claim 41, wherein the filters operatively retain a substantially monodisperse set of the microbeads in the fluid bath.
44. The system according to any one of claims 41 and 42, wherein the filters operatively divide the microbeads into one or more collections of microbeads, with each of the collections including a respectively monodisperse set of the microbeads.
45. The system according to claim 39, wherein the flow focusing apparatus further comprises a flow focusing body defining an interior chamber and an outlet portion, with the focused stream and the focusing stream being operatively delivered into intersection with one another in the chamber, and with the focusing stream and the focused stream operatively flowing out from the outlet portion of the flow focusing body.
46. The system according to claim 45, wherein the outlet portion of the flow focusing body is operatively located below a liquid level of the fluid bath.
47. The system according to any one of claims 45 and 46, wherein the focused stream is operatively focused by the focusing fluid, and wherein the focusing stream and the focused stream operatively flow out from the outlet portion as a single flow stream.
48. The system according to claim 47, wherein the focusing stream substantially surrounds the focused stream in the single flow stream.
49. The system according to claim 39, wherein the liquid-containing cell is operatively sealed relative to the outside environment.
50. The system according to claim 49, wherein the flow focusing apparatus operatively delivers the focused stream and the focusing stream, into intersection with one another, in the liquid-containing cell.
51. The system according to any one of claims 49 and 50, further comprising a volume of a gas at a predetermined pressure, operatively contained within the liquid-containing cell.
52. The system according to claim 51, further comprising a gas pressure source, wherein the liquid-containing cell is shaped to define an inlet valve, and wherein the gas pressure source operatively pressurizes the gas, via the inlet valve, in the liquid-containing cell.
53. The system according to any one of claims 51 to 52, wherein the liquid-containing cell is shaped to define a pressure safety valve, and wherein the pressure safety valve operatively releases a portion of the gas or the fluid bath, when the pressure exceeds a predetermined maximum safety pressure for the sealed liquid-containing cell.
54. The system according to claim 53, wherein the pressure safety valve is provided on, and in operative fluid relation with, the outlet port of the liquid-containing cell, and wherein the pressure safety valve operatively releases a portion of the fluid bath, when the pressure exceeds the predetermined maximum safety pressure.
55. The system according to any one of claims 51 to 54, wherein the gas comprises an inert gas.
56. The system according to any one of claims 51 to 55, wherein (i) the pressure of the gas is predetermined, in balance with operative flow rates for (ii) the focused stream through the polymer nozzle and (iii) the focusing stream through the focusing nozzle, so as to maintain the fluid bath at a substantially constant liquid level.
57. The system according to any one of claims 39 to 56, wherein the stirring bar comprises an electric stirring bar or a magnetic stirring bar.
58. The system according to any one of claims 39 to 57, wherein the liquid-containing cell is shaped to define a sealed orifice, with the sealed orifice being selectively openable, so as to recover solidified microbeads through the orifice, from the fluid bath.
59. A system for forming one or more concentrated volumes of microbeads, the system comprising:
(a) a fluid bath, a focusing fluid, and a polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium;
(b) a flow focusing apparatus comprising:
(i) a polymer nozzle operatively delivering a focused stream of the polymer solution and/or suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution;
with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath;
(c) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; and (d) a conduit in fluid communication between the outlet port and the focusing nozzle, so as to operatively recycle at least part of the volume of the focusing fluid operatively delivered out from the fluid bath, via the outlet port, as at least part of the focusing stream operatively delivered by the focusing nozzle.
(a) a fluid bath, a focusing fluid, and a polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium;
(b) a flow focusing apparatus comprising:
(i) a polymer nozzle operatively delivering a focused stream of the polymer solution and/or suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution;
with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath;
(c) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; and (d) a conduit in fluid communication between the outlet port and the focusing nozzle, so as to operatively recycle at least part of the volume of the focusing fluid operatively delivered out from the fluid bath, via the outlet port, as at least part of the focusing stream operatively delivered by the focusing nozzle.
60. The system according to any one of claims 39 to 59, wherein the medium comprises an organic solvent.
61. The system according to claim 60, wherein the organic solvent comprises chloroform or dichloromethane.
62. The system according to any one of claims 39 to 61, wherein the polymer is substantially hydrophobic.
63. The system according to any one of claims 39 to 62, wherein the polymer comprises a polystyrene powder or a derivative thereof.
64. The system according to any one of claims 39 to 63, wherein the focusing fluid comprises water.
65. The system according to any one of claims 39 to 64, wherein the polymer solution and/or suspension further comprises particles dissolved and/or dispersed in the medium, and wherein each of the microbeads binds an identifiable set of the particles.
66. The system according to claim 65, wherein the particles comprise fluorophores.
67. The system according to claim 65, wherein the particles comprise nanoparticles.
68. The system according to claim 67, wherein the nanoparticles comprise semiconductor nanoparticles, magnetic nanoparticles, metallic conductor nanoparticles, metal oxide nanoparticles, fluorescent nanoparticles, or phosphorescent nanoparticles.
69. The system according to claim 65, wherein the particles comprise quantum dots.
70. The system according to claim 65, wherein the particles comprise a combination of quantum dots and magnetic nanoparticles.
71. The system according to any one of claims 39 to 70, wherein the polymer solution and/or suspension has a concentration of about 0.04 by weight-weight percentage (4 wt %).
72. A system for forming one or more concentrated volumes of microbeads, the system being for use with a fluid bath, a focusing fluid, and a polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium, the system comprising:
(a) a flow focusing apparatus comprising:
(i) a polymer nozzle operatively delivering a focused stream of the polymer solution and/or suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution;
with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath; and (b) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; wherein the liquid-containing cell further comprises a stirring bar operatively maintaining the fluid bath under stirring, and wherein the fluid bath operatively allows the microbeads to solidify.
(a) a flow focusing apparatus comprising:
(i) a polymer nozzle operatively delivering a focused stream of the polymer solution and/or suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution;
with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath; and (b) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; wherein the liquid-containing cell further comprises a stirring bar operatively maintaining the fluid bath under stirring, and wherein the fluid bath operatively allows the microbeads to solidify.
73. A system for forming one or more concentrated volumes of microbeads, the system being for use with a fluid bath, a focusing fluid, and a polymer solution and/or suspension comprising a polymer dissolved and/or dispersed in a medium, the system comprising:
(a) a flow focusing apparatus comprising:
(i) a polymer nozzle operatively delivering a focused stream of the polymer solution and/or suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution;
with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath;
(b) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; and (c) a conduit in fluid communication between the outlet port and the focusing nozzle, so as to operatively recycle at least part of the volume of the focusing fluid operatively delivered out from the fluid bath, via the outlet port, as at least part of the focusing stream operatively delivered by the focusing nozzle.
(a) a flow focusing apparatus comprising:
(i) a polymer nozzle operatively delivering a focused stream of the polymer solution and/or suspension; and (ii) a focusing nozzle operatively delivering a focusing stream of the focusing solution;
with the flow focusing apparatus operatively delivering the focused stream and the focusing stream into intersection with one another, and with the flow focusing apparatus operatively flowing the focusing stream and the focused stream into the fluid bath, so as to form the microbeads in the fluid bath;
(b) a liquid-containing cell shaped to define an outlet port, with the liquid-containing cell operatively containing the fluid bath and operatively delivering a volume of the focusing fluid out from the fluid bath, via the outlet port, so as to concentrate the microbeads in the fluid bath; and (c) a conduit in fluid communication between the outlet port and the focusing nozzle, so as to operatively recycle at least part of the volume of the focusing fluid operatively delivered out from the fluid bath, via the outlet port, as at least part of the focusing stream operatively delivered by the focusing nozzle.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US97966707P | 2007-10-12 | 2007-10-12 | |
US60/979,667 | 2007-10-12 | ||
PCT/CA2008/001808 WO2009046540A1 (en) | 2007-10-12 | 2008-10-10 | Flow focusing method and system for forming concentrated volumes of microbeads, and microbeads formed further thereto |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2702367A1 true CA2702367A1 (en) | 2009-04-16 |
CA2702367C CA2702367C (en) | 2012-08-21 |
Family
ID=40548915
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2702367A Expired - Fee Related CA2702367C (en) | 2007-10-12 | 2008-10-10 | Flow focusing method and system for forming concentrated volumes of microbeads, and microbeads formed further thereto |
Country Status (6)
Country | Link |
---|---|
US (2) | US8551763B2 (en) |
EP (1) | EP2209549A4 (en) |
JP (1) | JP5628037B2 (en) |
CN (1) | CN101861203B (en) |
CA (1) | CA2702367C (en) |
WO (1) | WO2009046540A1 (en) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2580589C (en) * | 2006-12-19 | 2016-08-09 | Fio Corporation | Microfluidic detection system |
JP2010530912A (en) * | 2007-06-22 | 2010-09-16 | フィオ コーポレイション | Manufacturing system and method for polymer microbeads doped with quantum dots |
US8641399B2 (en) * | 2009-12-23 | 2014-02-04 | Husky Injection Molding Systems Ltd. | Injection molding system having a digital displacement pump |
AU2011248537B2 (en) | 2010-04-28 | 2014-04-17 | University Of Georgia Research Foundation, Inc. | Photochemical cross-linkable polymers, methods of marking photochemical cross-linkable polymers, methods of using photochemical cross-linkable polymers, and methods of making articles containing photochemical cross-linkable polymers |
US8721936B2 (en) * | 2011-04-21 | 2014-05-13 | University Of Georgia Research Foundation, Inc. | Devices and methods for forming non-spherical particles |
EP2731999A4 (en) | 2011-07-15 | 2015-09-23 | Univ Georgia | Permanent attachment of agents to surfaces containing c-h functionality |
US9439421B2 (en) | 2011-08-04 | 2016-09-13 | University Of Georgia Research Foundation, Inc. | Permanent attachment of ammonium and guanidine-based antimicrobials to surfaces containing -OH functionality |
CA2852999A1 (en) | 2011-10-14 | 2013-04-18 | University Of Georgia Research Foundation, Inc. | Photochemical cross-linkable polymers, methods of making photochemical cross-linkable polymers, methods of using photochemical cross-linkable polymers, and methods of making articles containing photochemical cross-linkable polymers |
WO2015075677A1 (en) * | 2013-11-21 | 2015-05-28 | Atomo Diagnostics Pty Limited | Fluid control in integrated testing devices |
CN104149219B (en) * | 2014-07-31 | 2017-04-26 | 中国科学院重庆绿色智能技术研究院 | Integrated powder body spheroidizing and classifying method |
US10088398B2 (en) | 2015-02-11 | 2018-10-02 | Emd Millipore Corporation | Stirred cell and method of using same |
CN106145198A (en) * | 2016-06-29 | 2016-11-23 | 中国科学技术大学 | Prepare the method and device of uranium oxide microsphere |
US10912373B2 (en) * | 2017-02-02 | 2021-02-09 | Gg Brands, Llc. | Makeup shields and methods of use |
US10639607B2 (en) | 2017-06-16 | 2020-05-05 | Matralix Pte Ltd | Systems and methods for preparing wax and lipid particles |
AT520184B1 (en) * | 2017-09-18 | 2019-02-15 | Zeta Biopharma Gmbh | Stirring head with identification device |
CN107910084B (en) * | 2017-11-21 | 2020-01-03 | 中国科学技术大学 | Uranium carbide nuclear fuel microsphere and preparation method thereof |
CN108853053B (en) * | 2018-09-11 | 2021-03-30 | 安徽万士生物制药有限公司 | Production method of iron dextran product capable of being rapidly disintegrated in pig oral cavity |
Family Cites Families (191)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1907455A (en) * | 1929-12-28 | 1933-05-09 | Petroleum Rectifying Co California | Method of contacting fluids |
US3539155A (en) * | 1968-06-19 | 1970-11-10 | Amicon Corp | Ultrafiltration batch cell |
US5244630A (en) | 1988-04-22 | 1993-09-14 | Abbott Laboratories | Device for performing solid-phase diagnostic assay |
ATE117829T1 (en) | 1988-05-24 | 1995-02-15 | Anagen Uk Ltd | MAGNETICALLY ATTRACTABLE PARTICLES AND PRODUCTION METHOD. |
DE4105400A1 (en) | 1991-02-21 | 1992-08-27 | Behringwerke Ag | DEFINED COATING WITH RECOMBINANT FUSION PROTEINS FROM CONSTANT FUSION PARTNER AND VARIABLE ANTIGEN IN DIAGNOSTIC TEST SYSTEMS |
JP3210360B2 (en) * | 1991-05-29 | 2001-09-17 | フロイント産業株式会社 | Seamless capsule manufacturing equipment |
EP0698101B1 (en) | 1993-05-05 | 2004-11-03 | Common Services Agency | Hepatitis-c virus type 4, 5 and 6 |
JPH07171302A (en) * | 1993-12-22 | 1995-07-11 | Chiyoda Corp | Plastic precipitating method and apparatus |
US6103379A (en) | 1994-10-06 | 2000-08-15 | Bar-Ilan University | Process for the preparation of microspheres and microspheres made thereby |
US5480540A (en) * | 1994-10-17 | 1996-01-02 | General Electric Company | Spray apparatus for separating solids from fluids |
US6340588B1 (en) | 1995-04-25 | 2002-01-22 | Discovery Partners International, Inc. | Matrices with memories |
DE19528029B4 (en) * | 1995-07-31 | 2008-01-10 | Chemagen Biopolymer-Technologie Aktiengesellschaft | Magnetic polymer particles based on polyvinyl alcohol, process for their preparation and use |
US6022500A (en) | 1995-09-27 | 2000-02-08 | The United States Of America As Represented By The Secretary Of The Army | Polymer encapsulation and polymer microsphere composites |
EP0852004B1 (en) | 1995-10-11 | 2011-01-19 | Luminex Corporation | Multiplexed analysis of clinical specimens |
US5837442A (en) | 1995-11-29 | 1998-11-17 | Roche Molecular Systems, Inc. | Oligonucleotide primers for amplifying HCV nucleic acid |
US5885470A (en) | 1997-04-14 | 1999-03-23 | Caliper Technologies Corporation | Controlled fluid transport in microfabricated polymeric substrates |
US6595202B2 (en) | 1996-05-13 | 2003-07-22 | Universidad De Sevilla | Device and method for creating aerosols for drug delivery |
US6189803B1 (en) | 1996-05-13 | 2001-02-20 | University Of Seville | Fuel injection nozzle and method of use |
US6116516A (en) | 1996-05-13 | 2000-09-12 | Universidad De Sevilla | Stabilized capillary microjet and devices and methods for producing same |
ES2140998B1 (en) | 1996-05-13 | 2000-10-16 | Univ Sevilla | LIQUID ATOMIZATION PROCEDURE. |
US6792940B2 (en) | 1996-05-13 | 2004-09-21 | Universidad De Sevilla | Device and method for creating aerosols for drug delivery |
US6196525B1 (en) | 1996-05-13 | 2001-03-06 | Universidad De Sevilla | Device and method for fluid aeration via gas forced through a liquid within an orifice of a pressure chamber |
US6299145B1 (en) | 1996-05-13 | 2001-10-09 | Universidad De Sevilla | Device and method for fluid aeration via gas forced through a liquid within an orifice of a pressure chamber |
US6405936B1 (en) | 1996-05-13 | 2002-06-18 | Universidad De Sevilla | Stabilized capillary microjet and devices and methods for producing same |
US6248378B1 (en) | 1998-12-16 | 2001-06-19 | Universidad De Sevilla | Enhanced food products |
US6187214B1 (en) | 1996-05-13 | 2001-02-13 | Universidad De Seville | Method and device for production of components for microfabrication |
US6386463B1 (en) | 1996-05-13 | 2002-05-14 | Universidad De Sevilla | Fuel injection nozzle and method of use |
US5800690A (en) | 1996-07-03 | 1998-09-01 | Caliper Technologies Corporation | Variable control of electroosmotic and/or electrophoretic forces within a fluid-containing structure via electrical forces |
US6582921B2 (en) | 1996-07-29 | 2003-06-24 | Nanosphere, Inc. | Nanoparticles having oligonucleotides attached thereto and uses thereof |
US6120666A (en) | 1996-09-26 | 2000-09-19 | Ut-Battelle, Llc | Microfabricated device and method for multiplexed electrokinetic focusing of fluid streams and a transport cytometry method using same |
US5817458A (en) | 1996-10-15 | 1998-10-06 | The Avriel Group, Amcas Division Inc. | Reagent system for detecting HIV-infected peripheral blood lymphocytes in whole blood |
US5714390A (en) | 1996-10-15 | 1998-02-03 | Bio-Tech Imaging, Inc. | Cartridge test system for the collection and testing of blood in a single step |
US5786219A (en) | 1996-10-28 | 1998-07-28 | Molecular Probes, Inc. | Microspheres with fluorescent spherical zones |
GB9707096D0 (en) * | 1997-04-08 | 1997-05-28 | Smithkline Beecham Plc | Novel device |
US5959291A (en) | 1997-06-27 | 1999-09-28 | Caliper Technologies Corporation | Method and apparatus for measuring low power signals |
US6066243A (en) | 1997-07-22 | 2000-05-23 | Diametrics Medical, Inc. | Portable immediate response medical analyzer having multiple testing modules |
JP3689333B2 (en) | 1997-08-08 | 2005-08-31 | アクゾ・ノベル・エヌ・ベー | Nucleic acid sequences that can be used as primers and probes to amplify and detect all subtypes of HIV-1 |
WO1999019000A1 (en) | 1997-10-11 | 1999-04-22 | The Research Foundation Of State University Of New York | Controlled size polymeric microspheres with superparamagnetic cores |
US6699723B1 (en) | 1997-11-25 | 2004-03-02 | The Regents Of The University Of California | Organo luminescent semiconductor nanocrystal probes for biological applications and process for making and using such probes |
EP0919568A1 (en) | 1997-12-01 | 1999-06-02 | Sorin Diagnostics S.r.l. | Escape mutant of the surface antigen of hepatitis B virus |
AU2021099A (en) | 1997-12-30 | 1999-07-19 | Caliper Technologies Corporation | Software for the display of chromatographic separation data |
WO1999036564A1 (en) | 1998-01-16 | 1999-07-22 | Luminex Corporation | Multiplexed analysis of clinical specimens apparatus and methods |
US6394952B1 (en) | 1998-02-03 | 2002-05-28 | Adeza Biomedical Corporation | Point of care diagnostic systems |
US6100541A (en) | 1998-02-24 | 2000-08-08 | Caliper Technologies Corporation | Microfluidic devices and systems incorporating integrated optical elements |
US7117188B2 (en) | 1998-05-01 | 2006-10-03 | Health Discovery Corporation | Methods of identifying patterns in biological systems and uses thereof |
CA2268997C (en) | 1998-05-05 | 2005-03-22 | National Research Council Of Canada | Quantum dot infrared photodetectors (qdip) and methods of making the same |
CA2331897C (en) | 1998-05-14 | 2008-11-18 | Luminex Corporation | Multi-analyte diagnostic system and computer implemented process for same |
WO1999064840A1 (en) | 1998-06-09 | 1999-12-16 | Caliper Technologies Corp. | Fluorescent polarization detection in microfluidic systems |
US7077328B2 (en) | 1998-07-31 | 2006-07-18 | Abbott Laboratories | Analyte test instrument system including data management system |
US6263286B1 (en) | 1998-08-13 | 2001-07-17 | U.S. Genomics, Inc. | Methods of analyzing polymers using a spatial network of fluorophores and fluorescence resonance energy transfer |
AU6142799A (en) | 1998-09-11 | 2000-03-27 | Amira Medical | Device for determination of an analyte in a body fluid intergrated with an insulin pump |
EP1115888B1 (en) | 1998-09-24 | 2008-03-12 | Indiana University Research and Technology Corporation | Water-soluble luminescent quantum dots and bioconjugates thereof |
US6498497B1 (en) | 1998-10-14 | 2002-12-24 | Caliper Technologies Corp. | Microfluidic controller and detector system with self-calibration |
US6261779B1 (en) | 1998-11-10 | 2001-07-17 | Bio-Pixels Ltd. | Nanocrystals having polynucleotide strands and their use to form dendrimers in a signal amplification system |
US6576155B1 (en) | 1998-11-10 | 2003-06-10 | Biocrystal, Ltd. | Fluorescent ink compositions comprising functionalized fluorescent nanocrystals |
US6333110B1 (en) | 1998-11-10 | 2001-12-25 | Bio-Pixels Ltd. | Functionalized nanocrystals as visual tissue-specific imaging agents, and methods for fluorescence imaging |
WO2000028598A1 (en) | 1998-11-10 | 2000-05-18 | Biocrystal Limited | Methods for identification and verification |
US6114038A (en) | 1998-11-10 | 2000-09-05 | Biocrystal Ltd. | Functionalized nanocrystals and their use in detection systems |
US6309701B1 (en) | 1998-11-10 | 2001-10-30 | Bio-Pixels Ltd. | Fluorescent nanocrystal-labeled microspheres for fluorescence analyses |
US6319607B1 (en) | 1998-11-10 | 2001-11-20 | Bio-Pixels Ltd. | Purification of functionalized fluorescent nanocrystals |
US6450189B1 (en) | 1998-11-13 | 2002-09-17 | Universidad De Sevilla | Method and device for production of components for microfabrication |
DE19906509C1 (en) * | 1999-02-17 | 2000-11-23 | Vorlop Klaus Dieter | Method and device for producing solid particles from a liquid medium |
ATE469699T1 (en) | 1999-02-23 | 2010-06-15 | Caliper Life Sciences Inc | MANIPULATION OF MICROPARTICLES IN MICROFLUID SYSTEMS |
US7166475B2 (en) | 1999-02-26 | 2007-01-23 | Cyclacel Ltd. | Compositions and methods for monitoring the modification state of a pair of polypeptides |
US20010055764A1 (en) | 1999-05-07 | 2001-12-27 | Empedocles Stephen A. | Microarray methods utilizing semiconductor nanocrystals |
WO2000068692A1 (en) | 1999-05-07 | 2000-11-16 | Quantum Dot Corporation | A method of detecting an analyte using semiconductor nanocrystals |
CA2373537A1 (en) | 1999-05-12 | 2000-11-16 | Aclara Biosciences, Inc. | Multiplexed fluorescent detection in microfluidic devices |
WO2000070080A1 (en) | 1999-05-17 | 2000-11-23 | Caliper Technologies Corp. | Focusing of microparticles in microfluidic systems |
US6592821B1 (en) | 1999-05-17 | 2003-07-15 | Caliper Technologies Corp. | Focusing of microparticles in microfluidic systems |
US6544732B1 (en) | 1999-05-20 | 2003-04-08 | Illumina, Inc. | Encoding and decoding of array sensors utilizing nanocrystals |
US20020051971A1 (en) | 1999-05-21 | 2002-05-02 | John R. Stuelpnagel | Use of microfluidic systems in the detection of target analytes using microsphere arrays |
US20060169800A1 (en) | 1999-06-11 | 2006-08-03 | Aradigm Corporation | Aerosol created by directed flow of fluids and devices and methods for producing same |
US6811668B1 (en) | 1999-06-22 | 2004-11-02 | Caliper Life Sciences, Inc. | Apparatus for the operation of a microfluidic device |
US6353475B1 (en) | 1999-07-12 | 2002-03-05 | Caliper Technologies Corp. | Light source power modulation for use with chemical and biochemical analysis |
WO2001013119A1 (en) | 1999-08-17 | 2001-02-22 | Luminex Corporation | Encapsulation of fluorescent particles |
WO2001017797A1 (en) | 1999-09-10 | 2001-03-15 | Caliper Technologies Corp. | Microfabrication methods and devices |
US20040267568A1 (en) | 1999-09-15 | 2004-12-30 | Mark Chandler | Creation of a database of biochemical data and methods of use |
AU7579900A (en) | 1999-09-15 | 2001-04-17 | Luminex Corporation | Creation of a database of biochemical data and methods of use |
US6978212B1 (en) | 1999-11-01 | 2005-12-20 | Smiths Detection Inc. | System for portable sensing |
US7037416B2 (en) | 2000-01-14 | 2006-05-02 | Caliper Life Sciences, Inc. | Method for monitoring flow rate using fluorescent markers |
US20020009728A1 (en) | 2000-01-18 | 2002-01-24 | Quantum Dot Corporation | Oligonucleotide-tagged semiconductor nanocrystals for microarray and fluorescence in situ hybridization |
US20020004246A1 (en) | 2000-02-07 | 2002-01-10 | Daniels Robert H. | Immunochromatographic methods for detecting an analyte in a sample which employ semiconductor nanocrystals as detectable labels |
US20030099940A1 (en) | 2000-02-16 | 2003-05-29 | Empedocles Stephen A. | Single target counting assays using semiconductor nanocrystals |
CA2399199A1 (en) | 2000-02-23 | 2001-08-30 | Ring-Ling Chien | Multi-reservoir pressure control system |
US6500622B2 (en) | 2000-03-22 | 2002-12-31 | Quantum Dot Corporation | Methods of using semiconductor nanocrystals in bead-based nucleic acid assays |
US6759235B2 (en) | 2000-04-06 | 2004-07-06 | Quantum Dot Corporation | Two-dimensional spectral imaging system |
US6773812B2 (en) | 2000-04-06 | 2004-08-10 | Luminex Corporation | Magnetically-responsive microspheres |
US6548264B1 (en) | 2000-05-17 | 2003-04-15 | University Of Florida | Coated nanoparticles |
WO2001089585A1 (en) | 2000-05-24 | 2001-11-29 | Biocrystal Ltd. | tLUORESCENT NANOCRYSTAL-LABELLED MICROSPHERES FOR FLUORESCENCE ANALYSES |
US7351376B1 (en) | 2000-06-05 | 2008-04-01 | California Institute Of Technology | Integrated active flux microfluidic devices and methods |
GB0013610D0 (en) | 2000-06-06 | 2000-07-26 | Secr Defence | Monitoring means |
US6494830B1 (en) | 2000-06-22 | 2002-12-17 | Guidance Interactive Technologies, Inc. | Handheld controller for monitoring/using medical parameters |
JP2002000271A (en) | 2000-06-28 | 2002-01-08 | Sanyo Electric Co Ltd | System, method, and database for analyzing microorganism |
ATE303597T1 (en) | 2000-07-07 | 2005-09-15 | Medmira Inc | HCV MOSAIC ANTIGEN COMPOSITION |
WO2002007064A2 (en) | 2000-07-17 | 2002-01-24 | Labnetics, Inc. | Method and apparatus for the processing of remotely collected electronic information characterizing properties of biological entities |
CA2314398A1 (en) | 2000-08-10 | 2002-02-10 | Edward Shipwash | Microarrays and microsystems for amino acid analysis and protein sequencing |
US20020182609A1 (en) | 2000-08-16 | 2002-12-05 | Luminex Corporation | Microsphere based oligonucleotide ligation assays, kits, and methods of use, including high-throughput genotyping |
US6934408B2 (en) | 2000-08-25 | 2005-08-23 | Amnis Corporation | Method and apparatus for reading reporter labeled beads |
US6681821B1 (en) * | 2000-09-18 | 2004-01-27 | Dominick Cirone | Protective bat cover |
US20020048425A1 (en) | 2000-09-20 | 2002-04-25 | Sarnoff Corporation | Microfluidic optical electrohydrodynamic switch |
EP2256834B1 (en) | 2000-10-04 | 2012-09-26 | The Board of Trustees of The University of Arkansas | Colloidal metal chalcogenide nanocrystals |
US6649138B2 (en) | 2000-10-13 | 2003-11-18 | Quantum Dot Corporation | Surface-modified semiconductive and metallic nanoparticles having enhanced dispersibility in aqueous media |
US6937323B2 (en) | 2000-11-08 | 2005-08-30 | Burstein Technologies, Inc. | Interactive system for analyzing biological samples and processing related information and the use thereof |
US6573128B1 (en) | 2000-11-28 | 2003-06-03 | Cree, Inc. | Epitaxial edge termination for silicon carbide Schottky devices and methods of fabricating silicon carbide devices incorporating same |
US6778724B2 (en) | 2000-11-28 | 2004-08-17 | The Regents Of The University Of California | Optical switching and sorting of biological samples and microparticles transported in a micro-fluidic device, including integrated bio-chip devices |
US20020083888A1 (en) | 2000-12-28 | 2002-07-04 | Zehnder Donald A. | Flow synthesis of quantum dot nanocrystals |
WO2002060275A1 (en) * | 2001-01-31 | 2002-08-08 | Kraft Foods Holdings, Inc. | Production of capsules and particles for improvement of food products |
CN1152055C (en) | 2001-03-20 | 2004-06-02 | 清华大学 | Surface cladding and radical functino modification method of magnetic microsphere, thus obtained microsphere and its application |
US7041468B2 (en) | 2001-04-02 | 2006-05-09 | Therasense, Inc. | Blood glucose tracking apparatus and methods |
JP2002311027A (en) | 2001-04-09 | 2002-10-23 | Hitachi Software Eng Co Ltd | Beads, manufacturing method of beads, flow cytometer, and program |
US20020164271A1 (en) | 2001-05-02 | 2002-11-07 | Ho Winston Z. | Wavelength-coded bead for bioassay and signature recogniton |
US6845327B2 (en) | 2001-06-08 | 2005-01-18 | Epocal Inc. | Point-of-care in-vitro blood analysis system |
US6905885B2 (en) | 2001-06-12 | 2005-06-14 | The Regents Of The University Of California | Portable pathogen detection system |
AU2002322348A1 (en) | 2001-06-28 | 2003-03-03 | Advanced Research And Technology Institute, Inc. | Methods of preparing multicolor quantum dot tagged beads and conjugates thereof |
EP1270073B1 (en) | 2001-06-28 | 2005-02-16 | Agilent Technologies, Inc. (a Delaware corporation) | Microfluidic system with controller |
WO2003006223A1 (en) * | 2001-07-10 | 2003-01-23 | University Technology Corporation | Devices and methods for the production of particles |
WO2003008937A2 (en) * | 2001-07-18 | 2003-01-30 | The Regents Of The University Of Michigan | Gas-focusing flow cytometer cell and flow cytometer detection system with waveguide optics |
EP2218762A3 (en) | 2001-07-20 | 2010-09-29 | Life Technologies Corporation | Luminescent nanoparticles and methods for their preparation |
US7060227B2 (en) | 2001-08-06 | 2006-06-13 | Sau Lan Tang Staats | Microfluidic devices with raised walls |
GB2378949B (en) | 2001-08-16 | 2005-09-07 | Morten Steen Hanefeld Dziegiel | Recombinant anti-plasmodium falciparum antibodies |
ATE470859T1 (en) | 2001-09-06 | 2010-06-15 | Straus Holdings Inc | FAST AND SENSITIVE DETECTION OF MOLECULES |
US7214428B2 (en) | 2001-09-17 | 2007-05-08 | Invitrogen Corporation | Highly luminescent functionalized semiconductor nanocrystals for biological and physical applications |
US7205048B2 (en) | 2001-09-17 | 2007-04-17 | Invitrogen Corporation | Functionalized fluorescent nanocrystal compositions and methods of making |
US7195913B2 (en) | 2001-10-05 | 2007-03-27 | Surmodics, Inc. | Randomly ordered arrays and methods of making and using |
US6966880B2 (en) | 2001-10-16 | 2005-11-22 | Agilent Technologies, Inc. | Universal diagnostic platform |
US7457731B2 (en) | 2001-12-14 | 2008-11-25 | Siemens Medical Solutions Usa, Inc. | Early detection of disease outbreak using electronic patient data to reduce public health threat from bio-terrorism |
US7341211B2 (en) * | 2002-02-04 | 2008-03-11 | Universidad De Sevilla | Device for the production of capillary jets and micro-and nanometric particles |
US7689899B2 (en) | 2002-03-06 | 2010-03-30 | Ge Corporate Financial Services, Inc. | Methods and systems for generating documents |
US7252928B1 (en) | 2002-03-12 | 2007-08-07 | Caliper Life Sciences, Inc. | Methods for prevention of surface adsorption of biological materials to capillary walls in microchannels |
ATE374598T1 (en) | 2002-03-15 | 2007-10-15 | Alrise Biosystems Gmbh | MICROPARTICLES AND METHOD FOR THE PRODUCTION THEREOF |
US20030194350A1 (en) | 2002-04-11 | 2003-10-16 | Siemens Information And Communication Networks | Public health threat surveillance system |
AU2003251890A1 (en) | 2002-07-15 | 2004-02-02 | Advanced Research And Technology Institute, Inc. | Rapid low-temperature synthesis of quantum dots |
WO2004014540A1 (en) | 2002-08-02 | 2004-02-19 | Capsulution Nanoscience Ag | Color coated layer-by-layer microcapsules serving as combinatory analysis libraries and as specific optical sensors |
US7267799B1 (en) | 2002-08-14 | 2007-09-11 | Detekt Biomedical, L.L.C. | Universal optical imaging and processing system |
NZ538348A (en) | 2002-08-19 | 2006-09-29 | Stout Solutions Llc | Bio-surveillance by threshhold analysis of symptom data captured by emergency services dispatchers |
JP4230741B2 (en) | 2002-08-30 | 2009-02-25 | 日立ソフトウエアエンジニアリング株式会社 | Purification method of semiconductor nanoparticles |
GB2393729A (en) | 2002-10-04 | 2004-04-07 | Nanomagnetics Ltd | Semiconductor nanoparticles |
AU2003275942A1 (en) | 2002-11-01 | 2004-05-25 | Technical University Of Denmark | A microfluidic system and a microdevice for velocity measurement, a method of performing measurements and use hereof |
US20040096363A1 (en) | 2002-11-18 | 2004-05-20 | Larry Porter | Point-of-care assay reader and analyzer |
TWI220162B (en) | 2002-11-29 | 2004-08-11 | Ind Tech Res Inst | Integrated compound nano probe card and method of making same |
AU2003302253B2 (en) | 2002-12-12 | 2007-06-28 | Nanosphere, Inc. | Direct SNP detection with unamplified DNA |
US7613510B2 (en) | 2002-12-12 | 2009-11-03 | Razvan Rentea | Biofeedback device displaying results on a cellular phone display |
US6905583B2 (en) | 2002-12-13 | 2005-06-14 | Aclara Biosciences, Inc. | Closed-loop control of electrokinetic processes in microfluidic devices based on optical readings |
JP4073323B2 (en) | 2003-01-23 | 2008-04-09 | 日立ソフトウエアエンジニアリング株式会社 | Functional beads, reading method and reading apparatus thereof |
US20040176704A1 (en) | 2003-03-04 | 2004-09-09 | Stevens Timothy A | Collection device adapted to accept cartridge for point of care system |
US20050014134A1 (en) | 2003-03-06 | 2005-01-20 | West Jason Andrew Appleton | Viral identification by generation and detection of protein signatures |
JP2006521278A (en) | 2003-03-11 | 2006-09-21 | ナノシス・インコーポレイテッド | Process for producing nanocrystals and nanocrystals produced thereby |
KR100890885B1 (en) | 2003-03-31 | 2009-03-31 | 에프. 호프만-라 로슈 아게 | Compositions and methods for detecting certain flaviviruses, including members of the japanese encephalitis virus serogroup |
WO2004111260A2 (en) | 2003-06-12 | 2004-12-23 | Bioarray Solutions, Ltd. | Immobilization of bead-displayed ligands on substrate surfaces |
US7115230B2 (en) | 2003-06-26 | 2006-10-03 | Intel Corporation | Hydrodynamic focusing devices |
EP1639660A4 (en) * | 2003-06-27 | 2009-12-02 | Ultracell Corp | Efficient micro fuel cell systems and methods |
EP1664772A4 (en) | 2003-08-04 | 2007-01-03 | Univ Emory | Porous materials embedded with nanospecies |
US7069191B1 (en) | 2003-08-06 | 2006-06-27 | Luminex Corporation | Methods for reducing the susceptibility of a peak search to signal noise |
US7298478B2 (en) | 2003-08-14 | 2007-11-20 | Cytonome, Inc. | Optical detector for a particle sorting system |
CN2640608Y (en) * | 2003-08-15 | 2004-09-15 | 同济大学 | Nozzle for preparing micronano particles |
US8346482B2 (en) | 2003-08-22 | 2013-01-01 | Fernandez Dennis S | Integrated biosensor and simulation system for diagnosis and therapy |
WO2005023923A2 (en) | 2003-09-04 | 2005-03-17 | Nanosys, Inc. | Methods of processing nanocrystals, and compositions, devices and systems including same |
US20070116868A1 (en) | 2003-09-24 | 2007-05-24 | The Regents Of The University Of California | Hybrid synthesis of core/shell nanocrystals |
US20050071199A1 (en) | 2003-09-30 | 2005-03-31 | Riff Kenneth M. | Aggregating patient information for use in medical device programming |
US7790473B2 (en) | 2003-11-05 | 2010-09-07 | The United States Of America As Represented By The Department Of Health And Human Services | Biofunctionalized quantum dots for biological imaging |
WO2005052996A2 (en) | 2003-11-19 | 2005-06-09 | William Marsh Rice University | Methods and materials for cdse nanocrystal synthesis |
US7309500B2 (en) * | 2003-12-04 | 2007-12-18 | The Board Of Trustees Of The University Of Illinois | Microparticles |
US7118627B2 (en) | 2003-12-04 | 2006-10-10 | Hines Margaret A | Synthesis of colloidal PbS nanocrystals with size tunable NIR emission |
CA2550153A1 (en) | 2003-12-12 | 2005-07-28 | Quantum Dot Corporation | Preparation of stable, bright luminescent nanoparticles having compositionally engineered properties |
AU2003292763A1 (en) | 2003-12-24 | 2005-07-14 | Amato Pharmaceutical Products, Ltd. | Process for producing microsphere and apparatus for producing the same |
EP1742729B8 (en) * | 2004-02-23 | 2010-02-03 | EyeSense AG | Process for production of ionically crosslinked polysaccharide microspheres |
US20050227370A1 (en) | 2004-03-08 | 2005-10-13 | Ramel Urs A | Body fluid analyte meter & cartridge system for performing combined general chemical and specific binding assays |
CA2566493A1 (en) | 2004-05-10 | 2005-11-24 | Evident Technologies | Iii-v semiconductor nanocrystal complexes and methods of making same |
US7335345B2 (en) | 2004-05-24 | 2008-02-26 | Drexel University | Synthesis of water soluble nanocrystalline quantum dots and uses thereof |
US7311861B2 (en) * | 2004-06-01 | 2007-12-25 | Boston Scientific Scimed, Inc. | Embolization |
CN1984708B (en) * | 2004-06-29 | 2014-01-29 | 皇家飞利浦电子股份有限公司 | Micro-spheres |
US7276720B2 (en) | 2004-07-19 | 2007-10-02 | Helicos Biosciences Corporation | Apparatus and methods for analyzing samples |
US7229690B2 (en) | 2004-07-26 | 2007-06-12 | Massachusetts Institute Of Technology | Microspheres including nanoparticles |
JP2008510852A (en) | 2004-08-17 | 2008-04-10 | インヴィトロジェン コーポレーション | Synthesis of highly luminescent colloidal particles |
TWI281691B (en) | 2004-08-23 | 2007-05-21 | Ind Tech Res Inst | Method for manufacturing a quantum-dot element |
US7524672B2 (en) | 2004-09-22 | 2009-04-28 | Sandia Corporation | Microfluidic microarray systems and methods thereof |
US7534489B2 (en) | 2004-09-24 | 2009-05-19 | Agency For Science, Technology And Research | Coated composites of magnetic material and quantum dots |
EP1817708A4 (en) | 2004-10-18 | 2014-08-27 | Wellstat Vaccines Llc | A systems and methods for obtaining, storing, processing and utilizing immunologic information of an individual or population |
US7405434B2 (en) | 2004-11-16 | 2008-07-29 | Cornell Research Foundation, Inc. | Quantum dot conjugates in a sub-micrometer fluidic channel |
CN1603011A (en) * | 2004-11-19 | 2005-04-06 | 中国科学技术大学 | Hardly soluble suspension liquid inject method and apparatus for preparing composite material sample room |
DE102004062573A1 (en) | 2004-12-24 | 2006-07-13 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Three-dimensional nano- and microstructured supports |
ES2257968B1 (en) * | 2005-01-28 | 2007-07-01 | Universidad De Sevilla | PROCEDURE AND DEVICE FOR OBTAINING MICRO AND NANOMETRIC SIZE PARTICLES. |
US20060173715A1 (en) | 2005-02-01 | 2006-08-03 | Hao Wang | Health information system and method |
WO2006132953A2 (en) | 2005-06-03 | 2006-12-14 | Bayer Healthcare Llc | Solar-powered integrated-diagnostic instrument |
WO2007002579A2 (en) | 2005-06-23 | 2007-01-04 | Bioveris Corporation | Assay cartridges and methods for point of care instruments |
WO2007011622A2 (en) | 2005-07-18 | 2007-01-25 | U.S. Genomics, Inc. | Microfluidic methods and apparatuses for sample preparation and analysis |
US20070081920A1 (en) | 2005-10-12 | 2007-04-12 | Murphy R S | Semi-disposable optoelectronic rapid diagnostic test system |
WO2008147382A1 (en) | 2006-09-27 | 2008-12-04 | Micronics, Inc. | Integrated microfluidic assay devices and methods |
WO2008089155A2 (en) | 2007-01-12 | 2008-07-24 | Holtzman Douglas A | Biomarker assays for the diagnosis of malaria in developing countries based on epo levels |
JP2010530912A (en) * | 2007-06-22 | 2010-09-16 | フィオ コーポレイション | Manufacturing system and method for polymer microbeads doped with quantum dots |
WO2009059404A1 (en) | 2007-11-05 | 2009-05-14 | University Health Network | Angiopoietin-1 and -2 biomarkers for infectious diseases that compromise endothelial integrity |
-
2008
- 2008-10-10 EP EP08837359.2A patent/EP2209549A4/en not_active Withdrawn
- 2008-10-10 US US12/682,710 patent/US8551763B2/en not_active Expired - Fee Related
- 2008-10-10 JP JP2010528254A patent/JP5628037B2/en not_active Expired - Fee Related
- 2008-10-10 CA CA2702367A patent/CA2702367C/en not_active Expired - Fee Related
- 2008-10-10 WO PCT/CA2008/001808 patent/WO2009046540A1/en active Application Filing
- 2008-10-10 CN CN200880116521.6A patent/CN101861203B/en not_active Expired - Fee Related
-
2013
- 2013-10-07 US US14/047,742 patent/US9695482B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP5628037B2 (en) | 2014-11-19 |
WO2009046540A1 (en) | 2009-04-16 |
US9695482B2 (en) | 2017-07-04 |
EP2209549A1 (en) | 2010-07-28 |
CN101861203A (en) | 2010-10-13 |
CA2702367C (en) | 2012-08-21 |
EP2209549A4 (en) | 2014-03-05 |
US20110081643A1 (en) | 2011-04-07 |
JP2011501769A (en) | 2011-01-13 |
US8551763B2 (en) | 2013-10-08 |
US20140038853A1 (en) | 2014-02-06 |
CN101861203B (en) | 2014-01-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2702367A1 (en) | Flow focusing method and system for forming concentrated volumes of microbeads, and microbeads formed further thereto | |
JP2011501769A5 (en) | ||
Azevedo et al. | Aqueous dispersions of nanobubbles: Generation, properties and features | |
Oh et al. | Hydrodynamic micro-encapsulation of aqueous fluids and cells via ‘on the fly’photopolymerization | |
JP5892708B2 (en) | Electrospray micro reaction field forming apparatus and chemical reaction control method | |
Varma et al. | Magnetic Janus particles synthesized using droplet micro-magnetofluidic techniques for protein detection | |
EP3456815A1 (en) | Aqueous solution capable of being administered to living body, and method for producing same | |
CN105612186B (en) | Reversed-phase polymerization method | |
JP2008183554A (en) | Method for producing dispersion liquid of organic fine particle, and organic fine particle obtained thereby | |
CN106040117A (en) | Method for preparing mono-dispersity calcium alginate microspheres based on emulsion liquid membrane mass transfer | |
Schneider et al. | Effects of chemical and physical parameters in the generation of microspheres by hydrodynamic flow focusing | |
JP2019504761A5 (en) | ||
US9156189B2 (en) | Systems and methods for high-throughput microfluidic bead production | |
US20090247730A1 (en) | Method of producing a polymer-processed organic fine particle dispersion | |
CN105013544A (en) | Micro-droplet fusion method based on hydrophilic cellosilk induction | |
JP2009256652A (en) | Method of producing organic pigment fine particle dispersion, and inkjet recording ink and paint using organic pigment fine particle obtained by the same | |
US10815316B2 (en) | Macroporous beads | |
US20160082134A1 (en) | Nanoparticle Photoacoustic Imaging Agents | |
CN107207637A (en) | It is related to the reversed-phase polymerization method of microfluidic device | |
JP2009041000A (en) | Pigment ink composition and image forming method using the same | |
CN108479729A (en) | Application of the low temperature liquid metallic microspheres in preparing adsorbing separation and analyzing high-molecular porous material | |
JP5843089B2 (en) | Method for synthesizing spherical or non-spherical polymer particles | |
Nimbalkar et al. | Improving the physiological relevance of drug testing for drug-loaded nanoparticles using 3D tumor cell cultures | |
JP2010083981A (en) | Method for manufacturing cage-type metal oxide modified with organic group | |
Chen-Jolly et al. | Supercritical continuous precipitation polymerization of acrylic acid in a droplet-based millifluidic device |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
MKLA | Lapsed |
Effective date: 20191010 |