WO2005079544A2 - Rainures d'alignement de plaques a puits multiples pour microparticules codees - Google Patents

Rainures d'alignement de plaques a puits multiples pour microparticules codees Download PDF

Info

Publication number
WO2005079544A2
WO2005079544A2 PCT/US2005/005743 US2005005743W WO2005079544A2 WO 2005079544 A2 WO2005079544 A2 WO 2005079544A2 US 2005005743 W US2005005743 W US 2005005743W WO 2005079544 A2 WO2005079544 A2 WO 2005079544A2
Authority
WO
WIPO (PCT)
Prior art keywords
microbeads
grooves
grating
plate
code
Prior art date
Application number
PCT/US2005/005743
Other languages
English (en)
Other versions
WO2005079544A9 (fr
WO2005079544A3 (fr
Inventor
James S. Sirkis
John A. Moon
Robert N. Brucato
Martin A. Putnam
Tuo Li
Joseph Traynor
Original Assignee
Cyvera Corporation
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Cyvera Corporation filed Critical Cyvera Corporation
Publication of WO2005079544A2 publication Critical patent/WO2005079544A2/fr
Publication of WO2005079544A3 publication Critical patent/WO2005079544A3/fr
Publication of WO2005079544A9 publication Critical patent/WO2005079544A9/fr

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/645Specially adapted constructive features of fluorimeters
    • G01N21/6452Individual samples arranged in a regular 2D-array, e.g. multiwell plates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502761Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277Apparatus
    • B01J2219/00497Features relating to the solid phase supports
    • B01J2219/005Beads
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277Apparatus
    • B01J2219/0054Means for coding or tagging the apparatus or the reagents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277Apparatus
    • B01J2219/0054Means for coding or tagging the apparatus or the reagents
    • B01J2219/00547Bar codes
    • B01J2219/005492-dimensional
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277Apparatus
    • B01J2219/0054Means for coding or tagging the apparatus or the reagents
    • B01J2219/00554Physical means
    • B01J2219/0056Raised or sunken areas
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277Apparatus
    • B01J2219/0054Means for coding or tagging the apparatus or the reagents
    • B01J2219/00572Chemical means
    • B01J2219/00576Chemical means fluorophore
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00718Type of compounds synthesised
    • B01J2219/0072Organic compounds
    • B01J2219/00722Nucleotides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06Fluid handling related problems
    • B01L2200/0605Metering of fluids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06Fluid handling related problems
    • B01L2200/0647Handling flowable solids, e.g. microscopic beads, cells, particles
    • B01L2200/0668Trapping microscopic beads
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0803Disc shape
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0809Geometry, shape and general structure rectangular shaped
    • B01L2300/0816Cards, e.g. flat sample carriers usually with flow in two horizontal directions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0809Geometry, shape and general structure rectangular shaped
    • B01L2300/0819Microarrays; Biochips
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0861Configuration of multiple channels and/or chambers in a single devices
    • B01L2300/0877Flow chambers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00Moving or stopping fluids
    • B01L2400/04Moving fluids with specific forces or mechanical means
    • B01L2400/0475Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure
    • B01L2400/0487Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure fluid pressure, pneumatics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5025Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures for parallel transport of multiple samples

Definitions

  • the present invention generally relates to a method and apparatus for processing information contained on microbeads, each microbead having an elongated body with a code embedded therein along a longitudinal axis thereof to be read by a code reading device; and more particularly to a method and apparatus for aligning the microbeads so the longitudinal axis thereof is in a fixed orientation relative to the code reading or other device.
  • microarrays have a low sample throughput but are capable of providing industry leading numbers of measurements per sample (upwards to 100,000 samples).
  • industry leading numbers of measurements per sample upwards to 100,000 samples.
  • Several technologies have been proposed to meet this challenge.
  • One example is printing microarrays in the bottom of wells of microtitre plates (GeneXP, Matrix). This technology is attractive because it preserves the microtitre format necessary for high sample throughput, but is limited in the number of spots that can be printed.
  • Gene XP for example, can print a maximum of 1024 spots.
  • GeneXP is limited to a total of 340 measurements per sample.
  • Other technologies that attempt to solve this problem include eTag (Aclara), fluorescent microbeads (Luminex, Quantum Dot), spatially ordered microbeads (Illumina), molecular multiplexed profiling (HGT), and others. Therefore, it would be desirable to obtain a coding element or platform that provides the capability of providing many codes (e.g., greater than 1 million codes), that can be made very small and/or that can withstand harsh environments. Moreover, it would be desirable to provide a method and apparatus to position and align such coding elements so as to better sense the chemical content and correlate it in relation to the code to determine information about the process.
  • the present invention provides a new and unique method and apparatus for aligning new and unique coding elements or microbeads, wherein each microbead has an elongated body with a code embedded therein along a longitudinal axis thereof to be read by a code reading or other detection device.
  • the method features the step of aligning the microbeads with a positioning device so the longitudinal axis of the microbeads is positioned in a fixed orientation relative to the code reading or other detection device.
  • the new and unique microbeads are not spherical, but instead have an elongated shape and may be cylindrical, cubic, rectangular, or any other elongated shape.
  • the microbeads are typically composed of silica glass with some germanium and/or boron doped region or regions that are photosensitive to ultraviolet light. Coded microbeads are individually identifiable via a single or series of spatially overlapping pitches written into them. The microbeads may be used in many different processes. After such processing, the microbeads have a resulting chemical content on the surface of each bead that is sensed and correlated in relation to the code contained with the microbead to determine information about the process. When used in an assay process, the microbeads are typically cylindrically (i.e. tubular) shaped glass beads and between 25 and 250 ⁇ m in diameter and between 100 and 500 ⁇ m long.
  • the code consists of a diffraction grating typically disposed along an axis of the microbead, there is a particular alignment required between the incident readout laser beam and the readout detector in two of the three rotational axes.
  • the two of the three rotational axes include the pitch of the microbead in the front-to-back direction and the yaw of the microbead in a side-to-side direction.
  • the third axis rotation about the center axis of the cylinder, is azimuthally symmetric and therefore does not require alignment.
  • the third axis is analogous to the roll axis.
  • the invention provides a method for aligning the microbeads in the two rotational axes to a fixed orientation relative to an incident laser beam and a readout camera, otherwise known as the code camera.
  • the invention further provides a method for rapidly aligning a large number of microbeads, between 1,000 and 1,000,000 microbeads or more, economically, and with the necessary tolerances.
  • the method is flexible as it relates to the size of the microbeads and can be integrated into a fully automated system, which prepares the microbeads for rapid readout by an automated code-reading machine.
  • the positioning device includes a plate with a series of parallel grooves, which could have one of several different shapes, including square, rectangular, v-shaped, semi-circular, etc., as well as a flat bottom groove with tapered walls.
  • the grooves are formed into an optically transparent medium such as borosilicate glass, fused silica, or plastic.
  • the depth of the grooves will depend on the diameter of the microbead but generally they will be between 10 and 125 ⁇ m, but may be larger as discussed hereinafter depending on the application.
  • the spacing of the grooves is optimal when it is between 1 and 2 times the diameter of the microbead, providing for both maximum packing density as well as maximum probability that a microbead will fall into a groove.
  • the width of grooves is optimal when the gap between the microbead and the walls of the grooves is sufficiently small to prevent the microbeads from rotating within the grooves by more than a few degrees.
  • the bottom of the groove must also be maintained flat enough to prevent the microbeads from rotating, by more than a few tenths of a degree, relative to the incident laser beam.
  • the grooved plate Another critical aspect of the grooved plate is the optical quality of the grooves. To prevent excess scatter of the readout laser beam, which could lead to low contrast between the code signal and the background scatter, it is important that the grooves exhibit high optical quality.
  • the beads can be read in the groove plate from the bottom of (i.e. below), from the top of (i.e. above), or from the side of the plate, depending on the application and type of microbead used.
  • Some advantages of the groove plate approach include: • Rapid simultaneous alignment of microbeads. Alignment rates ⁇ 1000's per second. • Once the microbeads are aligned, they can be read as many times as necessary to get a good reading or improve statistics.
  • the positioning device may includes a tube having a bore for receiving, aligning and reading the microbeads.
  • the present invention also provides an apparatus for aligning an optical identification element.
  • the optical identification element having an optical substrate having at least a portion thereof with at least one diffraction grating disposed therein, the grating having at least one refractive index pitch superimposed at a common location, the grating being embedded within a substantially single material, the grating providing an output optical signal when illuminated by an incident light signal, the optical output signal being indicative of a code, and being the result of passive, non-resonant scattering from said at least one diffraction grating when illuminated by said incident light signal, and the optical identification element being an elongated object with a longitudinal axis.
  • the apparatus also having an alignment device which aligns the optical identification element such that said output optical signal is indicative of the code.
  • the present invention also provides an optical element capable of having many optically readable codes.
  • the element has a substrate containing an optically readable composite diffraction grating having one or more collocated index spacing or pitches ⁇ .
  • the invention allows for a high number of uniquely identifiable codes (e.g., millions, billions, or more).
  • the codes may be digital binary codes and thus are digitally readable or may be other numerical bases if desired.
  • the elements may be very small "microbeads" (or microelements or microparticles or encoded particles) for small applications (about 1-1000 microns), or larger "macroelements" for larger applications (e.g., 1-lOOOmm or much larger).
  • the elements may also be referred to as encoded particles or encoded threads.
  • the element may be embedded within or part of a larger substrate or object.
  • the code in the element is interrogated using free-space optics and can be made alignment insensitive.
  • the gratings (or codes) are embedded inside (including on or near the surface) of the substrate and may be permanent non-removable codes that can operate in harsh environments (chemical, temperature, nuclear, electromagnetic, etc.).
  • the code is not affected by spot imperfections, scratches, cracks or breaks in the substrate.
  • the codes are spatially invariant. Thus, splitting or slicing an element axially produces more elements with the same code. Accordingly, when a bead is axially split-up, the code is not lost, but instead replicated in each piece.
  • Fig. 1 shows steps of a microbead platform assay process.
  • Fig. 2 is a side view of an optical identification element in accordance with the present invention.
  • Fig. 3 is a top level optical schematic for reading a code in an optical identification element in accordance with the present invention.
  • Fig. 4 is a perspective view of a grooved plate for use with an optical identification element, in accordance with the present invention.
  • Fig. 5 is a diagram of the flat grooves and an example of the dimensionality thereof in accordance with the present invention.
  • Fig. 6 is a perspective view of a plate with holes for use with an optical identification element, in accordance with the present invention.
  • Fig. 1 shows steps of a microbead platform assay process.
  • Fig. 2 is a side view of an optical identification element in accordance with the present invention.
  • Fig. 3 is a top level optical schematic for reading a code in an optical identification element in accordance with the present invention.
  • Fig. 4 is
  • FIG. 7 is a perspective view of a grooved plate for use with an optical identification element, in accordance with the present invention.
  • FIG. 8 is a diagram of a microbead mapper reading, in accordance with the present invention.
  • Fig. 8a is a diagram of a system for both detecting a material on and reading a code in a microbead, in accordance with the present invention.
  • Fig. 9 is a diagram of a plate having microbeads thereon in relation to an open plate format for detection and reading of the microbead in accordance with the invention.
  • Fig. 10 is a diagram of a starting point for handling microbeads for readout in a cuvette process in accordance with the invention.
  • Fig. 10 is a diagram of a starting point for handling microbeads for readout in a cuvette process in accordance with the invention.
  • FIG. 11 is a diagram of a second step in the readout process in accordance with the invention.
  • Fig. 12 is a diagram of the readout step in accordance with the invention.
  • Fig. 13 is a diagram of final steps in the cuvette process in accordance with the invention.
  • Fig. 14 is a diagram of an example of the cuvette showing its mount on a kinematic plate in accordance with the invention.
  • Fig. 15 is a diagram of an alternative embodiment of a cuvette showing a port for fluid filling/emptying using a pipette in accordance with the invention.
  • Fig. 16 is a diagram of an alternative embodiment of a cuvette showing an alternative port for fluid filling/emptying using a pipette in accordance with the invention.
  • Fig. 16 is a diagram of an alternative embodiment of a cuvette showing an alternative port for fluid filling/emptying using a pipette in accordance with the invention.
  • FIG. 17 is a diagram of a two zone cuvette showing a free region and a trapped region in accordance with the invention.
  • Fig. 18(a) is a diagram of steps for a conventional flow cytometer reader in a single pass cytometer process in accordance with the invention.
  • Fig. 18(b) is a diagram of steps for a disk cytometer reader in a multipass cytometer process in accordance with the invention.
  • Figs. 19(a), (b) and (c) show embodiments of a disk cytometer in accordance with the invention.
  • Fig. 20(a) show an embodiment of a disk cytometer having radial channels for spin drying in accordance with the invention.
  • Fig. 20(a) show an embodiment of a disk cytometer having radial channels for spin drying in accordance with the invention.
  • FIG. 20(b) show an alternative embodiment of a disk cytometer having a mechanical iris for providing a variable aperture for bead access to grooves in accordance with the invention.
  • FIG. 21 show an embodiment of a SU8 groove plate having 450 in accordance with the invention.
  • Fig. 21 show an embodiment of a SU8 cylindrical grooved plate having 450 x 65 microns beads in accordance with the invention.
  • Fig. 22 show an embodiment of an alignment tube in accordance with the invention.
  • Fig. 23 show an alternative embodiment of an alignment tube having a receiving flange in accordance with the invention.
  • Fig. 24 is an optical schematic for reading a code in an optical identification element, in accordance with the present invention.
  • FIG. 25(a) is an image of a code on a CCD camera from an optical identification element, in accordance with the present invention.
  • Fig. 25(b) is a graph showing an digital representation of bits in a code in an optical identification element, in accordance with the present invention.
  • Fig. 26 illustrations (a)-(c) show images of digital codes on a CCD camera, in accordance with the present invention.
  • Fig. 27 illustrations (a)-(d) show graphs of different refractive index pitches and a summation graph, in accordance with the present invention.
  • Fig. 28 is an alternative optical schematic for reading a code in an optical identification element, in accordance with the present invention.
  • FIG. 29 29, illustrations (a)-(b), are graphs of reflection and transmission wavelength spectrum for an optical identification element, in accordance with the present invention.
  • Figs. 30-31 are side views of a thin grating for an optical identification element, in accordance with the present invention.
  • Fig. 32 is a perspective view showing azimuthal multiplexing of a thin grating for an optical identification element, in accordance with the present invention.
  • Fig. 33 is side view of a blazed grating for an optical identification element, in accordance with the present invention.
  • Fig. 34 is a graph of a plurality of states for each bit in a code for an optical identification element, in accordance with the present invention.
  • FIG. 35 is a side view of an optical identification element where light is incident on an end face, in accordance with the present invention.
  • Figs. 36-37 are side views of an optical identification element where light is incident on an end face, in accordance with the present invention.
  • Figs. 38, illustrations (a)-(c), are side views of an optical identification element having a blazed grating, in accordance with the present invention.
  • Fig. 39 is a side view of an optical identification element having a coating, in accordance with the present invention.
  • Fig. 40 is a side view of whole and partitioned optical identification element, in accordance with the present invention.
  • Fig. 41 is a side view of an optical identification element having a grating across an entire dimension, in accordance with the present invention.
  • FIG. 42 illustrations (a)-(c), are perspective views of alternative embodiments for an optical identification element, in accordance with the present invention.
  • FIG. 43 illustrations (a)-(b), are perspective views of an optical identification element having multiple grating locations, in accordance with the present invention.
  • Fig. 44 is a perspective view of an alternative embodiment for an optical identification element, in accordance with the present invention.
  • Fig. 45 is a view an optical identification element having a plurality of gratings located rotationally around the optical identification element, in accordance with the present invention.
  • Fig.46 illustrations (a)-(e), show various geometries of an optical identification element that may have holes therein, in accordance with the present invention.
  • FIG. 47 illustrations (a)-(c), show various geometries of an optical identification element that may have teeth thereon, in accordance with the present invention.
  • Fig. 48 illustrations (a)-(c), show various geometries of an optical identification element, in accordance with the present invention.
  • Fig. 49 is a side view an optical identification element having a reflective coating thereon, in accordance with the present invention.
  • Fig. 50 illustrations (a)-(b), are side views of an optical identification element polarized along an electric or magnetic field, in accordance with the present invention.
  • Figs. 51 and 52 are diagrams of beads read from flat retro-reflector trays, in accordance with the present invention.
  • Figs. 53 and 54 are diagrams of beads read through V-grooves, in accordance with the present invention.
  • FIG. 1 shows, by way of example, steps of a microbead assay platform process which uses the microbead technology of the present invention.
  • the steps of the assay process shown in Figure 1 include a first step in which the microbeads are used or hybridized in a solution; a second step in which the microbeads are aligned or self-assembled in a desired manner; a third step in which the code and florescence in and/or on the microbeads are readout in solution; and a fourth step in which the information related to the code and florescence is processed in relation to data management and bioinformatics.
  • the present invention primarily relates to step 2 wherein the microbeads are uniquely aligned so the longitudinal axis of the microbeads is positioned in a fixed orientation relative to the code and florescence reading device, as well as relating to a lesser extent to step 3. It is important to note that the scope of the present invention is not intended to be limited to any particular type or kind of assay process or other process in which the microbead technology is used. The scope of the invention is intended to include embodiments in which the microbead technology of the present invention is used in many different processes.
  • the Microbead Element 8 Fig. 2 shows a diffraction grating-based optical identification element 8 (or encoded element or coded element) that comprises a known optical substrate 10, having an optical diffraction grating 12 disposed (or written, impressed, embedded, imprinted, etched, grown, deposited or otherwise formed) in the volume of or on a surface of the substrate 10 along the length or longitudinal axis L of the element 8, which is otherwise known hereinafter as the microbead.
  • the grating 12 is a periodic or aperiodic variation in the effective refractive index and/or effective optical absorption of at least a portion of the substrate 10.
  • the optical identification element 8 described herein is the same as that described in copending Patent Application Serial No.
  • the grating shown and described herein is provided by way of example.
  • the scope of the invention is not intended to be limited to the type or kind of grating 12 in the substrate, the type or kind of variations forming the same, or the manner or technique for disposing the grating 12 into the substrate 10.
  • the scope of the invention is intended to include gratings and techniques for disposing the same both now known in the art, as well as those developed in the future.
  • the substrate 10 has an inner region 20 where the grating 12 is located.
  • the inner region 20 may be photosensitive to allow the writing or impressing of the grating 12.
  • the substrate 10 has an outer region 18, which does not have the grating 12 therein.
  • the grating 12 is a combination of one or more individual spatial periodic sinusoidal variations (or components) in the refractive index that are collocated at substantially the same location on the substrate 10 along the length of the grating region 20, each having a spatial period (or pitch) A.
  • the resultant combination of these individual pitches is the grating 12, comprising spatial periods ( ⁇ l- ⁇ n) each representing a bit in the code.
  • the grating 12 represents a unique optically readable code, made up of bits, where a bit corresponds to a unique pitch ⁇ within the grating 12.
  • the code is determined by which spatial periods ( ⁇ l- ⁇ n) exist (or do not exist) in a given composite grating 12.
  • the code or bits may also be determined by additional parameters (or additional degrees of multiplexing), and other numerical bases for the code may be used, as discussed herein and/or in the aforementioned patent application.
  • the scope of the invention is not intended to be limited to the type or kind of code represented by the grating 12, or the manner or technique for reading or interpreting the same.
  • the scope of the invention is intended to include the grating represent codes, and/or or the manner or technique for reading or interpreting the same, both now known in the art, as well as those developed in the future.
  • the grating 12 may also be referred to herein as a composite or collocated grating. Also, the grating 12 may be referred to as a "hologram", as the grating 12 transforms, translates, or filters an input optical signal to a predetermined desired optical output pattern or signal.
  • the substrate 10 has an outer diameter Dl and comprises silica glass (SiO ) having the appropriate chemical composition to allow the grating 12 to be disposed therein or thereon. Other materials for the optical substrate 10 may be used if desired.
  • the substrate 10 maybe made of any glass, e.g., silica, phosphate glass, borosilicate glass, or other glasses, or made of glass and plastic, or solely plastic.
  • the optical substrate 10 made of a glass material is desirable. If a flexible substrate is needed, plastic, rubber or polymer-based substrate may be used.
  • the optical substrate 10 may be any material capable of having the grating 12 disposed in the grating region 20 and that allows light to pass through it to allow the code to be optically read.
  • the optical substrate 10 with the grating 12 has a length L and an outer diameter Dl, and the inner region 20 diameter D.
  • the length L can range from very small "microbeads" (or microelements, micro-particles, or encoded particles), about 1-1000 microns or smaller, to larger "macro beads” or “macroelements” for larger applications (about 1.0 - 1000 mm or greater).
  • the outer dimension Dl can range from small (less than 1000 microns) to large (1.0 - 1000 mm and greater).
  • Other dimensions and lengths for the substrate 10 and the grating 12 may be used within the spirit of the invention described herein.
  • the grating 12 may have a length Lg of about the length L of the substrate 10. Alternatively, the length Lg of the grating 12 maybe shorter than the total length L of the substrate 10.
  • the outer region 18 is made of pure silica (SiO 2 ) and has a refractive index n2 of about 1.458 (at a wavelength of about 1553 nm), and the inner grating region 20 of the substrate 10 has dopants, such as germanium and/or boron, to provide a refractive index nl of about 1.453, which is less than that of outer region 18 by about 0.005.
  • dopants such as germanium and/or boron
  • the grating region 20 may have an index of refraction that is larger than that of the outer region 18 or grating region 20 may have the same index of refraction as the outer region 18 if desired.
  • Fig. 3 The Code Reader or Detector 29 Fig. 3 shows a configuration for reading or detecting the code in the microbead 8 using a code reader or other detector device 29, which is used in step 3 of the process shown in Figure 1.
  • an incident light 24 of a wavelength ⁇ e.g., 532 nm from a known frequency doubled Nd: YAG laser or 632 nm from a known Helium-Neon laser, is incident on the grating 12 in the substrate 10.
  • Any other input wavelength ⁇ can be used if desired provided ⁇ is within the optical transmission range of the substrate (discussed more herein and/or in the aforementioned patent application).
  • a portion of the input light 24 passes straight through the grating 12, as indicated by an arrow 25.
  • the output light 27 may be a plurality of beams, each having the same wavelength ⁇ as the input wavelength ⁇ and each having a different output angle indicative of the pitches ( ⁇ l- ⁇ n) existing in the grating 12.
  • the input light 24 may be a plurality of wavelengths and the output light 27 may have a plurality of wavelengths indicative of the pitches ( ⁇ l- ⁇ n) existing in the grating 12.
  • the output light may be a combination of wavelengths and output angles.
  • the code reader or detector 29 has the necessary optics, electronics, software and or firmware to perform the functions described herein.
  • the detector reads the optical signal 27 diffracted or reflected from the grating 12 and determines the code based on the pitches present or the optical pattern, as discussed more herein or in the aforementioned patent application.
  • An output signal indicative of the code is provided on a line 31.
  • the Grooved Tray or Plate Fig. 4 shows one embodiment of a positioning device 200 for aligning the microbeads 8 so the longitudinal axis of the microbeads is in a fixed orientation relative to the code reading or other detection device.
  • the positioning device 200 is shown in the form of a tray or plate 200 having V-grooves 205 for aligning the microbeads 8 and is used in step 2 of the process shown in Figure 1.
  • the microbead elements 8 are placed in the tray 200 with V-grooves 205 to allow the elements 8 to be aligned in a predetermined direction for illumination and reading/detection as discussed herein.
  • the grooves 205 may have holes 210 that provide suction to keep the elements 8 in position.
  • the grooves in the groove plate 200 may be made in many different ways, including being formed by SU8 photoresistant material, mechanically machining; deep reactive ion etching; or injection molding.
  • One advantage of the injection molding approach is that the plate can be manufactured in volume at relatively low cost, and disposed of after the information about the beads is gathered in the assay process.
  • the groove plate may be made of glass, including fused silica, low fluorescence glass, borosilicate glass. Silicon is used because it is reflective so a reflective coating is typically not needed. Alternative, a mirror coating can be applied to the plate material to achieve the desired reflectivity.
  • the scope of the invention is not intended to be limited the manner or technique for forming the grooves in the groove plate, and is intended to include manners and techniques both now known or later developed in the future.
  • Fig. 5 Flat Grooves
  • the scope of the invention is not intended to be limited to any particular groove shape.
  • Fig. 5 shows a diagram a plate 300 having flat grooves 302 instead of V- grooves as shown in Fig. 3.
  • Some characteristics of the groove according to the present invention are as follows: •
  • the groove width (w) should be at least as wide as the diameter of the bead (D) but not larger than D + 15 ⁇ m.
  • the thickness of the depth of the groove (T) should be at least 0.5 times the diameter of the bead so that it sufficiently traps a bead once it falls into the groove even when it is subjected to mechanical agitation.
  • the depth should not exceed 1.5 times the diameter of the bead so as to prevent more than one bead from falling into the same groove location.
  • Groove plates have been made using a thick photoresist called SU8 and is available from Microchem.
  • the resist is both chemically inert and mechanically robust once fully cured.
  • the groove walls are formed by the resist material, which is deposited onto a glass or substrate. Advantages of this process include the ability to tailor the depth of groove by controlling the thickness of the resist material, and virtually every other geometric attribute through the design of the photo mask. Because it is photolithographic process, essentially any shape profile can be made. For example grooves can be made in simple rows, concentric circles, or spirals. Other features such as discrete wells, spots and cross hatches can be made as fiducial marks for tracking and positional registration purposes. The scope of the invention is also intended to include the grooves having a flat bottom as shown in Figure 5 with outwardly tapered walls.
  • Fig 6 The Holey Plate 674 Fig. 6 shows an alternative embodiment, wherein alignment may be achieved by using a plate 674 having holes 676 slightly larger than the elements 8 if the light 24 (Figs. 2 and 4) is incident along the grating axis 207.
  • the incident light indicated as 670 is reflected off the grating and exits through the end as a light 672 and the remaining light passes through the grating and the plate 674 as a line 678.
  • incident light 670 may be reflected out the side of the plate (or any other desired angle), as indicated by a line 680.
  • input light maybe incident from the side of the plate 674 and reflected out the top of the plate 474 as indicated by a line 684.
  • the light 672 may be a plurality of separate light beams or a single light beam that illuminates the entire tray 674 if desired.
  • FIG. 7 shows an alternative embodiment, wherein the V-groove plate discussed hereinbefore with Fig. 4 may be used for the end illumination/readout condition, hi this case, the grating 12 may have a blaze angle such that light incident along the axial grating axis will be reflected upward, downward, or at a predetermined angle for code detection. Similarly, the input light may be incident on the grating in a downward, upward, or at a predetermined angle and the grating 12 may reflect light along the axial grating axis for code detection.
  • Fig. 8 Microbead Mapper Readings
  • Fig. 8 shows microbeads 8 arranged on a plate 200 having grooves 205.
  • the microbeads 8 have three different codes (e.g. "41101", “20502", “41125”) using 16-bit, binary symbology, which may be read or detected using the reader or detector configuration described in relation to Fig. 3.
  • the codes in the beads are used to provide a cross reference to determine which probe is attached to which bead, thus allowing the researcher to correlate the chemical content on each bead with the measured fluorescence signal in Step 3 of the process shown in Figure 1.
  • Fig. 8 shows microbead Mapper Readings 8 arranged on a plate 200 having grooves 205.
  • the microbeads 8 have three different codes (e.g. "41101", “20502”, “41125”) using 16-bit, binary symbology, which may be read or detected using the reader or detector configuration described in relation to Fig. 3.
  • FIG. 8a shows a code reader 820 and a detector 808 that form part of a device generally indicated as 824 for obtaining information from the microbead 8 in Figure 8.
  • the codes in the microbeads 8 are detected when illuminated by incident light 24 from code excit 801 which produces a diffracted or output light signal 27 to a code reader 820, which includes the optics and electronics necessary to read the codes in each bead 8, as described herein and/or in the aforementioned copending patent application.
  • the code reader 820 provides a signal on a line 822 indicative of the code in each of the bead 8.
  • the incident light 24 may be directed transversely from the side of the grooved plate 200 (or from an end or any other angle) with a narrow band (single wavelength) and/or multiple wavelength source, in which case the code is represented by a spatial distribution of light and/or a wavelength spectrum, respectively, as described hereinafter and in the aforementioned copending patent application.
  • a narrow band single wavelength
  • multiple wavelength source in which case the code is represented by a spatial distribution of light and/or a wavelength spectrum, respectively, as described hereinafter and in the aforementioned copending patent application.
  • Other illumination, readout techniques, types of gratings, geometries, materials, etc. maybe used for the microbeads 8, as discussed hereinafter and in the aforementioned patent application.
  • an optical excitation signal 800 from excit source 803 is incident on the microbeads 8 on the grooved plate 200 and a fluorescent optical output signal 802 emanates from the beads 8 that have the fluorescent molecule attached.
  • the fluorescent optical output signal 802 passes through a lens 804, which provides focused light 806 to a known optical fluorescence detector 808.
  • other imaging optics may be used to provide the desired characteristics of the optical image/signal onto the fluorescence detector 808.
  • the detector 808 provides an output signal on a line 810 indicative of the amount of fluorescence on a given bead 8, which can then be interpreted to determine what type of chemical is attached to the bead 8.
  • the grooved plate 200 may be made of glass or plastic or any material that is transparent to the code reading incident beam 24 and code reading output light beams 27 as well as the fluorescent excitation beam 800 and the output fluorescent optical signal 802, and is properly suited for the desired application or experiment, e.g., temperature range, harsh chemicals, or other application specific requirements.
  • the code signal 822 from the bead code reader 820 and the fluorescent signal 810 from the fluorescence detector 808 are provided to a known computer 812.
  • the computer 812 reads the code associated with each bead and determines the chemical probe that was attached thereto from a predetermined table that correlates a predetermined relationship between the bead code and the attached probed, i addition, the computer 812 reads the fluorescence associated with each bead and determines the sample or analyte that is attached to the bead from a predetermined table that correlates a predetermined relationship between the fluorescence tag and the analyte attached thereto.
  • the computer 812 determines information about the analyte and/or the probe as well as about the bonding of the analyte to the probe, and provides such information on a display, printout, storage medium or other interface to an operator, scientist or database for review and/or analysis, consistent with shown in step 4 of Figure 1.
  • the sources 801, 803, the code reader 820, the fluorescence ⁇ y optics 804 and detector 808 and the computer 812 may all be part of one device known as an assay stick reader, which in that case would be generally indicated as 824.
  • the device 824 may have only one source beam which provides both the reflected optical signal 27 for determining the code and the fluorescence signal 802 for reading the tagged analyte attached to the beads 8.
  • the input optical signal has a common wavelength that performs both functions simultaneously, or sequentially, if desired.
  • the microbeads 8 may be coated with the desired probe compound, chemical, or molecule prior to being placed in the grooved plate 200. Alternatively, the beads 8 may be coated with the probe after being placed in the grooved plate 200.
  • the probe material may be an Oligo, cDNA, polymer, or any other desired probe compound, chemical, cell, or molecule for performing an assay.
  • the scope of the invention is not intended to be limited to using or detecting fluorescent molecule markers during the assay process.
  • embodiments of the invention are envisioned using and detection other types of molecular markers in other types ofprocesses.
  • Fig. 9 Open Format Approach
  • Fig. 9 shows the first, or open plate format, meaning there is no top to cover the microbeads 8 and the V-grooves 205.
  • the microbeads 8 are dispensed onto the plate 200 using, for example, a pipette tip or syringe tip, although the scope of the invention is not intended to be limited to the manner of depositing the microbeads on the plate.
  • the microbeads 8 may be then agitated by a sonic transducer (not shown), or manipulated with a mechanical wiper (not shown) or some form of spray nozzle (not shown) to encourage all the microbeads 8 to line up in the grooves 205.
  • microbead 8a, 8b there are always some microbeads, such as microbead 8a, 8b, as shown, that do not fall naturally into the grooves, and these must either be removed from the plate 200 or forced to fall into a groove 205.
  • the open format approach has the advantages that it consists of just the plate 200 having grooves 2005 and no other complicated features such as walls and a top, and possibly other chambers or channels to allow fluid flow and bubble removal. It also has the advantage that it can easily be made with a standard microscope slide, which is designed to fit all conventional microarray readers. However, the open format approach would most likely require the microbeads to be dried out prior to reading to prevent non-uniform and unpredictable optical aberrations caused by the uneven evaporation of the buffer solution.
  • Figs. 10-17 show the second mode which is called a closed format, that consists of not only of a groove plate but also a top and at least three walls to hold the solution and the microbeads in a cuvette-like device generally indicated as 500 as shown, for example, in Fig. 10.
  • the closed format approach provides a method for effectively distributing and aligning microbeads during the readout process, as described below:
  • the basic process for handling microbeads with a cuvette for readout consists of the following steps: (1) Fig. 10 shows a starting point for handling microbeads for a readout.
  • the microbeads 8 start in a bead test tube 502.
  • Typical test-tube volumes are typically 1.5 ml, although the scope of the invention is not intended to be limited to any particular volume.
  • the microbeads 8 will generally be in a liquid (usually water with a small amount of other buffer chemicals to adjust pH and possibly a small amount [ ⁇ 0.01%] of detergent.)
  • the bead test tube 502 contains the microbeads 8 in a solution generally indicated as 507, which forms part of step 1 of the process shown in Fig. 1.
  • Fig. 11 shows the bead tube 502 is coupled to a flange 504 of the cuvette 500, and the cuvette 500 is inverted so the beads flow onto the groove plate 503.
  • the cuvette 500 consists of two round flanges that accept test-tubes 502, 506, a transparent window 501, and an opposing groove plate 503.
  • Figure 14 shows a drawing of a prototype cuvette.
  • the groove plate outer dimensions can be any size, but typical microscope slide dimensions are convenient (e.g. 1" x 3").
  • the grooves are mechanically or laser cut lengthwise, and have dimensions that are chosen for the exact size of cylindrical microbead. For instance, for a 125 ⁇ m diameter bead, grooves of approximately 150 ⁇ m wide by 150 ⁇ m deep are used.
  • One tube 502 carries the microbeads 8 and a small amount of the carrier fluid or solution 507.
  • the second tube 506 may be larger and hold more of the fluid.
  • the purpose of the second tube 506 is to guarantee a certain fluid level in the next step.
  • Fig. 12 shows the readout step, in which, after the beads 8 are all (or nearly all) aligned in the groove plate 503 , the entire plate is moved (or alternatively the readout laser beam may be scanned, or some combination thereof) in order to read the codes of each bead, which forms part of step 3 of the process shown in Fig. 1.
  • Fig. 13 shows a final step, in which after the readout process the cuvette 500 is inverted to its original position and the beads 8 flow back into the original tube 502, which forms part of step 3 of the process shown in Fig. 1.
  • Fig. 14 shows an example of a cuvette generally indicated as 700 that is mounted on a kinematic base plate 710.
  • the cuvette 700 has a tube 702 for holding the solution with the beads and a top window 704 that is a 1 mm thick glass plate having dimensions of about 1" by 3".
  • the cuvette also has a bottom plate that is a transparent groove plate.
  • the location pins 712 and lever arm 714 hold the cuvette 700 in place on the kinematic plate 710.
  • Another advantage involves the potential to prevent microbeads from ever stacking up on top of each other, by limiting the space between the bottom and the top plate to be less than twice the diameter of the microbeads. Another advantage is that the cover keeps the fluid from evaporating.
  • Figs. 15-16 show alternative embodiments of the cuvette 500 shown in Figs. 10-14.
  • the microbeads 8 are injected from a hyperdermic needle 2001 into a cuvette 2000, 2000' by placing them near the edge of an opening 2002, 2002' and allowing the surface tension, or an induced fluid flow, to pull the microbeads into the cuvette 2000, 2000', where, because of the limited height between the floor and the ceiling of the cuvette 2000, 2000', they are confined to move around in a plane, albeit with all the rotational degrees of freedom unconstrained.
  • the microbeads 8 are quickly and sufficiently constrained by the grooves as the microbeads 8 fall into them.
  • the cuvette 2000' has a port 2003' for topping off the fluid level.
  • Fig. 17 Two Region Approach Fig. 17 shows an alternative embodiment of the closed approach, which involves sectioning the closed region into two regions, one region 2010 where the microbeads are free to move about in a plane, either in a groove or not, and a second region 2012 where the microbeads are trapped in one or more grooves 2014 and can only move along the axes indicated by arrow G of a groove 2014. Trapping the microbeads 8 in a groove 2014 is accomplished by further reducing the height of the interior chamber to the extent that the microbeads 8 can no longer hop out of a groove 2014.
  • the free region 2010 is used to pre-align the microbeads 8 into a groove, facilitating the introduction of
  • microbeads 8 into the trapped section 2012.
  • gravity can be used to pull the microbeads 8 along a groove 2014 from the free region 2010 to the trapped region 2012.
  • the microbeads 8 move to an end 2016 of the groove 2014 where they stop.
  • Subsequent microbeads 8 will begin to stack up until the groove is completely full of microbeads 8, which are stacked head to tail.
  • This has the advantage of packing a large number of microbeads into a small area and prevents the microbeads 8 from ever jumping out of the grooves.
  • This approach could also be used to align the microbeads 8 prior to injection into some form of flow cytometer, or a dispensing apparatus.
  • Figs. 18-23 The Cytometer Figs. 18-23 show methods and apparatuses related to using a cytometer.
  • Fig. 18(a) shows steps for a method related to a conventional (single pass) flow cytometer reader
  • Fig. 18(b) shows a method related to a disk cytometer reader (multipass).
  • the method generally indicated as 900 has a step 901 for providing beads and a solution similar to step 1 in Fig. 1; and a step 902 for reading information from the beads similar to steps 2 and 3 in Fig. 1.
  • the method generally indicated as 1000 has a step 1001 for providing beads and solution similar to step 1 in Fig.
  • a rotating disk 1003 (see Figs. 19(a), (b) and (c) and 20) is used for aligning the microbeads consistent with step 2 of the process shown in Fig. 1.
  • Fig. 19(a) shows an embodiment of a cytometer bead reader having a rotating disk generally indicated as 1250, having a disk platform 1252 with circumferential, concentric, grooves 1254 for aligning microbeads 8.
  • the rotating disk 1250 has various sectors for processing the microbeads, including a bead loading zone 1256, a bead removal zone 1258 and a readout zone 1260.
  • Fig. 19(b) shows an alternative embodiment of a rotating disk generally indicated as 1200, having a disk platform 1202 with planar groove plates 1204a, b, c, d, e, f that are shown with grooves oriented in any one or more different ways.
  • One or more of the planar groove plates 1204a, b, c, d, e, f may have an optional channel (See Fig. 20(a)) for fluid runoff, as shown, and a barrier for preventing the microbeads from flying off the plate.
  • FIG. 19(c) shows an alternative embodiment of a rotating disk generally indicated as 1280, having a disk platform 1282 with radial grooves 1284a, 1284b.
  • the disk platform 1282 has a bead loading zone 1286 in the center of the disk.
  • One advantage of this embodiment is that the opening of the bead loading zone 1286 will also serve to allow the release of air bubbles that will naturally collect in the center of the disk due the reduced density of the fluid, which results from the centrifugal force pushing the fluid radially outwardly.
  • the rotating disk 1280 has tight bead packing due to the centrifugal forces due to the spinning action of the disk.
  • the rotating disk 1280 has a wedge shape spacer 1288 that keeps the channel at a constant gap width and a wall 1290.
  • Fig. 20(a) shows an alternative embodiment of a rotating disk generally indicated as 1300 having narrow radial channels 1302 for spin drying so liquid is forced out of the circumferential grooves through the radial channels.
  • the plate 1300 may have a mechanical catcher 1320 coupled thereto for moving radially outwardly in direction 1320a if desired, for recirculating loose beads.
  • Fig. 20(b) show an alternative embodiment of a disk cytometer 1400 having a mechanical iris 1402 for providing a variable aperture for bead access to grooves in accordance with the invention.
  • Fig. 21 shows a rotating groove plate 1404 having 450 by 65 microns beads 8 arranged in the rotating SU8 circumferential channels 1406, each channel having corresponding channel walls 1408, 1410.
  • Continuous Mode - Process steps Consistent with that shown and described above, the following are the processing steps for a continuous mode of operation: 1. Dispense batch of microbeads onto plate. 2. Spin slowly while agitating the plate theta x and y to get microbeads into grooves. The agitation can be performed using rocking, ultrasound, airflow, etc. 3. Once a sufficient number of microbeads are in grooves, spin up plate or disk to remove excess microbeads (microbeads that did not go into a groove). 4. Spin plate or disk to read code and fluorescence off microbeads. 5.
  • microbeads To remove microbeads, purge with high velocity aqueous solution (enough to knock microbeads out of groove) and vacuum up, or spin microbeads off plate while they are not in a groove. 6. Inspect disk (probably with code camera) to verify that all microbeads have been removed. 7. Inject next batch of microbeads.
  • Figs. 22-23 The Alignment Tube 502
  • the microbeads 8 may be aligned in a tube 5020 that has a diameter that is only slightly larger than the substrate 10, e.g., about 1-50 microns, and that is substantially transparent to the incident light 24. hi that case, the incident light 24 may pass through the tube 5020 as indicated by the light 5000 or be reflected back due to a reflective coating on the tube 5020 or the substrate as shown by return light 504. Other techniques can be used for alignment if desired.
  • Fig. 23 shows the tube 5020 has an opening flange 5120 for receiving the microbeads 8.
  • Fig. 23 also shows an excitation laser 550, a diode laser 552 and a CCD camera 554 for gathering information from the bead 8 consistent with that discussed above.
  • Figs. 24-44 Reading The Microbead Code Figs. 24-44 show, byway of example, a method and apparatus for reading the code in the microbead 8. The scope of the invention is not intended to be limited in any way to manner in which the code is read, or the method of doing the same.
  • the reflected light 27 comprises a plurality of beams 26-36 that pass through a lens 37, which provides focused light beams 46-56, respectively, which are imaged onto a CCD camera 60.
  • the lens 37 and the camera 60, and any other necessary electronics or optics for performing the functions described herein, make up the reader or detector 29.
  • the image on the CCD camera 60 is a series of illuminated stripes generally indicated by reference label 120 indicating ones and zeros of a digital pattern or code of the grating 12 in the microbead 8. The ones are indicated by reference labels 122, 124, ..., 132.
  • reference labels 122, 124, ..., 132 are indicated by reference labels 122, 124, ..., 132.
  • lines generally indicated by reference label 68 on a graph generally indicated by 70 are indicative of a digitized version of the image shown in Fig. 25(a) as indicated in spatial periods ( ⁇ l- ⁇ n), which corresponds to the ones 122, 124, ..., 132 shown in Figure 25(a).
  • each of the individual spatial periods ( ⁇ l- ⁇ n) in the grating 12 is slightly different, thus producing an array of N unique diffraction conditions (or diffraction angles) discussed more hereinafter.
  • Eq. 1 is diffraction (or reflection or scatter) relationship between input wavelength ⁇ , input incident angle ⁇ i, output incident angle ⁇ o, and the spatial period ⁇ of the grating 12.
  • m is the "order" of the reflection being observed
  • n is the refractive index of the substrate 10.
  • Eq. 1 applies to light incident on outer surfaces of the substrate 10 which are parallel to the longitudinal axis of the grating (or the k B vector). Because the angles ⁇ i, ⁇ o are defined outside the substrate 10 and because the effective refractive index of the substrate 10 is substantially a common value, the value of n in Eq.
  • the output angle of reflection ⁇ o 37 degrees.
  • the output light 27 should fall within an acceptable portion of the Bragg envelope (or normalized reflection efficiency envelope) curve 200, as indicated by points 204,206 in Fig. 24, also defined as a Bragg envelope angle ⁇ B, as also discussed herein and/or in the aforementioned patent application.
  • the curve 200 maybe defined as:
  • the angle ⁇ i of the input light 24 should be set so that the angle ⁇ o of the reflected output light equals the input angle ⁇ i.
  • the thickness or diameter D (Fig. 2) of the grating 12 decreases, the width of the sin(x)/x function (and thus the width of the Bragg envelope) increases and, the coefficient to or amplitude of the sine 2 (or (sin(x)/x) 2 function (and thus the efficiency level across the Bragg envelope) also increases, and vice versa.
  • the wavelength ⁇ increases, the half-width of the Bragg envelope as well as the efficiency level across the Bragg envelope both decrease.
  • ⁇ n should be made as large as possible to maximize the brightness, which allows D to be made smaller.
  • is a reflection efficiency factor which is the value for x in the sinc 2 (x) function and where the value of sinc 2 (x) has decreased to a predetermined value from the maximum amplitude as indicated by points 204,206 on the curve 200 in Fig. 24.
  • the inventors have found th t the reflection efficiency is acceptable when ⁇ ⁇ I.39.
  • This value for ⁇ corresponds to when the amplitude of the reflected beam (i.e., from the 9 sine (x) function of Eqs. 3 & 4) has decayed to about 50% of its peak value.
  • sinc 2 ( ⁇ ) 0.5.
  • the digital code may be generated by selectively creating individual index variations (or individual gratings) with the desired spatial periods ⁇ l- ⁇ n.
  • Other illumination, readout techniques, types of gratings, geometries, materials, etc. may be used as discussed in the aforementioned patent application. Referring to Fig.
  • the length of the substrate 10 was 450 microns, the outer diameter Dl was 65 microns, the inner diameter D was 14 microns, ⁇ n for the grating 12 was about 10 " , nl in portion 20 was about 1.458 (at a wavelength of about 1550 nm), n2 in portion 18 was about 1.453, the average pitch spacing ⁇ for the grating 12 was about 0.542 microns, and the spacing between pitches ⁇ was about 0.36 % of the adjacent pitches ⁇ . Referring to Fig.
  • the pitch ⁇ of an individual grating is the axial spatial period of the sinusoidal variation in the refractive index nl in the region 20 of the substrate 10 along the axial length of the grating 12 as indicated by a curve 90 on a graph 91.
  • a sample composite grating 12 comprises three individual gratings that are co-located on the substrate 10, each individual grating having slightly different pitches, ⁇ l, ⁇ 2, ⁇ 3, respectively, and the difference (or spacing) ⁇ between each pitch ⁇ being about 3.0 % of the period of an adjacent pitch ⁇ as indicated by a series of curves 92 on a graph 94. Referring to Fig.
  • FIG. 27 illustration (c), three individual gratings, each having slightly different pitches, ⁇ l, ⁇ 2, ⁇ 3, respectively, are shown, the difference ⁇ between each pitch ⁇ being about 0.3% of the pitch ⁇ of the adjacent pitch as shown by a series of curves 95 on a graph 97.
  • the individual gratings in Fig. 27, illustrations (b) and (c) are shown to all start at 0 for illustration purposes; however, it should be understood that the separate gratings need not all start in phase with each other. Referring to Fig.
  • the overlapping of the individual sinusoidal refractive index variation pitches ⁇ l- ⁇ n in the grating region 20 of the substrate 10 produces a combined resultant refractive index variation in the composite grating 12 shown as a curve 96 on a graph 98 representing the combination of the three pitches shown in Fig. 27, illustration (b).
  • the resultant refractive index variation in the grating region 20 of the substrate 10 may not be sinusoidal and is a combination of the individual pitches ⁇ (or index variation).
  • the maximum number of resolvable bits N which is equal to the number of different grating pitches ⁇ (and hence the number of codes), that can be accurately read (or resolved) using side-illumination and side-reading of the grating 12 in the substrate 10, is determined by numerous factors, including: the beam width w incident on the substrate (and the corresponding substrate length L and grating length Lg), the thickness or diameter D of the grating 12, the wavelength ⁇ of incident light, the beam divergence angle ⁇ Rj and the width of the Bragg envelope ⁇ B (discussed more in the aforementioned patent application), and may be determined by the equation: ⁇ E N ⁇ ⁇ q. 6 2E» sin( ⁇ ,.)
  • the bits may be read/detected by providing a plurality of wavelengths and reading the wavelength spectrum of the reflected output light signal.
  • each bit (or ⁇ ) is defined by whether its corresponding wavelength falls within the Bragg envelope, not by its angular position Within the Bragg envelope 200.
  • the reflection wavelength spectrum ( ⁇ l- ⁇ n) of the reflected output beam 310 will exhibit a series of reflection peaks 695, each appearing at the same output Bragg angle ⁇ o.
  • Each wavelength peak 695 ( ⁇ l- ⁇ n) corresponds to an associated spatial period ( ⁇ l- ⁇ n), which make up the grating 12.
  • One way to measure the bits in wavelength space is to have the input light angle ⁇ i equal to the output light angle ⁇ o, which is kept at a constant value, and to provide an input wavelength ⁇ that satisfies the diffraction condition (Eq. 1) for each grating pitch ⁇ . This will maximize the optical power of the output signal for each pitch ⁇ detected in the grating 12.
  • the transmission wavelength spectrum of the transmitted output beam 330 (which is transmitted straight through the grating 12) will exhibit a series of notches (or dark spots) 696.
  • the transmitted light 330 may be detected at the detector/reader 308 (Fig. 28).
  • the optical signal levels for the reflection peaks 695 and transmission notches 696 will depend on the "strength" of the grating 12, i.e., the magnitude of the index variation n in the grating 12.
  • the bits may be detected by continuously scanning the input wavelength.
  • a known optical source 300 provides the input light signal 24 of a coherent scanned wavelength input light shown as a graph 304.
  • the source 300 provides a sync signal on a line 306 to a known reader 308.
  • the sync signal may be a timed pulse or a voltage ramped signal, which is indicative of the wavelength being provided as the input light 24 to the substrate 10 at any given time.
  • the reader 308 may be a photodiode, CCD camera, or other optical detection device that detects when an optical signal is present and provides an output signal on a line 309 indicative of the code in the substrate 10 or of the wavelengths present in the output light, which is directly related to the code, as discussed herein.
  • the grating 12 reflects the input light 24 and provides an output light signal 310 to the reader 308.
  • the wavelength of the input signal is set such that the reflected output light 310 will be substantially in the center 314 of the Bragg envelope 200 for the individual grating pitch (or bit) being read.
  • the source 300 may provide a continuous broadband wavelength input signal such as that shown as a graph 316.
  • the reflected output beam 310 signal is provided to a narrow band scanning filter 318 which scans across the desired range of wavelengths and provides a filtered output optical signal 320 through a lens 321 to the reader 308.
  • the scanning filter 318 provides a sync signal on a line 322 to the reader, which is indicative of which wavelengths are being provided on the output signal 320 to the reader and may be similar to the sync signal discussed hereinbefore on the line 306 from the source 300. In this case, the source 300 does not need to provide a sync signal because the input optical signal 24 is continuous.
  • the scanning filter may be located in the path of the input beam 24 as indicated by the dashed box 324, which provides the sync signal on a line 323.
  • the reader 308 maybe a known optical spectrometer (such as a known spectrum analyzer), capable of measuring the wavelength of the output light.
  • each readout wavelength is associated with a predetermined number of bits within the Bragg envelope. Bits (or grating pitches ⁇ ) written for different wavelengths do not show up unless the correct wavelength is used. Accordingly, the scope of the invention is intended to include the bits (or grating pitches ⁇ ) being read using one wavelength and many angles, many wavelengths and one angle, many wavelengths and many angles, or some combination thereof, as well as other techniques now known or later developed in the future, hi other words, the scope of the invention is not intended to be limited to the number of wavelengths or angles used to read the bits of the code. Referring to Fig.
  • the grating 12 may have a thickness or depth D which is comparable or smaller than the incident beam wavelength ⁇ .
  • This is known as a "thin" diffraction grating (or the full angle Bragg envelope is 180 degrees).
  • the half- angle Bragg envelope ⁇ B is substantially 90 degrees; however, ⁇ n must be made large enough to provide sufficient reflection efficiency, per Eqs. 3 and 4.
  • D* ⁇ n ⁇ /2 which corresponds to a ⁇ phase shift between adjacent minimum and maximum refractive index values of the grating 12.
  • the phase shift between adjacent minimum and maximum refractive index values of the grating 12 should approach a ⁇ phase shift; however, other phase shifts may be used.
  • the grating 12 is illuminated with the input light 24 oriented on a line 705 orthogonal to the longitudinal grating vector 705.
  • the input beam 24 will split into two (or more) beams of equal amplitude, where the exit angle ⁇ 0 can be determined from Eq. 1 with the input angle (normal to the longitudinal axis of the grating 12).
  • the +/-l st order beams corresponds to output beams 700,702, respectively;
  • the +/-2 n order beams corresponds to output beams 704,706, respectively;
  • the output beams 700-708 project spectral spots or peaks 710-718, respectively, along a common plane, shown from the side by a line 709, which is parallel to the upper surface of the substrate 10.
  • each different pitch corresponds to a different elevation or output angle which corresponds to a predetermined set of spectral peaks.
  • the presence or absence of a particular peak or set of spectral peaks defines the code.
  • the angle of the grating 12 is not properly aligned with respect to the mechanical longitudinal axis of the substrate 10, the readout angles may no longer be symmetric, leading to possible difficulties in readout.
  • the angular sensitivity to the alignment of the longitudinal axis of the substrate 10 to the input angle ⁇ i of incident radiation is reduced or eliminated, h particular, the input light can be oriented along substantially any angle ⁇ i with respect to the grating 12 without causing output signal degradation, due the large Bragg angle envelope.
  • the grating 12 can be oriented at any rotational (or azimuthal) angle without causing output signal degradation.
  • changing the incident angle ⁇ i will affect the output angle ⁇ o of the reflected light in a predetermined predictable way, thereby allowing for accurate output code signal detection or compensation.
  • the bits can also be multiplexed in an azimuthal (or rotational) angle ⁇ a of the substrate.
  • a plurality of gratings 750,752,754,756 each having the same pitch ⁇ are disposed in a surface 7011 of the substrate 10 and located in the plane of the subsfrate surface 7011.
  • the input light 24 is incident on all the gratings 750,752,754,756 simultaneously.
  • Each of the gratings provides output beams oriented based on the grating orientation.
  • the grating 750 provides the output beams 762,764
  • the grating 752 provides the output beams 766,768
  • the grating 754 provides the output beams 770,772
  • the grating 756 provides the output beams 774,776.
  • Each of the output beams provides spectral peaks or spots (similar to that discussed hereinbefore), which are located in a plane 760 that is parallel to the substrate surface plane 7011.
  • a single grating pitch ⁇ can produce many bits depending on the number of gratings that can be placed at different azimuthal (rotational) angles on the surface of the substrate 10 and the number of output beam spectral peaks that can be spatially and optically resolved/detected.
  • the number of bits can be multiplexed based on the number of grating pitches A and/or geometrically by the orientation of the grating pitches.
  • the edges of the substrate 10 no longer scatter light from the incident angle into the "code angular space", as discussed herein and/or in the aforementioned patent application.
  • a continuous broadband wavelength source may be used as the optical source if desired.
  • the pitches may be created at an angle ⁇ g (also known as a blaze angle). In that case, the input light 24 incident normal to the surface 792 will produce a reflected output beam 790 having an angle ⁇ o determined by Eq. 1 as adjusted for the blaze angle ⁇ g.
  • an additional level of multiplexing may be provided by having an optical code using other numerical bases, if intensity levels of each bit are used to indicate code information. This could be achieved by having a corresponding magnitude (or strength) of the refractive index change ( ⁇ n) for each grating pitch ⁇ .
  • intensity ranges are shown for each bit number or pitch ⁇ , providing for a Base-4 code (where each bit corresponds to 0,1,2, or 3). The lowest intensity level, corresponding to a 0, would exist when this pitch ⁇ is not present in the grating 12.
  • the next intensity level 450 would occur when a first low level ⁇ nl exists in the grating that provides an output signal within the intensity range corresponding to a 1.
  • the next intensity level 452 would occur when a second higher level ⁇ n2 exists in the grating 12 that provides an output signal within the intensity range corresponding to a 2.
  • the next intensity level 454, would occur when a third higher level ⁇ n3 exists in the grating 12 that provides an output signal within the intensity range corresponding to a 3.
  • the input light 24 may be incident on the substrate 10 on an end face 600 of the substrate 10.
  • the input light 24 will be incident on the grating 12 having a more significant component of the light (as compared to side illumination discussed hereinbefore) along the longitudinal grating axis 207 of the grating (along the grating vector k ⁇ ), as shown by a line 602.
  • the light 602 reflects off the grating 12 as indicated by a line 604 and exits the substrate as output light 608. Accordingly, it should be understood by one skilled in the art that the diffraction equations discussed hereinbefore regarding output diffraction angle ⁇ o also apply in this case except that the reference axis would now be the grating axis 207.
  • the input and output light angles ⁇ i, ⁇ o would be measured from the grating axis 207 and length Lg of the grating 12 would become the thickness or depth D of the grating 12.
  • a grating 12 that is 400 microns long would result in the Bragg envelope 200 being narrow. It should be understood that because the values of nl and n2 are close to the same value, the slight angle changes of the light between the regions 18,20 are not shown herein.
  • n ⁇ s the effective index of refraction of the substrate
  • is the input (and output wavelength)
  • is the pitch.
  • the code information is readable only in the spectral wavelength of the reflected beam, similar to that discussed hereinbefore for wavelength based code reading.
  • the input signal in this case may be a scanned wavelength source or a broadband wavelength source.
  • the code information may be obtained in reflection from the reflected beam 614 or in transmission by the transmitted beam 616 that passes through the grating 12.
  • n in sin ⁇ in n out sin ⁇ out Eq. 9
  • n m is the refractive index of the first (input) medium
  • n ou t is the refractive index of the second (output) medium
  • ⁇ in and ⁇ out are measured from a line 620 normal to the incident surface 600.
  • the grating region 20 of the substrate 10 will act as a known optical waveguide for certain wavelengths.
  • the grating region 20 acts as a "core” along which light is guided and the outer region 18 acts as a "cladding” which helps confine or guide the light.
  • such a waveguide will have a known "numerical aperture" ( ⁇ na) that will allow light 630 that is within the aperture ⁇ na to be directed or guided along the grating axis 207 and reflected axially off the grating 12 and returned and guided along the waveguide, h that case, the grating 12 will reflect light 632 having the appropriate wavelengths equal to the pitches ⁇ present in the grating 12 back along the region 20 (or core) of the waveguide, and pass the remaining wavelengths of light as the light 632'.
  • ⁇ na the grating region 20 act as an optical waveguide for wavelengths reflected by the
  • 3 ⁇ grating 12 allows incident light that is not aligned exactly with the grating axis 207 to be guided along and aligned with the grating 12 axis 207 for optimal grating reflection.
  • any standard waveguide may be used, e.g., a standard telecommunication single mode optical fiber (125 micron diameter or 80 micron diameter fiber with about a 8-10 micron diameter), or a larger diameter waveguide (greater than 0.5 mm diameter), such as is describe in U.S. Patent Application, Serial No. 09/455,868, filed December 6, 1999, entitled "Large Diameter Waveguide, Grating".
  • any type of optical waveguide may be used for the optical substrate 10, such as, a multi-mode, birefringent, polarization maintaining, polarizing, multi-core, multi-cladding, or microsturctured optical waveguide, or a flat or planar waveguide (where the waveguide is rectangular shaped), or other waveguides.
  • a multi-mode, birefringent, polarization maintaining, polarizing, multi-core, multi-cladding, or microsturctured optical waveguide or a flat or planar waveguide (where the waveguide is rectangular shaped), or other waveguides.
  • illustration (b) alternatively, the input light 24 maybe incident from the side and, if the grating 12 has the appropriate blaze angle, the reflected light will exit from the end face 652 as indicated by a line 654.
  • the grating 12 may have a plurality of different pitch angles 660,662, which reflect the input light 24 to different output angles as indicated by lines 664, 666.
  • the grating 12 may be impressed in the substrate 10 by any technique for writing, impressed, embedded, imprinted, or otherwise forming a diffraction grating in the volume of or on a surface of a substrate 10. Examples of some known techniques are described in US Patent No. 4,725,110 and 4,807,950, entitled “Method for Impressing Gratings Within Fiber Optics", to Glenn et al; and US Patent No.
  • the grating 12 may be partially or totally created by etching or otherwise altering the outer surface geometry of the substrate to create a corrugated or varying surface geometry of the substrate, such as is described in US Patent 3,891,302, entitled “Method of Filtering Modes in Optical Waveguides", to Dabby et al, which is incorporated herein by reference to the extent necessary to understand the present invention, provided the resultant optical refractive profile for the desired code is created.
  • the grating 12 maybe made by depositing dielectric layers onto the substrate, similar to the way a known thin film filter is created, so as to create the desired resultant optical refractive profile for the desired code.
  • Figs. 39-50 Alternative Microbead Geometries
  • Figs. 39-50 set forth microbead geometries consistent with that shown in Figs. 2-3.
  • the scope of the invention is intended to include the substrate 10 (and/or the element 8) having end-view cross-sectional shapes other than circular, such as square, rectangular, elliptical, clam-shell, D-shaped, or other shapes, and may have side-view sectional shapes other than rectangular, such as circular, square, elliptical, clam-shell, D- shaped, or other shapes.
  • 3D geometries other than a cylinder maybe used, such as a sphere, a cube, a pyramid or any other 3D shape.
  • the substrate 10 may have a geometry that is a combination of one or more of the foregoing shapes.
  • the shape of the element 8 and the size of the incident beam may be made to minimize any end scatter off the end face(s) of the element 8, as is discussed herein and/or in the aforementioned patent application.
  • the incident beam 24 may be oval shaped where the narrow portion of the oval is smaller than the diameter Dl, and the long portion of the oval is smaller than the length L of the element 8.
  • the shape of the end faces may be rounded or other shapes or may be coated with an antireflective coating. It should be understood that the size of any given dimension for the region 20 of the grating 12 may be less than any corresponding dimension of the substrate 10.
  • the dimensions of the grating 12 may be less than that of the subsfrate 12.
  • the grating 12 may be embedded within or part of a much larger substrate 12.
  • the element 8 may be embedded or formed in or on a larger object for identification of the object.
  • the dimensions, geometries, materials, and material properties of the subsfrate 10 are selected such that the desired optical and material properties are met for a given application.
  • the resolution and range for the optical codes are scalable by controlling these parameters as discussed herein and/or in the aforementioned patent application. Referring to Fig.
  • the substrate 10 may have an outer coating 799, such as a polymer or other material that may be dissimilar to the material of the substrate 10, provided that the coating 799 on at least a portion of the substrate allows sufficient light to pass through the substrate for adequate optical detection of the code.
  • the coating 799 may be on any one or more sides of the substrate 10.
  • the coating 799 may be a material that causes the element 8 to float or sink in certain fluids (liquid and/or gas) solutions.
  • the substrate 10 may be made of a material that is less dense than certain fluid (liquids and/or gas) solutions, thereby allowing the elements 8 to float or be buoyant or partially buoyant.
  • the substrate may be made of a porous material, such as controlled pore glass (CPG) or other porous material, which may also reduce the density of the element 8 and may make the element 8 buoyant or partially-buoyant in certain fluids.
  • CPG controlled pore glass
  • the grating 12 is axially spatially invariant.
  • the substrate 10 with the grating 12 shown as a long substrate 21
  • the limit on the size of the smaller substrates 30'-36' is based on design and performance factors discussed herein and/or in the aforementioned patent application.
  • one purpose of the outer region 18 (or region without the grating 12) of the substrate 10 is to provide mechanical or structural support for the inner grating region 20.
  • the entire substrate 10 may comprise the grating 12, if desired.
  • the support portion may be completely or partially beneath, above, or along one or more sides of the grating region 20, such as in a planar geometry, or a D-shaped geometry, or other geometries, as described herein and/or in the aforementioned patent application.
  • the non-grating portion 18 of the substrate 10 may be used for other purposes as well, such as optical lensing effects or other effects (discussed herein or in the aforementioned patent application).
  • the end faces of the substrate 10 need not be perpendicular to the sides or parallel to each other. However, for applications where the elements 8 are stacked end-to- end, the packing density may be optimized if the end faces are perpendicular to the sides.
  • illustrations (a)-(c) two or more substrates 10,250, each having at least one grating therein, may be attached together to form the element 8, e.g., by an adhesive, fusing or other attachment techniques. In that case, the gratings 12,252 may have the same or different codes.
  • the substrate 10 may have multiple regions 80,90 and one or more of these regions may have gratings in them. For example, there may be gratings 12,252 side-by-side (illustration (a)), or there may be gratings 82-88, spaced end-to-end (illustration (b)) in the substrate 10.
  • the length L of the element 8 may be shorter than its diameter D, thus, having a geometry such as a plug, puck, wafer, disc or plate.
  • the subsfrate 10 may have a plurality of the gratings 12 having the same codes written therein at numerous different angular or rotational (or azimuthal) positions of the substrate 10.
  • two gratings 550, 552, having axial grating axes 551, 553, respectively may have a common central (or pivot or rotational) point where the two axes 551,553 intersect.
  • the angle ⁇ i of the incident light 24 is aligned properly with the grating
  • the bead may be rotated as indicated by a line 559 and there may be many angular positions that will provide correct (or optimal) incident input angles ⁇ i to the grating.
  • illustrations (a), (b), (c), (d), and (e) the subsfrate 10 may have one or more holes located within the substrate 10.
  • holes 560 may be located at various points along all or a portion of the length of the subsfrate 10. The holes need not pass all the way through the subsfrate 10. Any number, size and spacing for the holes 560 may be used if desired.
  • holes 572 may be located very close together to form a honeycomb-like area of all or a portion of the cross-section
  • one (or more) inner hole 566 maybe located in the center of the substrate 10 or anywhere inside of where the grating region(s) 20 are located.
  • the inner hole 566 may be coated with a reflective coating 573 to reflect light to facilitate reading of one or more of the gratings 12 and/or to reflect light diffracted off one or more of the gratings 12.
  • the incident light 24 may reflect off the grating 12 in the region 20 and then reflect off the surface 573 to provide output light 577. Alternatively, the incident light 24 may reflect off the surface 573, then reflect off the grating 12 and provide the output light 575.
  • the grating region 20 may run axially or circumferentially 571 around the substrate 10.
  • the holes 579 maybe located circumferentially around the grating region 20 or transversely across the subsfrate 10.
  • the grating 12 maybe located circumferentially around the outside of the substrate 10, and there may be holes 574 inside the substrate 10.
  • the subsfrate 10 may have one or more protruding portions or teeth 570, 578,580 extending radially and/or circumferentially from the substrate 10.
  • the teeth 570, 578,580 may have any other desired shape. Referring to Fig.
  • the grating region 20 may have end cross-sectional shapes other than circular and may have side cross-sectional shapes other than rectangular, such as any of the geometries described herein for the subsfrate 10.
  • the grating region 20 may have a oval cross-sectional shape as shown by dashed lines 581, which may be oriented in a desired direction, consistent with the teachings herein. Any other geometries for the subsfrate 10 or the grating region 20 may be used if desired, as described herein. Referring to Fig.
  • the substrate 10 may be coated with a reflective coating 514 to allow incident light 510 to be reflected back to the same side from which the incident light came, as indicated by reflected light 512.
  • the substrate 10 can be electrically and/or magnetically polarized, by a dopant or coating, which may be used to ease handling and/or alignment or orientation of the substrate 10 and/or the grating 12, or used for other purposes.
  • the bead may be coated with conductive material, e.g., metal coating on the inside of a holey substrate, or metallic dopant inside the substrate, hi these cases, such materials can cause the substrate 10 to align in an electric or magnetic field.
  • the substrate can be doped with an element or compound that fluoresces or glows under appropriate illumination, e.g., a rare earth dopant, such as Erbium, or other rare earth dopant or fluorescent or luminescent molecule. In that case, such fluorescence or luminescence may aid in locating and/or aligning substrates.
  • a rare earth dopant such as Erbium, or other rare earth dopant or fluorescent or luminescent molecule.
  • Figure 55 hi particular, Figures 55(a), (b),(c) and (d) show an embodiment of the present invention that uses microtitre plates whose bottoms consist of flat or contoured groove plates.
  • beads are agitated to align themselves in the groove plates, and then codes and labels are read directly from the bottom of the microtitre plates with standard or custom fluorescence scanners.
  • This embodiment has the advantage of removing the bead transfer step, which in turn increases sample throughput and reduces the requisite investment in fluidic handling automation equipment.
  • the microtitre plate 1900 has straight grooves 1902 in the bottom that are about as wide as they are deep (1:1 aspect ratio) and can have a pitch of 1 to 200 microns.
  • the microtitre plate 1910 has circular grooves 1912 arranged concentrically.
  • the grooves maybe 100% to 200% of the bead diameter, and preferably about 120%.
  • the groove diameter should be about 32 microns.
  • the scope of the invention is not intended to be limited only to straight or concentric circular grooves, since embodiments are envisioned using grooves having other geometries, including diamond shaped, swervy, etc.
  • Figures 56-60 show a cell or fray design for loading and unloading beads during the bead alignment and interrogation process.
  • the design makes bead loading/unloading more convenient.
  • the goals are to be able to pipette the beads into the cell or tray; easily vacuum or wash the beads from the cell or tray; easily disassemble and clean the cell or tray; and provide an open cell architecture that lets bubbles out but keeps beads wet for hours.
  • Figures 56(a) and (b) Figures 56(a) and (b) show a side and top view of a cell or tray 2100 having four sides surrounding a glass plate or bottom 2102 with grooves 2104, and having a top 2106 hingeably coupled to the cell or tray 2100.
  • the cell or tray 2100 is stimulated, for example, using a magnetic stir bar, to aid the alignment of the beads 8 in the grooves 2104 on the bottom plate 2102 .
  • the top 2106 is closed when the beads 8 are aligned.
  • the cell or fray 2100 can be turned sideways and the beads 8 flushed out with a jet of liquid from a water providing device 2114.
  • Figures 59-60 Figure 59 shows an elevated perspective of the cell or tray 2100 with the cover down, while Figure 60 shows an elevated perspective of the cell or tray 2100 with the cover 2106 up.
  • Figure 61 Bead Alignment Device Having Narrow Groove Plate
  • Figure 61 shows an alternative embodiment in which the bead alignment device 2200 has a narrow window 2216. As shown, the grooves 2204 are in a section 2218 of the bottom plate, not across entire bottom, hi response to some stimulation, the beads (not shown) are corralled in narrow window 2016 and fall into alignment.
  • Figures 62-64 Bead Alignment Device Having Wide Window Figure 62 shows still another alternative embodiment generally indicated 2300, in which the grooves 2304 extend substantially along the entire base.
  • the solution having the microbeads (not shown) is provided to the bead alignment device 2300, the beads align themselves in the grooves. Consistent with that discussed above, typically the bead alignment device is stimulated to encourage bead movement into and alignment in the grooves.
  • Figures 65(a), (b), (c) Figure 65(a), (b). and (c) show an alternative embodiment of the alignment cell or tray in the form of a test tube or other container 2400, 2400'.
  • the grooves 2404 are arranged in the bottom of the test tube for aligning the beads contained in the liquid.
  • the container is shown having multiple levels of grooved platforms 2420, 2422, 2424, 2426, which may be perforated with holes to allow liquid and/or the beads 8 to flow between levels.
  • Figure 65(c) shows top views of various containers, which may have different geometric shapes, including circular, oval, square, rectangular. The scope of the invention is not intended to be limited to any particular container shape.
  • the term "microbead” is used herein as a label and does not restrict any embodiment or application of the present invention to certain dimensions, materials and/or geometries.
  • the dimensions and/or geometries for any of the embodiments described herein are merely for illustrative purposes and, as such, any other dimensions and/or geometries may be used if desired, depending on the application, size, performance, manufacturing requirements, or other factors, in view of the teachings herein.
  • any of the features, characteristics, alternatives or modifications described regarding a particular embodiment herein may also be applied, used, or incorporated with any other embodiment described herein.
  • the drawings herein are not drawn to scale.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Fluid Mechanics (AREA)
  • Dispersion Chemistry (AREA)
  • Hematology (AREA)
  • Clinical Laboratory Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)

Abstract

La présente invention a trait à un procédé et un appareil pour l'alignement d'éléments optiques ou microbilles dans lequel chaque microbille présente un corps de forme allongée avec un code incorporé selon un axe longitudinal de celui-ci pour être lu par un dispositif de lecture de code. Les microbilles sont alignées à l'aide d'un dispositif de positionnement de sorte que l'axe longitudinal des microbilles est positionné dans une orientation fixe par rapport au dispositif de lecture de code. Les microbilles sont typiquement des billes en verre de forme cylindrique entre 25 et 250 microns (νm) de diamètre et entre 100 et 500 νm de longueur, et comportent un code holographique incorporé dans la zone centrale de la bille qui est utilisé pour son identification du reste des billes dans un lot de billes avec plusieurs sondes chimiques différentes. Une référence croisée est utilisée pour déterminer quelle sonde est attachée à quelle bille, permettant ainsi la corrélation par le chercheur du contenu chimique sur chaque bille avec le signal de fluorescence mesuré. Etant donné que le code consiste en un réseau de diffraction typiquement disposé selon un axe, un alignement particulier est nécessaire entre le faisceau laser de lecture incident et le détecteur de lecture dans deux des trois axes de rotation. Le troisième axe effectuant une rotation autour de l'axe central du cylindre présente une symétrie azimutale et ne nécessite donc aucun alignement.
PCT/US2005/005743 2004-02-19 2005-02-22 Rainures d'alignement de plaques a puits multiples pour microparticules codees WO2005079544A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US54643504P 2004-02-19 2004-02-19
US60/546,435 2004-02-19

Publications (3)

Publication Number Publication Date
WO2005079544A2 true WO2005079544A2 (fr) 2005-09-01
WO2005079544A3 WO2005079544A3 (fr) 2006-09-28
WO2005079544A9 WO2005079544A9 (fr) 2007-09-20

Family

ID=34886267

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2005/005743 WO2005079544A2 (fr) 2004-02-19 2005-02-22 Rainures d'alignement de plaques a puits multiples pour microparticules codees

Country Status (1)

Country Link
WO (1) WO2005079544A2 (fr)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006102396A2 (fr) * 2005-03-22 2006-09-28 Applera Corporation Plaque haute densite creusee d'une gorge
US7659983B2 (en) 2003-01-22 2010-02-09 Electronics And Telecommunications Resarch Institute Hybrid random bead/chip based microarray
US7830575B2 (en) 2006-04-10 2010-11-09 Illumina, Inc. Optical scanner with improved scan time
US7872804B2 (en) 2002-08-20 2011-01-18 Illumina, Inc. Encoded particle having a grating with variations in the refractive index
US7898735B2 (en) 2002-09-12 2011-03-01 Illumina, Inc. Methods and systems for writing an optical code within or on a fiber substrate
US7901630B2 (en) 2002-08-20 2011-03-08 Illumina, Inc. Diffraction grating-based encoded microparticle assay stick
US7923260B2 (en) 2002-08-20 2011-04-12 Illumina, Inc. Method of reading encoded particles
US8081792B2 (en) 2003-08-20 2011-12-20 Illumina, Inc. Fourier scattering methods for encoding microbeads and methods and apparatus for reading the same
US20130302910A1 (en) * 2011-02-07 2013-11-14 Biocartis Sa Encoded microcarriers, assay system using them and method for performing an assay
WO2019147584A1 (fr) * 2018-01-24 2019-08-01 Illumina, Inc. Microscopie à éclairage structuré à balayage de ligne
WO2019147581A1 (fr) * 2018-01-24 2019-08-01 Illumina, Inc. Microscopie à éclairage structuré à dimensions réduite avec réseaux à motifs de nanopuits
CN112816411A (zh) * 2021-01-04 2021-05-18 武汉大学 基于弯曲波导传输损耗的折射率检测传感器、芯片及方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5837552A (en) * 1991-07-22 1998-11-17 Medifor, Ltd. Surface-enhanced analytical procedures and substrates
US6030581A (en) * 1997-02-28 2000-02-29 Burstein Laboratories Laboratory in a disk
US20020097658A1 (en) * 2000-12-08 2002-07-25 Worthington Mark O. Multiple data layer optical discs for detecting analytes
US20020155490A1 (en) * 2001-04-18 2002-10-24 Skinner Nigel G. Particle based assay system
US20030008323A1 (en) * 1999-04-15 2003-01-09 Ilya Ravkin Chemical-library composition and method

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5837552A (en) * 1991-07-22 1998-11-17 Medifor, Ltd. Surface-enhanced analytical procedures and substrates
US6030581A (en) * 1997-02-28 2000-02-29 Burstein Laboratories Laboratory in a disk
US20030008323A1 (en) * 1999-04-15 2003-01-09 Ilya Ravkin Chemical-library composition and method
US20020097658A1 (en) * 2000-12-08 2002-07-25 Worthington Mark O. Multiple data layer optical discs for detecting analytes
US20020155490A1 (en) * 2001-04-18 2002-10-24 Skinner Nigel G. Particle based assay system

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7872804B2 (en) 2002-08-20 2011-01-18 Illumina, Inc. Encoded particle having a grating with variations in the refractive index
US7901630B2 (en) 2002-08-20 2011-03-08 Illumina, Inc. Diffraction grating-based encoded microparticle assay stick
US7923260B2 (en) 2002-08-20 2011-04-12 Illumina, Inc. Method of reading encoded particles
US7898735B2 (en) 2002-09-12 2011-03-01 Illumina, Inc. Methods and systems for writing an optical code within or on a fiber substrate
US7659983B2 (en) 2003-01-22 2010-02-09 Electronics And Telecommunications Resarch Institute Hybrid random bead/chip based microarray
US8081792B2 (en) 2003-08-20 2011-12-20 Illumina, Inc. Fourier scattering methods for encoding microbeads and methods and apparatus for reading the same
WO2006102396A2 (fr) * 2005-03-22 2006-09-28 Applera Corporation Plaque haute densite creusee d'une gorge
WO2006102396A3 (fr) * 2005-03-22 2007-03-29 Applera Corp Plaque haute densite creusee d'une gorge
US7830575B2 (en) 2006-04-10 2010-11-09 Illumina, Inc. Optical scanner with improved scan time
US9310305B2 (en) * 2011-02-07 2016-04-12 Mycartis Nv Encoded microcarriers, assay system using them and method for performing an assay
US20130302910A1 (en) * 2011-02-07 2013-11-14 Biocartis Sa Encoded microcarriers, assay system using them and method for performing an assay
US10928322B2 (en) 2018-01-24 2021-02-23 Illumina, Inc. Structured illumination microscopy with line scanning
WO2019147581A1 (fr) * 2018-01-24 2019-08-01 Illumina, Inc. Microscopie à éclairage structuré à dimensions réduite avec réseaux à motifs de nanopuits
KR20200021472A (ko) * 2018-01-24 2020-02-28 일루미나, 인코포레이티드 라인 스캐닝을 이용한 구조화 조명 현미경법
CN111094933A (zh) * 2018-01-24 2020-05-01 伊鲁米纳公司 利用线扫描的结构化照明显微术
RU2736104C1 (ru) * 2018-01-24 2020-11-11 Иллюмина, Инк. Микроскопия структурированного освещения с линейным сканированием
WO2019147584A1 (fr) * 2018-01-24 2019-08-01 Illumina, Inc. Microscopie à éclairage structuré à balayage de ligne
KR102306769B1 (ko) 2018-01-24 2021-09-30 일루미나, 인코포레이티드 라인 스캐닝을 이용한 구조화 조명 현미경법
US11150455B2 (en) 2018-01-24 2021-10-19 Illumina, Inc. Reduced dimensionality structured illumination microscopy with patterned arrays of nanowells
US11650156B2 (en) 2018-01-24 2023-05-16 Illumina, Inc. Reduced dimensionality structured illumination microscopy with patterned arrays of nanowells
CN111094933B (zh) * 2018-01-24 2023-09-26 伊鲁米纳公司 利用线扫描的结构化照明显微术
US11933728B2 (en) 2018-01-24 2024-03-19 Illumina, Inc. Reduced dimensionality structured illumination microscopy with patterned arrays of nanowells
CN112816411A (zh) * 2021-01-04 2021-05-18 武汉大学 基于弯曲波导传输损耗的折射率检测传感器、芯片及方法

Also Published As

Publication number Publication date
WO2005079544A9 (fr) 2007-09-20
WO2005079544A3 (fr) 2006-09-28

Similar Documents

Publication Publication Date Title
CA2498933C (fr) Procede et appareil d'alignement de microbilles allongees de maniere a les interroger
US20060160208A1 (en) Multi-well plate with alignment grooves for encoded microparticles
EP1664782A2 (fr) Procede et dispositif servant a aligner des microbilles dans le but de les interroger
WO2005079544A2 (fr) Rainures d'alignement de plaques a puits multiples pour microparticules codees
US7901630B2 (en) Diffraction grating-based encoded microparticle assay stick
US8470605B2 (en) Optical reader for reading encoded microparticles
US7190522B2 (en) Chemical synthesis using diffraction grating-based encoded optical elements
US20040126875A1 (en) Assay stick
US7349158B2 (en) Diffraction grating-based encoded micro-particles for multiplexed experiments
AU2003265583B2 (en) Diffraction grating-based optical identification element
US7923260B2 (en) Method of reading encoded particles
US7900836B2 (en) Optical reader system for substrates having an optically readable code
WO2004025562A1 (fr) Procede et appareil d'etiquetage utilisant des elements d'identification optique codes a reseau de diffraction
CA2559801A1 (fr) Lecteur optique pour elements d'identification optique codes a base de reseaux de diffraction
WO2006076053A1 (fr) Procede et appareil d'alignement de microbilles en vue de leur interrogation
WO2004066210A1 (fr) Micro-reseau utilisant une bille/puce aleatoire hybride
WO2005029047A2 (fr) Baton de dosage de microparticules codees a base de reseau de diffraction

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE

122 Ep: pct application non-entry in european phase

Ref document number: 05723567

Country of ref document: EP

Kind code of ref document: A2