Patent Application
20120135449
For multiplexed applications, tissue samples or tissue microarrays (TMA) need to be stained with multiple molecular probes to investigate protein expression or spatial distribution quantitatively or qualitatively. The staining process is typically performed using time-consuming manual techniques that are susceptible to error. The reagents used in the staining process are often expensive and have limited shelf life thereby requiring special handling techniques.
Automated systems that use microscopic flow cells as reaction chambers for tissue samples or to monitor cellular activities under flow conditions exist. However, such systems have not been well adapted to use in tissue sample processing, lacking environmental control of the sample within the flow cell and requiring manual intervention.
Fluid flow rates of reagents (e.g., luminescent reagents) through the flow cell are difficult to control as a flow stream may cause turbulence within the small volume chamber, dislodging or damaging the sample. Also, peripheral external heating, (e.g., from a heated microscope stage), may cause non-uniform heating of the enclosed sample. Consequently, the temperature varies across the sample. Further, repeated reagent preparation, sample removal and replacement into the stage for image acquisition, require sample realignment and diminish reproducibility.
The invention generally relates to automated methods and devices that facilitate iterative staining of biological samples from imaging applications.
In some embodiments the methods include the steps of providing a small volume flow cell containing a biological sample, applying a stain to the biological sample, combining at least two precursor reagents to form an activated destaining agent and wherein the activated destaining agent decomposition rate is greater than or similar to the destaining reaction rate, flowing the destaining agent over the biological sample at a flow rate that is greater than the decomposition rate of the activated destaining agent, and releasing the sample from the flowcell wherein the integrity of the sample is intact. The process of staining, combining and flowing may be iteratively repeated.
In some embodiments a device for iterative staining of a biological sample is provided and comprises a flow cell in fluid communication with a premixer, wherein the volume capacity of the premixer is smaller than about five times the volume capacity of the flow cell.
In some embodiment the flow cell comprises a base configured to receive a tissue sample; a thermoelectric element; a gasket position between the base and the thermoelectric element; an inlet port in fluid communication with the premixer; and an outlet port; wherein one or both of the base and thermoelectric elements includes an image acquisition window. The flow cell may further comprise a degasser and a piezo-electric element.
These and other features, aspects, and advantages of the present invention will become better understood when the following detailed description is read with reference to the accompanying figures wherein.
The following detailed description is exemplary and not intended to limit the invention of the application and uses of the invention. Furthermore, there is no intention to be limited by any theory presented in the preceding background of the invention of the following detailed description of the figures.
To more clearly and concisely describe and point out the subject matter of the claimed invention, the following definitions are provided for specific terms, which are used in the following description and the appended claims.
The singular forms “a” “an” and “the” include plural referents unless the context clearly dictates otherwise. Approximating language, as used herein throughout the specification and claims, may be applied to modify any quantitative representation that could permissibly vary without resulting in a change in the basic function to which it is related. Accordingly, a value modified by a term such as “about” is not to be limited to the precise value specified. Unless otherwise indicated, all numbers expressing quantities of ingredients, properties such as molecular weight, reaction conditions, so forth used in the specification and claims are to be understood as being modified in all instances by the term “about.” Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques
As used herein, the term “biological sample” refers to a sample obtained from a biological subject, including sample of biological tissue or fluid origin obtained in vivo or in vitro. Such samples may be, but are not limited to, tissues, fractions, and cells isolated from mammals including, humans.
As used herein the term “lumiphore” refers to a chemical compound that demonstrates luminescence including chemoluminescence, bioluminescence, phosphorescence, and photoluminescence. Representative examples include, but are not limited to, luminol, lucigenin, acridans, acridinium esters, and dioxetanes, and fluorophores.
As used herein the term ‘oxidant” or “oxidizing agent” refers to a bleaching reagent that substantially inactivate a lumiphore. Representative oxidizing agents include active oxygen species, hydroxyl radicals, singlet oxygen, hydrogen peroxide, or ozone such as hydrogen peroxide, potassium permanganate, sodium dichromate, aqueous bromine, iodine-potassium iodide, or t-butyl hydroperoxide.
The present invention relates to an automated system and methods that operate with minimal operator intervention by eliminating the need to transfer samples (e.g., tissue samples on a slide within the flow cell). The disclosed systems and methods further eliminate the need to displace samples between the staining component and the imaging component. As such, in certain embodiments, the system allows a sample to be stained or labeled while in transit between a staining or heating or bleaching operation and an imaging operation by encapsulating the sample within a flow cell configured to allow iterative staining. This provides a more efficient use of the individual processing components, that is, the elimination of down-time which is an important consideration in sample integrity and testing.
In certain embodiments, the biological sample and glass slide support is encapsulated fully by the flow cell. The encapsulation of the biological sample and glass slide support minimizes both reagent volume and reagent dwell time within the system thereby saving on expensive reagents, such as fluorescence labeled antibodies, and minimizing reagent decomposition or side reactions. It also reduces variations in reagent metering and may reduce occurrences of reagent cross contamination. Automation of the imaging component eliminates or reduces steps associated with image alignment and remounting the sample after staining. The improvement in image registration facilitates formation of an accurate composite image.
In some embodiments, the device provides a means of temporarily encapsulating a biological sample, so that it can sequentially be: stained with a dye, imaged with any high resolution microscope, the fluorescent reporter bleached or quenched, then the cycle repeated.
The device provides a means of temporarily encapsulating a biological sample or standard glass pathology slide, allowing it to be moved between processing stations or environments (e.g. antigen retrieval step, AB-incubation step, agitation, heating, imaging station(microscope, camera, laser scanner), and dye bleaching step), while maintaining good control of spatial location and integrity of the sample. The sample can be simultaneously moved and processed.
Upon completion of an iterative molecular stain-image-bleach assay, the slide may then be released for subsequent processing, such as H&E staining, and archiving with mounting media and coverslip. In this manner the integrity of the sample and slide are preserved for further analysis or for reference. As used herein integrity refers to the ability of the sample to retain its shape, distribution, or other characteristics of its cellular compartments such as the cell nuclei useful in cellular assays. Integrity of the sample may also refer to maintaining the physical integrity of the cell such that essential cell signaling pathways are not interfered with such that the sample maybe subsequently stained or dyed using biomarker assays. To maintain integrity, temperature and exposure should be controlled and physical changes or damage to the sample must be minimized. Physical damage may be the result of turbulence in the flow chamber as well as during the transfer step including removal of the coverslip.
Automation may be achieved through computer control of one or more of the process steps involved in sequential staining such as addition of staining reagents and oxidant. Where the flow cell system is incorporated into a combined sample processing and image acquisition system, the image acquisition components (e.g., microscope or camera) may also be controlled by software such as a program written in LabVIEW or C.
In one embodiment as shown in
The flow cell may be a modular unit that is adapted to fit onto a standard microscope stage. Alternatively, the flow cell may be an integrated unit including a microscope stage. In some embodiments, the flow cell may be fixed on a microscope stage for the imaging process. This allows the sample to be exposed to a complete series of reagents without manual intervention thereby potentially eliminating realignment of the sample on the microscope stage for image acquisition or registration. This is particularly useful for multiplexed staining and imaging as images acquired after each staining step may be superimposed to form a composite image.
The flow cell may be used in a system that includes fluidic and temperature control subsystems to control fluidic delivery and solution temperature in the internal chamber of the flow cell. In one embodiment, the fluidic control system may further comprise reservoirs, flow sensors, mixing chambers, and degassers to prepare one or more reagents prior to injection into the flow cell. The advantage of such a system is to avoid the need of premixing and storing reagents that may have limited stability or shelf life. The fluidic control system is in fluidic communication with the inlet port and outlet port of the flow.
In certain embodiments, the flow cell, which may also be termed an encapsulation device, may include a slide-receiving member configured to receive a tissue sample positioned on a solid support such as a glass slide. The slide holder is compatible with a range of chemical and temperature variations. In one embodiment, the slide holder may consist of a base and a pin or tab system for securing the slide in the chamber.
The flow cell includes a gasket with a central opening configured to receive a tissue sample positioned on a slide. The gasket may be made of a deformable, chemically inert, rubber or plastic that retains the liquid applied to the flow chamber. The gasket may optionally include openings for the inlet and outlet ports. The central opening of the gasket maybe sized to maximize the field of view of the image acquisition window. The width, length, and depth of the gasket when placed into the flow cell may each be varied to achieve a predetermined internal volume of the flow cell. In some embodiments, the width and length of the gasket may be sized to conform to standard tissue section slides or microarray substrates. For example, in one embodiment, the central opening of the gasket can accommodate a tissue micro array that is 20 mm wide and 30 mm long. In certain embodiments, the gasket may have raised features in order to provide reliable compression and seal.
The inlet and outlet ports are preferably placed away from the image acquisition window. Thus, the inlet and outlet ports may be positioned in the gasket or upon the lid. The inlet and outlet ports are typically matched in size such that the in-flow rate and the out-flow rate are coordinated to achieve a desired rate of flow across the sample.
Referring further to
In some embodiments, the temperature control unit is integrated into the lid so that the internal chamber formed between a temperature control unit (e.g., a Peltier stack) and a slide is heated directly by the temperature control unit, instead of through the tissue slide. This configuration frees up the backside of the tissue slide for imaging.
In some embodiments, the invention further comprises a method for assisting in gas removal from the flow cell. As shown in
In some embodiments, the invention may further comprise a piezo-electric element connected to the flow chamber and capable of producing vibration within the flow chamber by conversion of low voltage electrical signals into acoustic energy. In a preferred embodiment the piezo-electric element maybe composed of a ceramic, quartz (SiO2) or barium titanate (BaTiO3). The configuration of the piezo-electric element provides ultrasonic agitation and influences the flow profile of reagents through the fluid chamber. This is particularly advantageous wherein the desired staining reaction is diffusion limited and conventional mechanical mixing is prohibited by the flow cell geometry.
A computer may control the various components of the flow cell system, including for example the thermal control unit, the premixer, the vibrational unit, and the pumps. Where the flow cell system is incorporated into a combined sample processing and image acquisition system, the image acquisition components (e.g., microscope or camera) may also be controlled by a computer.
Also provided herein are methods for processing and acquiring images from a biological sample adhered to a solid support (e.g., a tissue section fixed to a microscope slide). The methods include steps employing various alternative embodiments of the device selected for a particular application. Representative methods for iterative processing of biological samples are described in co-owned U.S. patent application Ser. No. 11/864,093, which is incorporated herein.
One representative method includes: (a) positioning a biological sample, such as a tissue section on a microscope slide, in a flow cell; (b) applying a fluorescent label or a lumiphore to the sample in a manner to allow sufficient contact time between the lumiphore and the sample which are typically in the range of 30 to 60 minutes depending on the concentration and type of label used; (c) applying a wash solution, for example an appropriate buffer solution to wash away any unbound fluorescent label or lumiphore; (d) acquiring an image of the labeled sample; (e) applying a chemical agent to destroy the lumiphore in step (b) by applying an oxidizing agent that substantially inactivates the lumiphore where a solution of the oxidizing agent is applied to the sample using a continuous flow process to minimize non-Laminar flow and dwell time within the flow cell resulting in an average dwell time of 1 to 5 minutes; (f) optionally acquiring an image of the sample, and (g) repeating steps (b)-(f) at least once.
Each of the applying steps may be accomplished by flowing a solution containing a particular reagent over the biological sample positioned within the flow cell. The following parameters may be controlled to enhance reactivity and, thereby, reduce reagent consumption (1) flow cell internal volume; (2) flow cell internal temperature; (3) timing of mixing of constituent parts of the oxidizing solution (e.g., hydrogen peroxide and sodium bicarbonate); (4) extent of agitation of the solutions as they pass the sample; and (5) bubble removal or degassing of the flow cell. Appropriate regulation of these parameters also may reduce sample degradation, permitting a single sample to yield more data.
The automated destaining step permits the operator to reprobe a single sample while maintaining the original registration. The addition of the oxidant results in destaining of the biological sample due to substantial removal of the signal produced by the lumiphore. Whether the destaining is accomplished by chemically altering the lumiphore or by detachment, the signal is reduced by at least 80% and preferably greater than 90%. This reduction in signal may be measured as the post-staining intensity at a particular wavelength relative to the initial absolute intensity of the stained biological to adjust for a concomitant reduction in background signal or autofluorescence resulting from the destaining step.
Small volume flow cells conserve valuable reagents. Where reagent diffusion is the rate-determining step, flow should correlate with the internal chamber volume. For example fluidic delivery to the flow cell may be adjusted based on the volume capacity of the chamber to allow for rapid, complete flushing of the chamber.
The flow cell provides a solid support for the test sample. The flow cell dimensions are constrained based on the solid support used. The height of the flow cell is based on the thickness of the sample. Where the sample is a tissue section, it may have a thickness between about 5 μm to about 100 μm. The tissue section may occupy 20 mm by 30 mm area. This results in a small internal chamber volume in the range of 10 μL to 1000 μL, preferably, 50 μL to 200 μL.
Decomposition may happen before a reagent is substantially removed from the flow cell. Turbulent flow with in the flow chamber improves surface reactivity and facilitates reagent byproducts (e.g., oxygen gas) removal. Accordingly, in some embodiments, the chamber may include an agitation element (e.g., acoustic piezoelectric component) that generates turbulence.
Although, many microarray staining processes proceed between 20° C. and 100° C., some systems may require significantly higher or lower temperatures with tight tolerance. Adsorption and desorption processes related to staining are temperature dependent and, therefore, in some embodiments, temperature uniformity is provided across the sample surface where the chemical interactions takes place.
For example, a stacked thermoelectric element may be introduced into or upon the chamber wherein current flowing through the elements may regulate chamber temperature, within a specified temperature range, through radiant heating of fluid within the chamber. Some systems may require a temperature tolerance of +/−5° C. while others may have a significantly tighter or less stringent temperature tolerance. In some embodiments, the thermoelectric element may optionally contain a heat sink to absorb and dissipate heat to facilitate temperature regulation.
Reagents used in multiplexing staining may have limited shelf life where by effectiveness of the reagents diminishes over time. This occurs when a reagent, produced by mixing two or more solutions to initiate a chemical reaction, may undergo partial decomposition or precipitation. This may lead to the formation of gas and other undesirable by products. In some embodiments, the solutions are completely mix at the molecular level by using a premixer to intersperses the reactants immediately before the reagent is introduced into the flow cell. Mixing times should be sufficient long to generate the reagent and sufficiently limited to prevent decomposition.
The premixer, which is positioned upstream of the flow cell, may be based on a chamber design or a tube design. The chamber design may include a small vessel with inlet and outlet ports and containing a mechanical mixer. The tube design may include a Y-adaptor into which the chemical reagents are driven at a predetermined flow rate. Alternatively, the tube design may include a physical barrier (e.g., micromesh or a spherical membrane positioned within the tube) or a nozzle that generates turbulence.
The premixer allows for mixing of the chemical reagents before introduction to the flow cell. The volume capacity of the flow cell is determined based on the decomposition rate of the chemical reagents and the desired flow rate of the chemical reagents or their reaction product through the flow chamber.
A peroxide solution decomposition rate at a given temperature equals −dC/dt=kC where C is peroxide concentration, t is time and k is the first order rate constant. Half-life of a first order reaction is independent of the starting concentration and is calculated as t ½=In(2)/k. Half-life of nth-order reactions can also be determined and is represented as:
t
1/2=2n-1−1/(n−1)k[A0]n-1.
Residence time within the flow cell is limited to less than the half-life of the reagent. Therefore the volume capacity of the flow cell is determined by: Vp<(V/t)(t ½) where (Vp) is the volume capacity of the flow cell and (V/t) is the flow rate.
An oxidant such as a hydrogen peroxide solution, which generates hydroperoxide anions, decomposes and forms oxygen gas within 5 minutes of preparation. Typically the volume capacity of the flow cell may range from 1 to 1000 μL, preferably 50 μL to 500 uL. To ensure the average dwelling time of reagents in the flow cell is less than 5 mins, the flow rate preferably ranges from 50 uL/min to 500 uL/min. Applying Vp<(V/t)(t ½), volume capacity of the premixer is limited to 5 to 5000 μL, preferable 250 μL to 2500 μL.
The premixer is in fluid communication with one or more reagent reservoirs. The reagent reservoirs act as storage devices for the reagents prior to deliver to the premixer. A flow controller allows for the transfer of a metered quantity of a reagent to the premixer. The delivery of more than one reagent can be done in a sequential order or in parallel, permitting accurate metering of the reagents and reducing reagent cross contamination.
In certain embodiments, the methods may be performed in a system that includes a flow cell configured to enable enhanced access to the sample through an image capture window. The image capture window may be defined by the substrate upon which the sample is set (e.g., microscope slide) or may include an optically transmissive material on the underside of the slide-receiving member.
Accordingly, the methods of the invention may be performed using a flow cell in which accessory devices, such as heating elements or agitation elements (e.g. an acoustic piezoelectric component) are positioned away from the image capture window through which a microscope, coupled to a camera, may capture images of the sample during the various phases of processing.
In one embodiment, 3 ml of a hydrogen peroxide buffer solution (3% H2O2, pH 10) is prepared in a premixer. The premixer is designed to be in physical communication with the flow cell such that, using continuous flow, the freshly prepared peroxide buffer is introduced into the flow chamber wherein residence time in the chamber is less than 5 mins. A typical flow rate is 250 μL/min and the volume of the flow chamber is less than 250 ul. The chamber further comprises a piezo-electric element.
As shown in
In certain embodiments, the flow cell containing the encapsulated biological sample may be moved between processing steps or stations using a robotic device. In certain embodiment, the sample may wait in a queue while the antibody incubates and is ultimately transferred to the imaging device. By using a robotic mechanism to move and process the sample, error may be reduced by allowing for more reproducibility in the staining and analysis process. Improvement in sample tracking and storage may also be achieved providing in certain embodiments, reduced testing cycle time.
This application is a continuation-in-part of U.S. patent application Ser. No. 12/061,044, filed on Apr. 2, 2008, which is herein incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12061044 | Apr 2008 | US |
| Child | 13365525 | US |
