1. Field of the Invention
This invention relates to sequential chemical reactions of which the polymerase chain reaction (PCR) is one example. In particular, this invention addresses methods and apparatus for performing chemical reactions simultaneously in a multitude of reaction mixtures and independently controlling the reaction in each mixture.
2. Description of the Prior Art
PCR is one of many examples of chemical processes that require a high level of temperature control of reaction mixtures with rapid temperature changes between different stages of the procedure. PCR itself is a process for amplifying DNA, i.e., producing multiple copies of a DNA sequence from a single strand bearing the sequence. PCR is typically performed in instruments that provide reagent transfer, temperature control, and optical detection of the product in a multitude of reaction vessels such as wells, tubes, or capillaries. The process includes a sequence of stages that are temperature-sensitive, different stages being performed at different temperatures and the temperature sequence being repeated in successive cycles.
While PCR can be performed in any reaction vessel, multi-well reaction plates and microfluidics devices with multiple channels are the reaction vessels of choice so that many strands of DNA can be replicated simultaneously. In many applications, PCR is performed in “real-time” and the reaction mixtures are repeatedly analyzed throughout the process, by the detection of light from fluorescently-tagged species in the reaction medium. In other applications, DNA is withdrawn from the medium for separate amplification and analysis. In multiple-sample PCR processes, a preferred arrangement is one in which each sample occupies one well of a multi-well plate or one channel of a multi-channel microfluidics device, and all samples in the plate or the microfluidics device are simultaneously equilibrated to a common thermal environment at each stage of the process.
Using a 96-well microplate with a sample in each well as an example, the plate is typically placed in contact with a metal block that is heated and cooled either by a Peltier heating/cooling apparatus or by a closed-loop liquid heating/cooling system that circulates a heat transfer fluid through channels machined into the block. In general, however, rapid changes in temperature that are uniform across all wells or channels are still difficult to achieve.
To address the need for rapid temperature changes in reaction systems that are retained in the wells of a microplate or in any plate or device that contains an array of individual sample receptacles, the various devices and methods disclosed herein involve the placement of a vapor chamber underneath the plate or device, plus heating elements, cooling elements, or both to allow or induce vaporization and condensation of a working fluid in the vapor chamber. The vapor chamber is arranged such that contact with the heated vapor of the working fluid, and condensation of the vapor when cooled, transfer heat into and draw heat from, respectively, the contents of each sample receptacle by conductive heat transfer between the walls of the vapor chamber and the walls of the receptacles. In certain embodiments of the invention, the top of the vapor chamber is in direct contact with the undersides of the receptacles, while in others an intermediary plate is placed between the undersides of the receptacles and the top of the vapor chamber. In embodiments in which the receptacles are wells and the vapor chamber and the wells are in direct contact, the top surface of the vapor chamber has depressions that are shaped and spaced to receive the wells, and to conform in contour with the undersides of the wells to the extent that the depressions are in direct and continuous contact with the wells. In embodiments in which an intermediary plate is included, the intermediary plate has depressions in its top surface that are shaped and spaced to receive, and that conform in contour to, the sample receptacles, while the bottom surface of the plate is contoured to provide maximal contact with the top surface of the vapor chamber. In many cases where an intermediary plate is used, the bottom surface of the intermediary plate and the top surface of the vapor chamber are both flat for convenience of construction and for low cost. In all embodiments, i.e., both those with the intermediary plate and those without, a single vapor chamber is arranged to control heat transfer into and out of a plurality of sample receptacles, and in many cases all receptacles, such as the wells of a microplate or other multi-well plate or all microchannels of a microfluidics device, serving as a heat spreader and cooling spreader among the various receptacles to achieve uniform and rapid temperature changes among the receptacles. Alternatively, a single vapor chamber can provide heat transfer into and out of a section of a well plate or microfluidics device, the section itself containing a plurality of wells or channels and the vapor chamber thereby spreading the thermal effects among all of the wells or channels with which it is in thermal contact.
Where the walls of the vapor chamber are in direct contact with the walls of the sample receptacles, best results will be achieved when the contours of contacting surfaces are identical in curvature (including no curvature in the case of flat surfaces) but curved in opposite directions. In the case of wells of a multi-well plate, surfaces of the vapor chamber that conform to the undersides of the wells will thereby achieve direct and continuous contact with the undersides of the wells, or at least with portions of the side walls of the wells to heights that will encompass the typical (or expected range of) depths of the reaction mixtures within the wells.
Vaporization and condensation of the working fluid are achieved by heating and cooling of the fluid through the use of heating elements, cooling elements, or both, that are externally controlled, i.e., turned on or off, and in some cases regulated, from outside the vapor chamber. In certain embodiments, a wick structure in the interior of the vapor chamber enhances the movement of the working fluid, particularly during condensation to promote the travel of the condensed fluid away from the reaction wells. In certain constructions, variable and independently controllable thermal coupling means are interposed between the heating element and the vapor chamber, or between the cooling element and the vapor chamber, or both.
These constructions and further variations are described in more detail below.
The vapor chamber that forms a component of each of the systems described herein is a hollow body with a closed internal cavity that contains a working fluid whose vaporization and condensation within the cavity serve as means for promoting or accelerating the transfer of heat out of the cavity into the reaction wells or into the cavity from the reaction wells. Thermal contact between the vapor chamber and the sample receptacles occurs in many cases at the top surface of the vapor chamber, either by direct contact with the undersides of the sample receptacles or through the intermediary plate. To accomplish this, the working fluid is generally partially vaporized so that it exists both in liquid and vapor form within the cavity. Heated vapors tend to rise within the cavity, and upon so doing to contact internal surfaces of cavity wall sections that are in direct contact with the walls of the sample receptacles. Condensation of the vapors at those surfaces releases heat from the vapor, and the released heat passes through the walls to heat the reaction mixtures within the receptacles. Conversely, vaporization at the walls draws heat from the receptacles into the cavity with the effect of cooling the reaction mixtures.
In certain embodiments that do not include an intermediary plate, the vapor chamber will have an array of depressions that conform to the sample receptacles, and that therefore extend downward into the internal cavity of the vapor plate. Structural integrity and rigidity of the vapor chamber can be reinforced by using depressions that are deep enough that their lower extremities contact or are fused to the floor of the vapor chamber. In other cases, a gap remains between the lower ends of the depressions and the floor of the chamber to provide additional space for circulation of the working fluid, whether in liquid or vapor form. In embodiments that include an intermediary plate, the vapor chamber can have a top surface that is flat or of any other contour since the vapor chamber does not directly contact the sample receptacles. For most efficient heat transfer, the intermediary plate will have top and bottom surfaces that are complementary in contour to the undersides of the wells and to the vapor chamber, respectively.
For those embodiments in which the sample receptacles are wells of a multi-well plate, the plate will generally be designed as a unitary structure that contains a planar array of wells connected by a deck portion, which is in many cases a flat horizontal portion that forms a continuous surface between all of the wells. In other cases, the deck portion is a network of webs or a flat surface that includes gaps. For manufacturing convenience, many well plates will have a continuous deck portion circling the rims of each of the wells, with no gaps in the deck portion or between the deck and the wells. In many cases, the wells will extend downward from the deck, with convex undersides extending below the deck. The shapes of the wells can vary widely. They can for example be those with hemispherical, elliptical, conical, frustoconical (i.e., truncated conical), cylindrical, or rectangular. For maximal response to temperature changes imposed through the walls of the wells, conical shapes are of particular interest since they offer a high ratio of lateral wall area to internal well volume and thus a large heat transfer area, and each well is readily emptied of liquid reaction media when desired.
Contact between the vapor chamber and the well plate for systems designed for use without an intermediary plate, or between the intermediary plate and the well plate for systems designed for use with an intermediary plate, can include the deck portion of the well plate, although inclusion of the deck portion is unnecessary. In many cases, therefore, only the sides of the reaction wells will be in contact with the vapor chamber or the intermediary plate for thermal transfer, and in many cases, contact need extend only a portion of the distance up the side wall of each reaction well. The reaction wells may thus be deeper than the corresponding depressions in the vapor chamber or the intermediary plate. Well plates with such reaction wells can be used, for example, when the reaction media to be retained within each well occupies only a portion of the well, since heat transfer need only occur as high as the height of the liquid medium in the well. Thus, example, the depths of the depressions can in some cases be one-third to five-sixths the depths of the reaction wells, or one-half to three-quarters the depths, and still provide rapid and effective temperature changes.
The intermediary plates when included will generally be of highly heat-conductive materials so that they will not significantly lower the rates of heat transfer in either direction. In many cases, the intermediary plate will also be of rigid construction to add to the stability and proper alignment of the well plate and the vapor chamber. Metals, for example copper, aluminum, and alloys thereof, are thus particularly useful as materials for intermediary plates.
Certain embodiments of the invention include two or more vapor chambers for further acceleration of heat transfer and to further promote uniformity of temperature among all of the sample receptacles. Two vapor chambers can be included, for example, with an intermediary plate of the type described above in between the two chambers. The lower vapor chamber can provide heat transfer to or from an underlying heating or cooling element.
Controllable heating of the working fluid, as well as controllable cooling, can be achieved by conventional heating and/or cooling elements of the types commonly used in biochemical or chemical laboratory equipment. Resistance heaters and Peltier (thermoelectric) modules are particularly convenient in view of their small size and localized effect. The heating and/or cooling elements can be placed at the sides of the vapor chamber, below the vapor chamber, or generally at any location that will result in rapid or optimal rates of heating and cooling for the particular protocol to be followed. Heat dissipation fins or heat sinks in general to accelerate cooling will also be of use in many cases.
The optimal working fluid is a fluid that provides high heat transfer, is readily volatilized and condensed, and flows readily over the wall surfaces of the vapor chamber. Fluids with high latent heat, high thermal conductivity, low liquid and vapor viscosities, and high surface tension will therefore be useful. Additional characteristics of value in many cases are thermal stability, wettability of wick and wall materials, and a moderate vapor pressure over the contemplated operating temperature range. Fluids that meet these characteristics can be organic or inorganic, the optimal choice depending on the contemplated temperature range. For PCR systems, a working fluid with a useful range of from about 50° C. to about 100° C., i.e., a fluid that is liquid at room (ambient) temperature and liquid at 100° C., at atmospheric pressure, will be most appropriate. Examples are acetone, methanol, ethanol, water, toluene, and any of these liquids with surfactants dissolved therein.
The partially vaporized working fluid can occupy the vapor chamber cavity on its own, or be mixed with a diluent gas that remains gaseous throughout the temperature cycling. Most efficient heat transfer however will often be achieved with an undiluted working fluid. Since the vapor chamber is a closed chamber, the heating and cooling of the working fluid will be accompanied by pressure changes. In many cases, particularly when the working fluid is undiluted it or essentially undiluted (i.e., diluted only with proportions of diluent gas that are small enough not to affect the diffusion rate of gaseous working fluid molecules throughout the cavity), it will be advantageous to select a working pressure range that will provide vaporization and condensation at temperatures that will match those of the temperature cycle that is sought for the samples in the reaction wells. The cavity can first be evacuated or partially evacuated, and the working fluid added in vapor form or in liquid form to vaporize upon entering the evacuated cavity, and resulting pressure will vary with the amount of working fluid thus introduced. Evacuation to less than 200 mm Hg, and in many cases less than 100 mm Hg or even less than 25 mm Hg, will be useful in many cases. The operating pressure range during the thermal cycling can then range from subatmospheric to atmospheric or superatmostpheric, although in many cases the pressure range over the full cycle will remain subatmospheric, such as for example between 200 mm Hg and 500 mm Hg. All pressures cited in this paragraph are absolute pressures.
As noted above, certain embodiments of the invention include a wicking means or wick structure in the vapor chamber. The wick structure can be a lining on a portion or all of the wall surface of the internal cavity of the vapor chamber, and aids in the flow of the working fluid over the internal surfaces of the vapor chamber to distribute the cooling and heating effects throughout the chamber cavity and thus increase the response to temperature changes and the uniformity of the temperature through the chamber and hence the sample receptacles. The wick structure thus promotes the flow of the condensate within the vapor chamber. Examples of wick structures are porous materials, typically made of metal foams, felts, or meshes of various pore sizes, in all cases lining the interior walls of the vapor chamber. Further examples are fibrous materials, notably ceramic fibers or carbon fibers. Wick structures can also be capillaries in the form of axial grooves in the vapor chamber wall, or a layer of dendritic metallic crystals such as copper dendrites.
The drawings provided herewith and the accompanying descriptions below are directed to systems where the sample receptacles are wells of a multi-well plate. Constructions in which the sample receptacles are channels of a microfluidics device are analogous.
The apparatus shown in
The vapor chamber 12 is a fully enclosed chamber with a hollow interior. A working fluid, when in liquid form, forms a shallow layer on the floor of the chamber whose liquid level 26 is below the lower ends of the depressions 24. When vaporized, the working fluid forms a vapor that rises to the upper regions of the chamber to contact the undersides 28 of the depressions 24. A wick structure 29 lines the interior wall surface of the chamber.
While the apparatus shown in
Changes in heating and cooling can be made more rapid by the interposition of controllable thermal couplings between the heating/cooling elements and the exterior surface of the vapor chamber. By “thermal coupling” is meant a substance or component that allows the passage of heat energy between the heating/cooling element(s) and the vapor chamber wall, and by “controllable thermal coupling” is meant a thermal coupling that can be switched at will from a high rate of heat flow to a low rate, and vice versa. Thus, when the apparatus is in a heating phase of a temperature cycle, a controllable thermal coupling at a heating element can be activated to a condition producing a high rate of heat transfer while the controllable thermal coupling at a cooling element is switched to a position in which the heat transfer rate is relatively low.
One means by which a controllable thermal coupling can be achieved is shown in
Another means of thermal coupling is shown in
A still further means is shown in
In the embodiment of
The structures shown in these Figures are merely illustrative; other examples and variations on the examples shown that utilize the central principles of a vapor chamber according to this invention will be readily apparent to those of skill in the art.
In the claims appended hereto, the term “a” or “an” is intended to mean “one or more.” The term “comprise” and variations thereof such as “comprises” and “comprising,” when preceding the recitation of a step or an element, are intended to mean that the addition of further steps or elements is optional and not excluded. All patents, patent applications, and other published reference materials cited in this specification are hereby incorporated herein by reference in their entirety. Any discrepancy between any reference material cited herein or any prior art in general and an explicit teaching of this specification is intended to be resolved in favor of the teaching in this specification. This includes any discrepancy between an art-understood definition of a word or phrase and a definition explicitly provided in this specification of the same word or phrase.
This application claims the benefit of U.S. Provisional Patent Application No. 61/483,439, filed May 6, 2011, the contents of which are incorporated herein by reference in their entirety.
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