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FIELD OF THE INVENTION
This invention relates to cuvettes in which reactions are undertaken in
liquids confined within the cuvette, and particularly those reactions
requiring carefully controlled temperatures and a rapid rate of heat
transfer to or from the cuvette.
BACKGROUND OF THE INVENTION
Although this invention is not limited to cuvettes used for nucleic acid
amplification, the background is described in the context of the latter,
as such amplification led to the invention.
Nucleic acid amplification generally proceeds via a particular protocol.
One useful protocol is that set forth in U.S. Pat. No. 4,683,195. Briefly,
that protocol features, in the case of DNA amplification, the following:
(1) A complete DNA double helix is optionally chemically excised, using an
appropriate restriction enzyme(s), to isolate the region of interest.
(2) A solution of the isolated nucleic acid portion (here, DNA) and
nucleotides is heated to and maintained at 92.degree.-95.degree. C. for a
length of time, e.g., no more than about 10 minutes, to denature the two
nucleic acid strands; i.e., cause them to unwind and separate and form a
template.
(3) The solution is then cooled through a 50.degree.-60.degree. C. zone to
cause a primer nucleic acid strand to anneal or "attach" to each of the
two template strands. To make sure this happens, the solution is held at
an appropriate temperature, such as about 55.degree. C. for about 15
seconds, in an "incubation" zone.
(4) The solution is then heated to and held at about 70.degree. C., to
cause an extension enzyme, preferably a thermostatable enzyme, to extend
the primer strand bound to the template strand by using the nucleotides
that are present.
(5) The completed new pair of strands is heated to 92.degree.-95.degree. C.
again, for about 10-15 seconds, to cause this pair to separate.
(6) Steps (3)-(5) are then repeated, a number of times until the
appropriate number of strands are obtained. The more repetitions, the
greater the number of multiples of the nucleic acid (here, DNA) that is
produced. Preferably the desired concentration of nucleic acid is reached
in a minimum amount of time.
A cuvette is usually used to hold the solution while it passes through the
aforementioned temperature stages. Depending upon the design given to the
cuvette, it can proceed more or less rapidly through the various stages. A
key aspect controlling this is the thermal transfer efficiency of the
cuvette--that is, its ability to transfer heat more or less
instantaneously to or from all of the liquid solution within the cuvette.
The disposition and the thermal resistance of the liquid solution itself
are usually the major aspects affecting the thermal transfer, since
portions of the liquid solution that are relatively far removed from the
heat source or sink, will take longer to reach the desired temperature.
The crudest and earliest type of cuvette used in the prior art is a test
tube, which has poor thermal transfer efficiency since (a) the walls of
the cuvette by being glass or plastic, do not transfer thermal energy
well, and (b) a cylinder of liquid has relatively poor thermal transfer
throughout the liquid. That is, not only does the liquid have low thermal
conductivity, but also a cylinder of liquid has a low surface to volume
ratio, that is, about 27 in.sup.-1 for a fill of about 100 .mu.l.
Still another problem in DNA amplification is the manner in which the
cuvette alows for ready removal of the liquid after reaction is complete.
A test tube configuration readily permits such removal. However,
modification of the cuvette to provide better thermal transfer efficiency
tends to reduce the liquid transferability. That is, a cuvette having
capillary spacing only, permits rapid heating of the contents. However,
the capillary spacing resists liquid removal.
RELATED APPLICATIONS
In commonly owned U.S. application Ser. No. 123,751 filed by Jeffrey L.
Helfer et al, entitled "Cuvette", there is disclosed a cuvette that solves
the aforementioned problems by providing for a thermal time constant for
the cuvette and water contained therein, that is no greater than about 10
seconds. That invention, however, did not account for the fact that
occasionally, the heating required for reactions in the cuvette generates
pressures that cause the thermal conductive wall of the cuvette to flex,
i.e., "dome" outward. Such flexing is unsatisfactory when it occurs, as it
can interfere with proper contact with the heating element. Such
interference, if it exists, reduces the rate at which thermal energy can
be transferred to or from the cuvette and thereby adversely affects the
thermal time constant of the fluid within the cuvette. Under the most
severe conditions, the "doming" effect can also cause the thermally
conductive wall to separate from the cuvette.
SUMMARY OF THE INVENTION
This invention provides a solution of the flexing problem noted above.
More specifically, this invention concerns a cuvette for controlled
reaction of components of a liquid involving cycling through temperatures
applied by a heater to the cuvette, the cuvette having a least one
liquid-confining chamber defined by two spaced-apart opposing walls each
providing a major surface of liquid contact; side walls connecting the two
opposing walls; and means permitting the introduction of liquid into, and
the removal of such liquid from, the chamber; one of the opposing walls
comprising a thermally conductive material as the sole structural
component, the thermal conductive material being exposed to the
environment to permit contact with an external heater or cooler. The
cuvette is improved in that the opposite one of the spaced-apart opposing
walls has a flexural strength that is sufficiently less than that of the
thermally conductive structural component, as to cause the opposite one of
the walls to flex under internal pressure, in lieu of the thermal
conductive structural component;
whereby the thermally conductive structural component substantially keeps
its initial shape and contact with the heater or cooler, when the cuvette
is applied to such heater/cooler.
Thus, it is an advantageous feature of the invention that a cuvette for
rapid thermal cycling is provided, featuring a heat transfer wall
sufficiently flexible as to flex under internal pressure, wherein means
are provided to prevent such flexing.
It is a related advantageous feature of the invention that such a cuvette
is provided wherein the wall opposite to the heat transfer wall is
deliberately constructed to undergo deformation to relieve internal
pressure, before the heat transfer wall becomes deformed.
Other advantageous features will become apparent upon reference to the
following detailed description of the preferred embodiments, when read in
light of the attached drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is an isometric view of a cuvette with respect to which the present
invention is an improvement;
FIG. 2 is a vertical section view taken generally along the mid-axis of the
cuvette of FIG. 1, and
FIG. 3 is a section view similar to that of FIG. 2, but illustrating the
invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The invention is described hereinafter for temperature cycling over a range
of at least about 35.degree. C., as is particularly useful in replicating
DNA strands. In addition, it is also useful for any kind of reaction of
liquid components and reagents that requires repetitive heating and
cooling of the cuvette within which the reaction is conducted. It is
further useful if the temperature range of cycling is more or less than
35.degree. C.
Orientations such as "up", "down", "above" and "below" are used with
respect to the cuvette as it is preferably used.
Turning first to FIGS. 1-2, a cuvette 30 is shown constructed as described
in the aforesaid commonly owned application. It comprises a
liquid-confining chamber 32 defined by two opposing walls 34 and 36, FIG.
2, spaced apart a distance t.sub.1. Such spacing is achieved by side walls
38 and 40, that join at opposite ends 42 and 44 of chamber 32. Most
preferably, the shape of side walls 38 and 40 is one of a gradual
concavity, so that they diverse at end 42, FIG. 1, at an angle of about
90.degree. C., and at a point halfway between ends 42 and 44, start to
reconverge again at an angle of about 90.degree.. Distance t.sub.1, FIG.
2, is selected such that such distance, when considered in light of the
shape of sidewalls 38 and 40, minimizes the quantity of liquid that is
retained in the cuvette upon removal of liquid. More specifically, that
distance is selected, given the shape shown for walls 38 and 40, so that
the capillary number (N.sub.ca) and the goucher number (N.sub.GO), both
standard terms known in the fluid management art, are each less than 0.05.
When so selected, momentum transfer particularly under a liquid-driven
transfer system, results in a majority removal of liquid from chamber 32.
Highly preferred values of t.sub.1 are between about 0.5 mm and about 2.5
mm.
Walls 34 and 36 provide the major surfaces in contact with the liquid. As
such, their surface area is selected such that, when considered in light
of the thickness of spacing t.sub.1, the surface-to-volume ratio for
chamber 32 is optimized for a high rate of thermal energy transfer. A
highly preferred example provides an exposed surface area of 2.4 cm.sup.2
(0.37 in.sup.2) for each of walls 34 and 36, with the surface from the
side walls providing a contact area of about 0.36 cm.sup.2. Most
preferably, therefore, the surface-to-volume ratio is between about 65
in.sup.-1 and about 130 in.sup.-1 for a fill volume of between 200 and 100
.mu.l, respectively.
Such a large fluid surface-to-volume ratio provides an advantage apart from
a rapid thermal energy transfer. It means that, for a given volume, a much
larger surface area is provided for coating reagents. This is particularly
important for reagents that have to be coated in separate locations on the
surface to prevent premature mixing, that is, mixing prior to injection of
liquid within the chamber. Also, the large reagent/fluid interface area
and short diffusion path provided by the large s/v ratio of the cuvette
provides rapid reagent dissolution without requiring external excitation
(such as shaking).
Therefore, one or more reagent layers (not shown) can be applied to the
interior surface of wall 36, in a form that will allow it to enter into a
reaction with liquid sample inserted into chamber 32. As used herein,
"layer" includes reagents applied as discrete dots.
A liquid access aperture 60 is formed in wall 36 adjacent end 42, FIG. 2.
The aperture has an upper portion 62 and a lower portion 64 that connects
the upper portion with chamber 32. Preferably at least portion 62 is
conical in shape, the slope of which allows a conical pipette P, FIG. 1,
to mate therewith.
At opposite end 44, an air vent 70 is provided, in a manner similar to that
described in U.S. Pat. No. 4,426,451. Most preferably, air vent 70 extends
into a passageway 72, FIG. 1, that is routed back to a point adjacent end
42, where it terminates in opening 74 adjacent access aperture 60.
To allow a single closure device to seal both the access aperture 60 and
opening 74 of the air vent, both of these are surrounded by a raised,
cylindrical boss 80. Any conventional closure mechanism is useful with
boss 80, for example, a stopper. Such stopper can have external threads
for engaging mating internal threads, not shown, on the boss, or it can be
constructed for a force fit within the boss 80.
The wall 34 opposite to wall 36 is the heat transfer wall, constructed with
a predetermined thermal path length and thermal resistance that will
provide a high rate of thermal energy transfer. Most preferably, such path
length (t.sub.2 in FIG. 2) is no greater than about 0.3 mm, and the
thermal resistance is no greater than about 0.01.degree. C./watt. These
properties are readily achieved by constructing wall 34 out of a thermally
conductive metal such as aluminum that is about 0.15 mm thick. Such
aluminum has a thermal resistance R, calculated as thickness
.chi..1/(conductivity K.surface area A), which is about 0.003.degree.
C./watt. (These values can be contrasted for ordinary glass of the same
thickness, which has a thermal resistance of about 0.24.degree. C./watt.)
Wall 34 can be secured to sidewalls 38 and 40 by any suitable means. One
such means is a layer 90, FIG. 2, which comprises for example a
conventional high temperature acrylic adhesive, and a conventional
polyester adhesive. Most preferably, layer 90 does not extend over the
surface area of wall 34, as such would greatly increase the thermal
resistance of wall 34, and possibly interfere with reactions desired
within chamber 32.
A cuvette constructed as described above for FIGS. 1-2, has been found to
produce a thermal time constant tau (.tau.) that is no greater than about
10 seconds. Most preferred are those in which .tau. is of the order of 3-8
seconds. When such a cuvette, filled with water, is heated along the
exterior of wall 34, and its temperature is measured at point Y, FIG. 2, a
thermal response curve is generated from 28.degree. C. to a final
temperature of 103.9.degree. C. The time it takes for the liquid therein
the reach a temperature of 76.degree. C. (the initial temperature of
28.degree. C. plus 63% of the difference (103.9-28)) is the value of tau
(.tau.). This derives (approximately) from the well-known thermal response
equation:
##EQU1##
Thus, if the time interval t in question equals tau, then e.sup.-t/.tau.
=e.sup.-1 .noteq.0.37. In such a case, T (t) (at t=tau) is the temperature
which is equal to the sum of the initial temperature plus 63% of (Final
Temperature - Initial Temperature).
For the above-described cuvette, tau is about 3.5 seconds, for the liquid
contained therein.
If the adhesive of layer 90 does extend over all the surface of wall 34,
then tau can be increased to as much as 7 or 8 sec.
A problem occasionally occurs with cuvette 30, particularly at the high
temperature end of the cycling. Pressure build-up occurs, due to thermal
expansion of fluids and air within the cuvette as well as the release of
gases dissolved in the liquid and the sealing of opening 60 as described
above. In the cuvette of FIG. 2, this causes wall 34 to tend to deform
outward, as indicated by the phantom line 34'. The outward deformation
creates a dome of thickness which prevents cuvette 30 from properly
resting on a flat heating element. That is, only a minor portion of
surface 34' remains in contact with the heating element. Such dome
formation thus reduces the rapid thermal transfer through wall 34 that is
desired.
In accord with the invention, FIG. 3, the aforementioned problems are
solved by a cuvette in which a part thereof, other than the thermally
conductive wall, becomes deformed to partially accommodate the pressure,
in order to maintain intimate contact between reaction vessel wall 34 and
the incubator. Parts similar to those previously described in FIGS. 1 and
2 bear the same reference numeral, to which the distinguishing suffix "a"
is appended.
Thus, cuvette 30a comprises opposite major walls 34a and 36a defining, with
side walls 40a (only one shown), a chamber 32a having a spacing t.sub.1.
These and the access aperture 60a and air vent 70a are generally
constructed as described above. To insure that wall 34a does not deform
under pressure, wall 36a is constructed to have a flexure strength that is
less than that of wall 34a. Specifically, this is preferably done as
follows: if wall 34a comprises aluminum that is about 0.15 mm thick, then
its flexure strength K at the center of flexure is determinable, based on
the following:
Deflection X is determined by the well-known equation
X=.alpha.Pa.sup.2 /Et.sup.3 (2)
where P=total applied load, E=plate modulus of elasticity, t=plate
thickness, and .alpha. is an empirical coefficient (usually equal to about
0.015). Rearranging,
P/X=Et.sup.3 /.alpha.a.sup.2. (3)
Because P/X is analogous to F/X which equals K (flexure strength), then
K.noteq.Et.sup.3 /.alpha.a.sup.2. (4)
This allows K to be calculated to be about 6.11.times.10.sup.6 dynes/mm.
For wall 36a to have a flexure strength less than that, for example a
value no greater than about 1.times.10.sup.6 dynes/mm, it need only
comprise a layer of polyethylene or polypropylene that is about 0.3 mm
thick (twice that of the aluminum wall 34a), to have a flexure strength of
about 8.3.times.10.sup.5 dynes/mm, calculated in the same manner. In such
a construction, wall 36a will dome upwardly as pressure, such as 12 psi,
is generated within chamber 32a, leaving wall 34a lying planar against the
heating element (shown in phantom as "E").
In use, the cuvette is filled to about point 44, FIG. 2, which provides a
fill of about 90%, with a liquid containing the desired sample for
reaction, for example, a solution of a DNA sequence that is to be
amplified. The device is then inserted into an appropriate incubator and
cycled through the necessary stages for the reaction.
Any suitable incubator is useful to cycle the cuvettes of this invention
through the desired heating and cooling stages. Most preferably, the
incubator provides stages that cycle through the temperatures described in
the "Background" above. A convenient incubator for doing this is described
in the aforesaid related application, the details of which are expressly
incorporated herein by reference. Preferably it is one having the
following stations: A preincubate station has heating means that delivers
a temperature of 95.degree. C. From there, the cuvette is pushed by
conventional pusher means onto a ring of constant temperature stations,
the first one of which is maintained at 55.degree. C. From this station
the cuvette is shuttled to the next adjacent, or second, station, which
heats it to 70.degree. C. This temperature is maintained for a period, and
accordingly the third station is also at that temperature. Next, a
short-time denaturing station (4th station) is encountered to denature the
newly replicated DNA, which station is maintained at 95.degree. C.
Stations 5-12 simply repeat twice more the cycles already provided by
stations 1 to 4. A moderate number of cycles through the incubator can
take place before the cuvette is removed. The number of cycles depends on
the concentration in the sample of the DNA sequence target desired to be
amplified, and the desired final concentration. After station no. 12, a
conventional transfer mechanism moves the cuvette off the ring for further
processing. (Both the injection of liquid into the cuvette and the removal
of liquid therefrom are done off-line, that is, outside of the incubator.)
The invention has been described in detail with particular reference to
preferred embodiments thereof, but it will be understood that variations
and modifications can be effected within the spirit and scope of the
invention.
* * * * *
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