AU2007284995A2 - Self-exciting, self-sensing piezoelectric cantilever sensor for detection of airborne analytes directly in air - Google Patents
Self-exciting, self-sensing piezoelectric cantilever sensor for detection of airborne analytes directly in air Download PDFInfo
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- AU2007284995A2 AU2007284995A2 AU2007284995A AU2007284995A AU2007284995A2 AU 2007284995 A2 AU2007284995 A2 AU 2007284995A2 AU 2007284995 A AU2007284995 A AU 2007284995A AU 2007284995 A AU2007284995 A AU 2007284995A AU 2007284995 A2 AU2007284995 A2 AU 2007284995A2
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Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
- G01N29/02—Analysing fluids
- G01N29/022—Fluid sensors based on microsensors, e.g. quartz crystal-microbalance [QCM], surface acoustic wave [SAW] devices, tuning forks, cantilevers, flexural plate wave [FPW] devices
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N29/00—Investigating or analysing materials by the use of ultrasonic, sonic or infrasonic waves; Visualisation of the interior of objects by transmitting ultrasonic or sonic waves through the object
- G01N29/02—Analysing fluids
- G01N29/036—Analysing fluids by measuring frequency or resonance of acoustic waves
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2291/00—Indexing codes associated with group G01N29/00
- G01N2291/02—Indexing codes associated with the analysed material
- G01N2291/025—Change of phase or condition
- G01N2291/0255—(Bio)chemical reactions, e.g. on biosensors
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- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
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- G01N2291/02—Indexing codes associated with the analysed material
- G01N2291/025—Change of phase or condition
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- G—PHYSICS
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- G01N2291/00—Indexing codes associated with group G01N29/00
- G01N2291/04—Wave modes and trajectories
- G01N2291/042—Wave modes
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- G—PHYSICS
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- G01N2291/00—Indexing codes associated with group G01N29/00
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- G01N2291/042—Wave modes
- G01N2291/0427—Flexural waves, plate waves, e.g. Lamb waves, tuning fork, cantilever
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- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- General Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
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Description
WO 2008/020903 WO 2008020903PC TIUS200 7/0 11402 SELF-EXCITING, SELF-SENSING PIEZOELECTRIC CANTILEVER SENSOR FOR DETECTION OF AIRBORNE ANALYTES DIRECTLY IN AIR CROSS REFERENCE TO RELATED APPLICATIONS [0001] The present application claims priority to U.S. Application No. 11/625,919, filed January 23, 2007, entitled "Self-Exciting, Self-Sensing Piezoelectric Cantilever Sensor", which is hereby incorporated by reference in its entirety. U.S. Application No. 11/625,919 claims priority to U.S. Provisional Patent Application No. 60/76 1,172, entitled "PIEZOELECTRIC CANTILEVER SENSORS," filed January 23, 2006, and U.S. Provisional Patent Application No. 60/807,020, entitled "PIEZOELECTRIC CANTILEVER SENSORS," filed July 11, 2006, both of which are hereby incorporated by reference in their entirety. The present application also claims priority to U. S. Provisional Patent Application No. 60/746,95 1, entitled "Detection of Airborne Pathogens Directly in Air," filed May 10, 2006, which is hereby incorporated by reference in its entirety.
TECHNICAL FIELD [0002] The technical field generally relates to sensors, and more specifically relates to piezoelectric cantilever sensors and to detecting and measuring analytes utilizing a piezoelectric cantilever sensor.
BACKGROUND
[0003] Cantilever sensors can be broadly divided into two categories, depending upbn dimensions of the sensor: micro-cantilevers and macro-cantilevers. Micro-cantilever sensors can be utilized in both static (bending) mode and dynamic (resonance) mode. In static mode, the deformation of the cantilever arm is measured to determine if an analyte (substance under analysis) is present. In dynamic mode, a resonance frequency is measured to determine if an analyte is present. Macro-cantilever sensors typically are not utilized in the static mode because bending of the cantilever arm is often limited. Macro-cantilever sensors can be utilized under liquid imumersion conditions or in a gas or vacuum. Typically, greater sensitivity is achievable 1- WO 2008/020903 WO 208/00903PCT/US2007!01 1402 when a cantilever sensor is utilized in a gas/vacuum than in a liquid. Liquid dampening tends to adversely affect sensitivity. However, measuring analytes in liquid medium has many practical applications.
[00041 One type of known micro-cantilever sensor is a silicon-based micro-cantilever sensor. A typical silicon-based micro-cantilever sensor comprises a micro-cantilever that acts as a resonator. The micro-cantilever is driven by an external actuator at the base of the microcantilever to generate vibrations in the resonator. Typically, the vibrations are detected by an external optical detector. One disadvantage of typical silicon-based micro-cantilevers is the complex external optical components required for detection. Further, optical detection means disadvantageously limit application of the micro-cantilever sensor to optically clear samples.
Another disadvantage is the weight and complexity added to the sensor due to the external actuator. Yet another disadvantage is that the external actuator can be located only at the base of the micro-cantilever, which limits its effectiveness in driving the cantilever's vibration. A further disadvantage of silicon-based micro-cantilever sensors is that they are mechanically fragile. Thus, silicon-based micro-cantilever sensors can not be used in high liquid flow rate environments. Further, typical silicon-based micro-cantilever sensors lose detection sensitivity in liquid media due to viscous damping.
[0005] Another type of know~n cantilever sensor is a quartz-based piezoelectric cantilever sensor. Quartz is a weak piezoelectric, and thus, much like silicon-based cantilever sensors, quartz-based piezoelectric cantilever sensors lose detection sensitivity in liquid media due to viscous damping. Further, the detection sensitivity of quartz-based sensors is limited by the planar geometry of the sensor.
[0006] Conventional piezoelectric cantilevers are known to be fabricated with a piezoelectric layer attached to a non-piezoelectric layer over part or the entire surface of the piezoelectric layer. In some conventional piezoelectric cantilevers, the piezoelectric layer is fixed at one end so that when the piezoelectric material is excited, the non-piezoelectric layer flexes to accommodate the strain caused in the piezoelectric material. When the frequency of excitation is the same as the natural frequency of the underlying mechanical structure, resonance occurs. This type of piezo electric cantilever sensor is known to operate at frequencies lower than about 100 kI~z at millimeter size. Currently, higher frequencies are obtainable only by making the cantilever sensor very short (less than 1.0 mm in length), very narrow (less than 0. 1 mm. in width), and very thin (less than 100 microns in thickness). However, reducing the dimensions of WO 2008/020903 PCT/US2007/011402 the cantilever sensor, particularly the width, thusly, makes the cantilever senor less usable in a liquid medium due to viscous damping. Damping increases inversely with square of cantilever width.
[0007] Most current bio-sensing technologies rely on fluorescence, lasers, fiber-opticsbased methods, quartz crystal microbalance technology, electrochemical enzyme immunoassays, and/or binding to metal particles. Most of these techniques are neither direct, nor quantitative.
Many of these techniques are also quite slow. In addition, most of the aforementioned techniques do not lend themselves to measurement of changes in mass, which may provide a convenient way to measure a variety of different parameters.
10008] A mass sensor based on resonance frequency requires three components, an actuator (driver), a resonator, and a detector. One example of a mass sensor is a silicon-based micro-cantilever, which can be easily integrated with existing silicon based methodologies. In a silicon-based micro-cantilever mass sensor, the micro-cantilever acts as the resonator and is driven by an external lead zirconate titanate (PZT) actuator at the base of the micro-cantilever to generate vibrations in the resonator, which may be detected by an external optical detector. For bio-detection, receptors are immobilized on the cantilever surface. Binding of antigens to the receptors immobilized on the cantilever surface increases the cantilever mass and causes a decrease in the resonance frequency. Detection of target molecules is achieved by monitoring the mechanical resonance frequency. In spite of the popularity of silicon-based micro-cantilevers, they rely on complex external optical components for detection. In addition, the PZT vibration driver adds to the weight and complexity of the sensor. Further, the external actuator can only be located at the base of the micro-cantilever, which greatly limits its effectiveness in driving the cantilever's vibration. The optical detection means also limits the application to optically clear.
samples.
[0009) In addition to mass detection, silicon-based micro-cantilevers have also been used as sensors for small molecules by detecting the stress generated on the cantilever by the adsorption of species onto receptors associated with the cantilever. Antibody or DNA receptors are coated on the surface of the micro-cantilevers to bind target biological molecules. The stress generated at the time of binding or unbinding of the target molecules to the receptors on the micro-cantilever surface induces a deflection of the micro-cantilever that may be detected by external optical components or by an adsorption-stress-induced DC voltage on a piezo-resistive coating layer on the cantilever surface.
[0010] Compared to silicon-based sensors, piezoelectric millimeter-sized cantilever sensors are not as bulky and complex. Piezoelectric devices are excellent transduction -3- WO 2008/020903 PCTiUS2007/011402 candidates because of their short response times and high piezoelectric coefficients. Because they are piezoelectric, both the driving and sensing of the mechanical resonance can be conveniently done electrically within the resonator. Currently, piezoelectric biosensors are based on commercially available quartz crystal microbalances (QCM), a disk device that uses thicknessmode resonance for sensing. Although quartz is a weak piezoelectric material, it is widely used as a layer thickness monitor in part due to the availability of large quartz single crystals to make the membranes. The typical mass detection sensitivity of a 5 MHz QCM that has a minimum detectable mass density (DMD) of 10- 9 g/cm 2 is about 10-8 g/Hz, about four orders of magnitude less sensitive than millimeter sized piezoelectric cantilevers.
10011] Microcantilevers exist that are about 100 microns length, a few tens of microns wide, and a few microns thick. Such microcantilevers are used in bending or in resonance mode for detection. The disadvantage of these microcantilevers is that their resonance characteristics are very strongly diminished due to viscous damping. Further, their use in liquid media has been accomplished at very low flow rates of microliters/min.
[0012] D. W. Carr and H. G. Craighead, "Fabrication of nanoelectromechanical systems in single crystal silicon using silicon on insulator substrates and electron beam lithography," vac. Sci. Technology. 15(6), 1997. pp 2760-2763, discloses the fabrication of beam sensors and multiple beam sensors in a mesh configuration of the order of a few hundred nanometers, and have achieved high resonant frequencies of 40 MHz. Copending US Application No. 11/659,919, filed January 23, 2007, entitled, "Self-Exciting, Self-Sensing Piezoelectric Cantilever Sensor" was co-invented by the present inventor and discusses the architecture and basic operation of millimeter sized piezoelectric-excited cantilever sensors in a liquid sample environment.
[0013] Therefore, there exists a need to improve the sensing capabilities of existing sensors and a need for the provision of sensors with an improved ability to perform detection of airborne species.
SUMMARY
[0014] A self-exciting and self-sensing piezoelectric cantilever sensing apparatus includes a piezoelectric layer and a non-piezoelectric layer attached to the piezoelectric layer such that a distal end of the non-piezoelectric layer extends beyond a distal end of the piezoelectric layer or a distal end of the piezoelectric layer extends beyond a distal end of the non-piezoelectric layer. That is, the piezoelectric layer is coupled to the non-piezoelectric layer such that the piezoelectric layer and the non-piezoelectric layer are not coextensive In various -4- WO 2008/020903 PCT/US2007/011402 configurations of the piezoelectric cantilever sensing apparatus, the piezoelectric layer, the nonpiezoelectric layer, or both are anchored to at least one base. Electrodes are operatively associated with the piezoelectric layer. The self-exciting, self-sensing piezoelectric cantilever sensor is utilized to sense mass change. To determine the mass of an analyte on the sensing apparatus, the resonance frequency of the mechanical member of the cantilever sensor is measured. The measured resonance frequency is compared with a baseline resonance frequency to determine a difference in frequency. The difference in frequency is indicative of a mass of an analyte on the sensing apparatus.
[0015] According to embodiments of the invention, detection of airborne pathogens in air, is accomplished without requiring sample collection in liquid or solid matrices. According to a one aspect, a method for airborne detection of target analytes, such as biological or chemical substance, is accomplished by exposing a sensing apparatus to the airborne analyte. A recognition entity, located on the sensing apparatus, binds to the analyte and is detectable while the analyte is present in a gas. Specific example recognition entities include chemical coatings for the detection of chemicals and immobilized antibodies for the detection of biologicals.
[0016] In one aspect of the invention, a sensing apparatus includes a sensor that includes a piezoelectric layer; a non-piezoelectric layer and a recognition entity located on either of the two layers. In a first embodiment, the sensor is a cantilever assembly that is fixed at only one end. Here, the piezoelectric layer is connected to a base and the non-piezoelectric layer is attached to the end of the piezoelectric layer in an overlap fashion. Electrodes are attached to the piezoelectric layer and are electrically driven to excite the piezoelectric layer to resonance. A recognition region on the non-piezoelectric layer attracts the analyte when exposed in a airflow and causes a change in mass of the cantilever that is formed by the combination of the piezoelectric and non-piezoelectric layers and the recognition area. The change in resonant frequency when the analyte is attached compared to a baseline resonant frequency is determined and the frequency shift is indicative of the amount of analyte held on the recognition entity.
[0017] The formation of the sensor may be changed to accommodate different frequency detection points. A second type of sensor involves the use of a beam type of sensor where the non-piezoelectric layer is attached to a base structure on both ends. The piezoelectric layer is placed on the non-piezoelectric layer and excited to resonance as mentioned above. A recognition entity on either of the non-piezoelectric or piezoelectric layers causes a mass change upon exposure to an aerosolized analyte and results in a frequency shift of the resonant frequency of the beam sensor. Thus, an analyte can be detected and its mass determined. A third WO 2008/020903 PCTiUS2007/011402 type of sensor is a variation of the beam sensor where the piezoelectric layer is the beam and the non-piezoelectric layer is attached onto the top of the beam.
[00181 An apparatus to detect airborne analytes includes an exposure tube containing a cantilever sensor attached to a nebulizer which aerosolizes the analyte so that the analyte exists in an airflow across the sensor. An analyzer measures the resonant frequency of the sensor and determines if and how much of the analyte is present in the airflow.
[0019] These and various other advantages and features of novelty that characterize the invention are pointed out with particularity in the claims annexed hereto and forming a part hereof. However, for a better understanding of the invention, its advantages, and the objects obtained by its use, reference should be made to the drawings which form a further part hereof, and to the accompanying descriptive matter, in which there is illustrated and described a preferred embodiment of the invention.
[0020] This Summary is provided to introduce a selection of concepts in a simplified form that are further described below in the Detailed Description. This Summary is not intended to identify key features or essential features of the claimed subject matter, nor is it intended to be used to limit the scope of the claimed subject matter.
BRIEF DESCRIPTION OF TBE DRAWINGS [0021] The foregoing summary, as well as the following detailed description, is better understood when read in conjunction with the appended drawings. For the purpose of illustrating a self-exciting, self-sensing piezoelectric cantilever sensor, there is shown in the drawings exemplary constructions thereof; however, a self-exciting, self-sensing piezoelectric cantilever sensor is not limited to the specific methods and instrumentalities disclosed. In the drawings: Figure 1 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor; Figure 2 is a cross-sectional view of an example self-exciting, self-sensing piezoelectric cantilever sensor depicting electrode placement regions for electrodes operationally associated with the piezoelectric layer; Figure 3 is a cross-sectional view of an example self-exciting, self-sensing piezoelectric cantilever sensor showing depicting example electrode placement within a base portion of the self-exciting, self-sensing piezoelectric cantilever sensor; -6- WO 2008/020903 PCTiUS2007/011402 Figure 4 is a cross-sectional view of an example self-exciting, self-sensing piezoelectric cantilever sensor showing depicting example electrode placement not within a base portion of the self-exciting, self-sensing piezoelectric cantilever sensor; Figure 5 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor wherein the distal end of the piezoelectric layer is flush with the distal end of the non-piezoelectric layer; Figure 6 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor wherein the distal end of the piezoelectric layer extends beyond the distal end of the non-piezoelectric layer and the proximate end of the piezoelectric layer extends beyond the proximate end of the non-piezoelectric layer; Figure 7 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor having two base portions; Figure 8 is an illustration of another example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor, wherein the piezoelectric layer is not attached to either base portion; Figure 9 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor having the piezoelectric layer anchored at two ends; Figure 10 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor wherein the piezoelectric layer comprises two portions, one of which is anchored; Figure 11 is another illustration of an example configuration of a self-exciting, selfsensing piezoelectric cantilever sensor wherein the piezoelectric layer comprises two portions, one of which is anchored; Figure 12 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor wherein the piezoelectric layer comprises two portions, neither which is anchored; WO 2008/020903 PCT/US2007/011402 Figure 13 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor having an anchored non-piezoelectric portion and a non-anchored piezoelectric portion Figure 14 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor, wherein the non-piezoelectric layer is not attached to either base portion; Figure 15 is illustration of another example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor wherein the piezoelectric portion has a different width than the piezoelectric portion; Figure 16 is an illustration of an example configuration of a self-exciting, self-sensing piezoelectric cantilever sensor comprising a piezoelectric layer and a non-piezoelectric layer, wherein the width, of the piezoelectric layer is less than the width of the non-piezoelectric layer 16, and the distal end of the piezoelectric layer extends beyond the distal end of the nonpiezoelectric layer and the proximate end of the piezoelectric layer extends beyond the proximate end of the non-piezoelectric layer; Figure 17 is a flow diagram of an example process for detecting an analyte utilizing the self-exciting, self-sensing piezoelectric cantilever sensor; Figure 18 is a plot of an example resonance spectrum of the configuration of the selfexciting, self-sensing piezoelectric cantilever sensor depicted in Figure 1, operated in air; Figure 19A shows a perspective view of a piezoelectric cantilever sensor useful in the methods of the present invention; Figure 19B shows an embodiment of an anchored piezoelectric-excited cantilever beam sensor useful in the methods of the present invention; Figure 19C shows an embodiment of a free-floating piezoelectric-excited cantilever beam sensor useful in the methods of the present invention; Figure 19D shows an embodiment of an anchored bimorph piezoelectric-excited cantilever beam sensor useful in the methods of the present invention; WO 2008/020903 PCT/US2007/011402 Figure 19E shows an embodiment of an overhang piezoelectric-excited cantilever beam sensor useful in the methods of the present invention; Figure 19F shows an embodiment of an anchored lead zirconate titanate (PZT) piezoelectric-excited cantilever beam sensor useful in the methods of the present invention; Figure 190 shows a schematic of an embodiment of a free-floating tip PEMC (ftPEMC) sensor in accordance with the present invention; Figure 20 is a resonance spectrum, in air, of a first embodiment of an overhang piezoelectric cantilever sensor, such as that shown in Figure 1 (see oPEMC#1 from Table 1 of Figure 47); Figure 21 is a resonance spectrum, in air, of a second embodiment of an overhang piezoelectric cantilever sensor shown in Figure 1 (see oPEMC#2 from Table 1 of Figure 47); Figure 22 is a resonance spectrum, in air, of a third embodiment of an overhang piezoelectric cantilever sensor shown in Figure 1 (see oPEMC#3 from Table 1 of Figure 47); Figure 23 is a resonance spectrum of a fourth embodiment of an overhang cantilever sensor as shown in Figure 1 (see oPEMC#4 from Table 1 of Figure 47); Figure 24 is a resonance spectrum of a fifth embodiment of an overhang cantilever sensor as shown in Figure 1 (see oPEMC#5 from Table 1 of Figure 47); Figure 25 shows a resonance spectrum plot of phase angle versus excitation frequency, in air of the anchored PEMCB sensor (aPEMCB, Figure 19B) excited at 1OOmV; Figure 26 shows the resonance characteristics of the free-floating PEMCB (fPEMCB#1, Figure 19C) sensor in air, using a plot of phase angle versus excitation frequency, at an excitation voltage of 100mV; WO 2008/020903 PCT/US2007/011402 Figure 27 shows a resonance spectrum of the anchored bimorph PEMCB (abPEMCB#1, Figure 19D) sensor in air, using a plot of phase angle versus excitation frequency, at an excitation voltage of 100mV; Figure 28 shows the resonance spectrum of an overhang PEMCB (oPEMCB#1), Figure 19E) sensor in air excited at a voltage of 100mV; Figures 11A-B show an apparatus used to implement airborne Bacillus anthracis detection; Figure 30A shows the results of detection experiments for detection of Bacillus anthracis in air; Figure 30B shows the results of detection experiments for detection of Bacillus anthracis in air with a control of inorganic particles; Figure 31 shows detection confirmation for the experiments of Figure Figure 33 shows a scanning electron micrograph of a sensor tested in accordance with the method of the present invention showing anthrax spores immobilized on the surface of the sensor; Figure 33 depicts a humidity infuser aspect of the present invention; Figure 34 is a flow diagram of a method of the present invention; Figure 35 is a notched configuration for a sensor; Figure 36 is a sandwiched configuration for a sensor; Figure 37 is an alternative sandwiched configuration for a sensor; Figure 38 is an alternative to Figure 19A for a sensor geometry; WO 2008/020903 PCT/US2007/011402 Figure 39 is another alternative configuration for Figure 19A of a sensor; Figure 40 is beam type configuration of Figure 19F; Figure 41 is an alternative configuration of Figure 19E; Figure 42 is an alternative configuration of Figure 19G; Figure 43 is an alternative configuration of Figure 42; Figure 44 is an alternative configuration of Figure 36; Figure 45 is a multiple layered sensor configuration where the layers are at least partially anchored in a base; Figure 46 is a configuration having an modified base; Figure 47 includes Table 1; Figure 48 includes Table 2; Figure 49 includes Table 3; and Figure 50 includes Table 4.
DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS [0022] A self-exciting, self-sensing piezoelectric cantilever sensor as described herein provides the ability to detect and measure extremely small amounts of an analyte. The selfexciting, self-sensing piezoelectric cantilever sensor can be utilized to detect and measure an analyte immersed in a liquid and an analyte contained in a gas or vacuum. In various example configurations, the self-exciting, self-sensing piezoelectric cantilever sensor comprises at least one piezoelectric layer and at least one non-piezoelectric layer, wherein the piezoelectric layer is coupled to the non-piezoelectric layer such that the piezoelectric layer and the non-piezoelectric layer are not coextensive. The piezoelectric layer, the non-piezoelectric layer, or both can be -11- WO 2008/020903 PCT/US2007/011402 coupled to at least one base. The piezoelectric layer and the non-piezoelectric layer can be of varying widths, lengths, and thicknesses.
[0023] The self-exciting, self-sensing piezoelectric cantilever sensor is utilizable to determine the mass of an analyte accumulated thereon. In an example embodiment, a portion of the self-exciting, self-sensing piezoelectric cantilever sensor is placed in a medium liquid, gas, vacuum). While in the medium, a resonance frequency of the self-exciting, self-sensing piezoelectric cantilever sensor is measured and compared to a baseline resonance frequency.
The difference in the measured resonance frequency and the baseline resonance frequency is indicative of an amount of mass of analyte accumulated bound, adsorbed, absorbed) on the self-exciting, self-sensing piezoelectric cantilever sensor.
[00241 Analytes can be directly or indirectly bound to the surface of the nonpiezoelectric portion of the self-exciting, self-sensing piezoelectric cantilever sensor. Binding of an analyte to the non-piezoelectric portion of the self-exciting, self-sensing piezoelectric cantilever sensor results in a change in mass of the self-exciting, self-sensing piezoelectric cantilever sensor, a change in stiffness of the self-exciting, self-sensing piezoelectric cantilever sensor, or a combination thereof. The changes in mass and/or stiffness are measurable as changes in resonance frequency, and can be monitored and measured by an appropriate analysis device, such as an operational amplifier, an impedance analyzer, a network analyzer, an oscillator circuit, or the like, for example. Resonance frequency changes, wherein at least a portion of the self-exciting, self-sensing piezoelectric cantilever sensor is immersed in a liquid, are detectable and measurable. Resonance frequency changes, wherein at least a portion of the self-exciting, self-sensing piezoelectric cantilever sensor is immersed in a gas or a vacuum, also are detectable and measurable.
[0025] The self-exciting, self-sensing piezoelectric cantilever sensor is operateable at high frequencies, such as, on the order of 0.1 MHz. to 6 MHz, for example. At these high frequencies, a Q factor (the ratio of the resonance peak frequency relative to the resonance peak width at half peak height), on the order of 10 to 100, under liquid immersion is obtainable. The self-exciting, self-sensing piezoelectric cantilever sensor is operateable at relative high frequencies in liquid media, gas media, and a vacuum. The self-exciting, self-sensing piezoelectric cantilever sensor thus provides extreme sensitivity to mass changes. The selfexciting, self-sensing piezoelectric cantilever sensor is especially suitable for analytes that are -12- WO 2008/020903 PCT/US2007/011402 present at very low concentrations in media such as in body fluids, water, and food materials, for example.
[0026] The self-exciting, self-sensing piezoelectric cantilever sensor described herein provides the ability to detect changes in mass accumulated thereon as small as 100 attogram/Hz (100x10 18 grams/Hertz) or less when immersed in a liquid media. Thus, with respect to detecting changes in mass, the self-exciting, self-sensing piezoelectric cantilever sensor is approximately 1 million times more sensitive than a quartz crystal micro-cantilever sensor, approximate 100,000 times more sensitive than standard analytical instruments, and about 10,000 times more sensitive than conventional, three-layer piezoelectric cantilever designs.
[0027] The self-exciting, self-sensing piezoelectric cantilever sensor permits detection of extremely small concentrations of analyte that bind to the non-piezoelectric portion thereof.
Utilizing the self-exciting, self-sensing piezoelectric cantilever sensor, pathogens and proteins are detectable at concentrations as low as a few pathogens/mL and, for proteins of average size kilo-Daltons, kDa), at less than 1 pathogen/mL. Furthermore, any analyte that binds to an organic or inorganic functional group on the non-piezoelectric portion is detectable. The selfexciting, self-sensing piezoelectric cantilever sensor is operable in media having relatively high flow rates. The piezoelectric cantilevers sensors is operable in media having flow rates of 0.5 to 10.0 mL/minute, which is approximately 1000 times the flow rate used successfully with known bending mode micro-cantilevers.
[0028] Various example applications of the piezoelectric cantilever include the detection of bioterrorism agents, such as Bacillus anthracis, the detection of food-borne pathogens, such as E. coli, the detection of pathogens in food and water, the detection of certain cell types in body fluids circulating tumor cells), the detection ofbiomarkers in body fluids proteins that mark specific pathophysiology- alpha-fetoprotein, beta-2-microglobulin, bladder tumor antigen, breast cancer marker CA-15-3, and other CAs (cancer antigens), calcitonin, carcinoembryonic antigen, and others), the detection of markers of explosives such as trinitrotoluene, the presence of dinitrotoluene, and the detection of airborne and waterborne toxins. The self-exciting, self-sensing piezoelectric cantilever sensor also can be used for the detection of biological entities at picogram levels, and for the detection of protein-protein interactions, both steady state and kinetic.
[0029] Pathogens, such as E-coli for example, are detectable utilizing the self-exciting, self-sensing piezoelectric cantilever sensor. Detection of a model protein, lipoprotein, DNA, -13- WO 2008/020903 PCTiUS2007/011402 and/or RNA at a concentration 1.0 fcmtogram per mL (10- 15 grams) and pathogens at 1 pathogen/mL, respectively is achievable by measuring directly in liquid using the self-exciting, self-sensing piezoelectric cantilever sensor immobilized with antibodies specific to the target analyte at a frequency of about 1 to 2 MHz. The self-exciting, self-sensing piezoelectric cantilever sensor is capable of detecting a target analyte without false positives or negatives even when contaminating entities are present. The self-exciting, self-sensing piezoelectric cantilever sensor described herein is particularly advantageous when utilized with a raw sample, and no preparation, concentrating step, and/or enrichment of any type. Detection of an analyte utilizing the self-exciting, self-sensing piezoelectric cantilever sensor can be conducted directly in raw samples under flow conditions, such as 0.5 to 10.0 mL/minute for example. If clean samples are available, such as in a laboratory environment, detection at 1 femtogram/mL is achievable. This sensitivity is approximately 100 times more sensitive than the sensitivity associated with known optical techniques.
[0030] As described below, the sensitivity of the self-exciting, self-sensing piezoelectric cantilever sensor is due in part to the geometric design thereof. The relative lengths and widths of the piezoelectric and non-piezoelectric layers of the self-exciting, self-sensing piezoelectric cantilever sensor determine the sensitivity, and also the shape of the peak of the frequency spectrum provided by the self-exciting, self-sensing piezoelectric cantilever sensor.
As described in more detail below, the self-exciting, self-sensing piezoelectric cantilever sensor comprises a piezoelectric layer and a non-piezoelectric layer coupled together such that a portion of the piezoelectric layer extends beyond the non-piezoelectric layer, or a portion of the nonpiezoelectric layer extends beyond the piezoelectric layer, or a combination thereof. Thus, the piezoelectric layer and the non-piezoelectric layer are not coextensive. That is, the self-exciting, self-sensing piezoelectric cantilever sensor is configured such that an entire surface of the nonpiezoelectric layer is not coupled to an entire surface of the piezoelectric layer.
[0031] The sensitivity of the self-exciting, self-sensing piezoelectric cantilever sensor is due in part to utilizing the piezoelectric layer of the cantilever sensor for both actuation and sensing and the electromechanical properties of the piezoelectric layer of the self-exciting, selfsensing piezoelectric cantilever sensor. At resonance, the oscillating cantilever concentrates stress in the piezoelectric layer toward a base portion of the self-exciting, self-sensing piezoelectric cantilever. This results in an amplified change in the resistive component of the piezoelectric layer, and a large shift in resonance frequency. Directing this stress to a portion of the piezoelectric layer having a low bending modulus more flexible) allows for exploitation -14- WO 2008/020903 PCTiUS2007/011402 of the associated shift in resonance frequency to detect extremely small changes in mass of the self-exciting, self-sensing piezoelectric cantilever sensor. For example, if both the piezoelectric layer and the non-piezoelectric layer of a piezoelectric cantilever sensor are anchored at the same end potted in epoxy), the sensor is less sensitive to changes in mass because the bending stress in the sensing piezoelectric layer proximal to the anchored end is lower compared to the case when only the piezoelectric layer is anchored. This is because the bending modulus of the two combined layers is higher than the case of anchoring the piezoelectric layer only. Bending modulus is the product of elastic modulus and moment of inertia about the neutral axis. And, moment of inertia is proportional to the cube power of thickness.
[0032] Figure 1 is an illustration of a self-exciting, self-sensing piezoelectric cantilever sensor 12 comprising a piezoelectric portion 14 and a non-piezoelectric portion 16. Piezoelectric portions are labeled with an uppercase letter p and non-piezoelectric portions are labeled with the uppercase letters np The self-exciting, self-sensing piezoelectric cantilever sensor 12 depicts an embodiment of an unanchored, overhang, self-exciting, self-sensing piezoelectric cantilever sensor. The self-exciting, self-sensing piezoelectric cantilever sensor 12 is termed "unanchored" because the non-piezoelectric layer 16 is not attached to the base portion The self-exciting, self-sensing piezoelectric cantilever sensor 12 is termed, "overhang" because the non-piezoelectric layer 16 extends beyond the distal tip 24 of the piezoelectric layer 14 to create an overhanging portion 22 of the non-piezoelectric layer 16. The piezoelectric portion 14 is coupled to the non-piezoelectric portion 16 via adhesive portion 18. The piezoelectric portion 14 and the non-piezoelectric portion overlap at region 23. The adhesive portion 18 is positioned between the overlapping portions of the piezoelectric portion 14 and the non-piezoelectric portion 16. The piezoelectric portion 14 is coupled to a base portion [0033] The piezoelectric portion 14 can comprise any appropriate material such as lead zirconate titanate, lead magnesium niobate-lead titanate solid solutions, strontium lead titanate, quartz silica, piezoelectric ceramic lead zirconate and titanate (PZT), piezoceramic-polymer fiber composites, or the like, for example. The non-piezoelectric portion 16 can comprise any appropriate material such as glass, ceramics, metals, polymers and composites of one or more of ceramics, and polymers, such as silicon dioxide, copper, stainless steel, titanium, or the like, for example.
[0034] The self-exciting, self-sensing piezoelectric cantilever sensor can comprise portions having any appropriate combination of dimensions. Further, physical dimensions can WO 2008/020903 WO 2081020903PCTiUS2007O1 1402 be non-uniform. Thus, the piezoelectric layer and/or the non-piezoelcotric layer can be tapered.
For example, the length Lp in Figure 1) of the piezoelectric portion piezoelectric portion 14) can range from about 0. 1 to about 10 mm. The length LNp in Figure 1) of the non-piezoelectric portion non-piezoelectric portion 16) can range from about 0. 1 to about mm. The overlap region overlap -region 23) can range from about 0. 1 to about 10 mun in length. The width Wp in Figure 1) of the piezoelectric portion piezoelectric portion 14), and the width WNp in Figure 1) of the non-piezoelectric portion non-piezoelectric portion 16), can range from about 0.1 nun to about 4.0 num. The width Wp in Figure 1) of the piezoelectric portion can differ from the width WNP in Figure 1) of the nonpiezoelectric portion as well. The thickness of the Tp in Figure 1) of the piezoelectric portion piezoelectric portion 14), and the thickness TNP in Figure 1) of the nonpiezoelectric portion non-piezoelectric portion 16), can range from about 0. 1 mun to about mim. The thickness Tp in Figure 1) of the piezoelectric portion also can differ from the thickness TNp in Figure 1) of the non-piezoelectric portion.
[00351 Figure 2 is a cross-sectional view of the self-exciting, self-sensing piezoelectric cantilever sensor 12 depicting electrode placement regions 26 for electrodes operationally associated with the piezoelectric portion 14. Electrodes can be placed at any appropriate location on the piezoelectric portion of the self-exciting, self-sensing piezoelectric cantilever sensor as indicated by brackets 26. For example, as shown in Figure 3, electrodes 28 can be coupled to the piezoelectric portion 14 within the base portion 20. Or, as depicted in Figure 4, electrodes 32 can be coupled to the piezoelectric portion 14 at any location not within the base portion 20 and not overlapped by the non-piezoelectric portion 16. Electrodes need not be placed symmetrically about the piezoelectric portion 14. In an example embodiment, one electrode can be coupled to the piezoelectric portion 14 within the base portion 20 and the other electrode can be coupled to the piezoelectric portion 14 not within the base portion 20. Electrodes, or any appropriate means inductive means, wireless means), can be utilized to provide an electrical signal to and receive an electrical signal from the piezoelectric portion 14. In an example embodiment, electrodes can be coupled to the piezoelectric portion 14 via a bonding pad or the like (depicted as elements 30 in Figure 3 and elements 34 in Figure Example bonding pads can comprise any appropriate material gold, silicon oxide) capable of immobilization of.a receptor material and/or an absorbent material appropriate for use in chemical sensing or for bio-sensing.
[00361 Electrodes can be placed at any appropriate location. In an example embodiment, electrodes are operatively located near a location of concentrated stress in the 16 WO 2008/020903 WO 2081020903PCTiUS2007O1 1402 piezoelectric layer 14. As described above, the sensitivity of the self-exciting, self-sensing piezoelectric cantilever sensor is due in part to advantageously directing (concentrating) the stress in the piezoelectric layer 14 and placing electrodes proximate thereto. The configurations of the self-exciting, self-sensing piezoelectric cantilever sensor described herein (and variants thereof) tend to concentrate oscillation associated stress in the piezoelectric layer 14. At resonance, in some of the configurations of the self-exciting, self-sensing piezoelectric cantilever sensor, the oscillating cantilever concentrates stress in the piezoelectric layer 14 toward the base portion 20. This results in an amplified change in the resistive component of the 'Piezoelectric layer 14, and a large shift in resonance frequency at the locations of high stress. Directing this stress to a portion of the piezoelectric layer 14 having a low bending modulus more flexible) allows for exploitation of the associated shift in resonance frequency to detect extremely small changes in mass of the self-exciting, self-sensing piezoelectric cantilever sensor.
Thus, in example configurations of the self-exciting, self-sensing piezoelectric cantilever sensor, the thickness of the piezoclectric layer 14 located near the base portion 20 is thinner than portions of the piezoelectric layer 14 flirther away from the base portion 20. This tends to concentrate stress toward the thinner portion of the piezoelectric layer 14. In example configurations, electrodes are located at or near the locations of the oscillation associated concentrated stress near the base portion of the self-exciting, self-sensing piezoelectric cantilever sensor. In other example configurations of the self-exciting, self-sensing piezoelectric cantilever sensor electrodes are positioned proximate the location of concentrated stress in the piezoelectric layer regardless of the proximity of the concentrated stress to a base portion of the self-exciting, self-sensing piezoelectric cantilever sensor.
[0)0371 The self-exciting, self-sensing piezoelectric cantilever sensor can be configured in accordance with a plurality of configurations, some of which are depicted in Figure 5 through Figure 16. It is to be understood however, that the configurations depicted herein do not represent all possible configurations, but rather a representative sample of configurations of the self-exciting, self-sensing piezoelectric cantilever sensor. Figure 5 is an illustration of an example configuration 36 of an unanchored self-exciting, self-sensing piezoelectric cantilever sensor wherein the distal end 40 of the piezoelectric portion 14 is flush with the distal end 38 of the non-piezoelectric portion 16. The self-exciting, self-sensing piezoelectric cantilever sensor 36 is termed "unanchored" because the non-piezoelectric portion 16 is not attached to the base portion 20. The piezoelectric portion 14 is coupled to the non-piezoelectric portion 16 via adhesive portion 18. The adhesive portion 18 is positioned between the overlapping portions of 17 WO 2008/020903 PCT/US2007/011402 the piezoelectric portion 14 and the non-piezoelectric portion 16. The piezoelectric portion 14 is coupled to a base portion [0038] Figure 6 is an illustration of an example configuration 42 of an unanchored selfexciting, self-sensing piezoelectric cantilever sensor wherein the distal end 44 of the piezoelectric portion 14 extends beyond the distal end 46 of the non-piezoelectric portion 16 and the proximate end 43 of the piezoelectric portion 14 extends beyond the proximate end 45 of the non-piezoelectric portion 16. The piezoelectric portion 14 is coupled to the non-piezoelectric portion 16 via adhesive portion 18. The adhesive portion 18 is positioned between the overlapping portions of the piezoelectric portion 14 and the non-piezoelectric portion 16. The piezoelectric portion 14 is coupled to the base portion [0039] The self-exciting, self-sensing piezoelectric cantilever sensor also can be configured to comprise multiple base portions. Example configurations of the self-exciting, selfsensing piezoelectric cantilever sensor comprising multiple base portions are depicted in Figure 7 through Figure 14. Configuring the self-exciting, self-sensing piezoelectric cantilever sensor to comprise multiple base portions is not intuitive because the expectation of one skilled in the art would be that affixation of both ends of the self-exciting, self-sensing piezoelectric cantilever sensor would provide a poor response as a result of the restrictions of the displacement of the self-exciting, self-sensing piezoelectric cantilever sensor as a result of its affixation to the multiple base portions. For configurations of the self-exciting, self-sensing piezoelectric cantilever sensor comprising two base portions, in an example embodiment, the stress of in the piezoelectric portion is measured, rather than the displacement of the piezoelectric portion.
Configuring the self-exciting, self-sensing piezoelectric cantilever sensor to comprise two base portions provides a stable and robust sensor that can perform under relatively high media flow conditions and provide excellent mass change sensitivity. Along with providing a mechanically robust self-exciting, self-sensing piezoelectric cantilever sensor that can withstand a relatively wide range of media flow conditions with minimal determination in performance, configuring the self-exciting, self-sensing piezoelectric cantilever sensor to comprise two base portions provides a fundamental frequency greater than 100 kHz) that is three to four times higher than a cantilever sensor having a single base portion and of similar dimensions.
[0040] Figure 7 is an illustration of an example configuration 48 of an anchored selfexciting, self-sensing piezoelectric cantilever sensor comprising two base portions 20, 50. The self-exciting, self-sensing piezoelectric cantilever sensor 48 is termed "anchored" because the -18- WO 2008/020903 PCT/US2007/011402 non-piezoelectric portion 16 is attached to the base portion 20. In the configuration depicted in the self-exciting, self-sensing piezoelectric cantilever sensor 48, both the proximate end 52 of the piezoelectric portion 14 and the proximate end 54 of the non-piezoelectric portion 16 are attached to the base portion 20. The piezoelectric portion and the non-piezoelectric portion can be attached to the base portion via any appropriate means. The distal end 58 of the nonpiezoelectric portion 16 also is attached to the base portion 50. The distal end 58 of the nonpiezoelectric portion 16 extends beyond the distal portion 56 of the piezoelectric portion 14. The piezoelectric portion 14 is coupled to the non-piezoelectric portion 16 via adhesive portion 18.
The adhesive portion 18 is positioned between the overlapping portions of the piezoelectric portion 14 and the non-piezoelectric portion 16.
[0041] Figure 8 is an illustration of an example configuration 60 of an anchored selfexciting, self-sensing piezoelectric cantilever sensor comprising two base portions 20, wherein the piezoelectric portion 14 is not attached to either base portion 20 or base portion In the configuration depicted in the self-exciting, self-sensing piezoelectric cantilever sensor the proximate end 62 of the non-piezoelectric portion 16 is attached to the base portion 20 and the distal end 64 of the non-piezoelectric portion 16 is attached to the base portion 50. The proximate end 62 of the non-piezoelectric portion 16 extends beyond the proximate end 66 of the piezoelectric portion 14 and the distal end 64 of the non-piezoelectric portion 16 extends beyond the distal end 68 of the piezoelectric portion 14. The piezoelectric portion 14 is coupled to the non-piezoelectric portion 16 via adhesive portion 18. The adhesive portion 18 is positioned between the overlapping portions of the piezoelectric portion 14 and the non-piezoelectric portion 16.
[0042] Figure 9 is an illustration of an example configuration 70 of an anchored selfexciting, self-sensing piezoelectric cantilever sensor comprising two base portions 20, comprising two piezoelectric portions 14, 72, and comprising two adhesive portions 18, 74. In the configuration depicted in the self-exciting, self-sensing piezoelectric cantilever sensor 70, the proximate end 76 of the piezoelectric portion 14 and the proximate end 78 of the nonpiezoelectric portion 16 are attached to the base portion 20. The distal end 80 of the piezoelectric portion 72 and the distal end 82 of the non-piezoelectric portion 16 are attached to the base portion 50. The proximate end 78 of the non-piezoelectric portion 16 extends beyond the proximate end 86 of the piezoelectric portion 72. The distal end 82 of the non-piezoelectric portion 16 extends beyond the distal end 84 of the piezoelectric portion 14. The distal end 84 of the piezoelectric portion 14 and the proximate end 86 of the piezoelectric portion 72 form a -19- WO 2008/020903 WO 2081020903PCTiUS2007O1 1402 space 88 therebetween. The piezoelectric portion 14 is coupled to the non-piezoelectric portion 16 via adhesive portion 18. The piezoelectric portion 72 is coupled to the non-piezoelectric portion 16 via adhesive portion 74. The adhesive portions 18 and 74 are positioned, respectively, between the overlapping portions of the piezoelectric portion 14 and the non-p iezoelectric portion 16, and the piezoelectric portion 72 and the non-piezoelectric portion 16.
[00431 In various alternate example configurations of the configuration 70 depicted in Figure 9, only one of the piezoelectric portions 14, 72 is attached to a respective base portion For example, in one example configuration as depicted in Figure 10, the piezoelectric portion 14 is attached to the base portion 20 and the piezoelectric portion 72 is not attached to the base portion 50. In another example configuration, as depicted in Figure 11, the piezoelectric portion 72 is attached to the base portion 50 and the piezoelectric portion 14 is not attached to the base portion 20. In yet another example configuration, as depicted in Figure 12, neither the piezoelectric portion 14 nor the piezoelectric portion 72 is attached to a respective base portion 50. In the various example configurations in which a piezoelectric layer comprises multiple portions, electrodes can be attached to any appropriate piezoelectric portion or portions. For example, in the example configuration depicted in Figure 9, Figure 10, Figure 11, and Figure 12, electrodes can be attached to piezoelectric portion 14, piezoelectric portion 72, or a combination thereof.
[00441 Figure 13 is an illustration of an example configuration 90 of an anchored selfexciting, self-sensing piezoelectric cantilever sensor comprising two base portions 20, wherein the piezoelectric portion 14 is attached to the base portion 20 and the non-piezoelectric portion 16 is attached to the base portion 50. The piezoelectric portion 14 is coupled to the nonpiezoelectric portion 16 via adhesive portion 18. The adhesive portion 18 is positioned between the overlapping portions of the piezoelectric portion 14 and the non-piezoelectric portion 16.
The distal end 98 of the non-piezoelectric portion 16 extends beyond the distal end 96 of the piezoelectric portion 14. The proximate end 92 of the piezoelectric portion 14 extends beyond the proximate end 94 of the non-piezoelectric portion 16.
[0045] Figure 14 is an illustration of an example configuration 100 of an anchored selfexciting, self-sensing piezoelectric cantilever sensor comprising two base portions 20, wherein the non-piezoelectric portion 16 is not attached to either base portion 20 or base portion In the configuration depicted in the self-exciting, self-sensing piezoelectric cantilever sensor 100, the proximate end 102 of the piezoelectric portion 14 is attached to the base portion 20 and 20 WO 2008/020903 WO 2081020903PCTiUS2007O1 1402 the distal end 104 of the piezoelectric portion 14 is attached to the base portion 50. The proximate end 102 of the piezoelectric portion 14 extends beyond the proximate end 106 of the non-piezoelectric portion 16 and the distal end 104 of the piezoelectric portion 14 extends beyond the distal end 108 of the non-piezoelectric portion 16. The piezoelectric portion 14 is coupled to the non-piezoelectric portion 16 via adhesive portion 18. The adhesive portion 18 is positioned between the overlapping portions of the piezoelectric portion 14 and the nonpiezoelectric portion 16.
[00461 Figure 15 is an illustration of an example configuration 110 of an unanchored self-exciting, self-sensing piezoelectric cantilever sensor comprising a piezoelectric portion 14 and a non-piezo electric portion 16, wherein the width, Wp, of the piezoelectric portion is less than the width, WNp, of the non-piezoelectric portion 16. The configuration 110 depicted in Figure 15 is similar to the configuration 12 depicted in Figure 1, with the exception that Wp is less than WNP. According, the self-exciting, self-sensing piezoelectric cantilever sensor depicts an embodiment of an unanchored, overhang, self-exciting, self-sensing piezo electric cantilever sensor. The piezoelectric portion 14 is coupled to the non-piezoelectric portion 16 via adhesive portion (adhesive portion not shown in Figure 15). The adhesive portion is positioned between the overlapping portions of the piezoelectric portion 14 and the non-piezoelectric portion 16. The piezoelectric portion 14 is coupled to a base portion [00471 Figure 16 is an illustration of an example configuration 112 of an unanchored self-exciting, self-sensing piezoelectric cantilever sensor comprising a piezoelectric portion 14 and a non-piezoelectric portion 16, wherein the width, Wp, of the piezoelectric portion is less than the width, WNp, of the non-piezo electric portion 16, and wherein the distal end 114 of the piezoelectric portion 14 extends beyond the distal end 116 of the non-piezoelectric portion 16 and the proximate end 118 of the piezoelectric portion 14 extends beyond the proximate end 120 of the non-piezoelectric portion 16. The configuration 112 depicted in Figure 16 is similar to the configuration 42 depicted in Figure 6, with the exception that Wp is less than WNp. The piezo electric portion 14 is coupled to the nion-piezoelectric portion 16 via adhesive portion (adhesive portion not shown in Figure 16). The adhesive portion is positioned between the overlapping portions of the piezoelectric portion 14 and the non-piezoelectric portion 16. The piezoelectric portion 14 is coupled to the base portion [00481 Figure 17 is a flow diagram of an example process for detecting an analyte utilizing the self-exciting, self-sensing piezoelectric cantilever sensor. The self-exciting, self- 21 WO 2008/020903 PCT/US2007/011402 sensing piezoelectric cantilever sensor is provided at step 120. The self-exciting, self-sensing piezoelectric cantilever sensor can be configured in accordance with the descriptions provided above, or configured in accordance with any appropriate variant is thereof. The self-exciting, self-sensing piezoelectric cantilever sensor is prepared to receive an analyte at step 122. In an example embodiment, an analyte attractor is applied to the non-piezoelectric portion of the selfexciting, self-sensing piezoelectric cantilever sensor. The attractor is specific to an analyte.
Thus the attractor will attract a target analyte and not attract other substances. For example, the non-piezoelectric portion of the self-exciting, self-sensing piezoelectric cantilever sensor can comprise an attractor for attracting bioterrorism agents, such as Bacillus anthracis, food-borne pathogens, such as E. coli, pathogens in food and water, cell types in body fluids circulating tumor cells), biomarkers in body fluids proteins that mark specific pathophysiology- alpha-fetoprotein, beta-2-microglobulin, bladder tumor antigen, breast cancer marker CA-15-3, and other CAs (cancer antigens), calcitonin, carcinoembryonic antigen, and others), markers of explosives such as trinitrotoluene, dinitrotoluene, airborne and waterborne toxins, biological entities, such as a protein, or a combination thereof, for example.
[0049] The self-exciting, self-sensing piezoelectric cantilever sensor is exposed to a medium at step 124. The medium can comprise any appropriate medium, such as a liquid, a gas, a combination of a liquid and a gas, or a vacuum, for example. The medium can exhibit a wide variety of flow conditions. If a target analyte is present in the medium, the target analyte will accumulate on the non-piezoelectric portion of the self-exciting, self-sensing piezoelectric cantilever sensor that has been treated with the attractor. As described above, accumulation binding) of the target analyte on the non-piezoelectric portion of the self-exciting, selfsensing piezoelectric cantilever sensor will result in a change in stiffness of the self-exciting, self-sensing piezoelectric cantilever sensor and/or an increase the mass of the self-exciting, selfsensing piezoelectric cantilever sensor, which will decrease the resonance frequency of the selfexciting, self-sensing piezoelectric cantilever sensor.
[0050] The resonance frequency of the self-exciting, self-sensing piezoelectric cantilever sensor is measure at step 126. The resonance frequency can be measured by any appropriate means, such as an operational amplifier, an impedance analyzer, a network analyzer, an oscillator circuit, or the like, for example. When the piezoelectric material of the piezoelectric portion of the self-exciting, self-sensing piezoelectric cantilever sensor is excited, the nonpiezoelectric portion of the self-exciting, self-sensing piezoelectric cantilever sensor flexes to 22 WO 2008/020903 WO 2081020903PCTiUS2007O1 1402 accommodate the strain caused in the piezoelectric material. When the frequency of excitation is the same as the natural frequency of the underlying mechanical structure, resonance occurs.
[0051] The measured resonance frequency is compared to a baseline resonance frequency at step 128. The baseline resonance frequency is the resonance frequency of the selfexciting, self-sensing piezoelectric cantilever sensor having no analyte accumulated thereon. If a difference in frequency (frequency shift) between the measured resonance frequency and the baseline resonance frequency is not measured (at step 130), it is determined, at step 132, that no analyte is detected. If a difference in frequency between the measured resonance frequency and the baseline resonance frequency is measured (at step 130), it is determined, at step 134, that an analyte is detected, an analyte is present in the medium. At step 136, the amount of mass of the analyte that has accumulated on the non-piezoelectric portion of the self-exciting, selfsensing piezoelectric cantilever sensor is determined in accordance with the frequency shift measured at step 130.
[00521 Various experiments have been conducted utilizing various configurations of the self-exciting, self-sensing piezoelectric cantilever sensor. Figure 18 is a plot 137 of an example resonance spectrum of the configuration 12 of the self-exciting, self-sensing piezoelectric cantilever sensor, depicted in Figure 1, operated in air. The width, Wp, and the width, WNp, were each approximately 2 mm. The plot 137 shows the phase angle (between the excitation voltage and the excitation current) versus excitation frequency, at an excitation voltage of 100 mV. The first resonance frequency mode 140 occurred approximately between 150 and 200 kHz and the second resonance frequency mode 142 occurred between 250 and 300 kHz. The resonance spectrum shows higher order characteristic peaks at approximately 980 kHz, 2.90 MHz and 4.60 MHz.
100531 Quality factors were determined as a ratio of the resonant frequency to the peak width at half the peak height. As a result, the quality factor is a measure of the sharpness of the resonant peaks. Experimentation has shown that the quality factor of the self-exciting, selfsensing piezoelectric cantilever sensor does not decrease significantly when the sensor is placed in different environments ranging from vacuum to liquid flow environments. Also, experimentation has shown that the Q values for the various configurations of the self-exciting, self-sensing piezoelectric cantilever sensor typically range between 10 and 70, depending upon the respective frequency mode where the peak is detected. The various configurations of the self-exciting, self-sensing piezoelectric cantilever sensor, when used in vacuum, air, and viscous -23 WO 2008/020903 PCTiUS2007/011402 environments, including flows, typically did not have more than a 20%-35% decrease in Q value.
This relatively small loss in the overall value of the quality factor reflects the ability of the selfexciting, self-sensing piezoelectric cantilever sensor to accurately detect chemicals and various biological items in viscous environments, including water and bloodstreams.
[0054] Experimentation has shown that the sensitivity of the self-exciting, self-sensing piezoelectric cantilever sensor is a function of the dimensions thereof. Specific changes in the geometry of the self-exciting, self-sensing piezoelectric cantilever sensor enhanced the sensor's mass change sensitivity, and thus, the sensor's response to the detection of low concentration of analyte. The resonance spectrum, a plot of phase angle versus excitation frequency, in air, showed dominant bending mode resonant peaks at 102 0.05, 970 0.05, and 1810 t 0.05 kHz, respectively. By changing the geometry of the of the self-exciting, self-sensing piezoelectric cantilever sensor, the sensor's resonance characteristics were enhanced. The corresponding bending resonant modes occurred at higher frequencies and had larger phase angles, suggesting that resonant peaks of the self-exciting, self-sensing piezoelectric cantilever sensor are more sensitive and are less dampened.
[0055] In an example experiment, the mass change sensitivity of the self-exciting, selfsensing piezoelectric cantilever sensor was measured. A known mass of paraffin wax was added to a glass surface of the self-exciting, self-sensing piezoelectric cantilever sensor and the change in resonant frequency was used to compute the mass sensitivity, expressed in g/Hz. Direct measurement was made of the mass change sensitivity in liquid; as well as the ratio of known mass to the change in resonant frequency in liquid before and after mass was added. The mass sensitivity of the resonant mode investigated under liquid was determined to be 1.5 x 10"15 g/Hz.
Application Of Piezoelectric Cantilever Sensors To The Detection Of Airborne Analvtes [00.56] Applicants has found no published information concerning the detection of a target analyte in a gas phase. The present invention addresses the detection of a target analyte in a gas phase by binding the analyte to a recognition entity within a sensor. The recognition entity exhibits an affinity for the target analyte. Examples of biological recognition entities include polyclonal and monoclonal antibodies, single-chain antibodies (scFvs), aptamer (synthetic DNA that is specially developed to detect a target molecule), recombinant and natural phage, and the like. In one embodiment, when using frequency transduction methods such as described herein, a detector makes use of immobilized antibodies as a recognition entity to detect concentrations of -24- WO 2008/020903 PCT/US2007/011402 airborne analytes. Immobilized antibodies are antibodies that are attached as a recognition entity onto the surface of a sensor that is used for airborne detection. This type of airborne detection provides a rapid and accurate detection of biological substances, such as pathogens including bacteria, virus, oocysts, prions, and spores, as well as non-biological substances, such as chemicals. Biological threats, such as bacteria, spores, and the like may be detected as well as chemical threats such as explosive or toxic chemicals.
[0057] In one aspect of the invention, airborne detection of a analyte using a recognition entity, such as described above, is performed by exposing a sensor having recognition entity, such as a coated surface of a sensor, to an airflow. The airflow may or may not contain the analyte. If the airflow does not contain the analyte, then no detection is expected.
However, if the analyte is present in the airflow then the analyte bonds to the recognition entity and affects characteristics of the sensor. The changed characteristics can be detected with a transducer that detects the presence of analyte now bonded to the sensor. Specifically, the transducer mechanism can operate via optical, frequency, capacitance, electrical conductivity, bending mode, or static mode cantilever. The transducer mechanism can determine the change in characteristic of the sensor as a result of the bonding of the analyte with the recognition entity.
As a result, the changed characteristic, size, frequency, mass, capacitance, electrical conductivity, bending mode, etc) can be detected and quantified. Once quantified, the amount of the analyte bonded to the recognition entity can be determined using calculation means known to those of skill in the art such as a computer, an embedded processor, or digital or analog circuitry.
One such transducer mechanism is frequency wherein the mechanical resonance of the sensor changes as analyte becomes bonded to the recognition surface of the sensor. Example embodiments using frequency transduction are presented below. However, other transduction mechanisms are possible as described above.
[0058] In one embodiment of frequency transduction for the detection of airborne analytes, piezoelectric-excited millimeter-sized cantilever (PEMC) sensors, because of their high sensitivity, are found by the inventors to be useful for the detection of airborne species. A PEMC surface prepared with a recognition entity, such as an antibodies or DNA molecules, will respond to the targeted analyte, which may be a pathogen, a protein, or a biomolecule. Such an event causes a change in the cantilever mass which manifests as a resonance frequency change, and can be monitored by an appropriate analyzer. Suitable analyzers may include, lock-in amplifiers, impedance analyzers, network analyzers or even an oscillator circuit.
[0059] In the present application, a technique for detection of an airborne pathogen is described. One aspect includes a method of contacting a target organism or molecule, in air, WO 2008/020903 WO 2081020903PCTiUS2007O1 1402 with a PEMC sensor including a recognition molecule to sense the presence of the target organism or molecule. One advantage of the present invention is that this can be carried out without having to collect the target organism or molecule in a liquid medium for sensing.
Traditional approaches deploy a sensor in a liquid environment. It is known that a dynamic sensing surface, such as an oscillating surface, resists the attachment of undesirable particulate contaminates. Since PEMC sensors are vibrating while in contact with the gas stream, only chemical bound attachment can occur thereby reducing or eliminating false positives from gas borne particulate contaminants in an airflow sample. This principle becomes an advantage of the current invention because the PEMC sensors can, by their operation, provide specificity in detection to the exclusion of contaminants.
100601 In one embodiment of this invention, the position and/or orientation of the sensor surface with respect to a flowing air stream in a low velocity flow region is specified.
Preferably, air flow velocities of about 0.01 to about 30 meter/second are used for detection. The low velocity flow region provides increased contact time between the target species and the sensor surface for binding. Contact time between the target species and the sensor surface can also be enhanced by the specific position or orientation of the sensor surface relative to the air flow. Preferably, the sensor surface is oriented substantially orthogonal to the air flow, though other orientations are also possible. Binding affinity of the spore to the antigen on the sensor may depend on local humidity. Keeping the humidity in the range of 10 to 95 provides sufficient binding and a value of 95% provides excellent binding affinity- While binding has been observed in the flow velocity range of 0.01 to 30 m/s, the lower end of this range shows higher binding kinetics. In some embodiments, an airflow velocity of 0.01 to 10 meters/second was an acceptable rate.
[00611 The methods of the present invention have been demonstrated to detect anthrax spores at concentrations as low as 40 spores per liter of air, measuring directly in air without the need for preparation of liquid or gel matrix based samnples.
[00621 Figures 1 9A- 190 show embodiments of various piezoelectric cantilever sensors which may be used in the methods of the present invention. It should be noted that the figures of the present application are not to scale unless otherwise indicated and that the figures are conceptual in presentation. In Figures 19A-1 9G, each sensor is comprised of a piezoelectric layer 14 (labeled an adhesive layer 18 (located between the overlapping portions of the piezoelectric layer and the non-piezoelectric layer), and a non-piezoelectric layer 16 (labeled NP) that includes a portion that extends as a tip. Base 20 is where the piezoelectric layer 14 is attached. Base 20 typically has electrodes (not shown) or some other similar means, associated 26 WO 2008/020903 PCT/US2007/011402 therewith for connection to the piezoelectric layer 14, though the electrodes need not be associated with the base 20 as long as the electrodes are connected to the piezoelectric layer 14.
The electrodes may be placed anywhere on the piezoelectric layer 14. There may also be a bonding pad that is made of gold, SiO 2 a material capable of immobilization of a receptor material, and/or an absorbent material appropriate for use in chemical sensing or for bio-sensing.
One of skill in the art will recognize that the designs described in Figures 19A-19G are only a subset of the possible geometries. Thus, variations of those designs are within the scope of the present application. For Example, the non-piezoelectric part of the sensor may be attached to the piezoelectric layer in one or many discrete numbers, either across the entire width of the piezoelectric layer or a part of it.
[0063] A cantilever or a beam (simple or composite) sensor is mechanically oscillated by AC electrical excitation of the PZT layer. When excitation frequency coincides with the mechanical resonance frequency or its higher modes, oscillation magnitude (deflection from equilibrium) is larger than at lower or higher frequency. Therefore at resonance the PZT experiences a higher stress level compared with levels present at non-resonance frequency. The stress level in the PZT varies along its length, and depends on the mode shape. The mode shape in turn also depends on the bending modulus of the cantilever. For example, referring to Figure 19A, bending modulus at section R is much higher than at Section S. Location of the exitation electrode solder point at or near the location of higher stress is advantageous as it gives a larger signal as measured by electrical impedance. The sensitivity of a free-end cantilever or a beam sensor is higher at higher resonance frequency. The various example structures illustrated in Figures 19A-19G and Figures 35- 46 are designed to achieve a dominant high-order resonance mode in the range of 60 kHz to 6 MHz. The location of the discrete non-piezoelectric layer can be designed such that certain high-order modes are enhanced, and non-flexural modes are reduced in intensity.
[0064] Piezoelectric layer 14 may be constructed out of lead zirconate titanate, lead magnesium niobate-lead titanate solid solutions, strontium lead titanate, quartz silica, piezoelectric ceramic lead zirconate and titanate (PZT) or Piezoceramic-polymer 1-3 fiber composites. The non-piezoelectric layer 16 may be constructed from ceramics, metals, polymers and composites of one or more of ceramics, metals, and polymers, such as silicon dioxide, copper, stainless steel, and titanium. Any known material for use in constructing the nonpiezoelectric layer of conventional piezoelectric cantilevers may be employed to construct the non-piezoelectric layer. The electrodes may be any suitable, conventional electrodes. In one -27 WO 2008/020903 PCT/US2007/011402 embodiment, the electrodes may be insulated or non-insulated depending on the exposure environment of the various piezoelectric cantilever sensors.
[0065] Detection is accomplished by measuring an oscillation a resonance frequency) of the apparatus and comparing the measured oscillation (resonance frequency) to a baseline oscillation (resonance frequency) to determine a frequency shift. The determined frequency shift may then be used to determine the presence of an analyte that adheres to a recognition entity deposited on one of the piezoelectric or non-piezoelectric layers of the sensor.
The combination of piezoelectric layer, the non-piezoelectric layer, and the recognition entity comprise the cantilever which oscillates when exited by electrodes attached to the piezoelectric layer.
[00661 One aspect of the invention is an apparatus and method for measuring any analyte that can be bound directly or indirectly to a surface. The binding of the analyte results in one or both of a mass change or a stiffness change. These changes can be measured as a resonance frequency change, and can be monitored by an appropriate analysis device, such as a lock-in amplifier, impedance analyzer, network analyzer or an oscillator circuit. Embodiments of the invention include novel geometric designs of the piezoelectric cantilever. Conventional piezoelectric cantilevers are fabricated with the piezoelectric layer attached to a nonpiezoelectric layer over an entire surface of the piezoelectric layer. In some conventional piezoelectric cantilevers, the piezoelectric layer is fixed at one end so that when the piezoelectric material is excited, the non-piezoelectric layer flexes to accommodate the strain caused in the piezoelectric material. When the frequency of excitation is the same as the natural frequency of the underlying mechanical structure, resonance occurs. This type of a cantilever sensor is good for operation at frequencies lower than about 100 kHz at millimeter size. Higher frequencies are possible only by making the cantilever very short (less than 1 mm).
[0067] Another version of a conventional piezoelectric cantilever includes the piezoelectric material is not affixed at one end. This is the so-called "unanchored piezoelectric cantilever." The unanchored piezoelectric cantilever presents its first bending mode resonance at over 100 kHz, while conventional anchored cantilevers present their first bending mode resonance at 2-60 kHz. The second bending mode resonance generally lies in the range of 200 kHz, and higher modes are present at 400 kHz, 800 kHz and potentially even higher frequencies.
[0068] Any mode that exhibits a Q value higher than 10 is convenient in a practical sense. Q values are the ratio of the resonance peak frequency relative to the resonance peak width at half peak height. Not all modes that show high Q value, however, provide sensitive detection. The difference in resonance frequency between air and water, and air and vacuum 28 WO 2008/020903 PCT/US2007/011402 gives a measure of sensitivity, as the differences in density cause a frequency shift in the resonance frequency. In many piezoelectric cantilever sensors, the change in media from air to vacuum causes a resonance frequency change of 4 to 25 kHz depending on the particular geometry of the sensor [0069] The relative length and widths of the piezoelectric and non-piezoelectric layers determines the sensitivity, and also the shape of the peak of the frequency spectrum provided by the sensor. This can be seen from the spectra of various piezoelectric cantilever sensors included as figures herein.
[0070] The instant invention permits detection of extremely small concentrations of analyte that will bind to the piezoelectric cantilever surface. In the examples, detection of pathogens and proteins has been demonstrated at low concentrations in air. Furthermore, any analyte that will bind to an organic or inorganic functional group on the PEMC surface can be detected. Thus, both chemical and biological agents can be detected in an airborne environment using the PEMC -based devices.
[0071] There are various potential applications for the cantilevers of the present invention, such as for the detection of bioterrorism agents, such as Bacillus anthracis, the detection of airborne pathogens, the detection of markers of explosives such as trinitrotoluene, such as the presence of dinitrotoluene, and the detection of airborne toxins. The piezoelectric cantilever of the present invention may also be used for the detection of biological entities at picogram levels, and for the detection of protein-protein interactions, both steady state and kinetic.
[0072] As an example use application, there are non-biological entities that have a high affinity to certain chemical coatings, and thus an airborne analyte sensor, such as the PEMC or PEMCB sensors, can be used in non-biological applications such as the detection of toxic or explosive chemicals. For example, a polymer coating of aSXFA-[poly(1-(4-hydroxy-4trifluoromethyl-5,5,5-trifluoro)pent-1- enyl)methylsiloxane] as a recognition entity may be used to detect 2,4-dinitrotoluene (DNT). Also, a molecularly imprinted polymers (MIPs) as a recognition entity may be used for detection of explosives such as trinitro toluene (TNT) and explosive signatures such as 2,4-dinitro toluene (2,4-DNT).
[0073] Figure 19A shows an embodiment 710 of an unanchored, overhang piezoelectric cantilever sensor (oPEMC). This sensor 710 is termed, "unanchored" since the non-piezoelectric layer 16 is not attached to the base. This sensor is termed, "overhang" because the nonpiezoelectric 16 layer extends beyond the distal tip of the piezoelectric layer 14 to create an overhanging portion of the non-piezoelectric layer 16 which is separated from the piezoelectric -29- WO 2008/020903 PCT/US2007/011402 layer by overlap region 18. The base 20 serves to hold the proximate end of the piezoelectric layer 14.
[0074] The present invention encompasses sensors having parts of all suitable dimensions. For example, each of the piezoelectric layer 14 non-piezoelectric layer 16 and overlap region 18 may range from 0.1 to 10 mm in length. The width of the piezoelectric layer 14 and the non-piezoelectric layer 16 may range from 0.1 mm to 4 mm for the lengths given above. The width of the piezoelectric layer 14 may differ from the width of the nonpiezoelectric layer 16 as well.
[0075] Typically an overhang piezoelectric cantilever sensor 710 has a nonpiezoelectric layer 16 between about 0.1 mm and about 10.0 mm in length, and between about 0.1 mm and about 4.0 mm in width. The piezoelectric layer 14 may be between about 0.1 mm and about 10.0 mm in length, or between about 0.25 and about 4.0 mm in width. Layer 18 corresponds to the overlap between layer 14 aid layer 16 and may be between about 0.1 mm and about 10 mm in length, or between about 0.1 and about 5.0 mm in length, depending on the specific construction of the overhang piezoelectric cantilever sensor.
[0076] The width of the overhang piezoelectric cantilever 710 sensor may be between about 0.1 mm and about 4.0 mm. The thickness of the piezoelectric cantilever 710 may be between about 0.1 mm and about 1.0 mm. Table 1 of Figure 47 illustrates several example dimensions of overhang PEMC devices that correspond to Figure 19A. In Table 1 of Figure 47, the length dimensions a, b, and c correspond to those of Figure 19A.
[0077] The overhang piezoelectric cantilever sensor 710 of the present invention generally exhibits a first bending mode resonance frequency mode peak at between 10-120 kHz, and a second bending mode resonance frequency mode peak at between 120 kHz-250 kHz.
[0078] Figures 19B-19F show various embodiments of piezoelectric-excited cantilever beam sensors in accordance with the present invention, which have been demonstrated to also provide successful sensing responses. The cantilever beam sensors include all of the same elements as the overhang sensor of Figure 19A, and, in addition, include a second base 50 to which at least one of the piezoelectric layer 14 and the non-piezoelectric layer 16 is also fixed.
In Figures 19B-19D, the non-piezoelectric layer 16 is affixed to both bases (20, 50) to form the "beam". In Figure 19E, the beam is formed by affixation of the piezoelectric layer 14 to the base affixation of the non-piezoelectric layer 16 to the piezoelectric layer 14 via the adhesive layer 18 and affixation of the non-piezoelectric layer 16 to the base 50. In the configuration 717 of Figure 19F, the beam is formed by affixation of the piezoelectric layer 14 to both bases (20, WO 2008/020903 PCTiUS2007/011402 [0079] Anchoring of the two ends of the piezoelectric and non-piezoelectric layers was accomplished using a 3 mm glass or tungsten rod. As long as the bending modulus of the support rod is much larger than the sensor beam, one observes excellent peak shapes. Other suitable methods for anchoring can also be employed.
[0080] The design of the cantilever beam sensors of Figures 19B-19F is not intuitive since the expectation of a skilled person would be that affixation of both ends of the beam would provide a poor response as a result of the restrictions of the displacement of the cantilever as a result of its affixation to the bases (20,50). In other words, in prior art cantilevers, one end of the cantilever was a free-end, i.e. not affixed to a base, in order to allow for a larger displacement of the cantilever during sensing in order to increase the response of the sensor.
[00811 Figure 19G depicts an alternative embodiment 719 to the overhang form of Figure 19A termed a free-floating tip PEMC (ftPEMC) sensor. Unlike the sensors in Figures 19B-19F, the Figure 19G construction has only one base 20 attachment. Performance results of this configuration and the other configurations are further discussed below.
[0082] Returning to the two base (20, 50) "beam" structures of Figures 19B-19F, it has been found that measurement of the stress in the piezoelectric layer, rather than the displacement of the piezoelectric layer, permits the use of cantilever "beam" sensors with both ends of the cantilever fixed to a base (20, 50). In addition, the cantilever beam sensors of the invention provide a higher fundamental mode (>100 kHz), stable and robust performance under flow conditions, and excellent mass change sensitivity which permits low sample concentration detection.
[0083] One advantage of the current invention is that the above Figure 19A- 19G designs are mechanically robust and withstand flow conditions with minimal deterioration in performance. A second advantage is that the fundamental frequency is three to four times higher than a sensor of similar dimensions in a cantilever configuration.
[0084] Figures 20-31, discussed below, show the results of various experiments conducted with different embodiments of overhang Piezoelectric-Excited Millimeter-sized Cantilever (oPEMC) sensors in accordance with the present invention. Table 1 of Figure 47 presents dimensions and resonant frequencies of overhang PEMC (oPEMC) devices. Figure 2 shows the typical resonance spectrum of a first embodiment of an overhang piezoelectric cantilever sensor, such as shown in Figure 19A, operated in air (see oPEMC#1 of Table 1 of Figure 47). A plot of phase angle versus excitation frequency, at an excitation voltage of 100 mV is shown in Figure 2. The first resonance frequency mode typically occurred between 150 and 200 kHz and the second resonance frequency mode occurred between 250 and 300 kHz. The -31- WO 2008/020903 WO 2081020903PCTiUS2007O1 1402 resonance spectrum shows higher order characteristic peaks at approximately 980 kHz, 2.90 MHz and 4.60 MHz for a composite PZT cantilever that is 2 min in width. As compared to a similar, unanchored piezoelectric cantilever configuration without an overhang, the base line up to 5 MHz was slightly more stable and the majority of the observed resonance frequencies were higher. Additionally, the quality factor of the 980 kHz characteristic peak was three times higher for the overhang embodiment, and the quality factor of the 4.60 MHz characteristic peak is a factor of two lower.
100851 Figure 21 shows a typical resonance spectrum of a second embodiment of an overhang piezoelectric cantilever sensor shown in Figure 1 9A, operated in air see oiPEMC#2 from Table I of Figure 47). Figure 21 shows a plot of phase angle versus excitation frequency, at an excitation voltage of 100 mV. The first resonance frequency mode typically occurred between 150 and 200 kI-z and the second resonance frequency mode occurred between 250 and 300 kHz. The resonance spectrum for this second embodiment of the overhang piezoelectric cantilever sensor shows higher order characteristic peaks at approximately 980 k~lz, 2.90 MHz and 4.60 MHz for a composite PZT cantilever that is 2 mun in width. The overhanging portion, section 16 of Figure 19A of this embodiment of the overhang piezoelectric cantilever sensor, is three times largler than the overhanging portion of oPEMC# 1, which may have caused some attenuation of the first resonance frequency mode and the resonance frequency mode that occurred between 850 -900 kHz.
[00861 Figure 22 shows the resonance spectrum of a third embodiment of anl overhang piezoelectric cantilever sensor, operated in air (see oPEMC43 from Table I of Figure 47). Figure 22 shows a piot of phase angle versus excitation frequency, at an excitation voltage of 100 mV.
The first resonance frequency mode typically occurred between 150 and 200 kHz, with no apparent second resonance frequency mode. The resonance spectrum for this embodiment of the overhang piezoelectric cantilever sensor shows higher order characteristic peaks at approximately 1. 81 MHz and 1.95 MHz for a composite PZT cantilever that is 1 mm in width.
As compared to an unanchored configuration without overhang, the resonant peak for the overhang configuration at 1.81 MHz becomes defined while all other peaks beyond 2.5 MHz become dampened.
[0087] Figure 23 shows the resonance frequency spectrum of a fourth embodiment of an overhang piezoelectric cantilever in accordance with the present invention (see oPEMC44 from Table I of Figure 47). The resonance frequency spectrum of Figure 23 was obtained using a 1 mmn wide overhang cantilever with a piezoelectric layer constructed of ceramic PZT. The 32- WO 2008/020903 PCT/US2007/011402 spectrum was obtained in air using a 100 mV signal to excite the cantilever. Characteristic peaks were obtained at 250 kHz, 650 kHz, 850 kHz, 1.65 MHz, and 4.65 MHz.
[0088] Figure 24 shows the resonance frequency spectrum of a fifth embodiment of an overhang piezoelectric cantilever in accordance with the present invention (se oPEMC#5 from Table 1 of Figure 47). The resonance frequency spectrum of Figure 24 was created using a 1 mm wide overhang cantilever with a piezoelectric layer constructed of ceramic PZT. By shortening section of the cantilever, more attenuated peaks were obtained for all listed frequencies. The spectrum was obtained in air using a 100 mV signal to excite the cantilever.
Characteristic peaks were obtained at 200 kHz, 1.0 MHz, 1.55 MHz, 1.90 MHz, and 4.50 MHz.
Additionally, the dimensions of this embodiment the overhang piezoelectric cantilever gave rise to a sensitive, resonant mode at 1.00 MHz.
[0089] In one embodiment, the piezoelectric cantilever sensors were fabricated from quartz silica and either piezoelectric ceramic lead zirconate and titanate (PZT) or piezoceramicpolymer 1-3 fiber composite. In one embodiment, the non-piezoelectric layer was constructed out of conventional materials such as ceramics, metals, polymers and composites of one or more of ceramics, metals, and polymers, such as silicon dioxide, copper, stainless steel, and titanium.
[0090] Table 2 of Figure 48 shows the quality factor of the corresponding resonant peaks listed in Table 1 of Figure 47 for the different piezoelectric cantilever sensors. The quality factors were determined as a ratio of the resonant frequency to the peak width at half the peak height. As a result, the quality factor is a measure of the sharpness of the resonant peaks. It has been shown in the experiments above that the quality factors of overhang piezoelectric cantilever sensors do not decrease significantly when the sensors are placed in different environments ranging from vacuum to air flow environments.
[0091] It is observed that the Q values for overhang piezoelectric cantilever sensors typically range between 10 and 70, depending upon the respective frequency mode where the peak is detected. The overhang piezoelectric cantilever sensors, when used in vacuum, air, and viscous environments, including flows, typically do not have more than a 20%-35% decrease in Q value.
[0092] The performance of the configurations of Figures 19B-19F are now considered.
Figure 25 shows a typical resonance spectrum, plot of phase angle versus excitation frequency, in air of the anchored Piezoelectric-Excited Millimeter-sized Cantilever Beam (aPEMCB) sensor 711 of Figure 19B excited at 1OOmV. The first peak is the fundamental resonant mode, which typically occurred in the frequency range 200 to 300 kHz. The second peak is the second resonant mode, which is usually in the frequency range 700 kHz to 1 MHz. The aPEMCB -33- WO 2008/020903 PCT/US2007/011402 resonant spectrum was measured by connecting the electrodes to an impedance analyzer (Agilent, HP4192A) that was interfaced to a personal computer for continuous measurement of impedance, phase angle and amplitude ratio in the frequency range of interest with an excitation voltage of 100 mV.
[0093] Figure 26 shows the resonance characteristics of the free-floating Piezoelectric- Excited Millimeter-sized Cantilever Beam (fPEMCB#I) sensor 712 of Figure 19C, in air, using a plot of phase angle versus excitation frequency, at an excitation voltage of 100mV. Typically, the fundamental resonance mode occurred between 200 kHz and 250 kHz, and the second mode frequency occurred between 800 kHz and 1 MHz. The quality factor for each resonant peak is list in Table 4 of Figure [0094] Figure 27 shows a typical resonance spectrum of the anchored bimorph Piezoelectric-Excited Millimeter-sized Cantilever Beam (abPEMCB#1) sensor 713 of Figure 19D, in air, using a plot of phase angle versus excitation frequency, at an excitation voltage of 100mV. The fundamental resonant frequency occurred at 200 kHz and the second mode at 700 kHz. The physical dimensions and quality factors for all of the sensor construction types are provided in Tables 3 and 4, respectively.
[0095] Figure 28 shows the resonance spectrum of an overhang beam PEMCB (oPEMCB# 1) sensor 715 of Figure 19E, in air, excited at a voltage of 100mV. The dimensions and resonant frequencies of the anchored, free-floating, and anchored bimorph and overhang PEMC sensors of Figures 19B, 19C, 19D and 19E respectively are tabulated in Table 3 of Figure 49. Here, it is seen that by varying the geometry of the PEMCB sensors, the peak positions of resonant frequencies can be tailored to specific needs. Thus, the position of the piezoelectric layer 14 and non-piezoelectric layer 16, as well as those layers being anchored or unanchored to the beam bases 20, 50, as well as the selection of which material comprises the beam allows a wide range of selection of resonant frequencies for determination of biological or chemical detection.
[0096] Table 3 of Figure 49 shows the physical dimensions of the PEMCB sensors used in Figures 25-28 in millimeters and the resonant frequency of the dominant modes in air. The length of PZT and glass is the dimension of the layer 14 and 16 respectively in Figures 19B-19F.
The width and thickness is the dimension of each layer. The PEMCB sensors were fabricated from piezoelectric ceramic lead zirconate and titanate (PZT) and quartz silica.
[0097] Another type of PEMC sensor having a different geometry from the dual-base cantilever beam devices just described is shown in Figure 19G and was also fabricated and tested. The new geometry 19, a free-floating tip PEMC sensor, (ftPEMC) was fabricated using a 34 WO 2008/020903 PCT/US2007/011402 127m thick PZT single sheet, and a 180pm thick quartz cover square. The PZT layer used is that same as the base sensor platform of Figure 19A. The cantilever free end was designed with the glass layer, 1.50 0.05 x 1 0.05 mm 2 (length x width), bonded at one end of the PZT layer, 4 0.05 x 1 0.05 mm (length x width), by a non-conductive adhesive. At the other end, 1.70 0.05 mm length of the PZT layer was epoxied into a glass tube. As a result, the cantilever free end has 0.8 mm of exposed PZT layer. Top and bottom electrodes were made on the 1.7 mm long PZT layer, before it was epoxied, using a 30 gauge copper wire soldered to BNC couplers.
The PZT layer at the cantilever free end was insulated with an 8 pm thick polyurethane layer.
The glass layer, 1.5 1 0.05 x 1 0.05 mm 2 provides a surface for antibody immobilization and antigen detection.
[0098] Any of the above-described PEMC or PEMCB devices can result in the formation of a sensor if a recognition entity, such as an antibody or a DNA, is coated on the surface of the PEMC or PEMCB device. With the proper coating, the resulting sensor coating will attract and bond to a targeted analyte, which may be an airborne pathogen, an airborne protein, or an airborne biological agent. In one embodiment, the direct detection of airborne Bacillus anthracis (BA) spores was explored using millimeter-sized PZT cantilever sensors (PEMC) coated with an immobilized BA antigen. The attachment of BA on the coated PEMC sensor is detected as a frequency change in the PEMC device due to the added mass of the BA because the attached BA affects the mass, and thus the mechanical resonance, of the cantilever device [0099] In one embodiment, an experimental apparatus included a horizontal tube with the PEMC sensor suspended vertically with its glass surface facing the air flow. The quartz surface was silanylated followed by immobilization of rabbit Anti-BA specific for the pathogen BA before exposure to a flowing air stream (11 cm/s) containing 42 to 278,000 spores/L-air. The BA was introduced upstream of the sensor using an axial flow nebulizer. The concentration of the BA solution in the nebulizer was measured using a Coulter Counter Multisizer II. The sensor was fabricated from a 2x5 mm PZT laminated with a 0.5 mm offset to 2x5 mm borosilicate glass anchored in a non-conductive epoxy base.
[0100] Figure 29A shows the apparatus 100 used to flow airborne Bacillus anthracis (BA) to PEMC-type sensor for detection of airborne BA. Supply air 110 (AO) conditioned to zero humidity is split into two streams. One stream uses air valve 110 (Al) and is used to feed nebulizer 121 a known concentration of BA in deionized water. The nebulizer 121 produces liquid particles of about 5 microns in size. A low shear nebulizer is used to prevent damage to the BA spores as they flow through the nebulizer. The liquid particles are carried by make-up air WO 2008/020903 PCTiUS2007/011402 from adjustable air valve 115 (A2) which is adjustable from about 1-200 Ipm though a 2" pipe.
In the configuration of Figure 29A, the two streams are mixed at mixer 123 and carry the aerosolized BA at a 1 m/s velocity although higher velocities are possible. The PEMC sensor is inserted in a "T-shaped" exposure tube assembly 125 in an orthogonal fashion, as shown in Figure 29B, is interfaced to an impedance analyzer 131 and a personal computer 135 that collects resonant frequency data every 30 seconds. The humidity and temperature of the flowing Bioaerosol is continuously monitored. Periodically, the exit stream is sampled using a commercial SASS 2000 air sampler 140, which provides a 5 ml liquid sample. These samples were either analyzed using a PEMC sensor in a separate apparatus or its particle size and distribution is determined using a Coulter counter. The SASS 2000 air sampler is monitored using an RS-232 interface to a personal computer 150.
[0101] Flow cell 125 in Figure 11 B comprises a gas flow input portion 1251, a gas flow body portion 1252, an exhaust opening portion 1253, and a sensor mounting portion 1253.
The sensor 1254 in the sensor mounting portion may be variably positioned in a vertical direction to adjust the depth of penetration if the sensor into the airflow through the body 1252.
In one embodiment, the sensor is oriented to expose the recognition entity of the cantilever sensor orthogonally to the direction of airflow to maximize exposure of the recognition entity to elements in the airflow.
[0102] Using the configuration of Figure 29A, a steady state frequency response of the sensor was achieved initially by flowing humid air (RH 85±3% and T 23±0.3 degrees C) at a flow rate of 2.4 1pm. Nebulizer charge was 10 million spores in 4 mL and nebulized for minutes which yielded gas phase concentration of 278,000 spores/L of air. The frequency of a PZT cantilever is a function of its mass and temperature, and the fluid dynamic properties of the surrounding gas. Upon exposure to airborne BA, resonance frequency decreased 700 Hz due to spore attachment to the coated cantilever device. Post-detection, the sensor was immersed in PBS for confirmation of BA attachment by releasing the attached BA using a low pH buffer. The frequency change resulting from the release of the spores was 350 Hz. The frequency change due to temperature and moisture effects were 60 Hz per degree C and 2 Hz per of relative humidity (RH).
[01031 PEMC sensors can have a sensitivity of 10 femtogram depending upon construction and the vibration mode used for detection. For the results of Figure 30A, two sensors were used. Sensor 1 when exposed to flowing BA spores at concentration of 278,000 spores per Liter of air (Humidity 95%, 24 and gave a 760 Hz response. Using the same spore concentration, Sensor 2 gave nearly an identical response of 760 Hz shift. Figure 30A also -36- WO 2008/020903 PCTiUS2007/011402 shows excellent repeatability between separate runs with different sensors of similar construction when the same mode is used for detection. Thus, successful, quantitative, and repeatable detection of BA spores was observed.
[0104] Figure 12 B shows the results of exposing four sensors. Sensor 1 (1006) and Sensor 2 (1008) were prepared with a recognition entity that would detect BA spores. Control sensors 1002 and 1004 were likewise prepared with the same recognition entity. Figure depicts the consistency of results between sensor 1 and sensor 2 in detecting spores in an 278,000 spores per liter gas environment. Sensor plot 1002 depicts a sensor response to a controlled injection of inorganic particulates of aluminum silicate particles in the 0.2 to 0.6 micrometer size. The sensor plot 1002 indicates that there was no substantive response as expected. Sensor plot 1004 depicts a sensor response to a clean air environment. Note that there is no substantive response as expected. This evinces that detection of analytes using the PEMC/PEMCB sensors is very specific to the recognition entity used and that the sensors thus configured are insensitive to non-target substances.
[0105] The PEMC sensor responds to changes in mass, temperature and fluid density.
Fluctuations in system temperature, humidity (mass and density effects) and pressure (density) can mask the detection of the pathogen. Design of the PEMC sensor minimizes these masking effects. It is noted that the frequency of the PEMC device responded within the time for the spores to travel from the nebulizer to the sensor. The time to detect the BA is on the order of 2 minutes.
[0106] As mentioned above, confirmation of the detection of BA attachment to the PEMC sensor was performed by release in low pH buffer. Direct microscopic observation was also used as confirmation. In the low pH buffer confirmation, the ratio of the attachment to the release of 2:1 is consistent with that reported by others for air versus liquid mass change.
Confirmation of the BA aerosolization was confirmed via particle size analysis of the nebulizer feed and of the exhaust captured by a air sampler device (SASS 200) in the configuration of Figure 29A. The SASS 2000 captures approximately 30% of the inlet airborne BA. The results of detection confirmation are given in Figure 31.
[0107] After performing the experiments shown in Figure 30A, the sensor that was exposed to 278,000 spores per liter of air sample, was inserted in a release buffer (with a pH 2.2) and the resonant frequency was measured. At this pH, the antigen is released from the sensor surface and the reduced mass increases the resonance frequency confirming that the reduction in frequency was indeed due to BA attachment. This confirmation is shown in Figure 31.
-37- WO 2008/020903 PCT/US2007/011402 [0108] An additional confirmation of the attachment of BA was provided by direct microscopic examination. The scanning electron micrograph of Figure 33 shows a broken cantilever used in one of the airborne anthrax detection experiments. The sensor was broken to enable mounting on a SEM pedestal mount and was then used for microscopic analysis. The top panel of Figure 33 shows the presence of anthrax spores used in detection in the region of the sensor surface indicated in the bottom panel. These micrographs show that the anthrax antigen binds to the antibody which is chemically immobilized on the sensor surface.
[0109] As noted earlier, since PEMC sensors are vibrating while in contact with the gas stream, only chemical bound attachment can occur thereby reducing or eliminating false positives from gas borne particulate contaminants in an airflow sample. Gas phase experiments were conducted with 0.2 to 6.0 micron clay particles as inert contaminates. It was observed that no change in sensor output was seen from exposure to the contaminants. This also confirms that inert contaminates do not attach to the PEMC surface during operation.
[0110] Thus it can see understood and shown by example that the sensors of the present invention may be used for the detection of bioterrorism agents, the detection of airborne pathogens, the detection of markers of TNT such as DNT, the detection of airborne toxins, and the detection of any other target analyte that will bind to suitably prepared PEMC or PEMCB surface. The sensors of the present invention can also be implemented in sensor arrays wherein a plurality of sensors are arranged in a single device for sensing a plurality of different analytes simultaneously. In this manner, the sensors of the present invention can be used, for example, to identify unknown species in a gas, or to indicate the presence of a plurality of different analytes in a gas.
[0111] As noted above, detection is affected by humidity. Specifically, very low humidity adversely affects binding affinity. Thus, it is advantageous to include humidification in association with an airborne analyte sensor. Figure 33 depicts a configuration using the airborne sensor of Figure 29B. In this embodiment, a gas pump 305 has an air inlet to intake air from an air sample, such as a chamber, a vessel, or a room, and pump the air intake to a humidifier 310.
The humidifier 310 adds an amount of humidity to the pumped air so that the PEMC or PEMCB sensor in the flowcell 125 reacts well to target analytes contained in the air intake. The PEMC/PEMCB flowcell 125 then exhausts the air 315 to a safe location. The sensor in the flowcell 125 is measured using an impedance analyzer 131 and a personal computer 135 that collects resonant frequency data from the flowcell. Figure 33 is simple application of the PEMC/PEMCB sensor in the flowcell for airborne detection of an analyte.
-38 WO 2008/020903 PCT/US2007/011402 10112] Figure 34 depicts a flow diagram of a method involving aspects of the invention.
The method concerns the detection of an airborne analyte using PEMC-type sensors (including PEMC and PEMCB types). The method starts with providing an PEMC type sensor in step 2120.
These sensors can include any of the types shown in Figures 19A-19G and variants thereof.
These type include the single base cantilever types shown in Figures 19A and 19G, the dual base beam type sensors having a non-piezoelectric beam as shown in Figures 19B-19D, the beam type sensor having a piezoelectric beam as in Figure 19F, and the overlapped layer structure shown in Figure 19E.
[0113] Next, an aerosolized target analyte is passed over the sensor in an airflow in step 2122. Here, it is preferable if the recognition entity which attracts the analyte is oriented orthogonally to the airflow having the analyte. Exposure to the airflow allows the recognition entity to capture target analytes. Next, the PEMC sensor is excited via the electrodes into oscillation in step 2124. The oscillation frequency of the cantilever or beam assembly is dependent upon the mass of the assembly which includes the analyte collected by the recognition entity. The oscillation frequency, the resonant frequency of the cantilever assembly) of the sensor is measured in step 2126. The measured oscillation frequency of the cantilever assembly is then compared to a natural (resonant) baseline frequency of the cantilever assembly in step 2128. Such comparisons can be made with calculation means that includes a personal computer, an embedded processor, analog or digital circuits, or a hand calculation.
[0114] A frequency shift is detected in decision step 2130. If no frequency shift is detected as in step 2132, then a determination is made that no analyte is present on the recognition entity. This may result if the airflow sample is pure or if the recognition entity is not compatible with any analyte within the airflow. If a frequency shift is detected, a determination is made at step 2134 that the target analyte is detected. Further, the specific amount of analyte the mass of the analyte deposited on the recognition entity) is determined in step 2136. This step is performed by examining the magnitude of the frequency shift and correlating that magnitude with a mass of the analyte needed to change the resonant frequency of the PEMC sensor. Note that no special preparations were performed as are need in the case of a liquid-based sampling of an analyte. Also, no special concentrating step or enrichment steps are included in the above method as compared to liquid-based analyte detections.
[0115] To provide quality control or more accuracy of the detection of an analyte, a comparison, not shown in Figure 33, is made between a control sensor and the measurement sensor that detects the analyte. For example, a control sensor is preferably identical to the measurement sensor except that the control sensor does not have the recognition entity for the -39- WO 2008/020903 PCT/US2007/011402 target analyte. When exposed to the same airflow as the measurement sensor, the control sensor resonant frequency change can be differenced from the resonant frequency of the measurement sensor to provide an accurate result.
Additional Sensor Configurations [0116] All of the configurations of Figures 35-47 are useful for the construction of sensors which can be used for the detection of analytes in gas or liquid mediums as are the configurations of Figures 19A-19G. Thus, the application of the configurations of Figures 35-47 is similar to that discussed herein for the detection of airborne chemicals or biologicals. Figures 35-47 share some characteristics with those of Figures 19A-19G. For example, where indicated, a base element 20 is present where an attachment is made to either a piezoelectric 14 type of element or a non-piezoelectric 16 type of element. The adhesive layer 18 separates a P type layer 14 from a NP type layer 16. Figures 35-47 depict electrodes 28 connected to at points 30 to various locations of the piezoelectric 14 type of element for excitation of the cantilever structure or beam structure. Figures 35-47 indicate the wide range of configurations that can be implemented.with PEMC and PEMCB devices. A brief description of each follows.
[01171 Figure 35 depicts a configuration ofa PEMC or PEMCB sensor where the NP section 16 is contiguous with P section 14. The thickness of the NP layer 16 can vary along length of the NP layer 14 and TNp can be designed to support a sensitive sensor. In this configuration, the modulus of bending is in the NP layer 14 notched area is less than that of the thicker portion of the NP layer 14. Although only a free-end cantilever arm comprising a P and NP layer are shown, the configuration of Figure 35 may be duplicated in mirror form about the center line A-A. This mirror duplication of Figure 35 depicts a symmetry for a beam type (PEMCB) sensor. There are several instances of a centerline depiction in Figures 35-47 where the geometry depiction can be either a free-end cantilever or a beam type configuration of sensor.
In addition, all of the basic information about electrode wire 28 and contact 30 placement and the width of the notch applies to this configuration and to all others.
[0118] Figure 36 depicts two layers of NP 16; one at the top and one at the bottom, which can be used effectively if the Bending Modulus (EI) of NP1 is not equal to that ofNP2 Here, the designations NP 1 and NP2 on Figure 36 indicate that the two NP layers may differ in geometry as well as material. For example, NP1 can be smaller or a different shape than NP2.
Also NP1 can be made of glass whereas NP2 is made of ceramic. As in Figure 35, the mirror image around centerline A-A would create a beam configuration. In this case, the distance X is greater than or equal to 0, meaning that P can be contiguous to the mirror anchor or it could be two separate pieces. In the case where X>0, you could excite one or BOTH pieces of P but in WO 2008/020903 PCTiUS2007/011402 the later case the two excitations could be synchronized. Figure 37 depicts a configuration similar to Figure 36 except for two aspects. In Figure 36, NP1 NP2 because having P1 and P2 creates an axis of symmetry. The mirror image around A-A creates a beam configuration. In this case, X is greater than or equal to zero. This means that P can be contiguous to the mirror anchor OR it could be two separate pieces. In the case where X>0, you could excite one or both pieces of P but in the later case, the two excitations would preferably be synchronized.
[0119] Figure 38 depicts a configuration similar to Figure 19A with the exception of an additional piece of NP 16 type material. The advantage of this structure over Figure 19A is that more control over the position of the resonant frequency peak may be achieved and the configuration can be effective in dampening unwanted modes. NP1 16 can be equal or unequal to NP2 16 depending on the desired properties. The free-end cantilever configuration of Figure 38 could be converted to a beam configuration by simply fixing the distal end of NP2 into a base element. Note also, that the portion labeled NP2 in Figure 38 could be created simply by removing the electrodes (laser ablation, chemical etching, etc.) from a section of P type material and using an unexcitable portion of P type material.
[0120] Figure 39 depicts a configuration similar to Figure 19A with the exception of the addition of NP 1. Here, NP 1 connects to base 20 instead of a P type of layer. This configuration offers an improved signal because, unlike the Figure 19A configuration, the proximal end of P is not constrained so that some of its signal energy is not dissipated thereby generating a larger signal. Stated differently, some of the signal energy from Figure 19A may be lost because the proximal end is constrained. The configuration of Figure 39 represents an improvement over that of Figure 19A. As in the configurations of Figures 35-37, a beam configuration can be created by adding the mirror image around centerline A-A.
[0121] Figure 40 depicts a configuration similar to the structure of Figure 19F with the exception of the addition of the reversal of the P and NP regions and the addition of the P type of layer 14. This configuration may offer an improved signal because the proximal end' of P is not constrained such some of its signal energy may not be dissipated. Thus, a larger signal is generated. Figure 41 depicts a configuration similar to that of Figure 19E with the exception of the addition ofNP1. This configuration may offer an improved signal because the proximal end of P is not constrained such some of its signal energy may not be dissipated. Thus, a larger signal is generated. Figure 42 depicts a configuration similar to Figure 19G with the exception that the Bending Modulus (El) of the NP layer varies as a function of the length L. By varying this parameter, an enhancement in sensitivity by increasing the stress concentrated at the position of the electrodes is achieved. One practical way to achieve this would be as shown in -41 42 Figure 43 where the NP layer is composed of multiple discrete segments which can vary in width along with adjacent sections that are empty space or an alternate material of a lower modulus. A beam configuration is created by adding the mirror image around A-A in either of Figures 42 or 43.
00 0 [0122] Figure 44 is a configuration that is similar to Figure 36 except that the top NP layer has a Bending Modulus (El) that varies as a function of length and a bottom layer that varies as a function of length. This is effectively the mirror image 00 N of Figure 43 but where the bottom layer is different than the top layer to create a 0 10 resonant structure. In Figure 44, the top and bottom layers could be identical, but 0 c-i only if the P layer were a sandwich construction as shown in Figure 37. Figure is a configuration that concentrates stress sufficiently at the point of the electrodes to create a sensitive response. However, it gives a more stable response due to the position of NP 16. A beam can structure can be created by mirroring around the A-A centerline. Figure 46 is a configuration that is useful for manufacturability because of the abbreviated base 20. However, it provides more unwanted vibration modes. A beam structure is created by mirroring about the A-A centerline.
[0123] It is to be understood, however, that even though numerous characteristics and advantages of the present invention have been set forth in the foregoing description, together with details of the structure and function of the invention, the disclosure is illustrative only, and changes may be made in detail, especially in matters of shape, size and arrangement of parts within the principles of the invention to the full extent indicated by the broad general meaning of the terms in which the appended claims are expressed.
[0124] In the specification the term "comprising" shall be understood to have a broad meaning similar to the term "including" and will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. This definition also applies to variations on the term "comprising" such as "comprise" and "comprises." 42A S[0125] The reference to any prior art in this specification is not, and should not be F1 taken as an acknowledgement or any form of suggestion that the referenced prior art forms part of the common general knowledge in Australia.
00 00 0q
Claims (19)
1. A method for detection of a target analyte comprising the steps of: 00 providing a sensor comprising; a piezoelectric layer having a first end and a second end, the first end 00 5 proximate to and attached to a first base; a non-piezoelectric layer having a first end and a second end, wherein a portion of the non-piezoelectric layer overlaps and is attached to the piezoelectric layer; a recognition entity associated with the non-piezoelectric layer, wherein the combination of the piezoelectric layer, the non-piezoelectric layer, and the recognition entity comprising a cantilever portion; and electrodes operatively attached to the piezoelectric layer, wherein electrical stimulation from the electrodes causes the cantilever portion to oscillate; mounting the sensor in a media flow; exposing the recognition entity of the cantilever to the target analyte in the media flow; measuring an oscillation frequency of the cantilever; and comparing the measured oscillation frequency to a baseline oscillation frequency to determine a frequency shift indicative of a presence of the target analyte on the recognition entity.
2. The method of claim 1, wherein providing a sensor further includes providing a sensor wherein the piezoelectric layer comprises both piezoelectric and non-piezoelectric portions arranged linearly. 44
3. The method of claim 1 or claim 2, wherein providing a sensor further includes providing a sensor wherein the non-piezoelectric layer comprises a plurality of linearly 00 arranged and spaced non-piezoelectric portions.
4. The method of any one of claims 1 to 3, further comprising: determining an amount of the target analyte present on the recognition entity. 00 The method of any one of claims 1 to 4, wherein providing a sensor further comprises C providing the sensor wherein the recognition entity is selected from one of the group consisting of antibodies, DNA molecules, aptamers, phage and biochemical reagents and wherein the selection is one of the group consisting of naturally and synthetically constituted.
6. The method of any one of claims 1 to 5, wherein the recognition entity is an antibody that recognizes and binds the target analyte.
7. The method of claim 6, wherein the target analyte is chemically immobilized on the cantilever sensor surface by binding with the antibody.
8. The method of any one of claims 1 to 7, wherein exposing the recognition entity of the cantilever to the target analyte comprises exposing the recognition entity to one of the group consisting of a biological substance and a chemical substance in the medium.
9. The method of any one of claims I to 8, further comprising: providing a plurality of sensors in a sensor array, wherein each of the plurality of sensors in the array is exposed to the medium to detect one at least one analyte.
10. The method of claim 9, wherein the at least one analyte is detected by measuring a plurality of frequency shifts, one frequency shift for each provided sensor.
11. An apparatus for detecting a target analyte, the apparatus comprising: 00 a sensor comprising; a first layer having a first end and a second end, the first end proximate to and attached to a first base; 00 C' 5 a second layer having a first end and a second end, wherein a portion of the O second layer overlaps and is attached to the first layer, and wherein the first layer is selected from the group consisting of a piezoelectric material and a non-piezoelectric material and the second layer is a different material from the first layer; a recognition entity associated with the second layer, wherein the combination of the first layer, the second layer, and the recognition entity comprises a cantilever portion; and electrodes operatively attached to the piezoelectric material, wherein electrical stimulation from the electrodes causes the cantilever portion to oscillate; an analyzer that collects resonant frequency data from the sensor, wherein the analyzer compares the measured resonant frequency of the sensor to a baseline resonant frequency to determine a frequency change, the frequency change indicating an amount of mass of the target analyte collected on the recognition entity of the sensor.
12. The apparatus of claim 1 i, further comprising an array of sensors, each sensor in the array providing frequency information to the analyzer for a determination of the presence and amount of at least one analyte.
13. A method of detecting an analyte, the method comprising: coating a surface of a cantilever detection device with immobilized antibodies, the cantilever detection device having a base resonant frequency; 46 exposing the coated surface to a media flow, wherein an analyte compatible with the immobilized antibodies binds to the coated surface if the a media flow contains the analyte; 00 measuring the resonant frequency of the of the cantilever detection device; determining an amount of analyte that bonds to the recognition entity. 00 N 5 14. The method of claim 13, wherein the recognition entity comprises one of the group consisting of an immobilized antibody, an aptamer, a recombinant phage, and a DNA Smolecule, the method further comprising using a transducer mechanism coupled with calculation means to determine the amount of the analyte that bonds to the recognition entity. The apparatus of claim 11 or claim 12, wherein the piezoelectric layer comprises two piezoelectric layers.
16. The apparatus of any one of claims 11, 12 and 15, wherein the non-piezoelectric layer comprises a plurality of linearly arranged and spaced non-piezoelectric portions.
17. The apparatus of any one of claims 11, 12, 15 and 16, wherein electrical excitation of the electrodes causes a mechanical oscillation in the piezoelectric layer, wherein oscillations at resonance subject the sensor to higher stress levels than oscillations at non-resonance; and wherein electrode attachment to the piezoelectric layer is proximate to a point on the piezoelectric layer indicative of an increased electrical impedance in the piezoelectric layer as compared other points in the piezoelectric layer.
18. The apparatus of claim 17, wherein the increased electrical impedance is indicative of a respective increased stress on the piezoelectric layer.
19. The apparatus of any one one of claims 11, 12 and 15 to 18, wherein enhanced detection of the target analyte is achieved by varying a bending modulus of the sensor to enhance stress and electrical impedance at a point of electrode attachment. 47 The apparatus of any one of claims 11, 12 and 15 to 19, wherein enhanced detectably _of the target analyte is achieved by selecting a geometry of the piezoelectric layer and a 00 geometry of the non-piezoelectric layer to achieve at least one dominant higher order mode of the sensor at a location of the electrodes, wherein the at least one dominant higher order tt 5 mode is a function of impedance and quality factor at resonance. 00 C 21. The apparatus in accordance with claim 20, wherein: non-flexural modes of the sensor are reduced in an amplitude intensity as compared to the at least one higher order mode; and non-flexural modes provide no perceivable contribution to the impedance at the flexural mode resonance at the location of the electrodes.
22. A method for detection of a target analyte substantially as hereinbefore described with reference to the accompanying drawings.
23. An apparatus for detecting a target analyte substantially as hereinbefore described with reference to the accompanying drawings.
24. A method of detecting an analyte substantially as hereinbefore described with reference to the accompanying drawings.
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US60/807,020 | 2006-07-11 | ||
PCT/US2007/011402 WO2008020903A2 (en) | 2006-05-10 | 2007-05-10 | Self-exciting, self-sensing piezoelectric cantilever sensor for detection of airborne analytes directly in air |
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AU2007284995A2 true AU2007284995A2 (en) | 2009-02-12 |
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AU2007284995A Abandoned AU2007284995A1 (en) | 2006-05-10 | 2007-05-10 | Self-exciting, self-sensing piezoelectric cantilever sensor for detection of airborne analytes directly in air |
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JP (1) | JP5225981B2 (en) |
AU (1) | AU2007284995A1 (en) |
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WO (1) | WO2008020903A2 (en) |
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US7497133B2 (en) | 2004-05-24 | 2009-03-03 | Drexel University | All electric piezoelectric finger sensor (PEFS) for soft material stiffness measurement |
US8171795B1 (en) | 2006-01-23 | 2012-05-08 | Drexel University | Self-exciting, self-sensing piezoelectric cantilever sensor for detection of airborne analytes directly in air |
US8481335B2 (en) | 2006-11-27 | 2013-07-09 | Drexel University | Specificity and sensitivity enhancement in cantilever sensing |
US8927259B2 (en) | 2006-11-28 | 2015-01-06 | Drexel University | Piezoelectric microcantilever sensors for biosensing |
US7992431B2 (en) | 2006-11-28 | 2011-08-09 | Drexel University | Piezoelectric microcantilevers and uses in atomic force microscopy |
EP2115448A4 (en) | 2007-02-01 | 2013-01-30 | Univ Drexel | A hand-held phase-shift detector for sensor applications |
US8241569B2 (en) | 2007-11-23 | 2012-08-14 | Drexel University | Lead-free piezoelectric ceramic films and a method for making thereof |
US8741663B2 (en) | 2008-03-11 | 2014-06-03 | Drexel University | Enhanced detection sensitivity with piezoelectric sensors |
AU2009246115A1 (en) | 2008-05-16 | 2009-11-19 | Drexel University | System and method for evaluating tissue |
JP5463788B2 (en) * | 2009-08-18 | 2014-04-09 | 富士通株式会社 | Ion analyzer and ion analysis method |
US8722427B2 (en) | 2009-10-08 | 2014-05-13 | Drexel University | Determination of dissociation constants using piezoelectric microcantilevers |
WO2013023215A1 (en) * | 2011-08-11 | 2013-02-14 | William Marsh Rice University | Methods for sensitive and rapid detection of molecules |
WO2013064157A1 (en) | 2011-11-04 | 2013-05-10 | Danmarks Tekniske Universitet | Resonant fiber based aerosol particle sensor and method |
JP6150671B2 (en) * | 2013-08-22 | 2017-06-21 | オリンパス株式会社 | Gas sensor |
JP6392679B2 (en) * | 2015-02-09 | 2018-09-19 | オリンパス株式会社 | Gas sensor |
JP6671471B2 (en) * | 2015-07-13 | 2020-03-25 | イントレピッド ヴィジョンズ インコーポレーテッドIntrepid Visions Inc. | System and method for micro-cantilever actuation with base excitation |
KR101819969B1 (en) | 2016-04-15 | 2018-01-19 | 전남대학교산학협력단 | Pdms polymer cantilever structure for improving reliavility of piezoresistive sensor |
BG112997A (en) | 2019-09-17 | 2021-03-31 | "Амг Технолоджи" Оод | Gas monitoring device |
CN112834570B (en) * | 2020-12-30 | 2023-09-22 | 中国航空工业集团公司金城南京机电液压工程研究中心 | Gas-liquid two-phase detection device and method based on self-excitation type piezoelectric element |
CN112736187B (en) * | 2020-12-30 | 2024-02-02 | 中国航空工业集团公司金城南京机电液压工程研究中心 | Exhaust device and method based on self-excitation type piezoelectric element |
CN112834571B (en) * | 2020-12-30 | 2023-07-21 | 中国航空工业集团公司金城南京机电液压工程研究中心 | Gas-liquid two-phase detection device and method based on separate excitation type piezoelectric element |
CN113294411B (en) * | 2021-04-29 | 2023-11-07 | 中国航空工业集团公司金城南京机电液压工程研究中心 | Exhaust device and method based on voice coil element |
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JP3545269B2 (en) * | 1998-09-04 | 2004-07-21 | 日本碍子株式会社 | Mass sensor and mass detection method |
US7458265B2 (en) * | 2003-10-27 | 2008-12-02 | Drexel University | Piezoelectric cantilever sensors |
KR100613398B1 (en) * | 2003-11-25 | 2006-08-17 | 한국과학기술연구원 | Element detecting system using cantilever, method for fabrication of the same system and method for detecting micro element using the same system |
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- 2007-05-10 AU AU2007284995A patent/AU2007284995A1/en not_active Abandoned
- 2007-05-10 EP EP07809068A patent/EP2032976A1/en not_active Withdrawn
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- 2007-05-10 WO PCT/US2007/011402 patent/WO2008020903A2/en active Application Filing
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WO2008020903A3 (en) | 2009-02-05 |
JP5225981B2 (en) | 2013-07-03 |
AU2007284995A1 (en) | 2008-02-21 |
JP2009536738A (en) | 2009-10-15 |
EP2032976A1 (en) | 2009-03-11 |
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