US20050192489A1 - Swallowable data recorder capsule medical device - Google Patents

Abstract

The present invention provides a swallowable data recorder medical device. The swallowable data recorder medical device includes a capsule including a sensing module for sensing a biologic condition within a body. A recording module is provided including an atomic resolution storage device. The recording module is electrically coupled to the sensing module for recording data representative of the sensed biologic condition in the atomic resolution storage device. A power supply is coupled to the recording module.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
• This patent application is related to Non-Provisional U.S. Patent DISPENSER CAPSULE MEDICAL DEVICE,” having Attorney Docket No. 10002323-1; which is filed on even date herewith, is assigned to the same assignee as the present application, and is herein incorporated by reference.
THE FIELD OF THE INVENTION
• The present invention relates to intrabody sensors, and in particular an ingestible data recorder capsule medical device which senses and records information within a body.
BACKGROUND OF THE INVENTION
• Obtaining information about biologic conditions on the inside of the body poses at least two basic issues. First, one must place a sensing device in the body at the desired location. For example, to obtain data about biologic conditions on the large intestine or colon, one must insert a sensor at that location. Second, the data obtained must be transmitted from the internal location to a remote location outside of the human body for processing, storage and/or analysis.
• In one example, a conventional endoscope inserted within a colon can obtain internal information about the colon, such as an image of any polyps in the colon, and then transmit that image to a remote location for real time viewing and/or storage. Unfortunately, use of an endoscope is quite invasive requiring insertion of a probe within the colon and simultaneous extension of communication lines from the probe to a location outside of the colon. Moreover, in addition to manual insertion, this method requires manually maintaining the position of the sensing device, e.g. probe, within the body. Accordingly, only locations within the body that are reachable by insertable probes can be monitored using this method.
• In another example, an inert, ingestible medical capsule is known which is capable of sensing temperature within the digestive tract and then transmitting that temperature data to a receiver located remotely outside of the body. Since the capsule is inert, i.e. non-digestible, the capsule can be reused for subsequent procedures. Use of this medical capsule requires the patient to be located closely to the remote data receiver for an extended period of time to insure that the sensed data is properly transmitted to the remote receiver.
• Perhaps more importantly, this conventional capsule is limited to sensing a single type of data, e.g. temperature. Moreover, the amount of data recorded remotely is limited by the size and strength of components located within the capsule, such as the size and amount of memory storage available within the capsule, the size and strength of transmitter in the conventional capsule, as well as by the associated wireless communication technique. Naturally, these constraints artificially limit the amount and types of biologic data that could otherwise be sensed and recorded throughout the digestive tract since the biologic information available is virtually limitless.
• Accordingly, conventional intrabody sensors have several limitations. First, manual insertion of sensors limit the number and type of body locations that can be monitored and also require extensive remote (i.e. outside of the body) equipment support during the procedure. Second, more mobile sensors, such as ingestible capsules, require a remote receiver for receiving data transmitted from the capsule. This requirement forces the patient to remain relatively stationary for a protracted period of time during the procedure, or forces the patient to wear some form of remote receiver. Finally, the conventional capsule is limited in the amount and type of data sensed and recorded.
SUMMARY OF THE INVENTION
• The present invention provides a swallowable data recorder medical device. The swallowable data recorder medical device includes a capsule enclosing a sensing module for sensing a biologic condition within a body. A recording module is provided including an atomic resolution storage device. The recording module is electrically coupled to the sensing module for recording data representative of the sensed biologic condition in the atomic resolution storage device. A power supply is coupled to the recording module.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a schematic illustration of one exemplary embodiment of a swallowable data recorder capsule medical device, according to the present invention.
• FIG. 2 is a sectional view of a digestive tract of a human body showing the travel path of a swallowable data recorder capsule medical device, according to an embodiment of the present invention.
• FIG. 3 is a block diagram of a swallowable data recorder capsule, according to an embodiment of the present invention.
• FIG. 4 is a side view illustrating one exemplary embodiment of a storage device used in a swallowable data recorder capsule medical device in accordance with the present invention.
• FIG. 5 is a simplified schematic diagram illustrating one exemplary embodiment of storing information within the storage device illustrated inFIG. 4.
• FIG. 6 is a top view illustrating one exemplary embodiment of a storage device used in a swallowable data recorder in accordance with the present invention taken along lines6-6 ofFIG. 4.
• FIG. 7 is a diagram illustrating one exemplary embodiment of field emitters reading from storage areas of the storage device ofFIG. 4.
• FIG. 8 is a perspective view of a swallowable data recorder capsule incorporating an image detector array, according to an embodiment of the present invention.
• FIG. 9 is a perspective view of a sensor array of a swallowable data recorder capsule, according to an embodiment of the present invention.
• FIG. 10 is a schematic illustration of the swallowable data recorder capsule ofFIG. 9.
• FIG. 11 is a schematic illustration of a swallowable data recorder capsule incorporating a video recorder module, according to an embodiment of the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
• In the following detailed description of the preferred embodiments, reference is made to the accompanying drawings which form a part hereof, and in which is shown by way of illustration specific embodiments in which the invention may be practiced. It is to be understood that other embodiments may be utilized and structural or logical changes may be made without departing from the scope of the present invention. The following detailed description, therefore, is not to be taken in a limiting sense, and the scope of the present invention is defined by the appended claims.
• The present invention provides a swallowable data recorder capsule medical device which internally senses and internally records information about biologic conditions within the digestive tract of a body. The capsule is inert and therefore ingestible and passable through the digestive tract without being consumed. Accordingly, the swallowable sensor and recorder optimally is used in sensing and recording information about the digestive tract or about chemical conditions or conditions within the digestive tract that are indicative of conditions in other organs (e.g., skin). Preferably all of the biologic information sensed within the digestive tract is recorded immediately in an atomic resolution storage device or atomic resolution memory within the capsule while the capsule is in the digestive tract. The sensed data is conveniently retrievable from the atomic resolution storage device memory after the capsule is captured outside of the body.
• The atomic resolution storage device memory used in the swallowable data recorder capsule medical device according to the present invention is subminiature in size, allowing it to be contained within a swallowable capsule, has low power requirements, and provides for non-volatile storage of large amounts of data, including video. The term “atomic resolution storage device” memory as used herein is defined as a non-volatile memory storage device capable of storing a large volume of data, such as megabytes to gigabytes of data points, within a relatively small storage area and requiring very low power consumption. The atomic resolution storage device includes a field emitter, a storage medium, and a micromover and associated circuitry for the reading and writing of data. Preferably, the atomic resolution storage device includes a plurality of spaced apart field emitters, wherein each field emitter is responsible for a number of storage areas on the storage medium.
• As shown generally inFIG. 1, a swallowable data recorder capsulemedical device10 of the present invention includes a capsule housing orcapsule shell12 containingsensing module14 andrecording module16. Capsule10 is readily ingestible within a digestive tract of a human body and is inert (i.e. non-digestible) so thatcapsule10 passes through the digestive tract without being consumed.Sensing module14 senses one or more predetermined biologic condition(s) within the human body such as temperature, pH, biological/chemical constituents, and/or visually recognizable landmarks internally within the human body, etc.Recording module16 records, withincapsule10, a digital representation of the data sensed bysensing module14. Accordingly, after ingestion,capsule10 senses one or more predetermined biologic conditions within a digestive tract of the human body and then stores that biologic information “on-board” withincapsule10 as data inrecording module16. In one preferred embodiment, the stored data is retrieved aftercapsule10 is captured outside of the human body.
• FIG. 2 showscapsule10 in association withhuman body30 includingdigestive tract32 havingmouth34,esophagus36,stomach38,small intestine40,large intestine42, andrectum44. Once ingested withinmouth34,inert capsule10 travels the full path ofdigestive tract32 untilcapsule10 is captured upon exiting atrectum44. Each of the named locations within the human body represents examples of locations at whichcapsule10 can sense and record data regarding biologic conditions. Of course, operation ofcapsule10 is not limited to use in the named locations ascapsule10 can sense and record data anywhere withindigestive tract32. More importantly,recording module16 has sufficient capacity to store data from multiple locations withindigestive tract34 and regarding several biologic parameters.
• Capsule10, particularly itsshell12, preferably is made of or coated with one or more of the following inert materials: Teflon (i.e., polytetrafluouroethylene); glass; ceramic; or other materials known to those skilled in the art. Other suitable materials will become apparent to those skilled in the art after reading the present application.Capsule10 preferably has a size as large as the digestive tract will allow, such as five millimeters in diameter, and preferably has a generally rounded oblong shape, as shown inFIG. 1. However, other shapes and sizes can be used (e.g., a smaller capsule), provided that the shapes are readily passable throughdigestive tract34 and can adequately house the required sensing andrecording module14,16.
• Capsule10 is capable of continuously sensing biologic conditions and continuously recording that sensed data within thecapsule10. Alternatively, each of the sensing and recording functions can be selectively controlled using remote wireless communication techniques for selective activation at a predetermined body location or at a predetermined point in time. Accordingly, as shown inFIG. 2,capsule10 optionally comprises a larger system includingwireless communication system20 with transmitter/receiver21 that operates (i.e., communicates) with a transmitter/receiver (not shown) incorporated incapsule10. Finally,capsule10 optionally continuously senses biologic conditions and then records data or only selectively records data (representative of those conditions) upon the sensed data reaching a predetermined value of one or more predetermined parameters (e.g., temperature, pH, etc.).
• FIG. 3 is a block diagram illustrating one exemplary embodiment of swallowabledata recorder capsule10, illustratingcapsule10 in greater detail. As shown inFIG. 3,recorder capsule10 includessensors50,52,controller54,memory56, optionalprogrammable logic58,power supply60, andcommunication interface62. Communications interface62 may include one or more of the following types of communication modules:radiofrequency64; ultrasonic66; and/or infrared68. Other suitable communication modules will become apparent to those skilled in the art after reading the present application. Finally, atleast memory56, and preferably alsocontroller54 and/orprogrammable logic58 are embodied on arecording module70, and preferably on a silicon-basedmodule70 in one or more semiconductor chips.
• Sensors50,52 further definesensing module14 ofFIG. 1.Sensors50,52 define multiple sensors that are arranged about an outer surface ofcapsule10 in a desired predetermined orientation to expose each sensor to a targeted bodily condition or landmark target within the human body. Each sensor can comprise a single type of sensor such as an image detector or a different type of sensor (e.g. chemical, electrical, temperature, etc.). For example, chemical detectors detect the presence of many substances, such as the concentration of glucose, which is relevant to treatment of diabetes patients.
• Controller54 regulates communication betweensensors50,52 andmemory54, communication betweenmemory54 and any remote controllers outside of the human body, and communication with programmable logic component(s)58. Finally,controller54 operably controlscommunication interface62 and preferably includes a central processing unit or one or more other devices capable of performing a sequence of logical operations. In one preferred embodiment,controller54 is a microprocessor. In another embodiment,controller54 includes one or more logic gates located withinmemory56.
• Memory orstorage device56 is preferably an ultra-high capacity storage device, and which is more preferably of a silicon-based construction. In one preferred embodiment,memory56 is an atomic resolution storage device capable of storing a large volume of data, such as megabytes to gigabytes of data points, within a relatively small storage area. The atomic resolution storage device is a low power consumption storage device, requiring only about 0.1 watts or less to operate. In one preferred embodiment,ARS module70 has a size of about 1 square millimeter, suitable to be carried within a swallowable medical capsule. In addition, ARS module can include its own modules that correspond to the functions ofprogrammable logic58 and/orcontroller54. Finally, other subminiature memory devices, known to those skilled in the art, that have a high storage capacity with relatively low power consumption can be used in place of ARS module. However, these alternative devices may limit the volume and quality of data recorded since these devices will not be as powerful asARS module70 relative to the power consumption requirements and amount of memory storage.
• One atomic resolution storage device suitable for use in the swallowable data recorder capsule medical device according to the present invention is disclosed in U.S. Pat. No. 5,557,596 to Gibson et al., issued Sep. 17, 1996, entitled “Ultra-High Density Storage Device.” Other suitable ultra-high density storage devices suitable for use asmemory56 with the swallowable data recorder capsule medical device according to the present invention will become apparent to those skilled in the art after reading the present application. One exemplary embodiment of a suitable ultra-high density storage device (i.e., atomic resolution storage device) suitable for use asmemory56 with the swallowable data recorder capsule medical device according to the present invention is disclosed in further detail later in this application.
• Asuitable power supply58 includes a lithium-ion battery, which is relatively non-toxic, as well as other power supplies suitable for in vivo environments.
• Communication interface62 includes a suitable transmission technology, preferable wireless (e.g. ultrasonic, radiofrequency, etc.), that readily permits communication to and fromcapsule10 while capsule is indigestive tract34 and remote transmitter/receiver21 (FIG. 1) is located remotely outside of the body. However,infrared port68 is preferably used for communicating withcapsule10 aftercapsule10 is captured from the body to retrieve sensed data frommemory56. Likewise,infrared port68 preferably is used for programmingcontroller54,memory56, and/orlogic component58 prior to insertion ofcapsule10 within the body to determine the manner in whichsensors50,52 will operate and communicate withmemory56 viacontroller54.
• In use,sensors50,52 ofcapsule10 sense biologic data withindigestive tract34 and the sensed data is passed throughcontroller54 for storage inmemory56. The sensed data is stored inmemory56 and retrieved viacommunication interface62 after capture ofcapsule10 upon exitingdigestive tract34. Finally,wireless communication system20 optionally is used in addition to, or as an alternative to,controller54 andmemory56 to facilitate and retrieving storing sensed data. The most significant aspect ofcapsule10 is recordingmodule16 includingmemory56, which permits internally recording within capsule10 a profile of one or more biologic parameters throughout the entire digestive tract. This feature eliminates the need for transmission of data to a remote receiver as well as expands the type and amount of biologic data sensed and recorded.
• FIGS. 4 through 7 disclose one exemplary embodiment of an atomic resolution storage device capable of storing megabytes to gigabytes of information in a small storage area. For a further discussion of an atomic resolution storage device, see U.S. Pat. No. 5,557,596, entitled, “Ultra-High Density Storage Device”, by Gibson et al. and assigned to Hewlett-Packard Company, which is incorporated herein by reference.
• FIG. 4 illustrates a side cross-sectional view ofstorage device100.Storage device100 is one exemplary embodiment ofstorage device recorder54 includingmemory56.Storage device100 includes a number of field emitters, such asfield emitters102 and104,storage medium106 including a number of storage areas, such asstorage area108, andmicromover110.Micromover110scans storage medium106 with respect to the field emitters or vice versa. In one preferred embodiment, each storage area is responsible for storing one bit of information.
• In one embodiment, the field emitters are point emitters having relatively very sharp points. Each point emitter may have a radius of curvature in the range of approximately1 nanometer to hundreds of nanometers. During operation, a pre-selected potential difference is applied between a field emitter and its corresponding gate, such as betweenfield emitter102 andgate103 surrounding it. Due to the sharp point of the emitter, an electron beam current is extracted from the emitter towards the storage area. Depending on the distance between the emitters and thestorage medium106, the type of emitters, and the spot size (bit size) required, electron optics may be utilized to focus the electron beams. A voltage may also be applied to thestorage medium106 to either accelerate or decelerate the field-emitted electrons or to aid in focusing the field-emitted electrons.
• In one embodiment, casing120 maintainsstorage medium106 in a partial vacuum, such as at least 10⁻⁵torr. It is known in the art to fabricate such types of microfabricated field emitters in vacuum cavities using semiconductor processing techniques. See, for example, “Silicon Field Emission Transistors and Diodes,” by Jones, published in IEEE Transactions on Components, Hybrids and Manufacturing Technology, 15, page 1051, 1992.
• In the embodiment shown inFIG. 4, each field emitter has a corresponding storage area In another embodiment, each field emitter is responsible for a number of storage areas. As micromover110scans storage medium106 to different locations, each emitter is positioned above different storage areas. Withmicromover110, an array of field emitters can scan overstorage medium106.
• As will be described, the field emitters are responsible to read and write information on the storage areas by means of the electron beams they produce. Thus, field emitters suitable for use instorage device100 are the type that can produce electron beams that are narrow enough to achieve the desired bit density on the storage medium, and can provide the power density of the beam current needed for reading from and writing to the medium. A variety of ways are known in the art that are suitable to make such field emitters. For example, one method is disclosed in “Physical Properties of Thin-Film Field Emission Cathodes With Molybdenum Cones,” by Spindt et al, published in the Journal of Applied Physics, Vol. 47, No. 12, December 1976. Another method is disclosed in “Fabrication and Characteristics of Si Field Emitter Arrays,” by Betsui, published in Tech. Digest 4^thInt. Vacuum Microelectronics Conf., Nagahama, Japan, page 26, 1991.
• In one embodiment, there can be a two-dimensional array of emitters, such as 100 by 100 emitters, with an emitter pitch of 50 micrometers in both the X and the Y directions. Each emitter may access tens of thousands to hundreds of millions of storage areas. For example, the emitters scan over the storage areas with a periodicity of about 1 to 100 nanometers between any two storage areas. Also, all of the emitters may be addressed simultaneously or sequentially in a multiplexed manner. Such a parallel accessing scheme significantly reduces access time, and increases data rate of the storage device.
• FIG. 5 shows the top view ofstorage medium100 having a two-dimensional array of storage areas and a two-dimensional array of emitters. Addressing the storage areas requires external circuits. One embodiment to reduce the number of external circuits is to separate the storage medium into rows, such asrows140 and142, where each row contains a number of storage areas. Each emitter is responsible for a number of rows. However, in this embodiment, each emitter is not responsible for the entire length of the rows. For example,emitter102 is responsible for the storage areas withinrows140 through142, and withincolumns144 through146. All rows of storage areas accessed by one emitter are connected to one external circuit. To address a storage area, one activates the emitter responsible for that storage area and moves that emitter by micromover110 (shown inFIG. 4) to that storage area. The external circuit connected to the rows of storage areas within which that storage area lies is activated.
• Micromover110 can also be made in a variety of ways, as long as it has sufficient range and resolution to position the field emitters over the storage areas. As a conceptual example,micromover110 is fabricated by standard semiconductor microfabrication process to scanstorage medium106 in the X and Y directions with respect tocasing120.
• FIG. 6 shows the top view of the cross section6-6 inFIG. 4, illustratingstorage medium106 held by two sets of thin-walled microfabricated beams. The faces of the first set of thin-walled beams are in the Y-Z plane, such as112 and114. Thin-walled beams112 and114 may be flexed in the X direction allowingstorage medium106 to move in the X direction with respect tocasing120. The faces of the second set of thin-walled beams are in the X-Z plane, such as116 and118. Thin-walled beams116 and118 allowstorage medium106 to move in the Y direction with respect tocasing120.Storage medium106 is held by the first set of beams, which are connected to frame122.Frame122 is held by the second set of beams, which are connected tocasing120. The field emitters scan overstorage medium106, orstorage medium106 scans over the field emitters in the X-Y directions by electrostatic, electromagnetic, piezoelectric, or other means known in the art. In this example,micromover110 movesstorage medium106 relative to the field emitters. A general discussion of such microfabricated micromover can be found, for example, in “Novel Polysilicon Comb Actuators for XY-Stages,” published in the Proceeding of MicroElectro Mechanical Systems1992, written by Jaecklin et al.; and in “Silicon Micromechanics: Sensors and Actuators on a Chip”, by Howe et al., published in IEEE Spectrum, page 29, in July 1990.
• In another embodiment, the electron beam currents are rastered over the surface ofstorage medium106 by either electrostatically or electromagnetically deflecting them, such as by electrostatic deflectors or electrodes125 (shown inFIG. 4) positioned adjacent toemitter104. Many different approaches to deflect electron beams can be found in literature on Scanning Electron Microscopy and will not be further described in this specification.
• In one method, writing is accomplished by temporarily increasing the power density of the electron beam current to modify the surface state of the storage area. Reading is accomplished by observing the effect of the storage area on the electron beams, or the effect of the electron beams on the storage area. For example, a storage area that has been modified can represent a bit1, and a storage area that has not been modified can represent a bit0, and vice versa. In fact, the storage area can be modified to different degrees to represent more than two bits. Some modifications may be permanent, and some modifications may be reversible. The permanently modified storage medium is suitable for write-once-read-many memory (WORM).
• In one embodiment, the basic idea is to alter the structure of the storage area in such a way as to vary its secondary electron emission coefficient (SEEC), its back-scattered electron coefficient (BEC), or the collection efficiency for secondary or back-scattered electrons emanating from the storage area. The SEEC is defined as the number of secondary electrons generated from the medium for each electron incident onto the surface of the medium. The BEC is defined as the fraction of the incident electrons that are scattered back from the medium. The collection efficiency for secondary/back-scattered electrons is the fraction of the secondary/back-scattered electrons that is collected by an electron collector, typically registered in the form of a current.
• Reading is typically accomplished by collecting the secondary and/or back-scattered electrons when an electron beam with a lower power density is applied tostorage medium106. During reading, the power density of the electron beam should be kept low enough so that no further writing occurs.
• One embodiment ofstorage medium106 includes a material whose structural state can be changed from crystalline to amorphous by electron beams. The amorphous state has a different SEEC and BEC than the crystalline state, which leads to a different number of secondary and back-scattered electrons emitted from the storage area. By measuring the number of secondary and back-scattered electrons, one can determine the stage of the storage area. To change from the amorphous to crystalline state, one increases the beam power density and then slowly decreases it. This heats up the amorphous and then slowly cools it so that the area has time to anneal into its crystalline state. To change from crystalline to amorphous state, one increases the beam power density to a high level and then rapidly decreases the beam power. To read from the storage medium, a lower-energy beam strikes the storage area. An example of such type of material is germanium telluride (GeTe) and ternary alloys based on GeTe. Similar methods to modify states using laser beams as the heating source have been described in “Laser-induced Crystallization of Amorphous GeTe: A Time-Resolved Study,” by Huber and Marinero, published inPhysics Review B 36, page 1595, in 1987, and will not be further described here.
• There are many preferred ways to induce a state change instorage medium106. For example, a change in the topography of the medium, such as a hole or bump, will modify the SEEC and BEC of the storage medium. This modification occurs because the coefficients typically depend on the incident angle of the electron beam onto the storage area. Changes in material properties, band structure, and crystallography may also affect the coefficients. Also, the BEC depends on an atomic number, Z. Thus, one preferred storage medium has a layer of low Z material on top of a layer of high Z material or vice versa, with writing accomplished through ablating some of the top layer by an electron beam.
• FIG. 7 shows schematically the field emitters reading fromstorage medium106. The state ofstorage area150 has been altered, while the state ofstorage area108 has not been altered. When electrons bombard a storage area, both secondary electrons and back-scattered electrons will be collected by the electron collectors, such aselectron collector152. An area that has been modified will produce a different number of secondary electrons and back-scattered electrons, as compared to an area that has not been modified. The difference may be more or may be less depending on the type of material and the type of modification. By monitoring the magnitude of the signal current collected byelectron collectors152, one can identify the state of and, in turn, the bit stored in, the storage area.
• Field emitters may be noisy with the magnitude of the electron beam current varying with respect to time. Moreover, the gap distance between the tips of the emitters and the surface of the storage medium may vary. If the information stored were based on tunneling current, then the gap distance may be extremely crucial. However, the application presently disclosed depends on field emitters, and not directly on the emitted electron beam current, but rather on the effect of the beam. At least two ways may be used to alleviate the problem of the emitters being noisy. One way is to connect constantcurrent source154 tofield emitter102. This source will control the power density of electron beamcurrent beam156. Although this method would not help storage techniques using the magnitude of the field emitted current as the signal, this method reduces the field emitter noise significantly. Another way to alleviate the field-emitter noise is to separately measure the emitted electron beam current and use it to normalize the signal current. As the electron beam current varies, the signal current varies correspondingly. On the other hand, the normalized signal current remains the same to indicate the state of the storage area.
• FIG. 8 is a perspective view ofcapsule10 in which sensor array80 further definessensors50,52 and includessensors80A,80B,80C,80D,80E, and80F. Eachsensor80A-80F can represent a single type of sensor such as an image detector or a different type of sensor (e.g. chemical, electrical, temperature,etc.). Alternatively, multiple sensors (e.g. sensors80C,80D) can represent a single type of sensor. Sensor array80 is arranged to sense data along the six cardinal directions using the classical major and minor axes of the generally elliptical-shapedcapsule10. However, sensor array80 can include more or less than six sensors and need not be oriented along the six cardinal directions but along other multi-directional orientations as desired. Accordingly, sensor array80 illustrates that multiple sensors are arranged about the capsule surface in a desired predetermined orientation that is expected to expose each sensor, or the full array, to a targeted bodily condition or landmark within the human body.
• FIG. 9 is perspective view ofcapsule10, in whichsensor module90 further definessensor50 and includessensors92,94,96. Eachsensor92,94,96 represents the same type of sensor. Alternatively, as shown inFIG. 10,sensor array90 may includesensors92,94,96 which each comprise a different type of sensor. For example,sensor92 comprises a biologic condition sensor (e.g. pH),sensor94 comprises an electrical sensor (e.g. temperature), andsensor96 comprises a chemical sensor (e.g. sodium and/or potassium).
• Sensing module90 preferably is a silicon-based module, which includes various cavities filled with the desired type of sensing substance and/or circuitry to form eachsensor92,94,96. For example,sensor90 preferably is constructed from a silicon surface bearing a chemically sensitized film for eachsensor92,94,96, wherein the film reacts upon the presence of a particular biologic constituent, producing an electrical response in the silicon surface that is recorded in memory as sensed data.Suitable sensor modules90 are known in the art, such as are available from Agilent Technologies (e.g., an Agilent 2100 bioanalyzer).
• For example, using thesetechniques sensor92 can be selected to sense absolute values of pH, or sense pH only below a certain value, e.g. 5.Sensor92 also could be selected to sense any pH value to provide continuously variable data on pH.
• Alternatively,sensor92 could sense the presence of any expected digestive tract constituent such as bile fluids, or any unexpected digestive tract constituent such as blood, or cancer cells. For example, one of thesensors92,94,96 could be chemically sensitive to cancer cells. Upon a sensor detecting a cancer cell constituent, the data is recorded. After retrieving the data outside of the body, the location indigestive tract34 is determined based on the character of the sensed data and is used to target future diagnostic and/or therapeutic techniques to that location. Alternatively, radiographic or wireless communication techniques can be used to identify the location ofcapsule10 upon the sensed data triggering a transmission signal to a remote receive.
• This type ofsensor array90 conveniently permits a large number of the same type or different type of sensors to be placed on small electrically communicable module. This arrangement is preferred where many different types of tests must be performed. For example, in investigative research, comprehensive information can be gathered about many biologic conditions with one pass ofcapsule10, rather than checking for a single biologic condition with each pass ofcapsule10.
• FIG. 11 is a perspective view of a data recorder capsule of the present invention including a video and illumination capsule in whichsensors50,52 further include avideo module102 and illumination module104 (e.g., a light emitting diode), in which video images are received byvideo module102 andillumination module104 acts to illuminate the subject under investigation. While not shown inFIG. 7,video module102 andillumination module104 are connected to the remainder of the system shown inFIG. 3. Subminiature video receiving and illumination devices known to those skilled in the art can be used. The high capacitystorage device memory56 allows for large amounts of video data to be stored incapsule10.
• As shown inFIG. 11, this embodiment also optionally further includesmagnetic member106 withincapsule10 and remote magnetic positioner108 (for placement outside of the body) to assist inpositioning capsule10 withindigestive tract34 to obtain a desired image usingvideo module102. To orientcapsule10 withindigestive tract34,magnetic positioner108 is manipulated outside the body to directcapsule10 into a desired orientation.Magnetic member106 andmagnetic positioner108 can be incorporated into any of the other embodiments ofcapsule10 described herein.
• A swallowable medical capsule of the present invention has many advantageous features. Foremost, after sensing biologic conditions within a digestive tract, the capsule immediately records that sensed biologic data in memory within the capsule while still in the digestive tract. The sensed data is retrieved later after the capsule is captured upon exit from the digestive tract.
• The ultra large storage capacity of the memory within the capsule along with the use of silicon-based surface sensing modules (or other types of sensors, e.g., imaging) permits large volumes of many different types of biologic conditions to be sensed and recorded internally for later study. In addition, this internal recording feature alleviates the prior art need to immediately transmit sensed data from the capsule inside the digestive tract to a receiver remotely located away from the capsule outside of the body. Accordingly, a patient no longer must remain in close proximity to a receiving device during the time period that the capsule is within the human body. Rather, the patient can move freely, making more likely that such a capsule will be used. Nevertheless, for ultimate flexibility, the internal recording ability also can be used at the same time as known wireless data transmission techniques to both immediately transmit sensed data to a remote location and to record the data internally within the capsule. Finally, unlike the use of endoscopes, use of the capsule is essentially non-invasive, which will likely cause more patients to agree to a diagnostic sensing procedure using the capsule. The capsule may also be implanted at a desired location within a body for long periods of time, sense and record data, and be removed at a later date for data retrieval and analysis.
• Although specific embodiments have been illustrated and described herein for purposes of description of the preferred embodiment, it will be appreciated by those of ordinary skill in the art that a wide variety of alternate and/or equivalent implementations calculated to achieve the same purposes may be substituted for the specific embodiments shown and described without departing from the scope of the present invention. Those with skill in the chemical, mechanical, electromechanical, electrical, and computer arts will readily appreciate that the present invention may be implemented in a very wide variety of embodiments. This application is intended to cover any adaptations or variations of the preferred embodiments discussed herein. Therefore, it is manifestly intended that this invention be limited only by the claims and the equivalents thereof.

Claims (21)

1-22. (canceled)

23. A method of recording data internally within a human body comprising:

ingesting an inert capsule within a digestive tract of a human body;

sensing a predetermined type of biological condition within the digestive tract with a sensor disposed within the capsule; and

recording the sensed biologic condition as data in an atomic resolution storage device memory module within the capsule while the capsule is in the digestive tract.

24. The method ofclaim 23, further comprising:

retrieving the sensed data from memory module when the capsule is outside of the human body.

25. The method ofclaim 24, wherein the retrieving step the further comprises the step of:

capturing the capsule after passage of the capsule through the digestive tract.

26. The method ofclaim 23, further comprising the step of:

transmitting the data from the capsule to a location outside of the human body while the capsule is within the human body.

27. The method ofclaim 23, wherein the sensing step further comprises the step of:

obtaining an image of a predetermined body location within the digestive tract.

28. The method ofclaim 24, wherein the obtaining step further comprises:

arranging a magnetic member in the capsule prior to the ingesting step;

arranging a magnet positioner outside the body; and

magnetically manipulating the relative position and orientation of the capsule within the digestive tract by using the magnet positioner to move the magnetic member in the capsule.

29. The method ofclaim 23, wherein the sensing step further comprises the step of:

exposing a chemical sensor array on the surface of the capsule to sense one or more chemical conditions in the digestive tract.

30. The method ofclaim 29, wherein the exposing step further comprises the step of:

sensing at least one of a relative amount and an absolute amount of at least one or more digestive tract constituents.

31. The method ofclaim 30, wherein the sensing step further comprises the step of:

sensing a pH of the digestive tract constituents.

32. The method ofclaim 23, wherein the sensing step further comprises the step of:

exposing an electrically based sensor in the capsule to sense biologic conditions.

33. The method ofclaim 32, wherein the exposing step further comprises the step of:

sensing a temperature within the digestive tract.

34. The method ofclaim 23, further comprising the step of:

performing the sensing step at a predetermined body location within the digestive tract that corresponds to a known location for the predetermined biologic condition.

35. The method ofclaim 34, further comprising the step of:

identifying the passage of the capsule at a predetermined body location within the digestive tract using at least one of a radiographic technique and an ultrasonic technique.

36. The method ofclaim 23, wherein the recording step further comprises the step of:

recording sensed data continuously within the digestive tract.

37. The method ofclaim 23, wherein the recording step further comprises the step of:

initiating and maintaining recording of the sensed data when the sensed data reaches a predetermined value of a predetermined biologic condition.

38. A method of recording data about biological conditions within a human body, the method comprising:

placing a capsule within a digestive track of a human body, the capsule including a sensor and a storage device comprising an atomic resolution storage device;

sensing a biological condition within the human body with the sensor; and

performing one or more logical operations using the sensed biological condition; and

selectively recording the sensed biological condition to the storage device based upon the logical operations.

39. The method ofclaim 38, wherein sensing a biological condition comprises:

receiving video of the biological condition via a video receiver.

40. The method ofclaim 38, wherein performing one or more logical operations comprises:

accessing programmable logic from the storage device.

41. The method ofclaim 38, wherein selectively recording the sensed biological condition comprises:

generating an electron beam current; and

bombarding a storage area of the atomic resolution storage device with the electron beam current to record data representative of the sensed biological condition.

42. The method ofclaim 41, further comprising:

positioning the storage area to be bombarded by the electron beam current.

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