US20230131362A1 - Intraosseous implanted biological sensor - Google Patents

Abstract

A method and system for monitoring analytes in the circulatory system of an individual is provided. A biological sensor is implanted in the bone marrow of a patient and may be self contained within a housing. The biological sensor measures physiological parameters of a patient, including analytes, on a fixed or adjustable schedule. The biological sensor includes a control unit having a transmitter and an energy source for providing energy to the control unit. The biological sensor may be used to adjust other medical treatments and devices in a closed or semi closed loop mechanism and/or predict patient treatment.

Description

RELATED APPLICATIONS AND CLAIM OF PRIORITY
• This patent document is a continuation of U.S. Pat. Application No. 16/976,104 filed Aug. 27, 2020, which is a national phase entry of International Application No. PCT/US2019/021559 filed Mar. 11, 2019, which claims priority to U.S. Provisional Pat. Application No. 62/641,737 filed Mar. 12, 2018. The disclosures of the listed applications are fully incorporated into this document by reference.
FIELD OF THE INVENTION
• The invention relates to the field of biological sensors. More particularly, the invention relates to an intraosseous implantable biological sensor.
BACKGROUND OF THE INVENTION
• Biological sensors are known. However, what is needed is a biological sensor that can be implanted into the bone marrow for long-term to assaying of circulating active and inactive substances which relate to physiologic and pathologic processes.
BRIEF SUMMARY OF THE INVENTION
• The foregoing need is addresses by the intraosseous implantable biological sensor in accordance with the invention.
• The method and system in accordance with the invention monitors analytes in the circulation by providing a biological sensor that is embedded in the bone marrow of a patient and may be self contained within a housing. The functional system is entirely embedded within a patient’s body. The biological sensor may measure physiological parameters of a patient, including analytes, on a fixed or adjustable schedule.
• The biological sensor includes a control unit having a transmitter and an energy source for providing energy to the control unit. The biological sensor may be used to adjust other medical treatments and devices in a closed or semi closed loop mechanism or predict patient treatment.
• The biological sensor includes a membrane that can be used to access component in the biological sensor to replace or replenish them a system by use of a temporary external attachment using a catheter or other delivery device. The biological sensor may be easily removed from the implantation site and its component parts removed and/or replaced in whole or in part.
• The housing of the biological sensor may be coated with a biocompatible or inert material or may comprise a biocompatible or inert material.
• The biological sensor may also include an integrated treatment system for providing treatment to a patient based on the data received from the sensing units. Alternatively, the treatment system may be implanted in another surgical site or may be external to the patient but connectable to the patient by catheters, tubing and the like for delivery of medications. The treatment may be initiated by the control unit immediately upon receiving data from the sensing units or may be varied over time based on data received from the sensing units. Alternatively, treatment may be suggested, i.e. on the display of an external computing system, but not activated.
• The biological sensor may also include an embedded energy source and control unit including a transmitter. Alternatively, the energy source and/or transmitter are separate from the biological sensor.
• The control unit may be integrated into the biological sensor or may be external to the biological sensor positioned in another part of the body or alternatively external to the body. The control unit may adjust the parameters of system and monitor settings by use of wireless command.
• The sensor for measuring analytes in accordance with the invention includes a housing having an interior; a housing control unit positioned within the housing and having a transmitter and a receiver; an energy source positioned within the housing for providing energy to the control unit; one or more sensing units disposed at least partially within the housing and extending from the housing into a bone marrow of a patient; and a membrane covering a part of the housing that is configured to allow access to the interior of the housing.
• The sensor further includes an ancillary control unit located remotely from the sensor and in communication with the housing control unit. The ancillary control unit has a display for displaying information received from the sensing units through the housing control unit.
• The housing control unit may receives a signal from the one or more sensing units and transmits to the ancillary control unit. The ancillary control unit includes a display and the signal includes patient analyte data that may be displayed on the display.
• The housing control unit is configured to receive a signal from the at least one or more sensing units, the signal including patient analyte data and may transmit instructions to the at least one or more sensing units to measure analytes data on a fixed or adjustable schedule. Alternatively, the housing control unit may receive a signal from the at least one or more sensing units and transmit it to the ancillary control unit and the ancillary control unit transmits instructions to the one or more sensing units to adjust the measurement of analytes. The ancillary control unit or the housing control unit may also transmit instructions to a treatment system to deliver medications to the patient based on the patient analyte data contained within the signal. The treatment system may be housed within the housing or located remotely from a site where the sensor is implanted.
• The one or more sensing units may be removable and replaceable and/or capable of being restored or reconditioned through the housing membrane.
• The sensor includes a replaceable or renewable energy source selected from one or more replaceable batteries or a self generating system which uses a process such as motion or vascular flow, body heat, or chemical reaction.
• These and other aspects of the biological sensor will be further described herein.
BRIEF DESCRIPTION OF THE DRAWINGS
• For a better understanding of the invention, and to show how the same may be carried into effect, reference will now be made, by way of example, to the accompanying drawings, in which:
• FIG.1 is an illustration depicting a pelvis identifying a location site for implanting the sensor in accordance with the invention.
• FIG.2 is a schematic diagram of the sensor in accordance with the invention.
DETAILED DESCRIPTION OF THE INVENTION
• Referring toFIGS.1 and2 the intraosseous implantable biological sensor in accordance with the invention will now be described. Thesensor10 broadly includes ahousing12, one or moresensing units14, acontrol unit16 and an energy source18. Thehousing12 includes amembrane20 thereon that allows replacement and/or replenishment of individual parts, such assensing units14. An ancillary processing device/control unit22 can also be utilized and may integrated into the sensor or positioned and used at a remote location.
• Sensor10 may direct automated and semi automated treatment techniques such as closed, and partially closed loop infusions. The insertion into the marrow space allows measurement through small blood channels while allowing thesensor10 to be fixed directly to tissue. In addition, thesensor10 is embedded (implanted) so that the skin and subcutaneous tissues cover it allowing minimal external compromise.
• Sensing units14 may include optical, enzymatic, calorimetry, thermal, spectroscopy, or “lab on a chip.” A portion of thesensing units14 are housed within the sensor housing and a portion thereof may project into thebone marrow26 of a patient. Alternatively, the distal end of the sensing units may be flush with thehousing12 but housing may contain an opening30 that exposes the sensing units to the bone marrow These may be in a combined modality and other non specified technologies may also be used. The device may measure one or more analytes over various time cycles. These may be fixed or controlled externally by a wireless method to adjust the timing of thesensor10.
• Control unit16 may include a receiver for receiving a signal from the sensing units that includes physiological data of the patient. Thecontrol unit16 may also includes a transmitter that may transmit the signal to a remotely located ancillary processing device22 for analysis. The processing device22 may include a display screen for displaying the analyzed data to monitor the condition of the patient. Data generated from thesensing units14 may alter treatment settings of respirators, dialysis systems, pacemakers, defibrillators and intravenous, intraarterial, interstitial, cerebrospinal and subcutaneous injections and infusions as well as alteration and adjustment of other medical devices or treatments.Control unit16 may include memory having a data base of knowledge including known normative data related to interpreting the analyte data received from the sensing units.Control unit16 receives a signal from the sensing units which contains patient physiological parameters and analyzes the physiological parameters and other data obtained from thesensing units14.Control unit16 analyzes the data (i) in isolation as it is received; (ii) in the context of measurement and analysis based on the past history of the patient, which is stored in memory; or (iii) cross-references the patient data in the signal and cross-references it with the known normative data in the database. Alternatively,control unit16 transmit the signal to a remotely located ancillary processing/control unit22. The processing unit22 optionally includes adisplay device24 for displaying the output. Thecontrol unit16 or the ancillary processing unit22 can also include information related to goal-directed therapies associated with particular disease states for providing suggested goal-directed treatments based on the cross-referencing step and outputs a suggested treatment by transmitting it wirelessly or by wire to atreatment system28. Thetreatment system28 may include one or more medications for delivering the medications to a patient.
• In addition thesensing units14 could monitor potentially toxic substances such as inhalants or injurious materials allowing rapid treatment, for example antidotes. Such treatment could be integrated with a separate embedded structure and could be initiated by a signal from the sensor. This treatment component could be embedded in themarrow26 or another part of the body.
• Energy source18 may include one or more replaceable batteries or a self generating system which uses a process such as motion or vascular flow, body heat, or chemical reaction. These in combination with other sources known to those of skill in the art may also be used.
• Thesensor10 is configured to measure and record numerous analytes including but not limited to biochemical, hormonal, inflammatory, hematologic, genetic/nucleic acid and physiologic concentrations, vascular pressures, flow rates, pharmacologic concentrations, degradation products, pH, oxygen, carbon dioxide, toxic exposures, metabolic factors such as glucose, lactate, electrolytes; hormones such as cortisol, insulin, epinephrine; drug and drug metabolites; other therapeutic substances such as monoclonal antibodies, ligands, and chemotherapeutic agents; hematologically active substances such coagulants and anticoagulants; DNA, RNA and nucleic acid containing substances.
• Thesensor10 may be implanted by surgical insertion and remain without extension through the skin. The area of implantation is pelvic and usually the ileum but not restricted to these sites. Thehousing12 may comprise biologically inert or biocompatible material such as polymers, stainless steel, silicone and the like. Thehousing membrane20 is porous so as to allow contact with the marrow circulation without producing inflammation and/or rejection. Regeneration of thesensing units14 could be through injection or insertion of new material through temporary use of a catheter or needle into the device or alternatively extraction of the sensing units and replacement such as in a self contained form. Those of skill in the art will also appreciate that although long-term use is contemplated the entire sensor may be replaced or individual parts such as the energy source18 orcontrol unit16 may be replaced or replenished.
• While the invention has been described with reference to the specific embodiments thereof, those skilled in the art will be able to make various modifications to the described embodiments of the invention without departing from the true spirit and scope of the invention. The terms and descriptions used herein are set forth by way of illustration only and are not meant as limitations. Those skilled in the art will recognize that these and other variations are possible within the spirit and scope of the invention as defined in the following claims and their equivalents.

Claims (11)

What is claimed:

1. A sensor for measuring analytes comprising:

a housing having an interior;

a housing control unit positioned within the housing and having a transmitter and a receiver;

an energy source positioned within the housing for providing energy to the control unit;

one or more sensing units positioned at least partially within the housing and extending from the housing into a bone marrow of a patient, the sensing units in communication with the control unit;

a porous membrane covering a part of the housing that is configured to allow access to the interior of the housing.

2. The sensor ofclaim 1 further comprising an ancillary control unit located remotely from the sensor and in communication with the housing control unit, the ancillary control unit having a display.

3. The sensor ofclaim 2 wherein a signal from the one or more sensing units is received by the housing control unit and transmitted to the ancillary control unit.

4. The sensor ofclaim 3 wherein said signal transmitted to the ancillary control unit includes patient data that may be displayed on the display.

5. The sensor ofclaim 1 wherein the control unit is configured to receive a signal from the at least one or more sensing units, said signal including patient analyte data and transmit instructions to said at least one or more sensing units to measure analytes data on a fixed or adjustable schedule.

6. The sensor ofclaim 1 wherein the one or more sensing units are removable and replaceable.

7. The sensor ofclaim 1 further comprising a treatment system for providing medication to the patient, the treatment system housed within the housing or located remotely from a site where the sensor is implanted.

8. The sensor ofclaim 7 wherein the control unit is configured to receive a signal from the at least one or more sensing units, said signal including patient analyte data and transmit instructions to the treatment system to deliver medication to the patient based on the patient analyte data included in the at least one or more sensing units signal.

9. The sensor ofclaim 1 wherein the energy source is selected from one or more replaceable batteries or a self generating system which uses a process such as motion or vascular flow, body heat, or chemical reaction.

10. The sensor ofclaim 1 wherein the analytes are selected from biochemical, hormonal, inflammatory, hematologic, genetic/nucleic acid and physiologic concentrations, vascular pressures, flow rates, pharmacologic concentrations, degradation products, pH, oxygen, carbon dioxide, toxic exposures, metabolic factors such as glucose, lactate, electrolytes; hormones such as cortisol, insulin, epinephrine; drug and drug metabolites; other therapeutic substances such as monoclonal antibodies, ligands, and chemotherapeutic agents; hematologically active substances such coagulants and anticoagulants; DNA, RNA and nucleic acid containing substances.

11. The sensor ofclaim 1 wherein the sensor is implantable in a pelvic region of a patient.

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