Pressure sensor element to measure contact stress

• US 4,967,764 A
• Filed: 10/24/1988
• Issued: 11/06/1990
• Est. Priority Date: 10/24/1988
• Status: Expired due to Term

• Current Assignee: United States Department Of Health And Human Services (Government of the United States of America)
• Original Assignee: United States Department Of Health And Human Services (Government of the United States of America)
• Inventors: Basser, Peter J.
• Primary Examiner(s): Sykes, Angela D.
• Application Number:
  US07/261,303
• Time in Patent Office: 743 Days
• Field of Search: 128/653-654, 128/748, 128/774, 128/782, 128/653 A, 128/653 R, 424/4, 424/9, 436/173, 436/806
• US Class Current: 600/587
• CPC Class Codes: A61B 5/03 Detecting, measuring or recording fluid pressure within the body other than blood pressure, e.g. cerebral pressure; Measuring pressure in body tissues or organs A61B5/205 takes precedence
• CPC Class Codes: G01L 1/005 by electrical means and not provided for in G01L1/06 - G01L1/22
• CPC Class Codes: G01R 33/28 Details of apparatus provided for in groups G01R33/44 - G01R33/64
• CPC Class Codes: G01R 33/465 applied to biological material, e.g. in vitro testing

Abstract

A biological inplantable pressure sensor element comprises a fixed volume pouch formed by a sealed, flexible, impermeable membrane comprising therewithin a gel mass contained in a gel volume, said gel being hydrated with an aqueous solution comprising an agent having at least a first and a second NMR-detectable form, the proportion of the first to the second form of the agent in the gel volume being determined by their electrolytic interaction with the gel, whereby when an external pressure is applied to the sensor element a d(chemical shift)/d(σ/K) greater than 0.0001 ppm is attained, wherein σ is the external pressure and K is the modulus of the gel. A kit contains sterile, individually wrapped sensor elements.

A method of measuring in vivo contact stress applied to an implanted pressure sensor element, comprises implanting the pressure sensor of the invention into a situs of a subject in need of such measurement, non-invasively subjecting the subject situs to a nuclear magnetic resonance source effective to detect said NMR-detectible agent, obtaining the NMR spectrum of said agent, obtaining the chemical shifts from the spectrum, repeating steps (b) to (d) at least once at a desired time interval, comparing the chemical shifts obtaining in step (d) at different time intervals, and calculating the contact stress applied to said sensor element at a desired time from a correlation of observed chemical shifts for normalized stresses (σ/K) for the sensor element.

A method of measuring in vitro contact stress applied to a pressure sensor element, comprises placing the stress sensor element of the invention in contact with a biological tissue in culture, non-invasively subjecting the biological tissue to a nuclear magnetic resonance source effective to detect said NMR-detectible agent, obtaining the NMR spectrum of said agent, obtaining the chemical shifts from the spectrum, repeating steps (b) to (d) at least once at a desired time interval, comparing the chemical shifts obtained in step (d) at different time intervals, and calculating the contact stress applied to said sensor element at a desired time from a correlation of observed chemical shifts to normalized stresses (σ/K) for the sensor element.

Claims

1. A biologically implantable pressure sensor element, comprising

a fixed membrane volume pouch formed from a sealed, flexible, liquid- and ion-impermeable, heat-permeable membrane comprising therewithin an aqueous solution comprising an agent having at least first and second NMR-detectable forms, and a polyelectrolyte gel mass contained in a gel volume comprised in the membrane volume, the gel being placed in contact and hydrated with the solution, wherein the solution is comprised in at least a first compartment defined by the gel volume and a second compartment defined by the membrane volume which is external to the gel volume, the proportion of the first to the second form of said agent in said gel volume being determined by an electrolytic interaction thereof with the gel, whereby when an external contact pressure is applied to the sensor element a d(chemical shift)/d(σ

/K) greater than about 0.0001 ppm is attained, wherein σ

is the external pressure and K is the modulus of the gel.

2. The sensor element of claim 1, wherein

the membrane is non-biodegradable, physiologically-acceptable membrane.

3. The sensor element of claim 1, wherein

the NMR-detectable agent is a polyelectrolyte.

4. The sensor element of claim 1, wherein

the NMR-detectable agent is a fluorinated aminoacid.

5. The pressure sensor element of claim 1, wherein

the polyelectrolyte comprises partially hydrolyzed polyacrylamide.

6. The pressure sensor element of claim 1, wherein

the proportion of gel:

solution is about 1;

10 to 10;

1 and

the NMR-detectable agent is present in the solution in an amount of about 1×

10^-5 to 3.0M.

7. A kit, comprising

1 to 100 biologically implantable pressure sensor elements, each element comprising a fixed membrane volume pouch formed from a sealed, flexible, liquid- and ion-impermeable, heat-permeable membrane comprising therewithin an aqueous solution comprising an agent having at least first and second NMR-detectable forms, and a polyelectrolyte gel mass contained in a gel volume comprised in the membrane volume, the gel being placed in contact and hydrated with the solution, wherein the solution is comprised in at least a first compartment defined by the gel volume and a second compartment defined by the membrane volume which is external to the gel volume, the proportion of the first to the second form of said agent in said gel volume being determined by an electrolytic interaction thereof with the gel, whereby when an external contact pressure is applied to the sensor element a d(chemical shift)/d(σ

/K) greater than about 0.0001 ppm is attained, wherein σ

is the external pressure and K is the modulus of the gel.