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US4681119A Expired / Lapsed US ⏱️ 0.0 years remaining

Method of production and use of microbubble precursors

Assignee: Bayer Pharma AG
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Filing: 1986-04-22
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Granted: 1987-07-21
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Expires: 2006-04-22
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Abstract

Abstract In the inventive method, microbubbles are formed in body liquid or carrier liquid, for example within the genitourinary or digestive systems in order to alter the transmission characteristics thereof to electromagnetic and sonic waves transmitted therethrough, by dissolving therein a solid particulate material, preferably as a suspension in a carrier liquid in which the particulate material is at least temporarily stable, the particles of which are substantially free of microbubbles and have a plurality of gas-filled voids communicating with the surface of the particles and providing nuclei for microbubble formation and the ratio of the mass of the particles to the volume of gas in the voids is sufficient to render the liquid in which the particulate material is dissolved supersaturated with respect to the gas in the voids in the area of the liquid surrounding the microbubbles when they are formed.

Inventors

  • 👤 Julia S. Rasor
  • 👤 Ernest G. Tickner

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 09:44
CPC Classifications
A; A61; A61K; A61K49/00; A61K49/22; A61K49/222; A61K49/223; A61B; A61B8/00; A61B8/06; A61B8/48; A61B8/481

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 167 words
In a method for altering the transmission characteristics of a liquid-filled region of the body other than the cardiovascular system to an electromagnetic or elastic wave transmitted therethrough by dispersing in the liquid an amount of microbubbles effective to substantially alter such transmission characteristics of the liquid in the area thereof containing the microbubbles, wherein the microbubbles are formed by dissolving in the liquid a solid which is particulate, is substantially free of microbubbles, and consists predominantly of particles which have a plurality of gas-filled voids communicating with the surface of the particles and a plurality of nuclei for microbubble formation and the ratio of the mass of the particles to the volume of gas in the voids is sufficient to render the liquid in which the particulate material is dissolved supersaturated with respect to the gas in the voids in the area of the liquid surrounding the microbubbles, the improvement wherein the liquid is sterile water or sterile aqueous galactose solution and the solid is galactose.
Claim 2
Dependent Claim 167 words
In a method for altering the transmission characteristics of a liquid-filled region of the body other than the cardiovascular system to an electromagnetic or elastic wave transmitted therethrough by dispersing in the liquid an amount of microbubbles effective to substantially alter such transmission characteristics of the liquid in the area thereof containing the microbubbles, wherein the microbubbles are formed by dissolving in the liquid a solid which is particulate, is substantially free of microbubbles, and consists predominantly of particles which have a plurality of gas-filled voids communicating with the surface of the particles and a plurality of nuclei for microbubble formation and the ratio of the mass of the particles to the volume of gas in the voids is sufficient to render the liquid in which the particulate material is dissolved supersaturated with respect to the gas in the voids in the area of the liquid surrounding the microbubbles, the improvement wherein the liquid is sterile water or sterile aqueous galactose solution and the solid is galactose.
Claim 3
Dependent Claim 15 words
The method according to claim 1, wherein the liquid is about 20% wt./vol. galactose solution.
Claim 4
Dependent Claim 12 words
The method according to claim 1, wherein the solid is α-D(+) galactose.
Claim 5
Dependent Claim 34 words
The method according to claim 1, wherein within 5-10 minutes prior to use the galactose is added to the water or galactose solution and the mixture shaken to yield a suspension of the microbubbles.
Claim 6
Dependent Claim 21 words
The method according to claim 4, wherein the solid is α-D(+) galactose wherein the liquid is about 20% wt./vol. galactose solution.
Claim 7
Dependent Claim 17 words
A method according to claim 1, wherein the liquid filled region is part of the digestive system.
Claim 8
Dependent Claim 17 words
A method according to claim 1, wherein the liquid filled region is part of the urinary system.
Claim 9
Dependent Claim 17 words
A method according to claim 1, wherein the liquid filled region is part of the reproductive system.
Claim 10
Independent Claim 185 words
A method of enhancing ultrasonic images in a liquid filled region of the body other than the cardiovascular system of a living test subject, comprising the steps of: (a) forming a fluid injectable suspension of: (i) particulate galactose which is substantially free of microbubbles, whose paarticles are aggregates having gas filled voids therebetween of smaller particles having an average size in the range of from 1 to 250 micrometers, with the ratio of the mass of the smaller particles to the volume of gas in the voids therebetween effective to render blood in which the particulate solid is dissolved supersaturated with respect to the gas in the area of the blood surrounding the microbubbles when they form therein; in (ii) an amount of sterile water or a sterile galactose solution in which the solid galactose is at least temporarily stable; (b) injecting a unit dosage amount of the fluid injectable suspension into the liquid-filled region of the test subject, thereby forming a cloud of microbubbles in the liquid therein; and (c) obtaining an ultrasonic image of the liquid-filled region opposite a location containing said microbubbles.
Claim 11
Independent Claim 185 words
A method of enhancing ultrasonic images in a liquid filled region of the body other than the cardiovascular system of a living test subject, comprising the steps of: (a) forming a fluid injectable suspension of: (i) particulate galactose which is substantially free of microbubbles, whose paarticles are aggregates having gas filled voids therebetween of smaller particles having an average size in the range of from 1 to 250 micrometers, with the ratio of the mass of the smaller particles to the volume of gas in the voids therebetween effective to render blood in which the particulate solid is dissolved supersaturated with respect to the gas in the area of the blood surrounding the microbubbles when they form therein; in (ii) an amount of sterile water or a sterile galactose solution in which the solid galactose is at least temporarily stable; (b) injecting a unit dosage amount of the fluid injectable suspension into the liquid-filled region of the test subject, thereby forming a cloud of microbubbles in the liquid therein; and (c) obtaining an ultrasonic image of the liquid-filled region opposite a location containing said microbubbles.
Claim 12
Dependent Claim 15 words
The method according to claim 9, wherein the liquid is about 20% wt./vol. galactose solution.
Claim 13
Dependent Claim 12 words
The method according to claim 9, wherein the solid is α-D(+) galactose.
Claim 14
Dependent Claim 34 words
The method according to claim 9, wherein within 5-10 minutes prior to use the galactose is added to the water or galactose solution and the mixture shaken to yield a suspension of the microbubbles.
Claim 15
Dependent Claim 21 words
The method according to claim 12, wherein the solid is α-D(+) galactose wherein the liquid is about 20% wt./vol. galactose solution.
Claim 16
Dependent Claim 17 words
A method according to claim 13, wherein the liquid filled region is part of the digestive system.
Claim 17
Dependent Claim 17 words
A method according to claim 13, wherein the liquid filled region is part of the urinary system.
Claim 18
Dependent Claim 17 words
A method according to claim 13, wherein the liquid filled region is part of the reproductive system.

References Cited (Backward Citations)

US4466442A Cited
US4572203A Cited
US4615879A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-07-20 1991-01-19 1991-07-21 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-07-20 1995-01-19 1995-07-21 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-07-20 1999-01-19 1999-07-21 $7700.00 Window Closed / Lapsed

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