TRANSMISSION MEDIUM FOR ULTRASONIC DIAGNOSIS

• US 20110252889A1
• Filed: 04/18/2011
• Published: 10/20/2011
• Est. Priority Date: 10/02/2001
• Status: Active Grant

• Current Assignee: Idemitsu Kosan Company Limited
• Original Assignee: Idemitsu Kosan Company Limited
• Inventors: TSUBOUCHI, Toshiyuki, AOYAMA, Shoji, FUKUHARA, Mikio
• Granted Patent: US 8,292,813 B2
• Time in Patent Office: Days
• US Class Current: 73/600
• CPC Class Codes: G01N 29/28 providing acoustic coupling , e.g. water impedance matching G10K11/02

Abstract

Provided is a method of ultrasound diagnosis, wherein the method includes: coating a surface of a specimen with a transmission medium; and performing the ultrasound diagnosis, wherein the transmission medium has a viscosity of at least 1,000 mPa·s at 25° C. and contains a hydrocarbon compound.

Claims

1-3. -3. (canceled)

4. A method of ultrasound diagnosis, wherein the method comprises:

coating a surface of a specimen with a transmission medium; and

performing the ultrasound diagnosis,

wherein the transmission medium has a viscosity of at least 1,000 mPa·

s at 25°

C. and comprises a hydrocarbon compound.

5. The method according to claim 4, wherein said performing the ultrasound diagnosis comprises:

transmitting an ultrasonic wave through the transmission medium to the specimen; and

analyzing the ultrasonic wave received through the transmission medium from the specimen.

6. The method according to claim 5, wherein the ultrasonic wave is at least one ultrasonic wave selected from the group consisting of a transverse wave, a shear horizontal wave, a shear vertical wave, and a longitudinal wave.

7. The method according to claim 4, wherein the hydrocarbon compound comprises a quaternary carbon.

8. The method according to claim 4, wherein the hydrocarbon compound comprises a cyclic structure.

9. The method according to claim 4, wherein the hydrocarbon compound comprises a quaternary carbon and a cyclic structure.

10. The method according to claim 4, wherein the hydrocarbon compound comprises a cyclic structure comprising a saturated ring selected from the group consisting of a cyclohexane ring, a decalin ring, a cyclopentane ring, a bicyclo[2,2,1]heptane ring, a bicyclo[2,2,2]octane ring, a bicyclo[3,2,1]octane ring, and a bicyclo[3,3,0]octane ring.

11. The method according to claim 4, wherein the hydrocarbon compound comprises a cyclic structure comprising an aromatic ring selected from the group consisting of a benzene ring, a naphthalene ring, an anthracene ring, a fluorene ring, an indan ring, and an acenaphthene ring.

12. The method according to claim 4, wherein the hydrocarbon compound is selected from the group consisting of dipentene oligomer hydride, polybutene, dicyclopentadiene oligomer hydride, dicyclopentadiene-styrene oligomer hydride, polyphenyl ether, styrene oligomer, styrene oligomer hydride, α

-methylstyrene oligomer, α

-methylstyrene oligomer hydride, and mixtures thereof.

13. The method according to claim 4, wherein the hydrocarbon compound is 2-methyl-3-methyl-2[(3-methylbicyclo[2,2,1]kept-2-yl)methyl]bicyclo[2,2,1]-heptane.

14. The method according to claim 4, wherein the hydrocarbon compound is 3-methyl-2-[(3-methylbicyclo[2,2,1]hept-2-yl)methyl]-2-[2,3-dimethylbicyclo-[2,2,1]kept-2-yl]methyl]bicyclo[2,2,1]heptane.

15. The method according to claim 4, wherein the hydrocarbon compound is a mixture of 2-methyl-3-methyl-2[(3-methylbicyclo[2,2,1]hept-2-yl)methyl]bicyclo[2,2,1]-heptane and 3-methyl-2-[(3-methylbicyclo[2,2,1]hept-2-yl)methyl]-2-[2,3-dimethylbicyclo-[2,2,1]hept-2-yl ]methyl]bicyclo[2,2,1]heptane.

16. The method according to claim 4, wherein the transmission medium has a viscosity of 1,000-300,000 mPa·

s at 25°

C.

17. The method according to claim 4, wherein the transmission medium has a viscosity of 1,000-150,000 mPa·

s at 25°

C.

18. The method according to claim 4, wherein the transmission medium further comprises an ether compound comprising a cyclic structure.

19. The method according to claim 4, wherein the ether compound comprises a cyclic structure comprising a saturated ring selected from the group consisting of a cyclohexane ring, a decalin ring, a cyclopentane ring, a bicyclo[2,2,1]heptane ring, a bicyclo[2,2,2]octane ring, a bicyclo[3,2,1]octane ring, and a bicyclo[3,3,0]octane ring.

20. The method according to claim 4, wherein the ether compound comprises a cyclic structure comprising an aromatic ring selected from the group consisting of a benzene ring, a naphthalene ring, an anthracene ring, a fluorene ring, an indan ring, and an acenaphthene ring.

21. The method according to claim 4, wherein the transmission medium further comprises an ester compound comprising a cyclic structure.

22. The method according to claim 4, wherein the ester compound comprises a cyclic structure comprising a saturated ring selected from the group consisting of a cyclohexane ring, a decalin ring, a cyclopentane ring, a bicyclo[2,2,1]heptane ring, a bicyclo[2,2,2]octane ring, a bicyclo[3,2,1]octane ring, and a bicyclo[3,3,0]octane ring.

23. The method according to claim 4, wherein the ester compound comprises a cyclic structure comprising an aromatic ring selected from the group consisting of a benzene ring, a naphthalene ring, an anthracene ring, a fluorene ring, an indan ring, and an acenaphthene ring.