IP Library Granted Patent US 12,390,112
Granted Patent B2
US 12,390,112 · App. 17/023,108 · Granted Aug 19, 2025

Atherosclerotic plaque detection

Inventors: Karlheinz Peter (Hawthorne, AU); Nay Min Htun (South Yara, AU); Yung-Chih Chen (Box Hill South, AU)
Assignee: BAKER HEART AND DIABETES INSTITUTE
A61B5/0086A61B5/0071A61B5/0084A61B5/02007A61B5/7246A61B5/725A61B5/7275A61B5/7282A61B2576/02
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,390,112
App. No.
17/023,108
Granted
Aug 19, 2025
Kind
B2
Abstract

An apparatus detects atherosclerotic plaques. The apparatus includes an electronic processing device that determines a level of fluorescence sensed by a sensor at a second infrared wavelength in response to exposure of at least part of an artery to radiation at a first infrared wavelength and determines a fluorescence indicator using the level of fluorescence. The fluorescence indicator is indicative of the presence, absence, or degree of an atherosclerotic plaque.

Claims (148)

1. An apparatus for detecting atherosclerotic plaques, the apparatus comprising:

a) a radiation source for generating radiation to thereby expose at least part of an artery to radiation at a first infrared wavelength, wherein the first infrared wavelength is in a range from 600 nm to 900 nm;

b) a sensor configured to sense radiation emitted from at least part of the artery at a second infrared wavelength;

c) an electronic processor configured to:

i) determine a level of autofluorescence sensed by the sensor at the second infrared wavelength in response to exposure of at least part of the artery to radiation at the first infrared wavelength; and

ii) determine a fluorescence indicator using the level of autofluorescence, the fluorescence indicator being indicative of a presence, absence, degree or vulnerability of an atherosclerotic plaque.

2. The apparatus according to claim 1 , wherein:

a) the radiation source comprises a laser;

b) the sensor comprises an infrared photodetector; and/or

c) the apparatus comprises optics for focusing radiation.

3. The apparatus according to claim 1 , wherein the apparatus comprises a catheter comprising one or more optical fibers extending between proximal and distal ends, the distal end being for insertion into the artery, and the radiation source and sensor being coupled to the proximal end.

4. The apparatus according to claim 1 , wherein the apparatus comprises a bandpass filter.

5. The apparatus according to claim 1 , wherein the first infrared wavelength is selected from the group consisting of:

a) 650 nm±50 nm;

b) 700 nm±50 nm;

c) 750 nm±50 nm;

d) 800 nm±50 nm;

e) 850 nm±50 nm;

f) 650 nm−850 nm;

g) 700 nm−850 nm;

h) 750 nm−850 nm;

i) 800 nm−850 nm;

j) 650 nm−800 nm;

k) 700 nm−800 nm;

l) 750 nm−800 nm;

m) 650 nm−700 nm;

n) 650 nm−750 nm;

o) 650 nm−800 nm;

p) 700 nm−750 nm;

q) 685 nm; and

r) 785 nm.

6. The apparatus according to claim 1 , wherein the second infrared wavelength is selected from the group consisting of:

a) different to the first infrared wavelength; and

b) longer than the first infrared wavelength.

7. The apparatus according to claim 1 , wherein the second infrared wavelength is selected from the group consisting of:

a) 700 nm±50 nm;

b) 750 nm±50 nm;

c) 800 nm±50 nm;

d) 850 nm±50 nm;

e) 900 nm±50 nm;

f) 950 nm±50 nm;

g) 1000 nm±50 nm;

h) 1050 nm±50 nm;

i) 1100 nm±50 nm;

j) 700 nm−1150 nm;

k) 750 nm−1150 nm;

l) 800 nm−1150 nm;

m) 850 nm−1150 nm;

n) 900 nm−1150 nm;

o) 950 nm−1150 nm;

p) 1000 nm−1150 nm;

q) 1050 nm−1150 nm;

r) 1100 nm−1150 nm;

s) 700 nm−1100 nm;

t) 750 nm−1100 nm;

u) 800 nm−1100 nm;

v) 850 nm−1100 nm;

w) 900 nm−1100 nm;

x) 950 nm−1100 nm;

y) 1000 nm−1100 nm;

z) 1050 nm−1100 nm;

aa) 700 nm−1050 nm;

bb) 750 nm−150 nm;

cc) 800 nm−1050 nm;

dd) 850 nm−150 nm;

ee) 900 nm−150 nm;

ff) 950 nm−150 nm;

gg) 1000 nm−150 nm;

hh) 700 nm−1000 nm;

ii) 750 nm−1000 nm;

jj) 800 nm−1000 nm;

kk) 850 nm−1000 nm;

11 ) 900 nm−1000 nm;

mm) 950 nm−1000 nm;

nn) 700 nm−950 nm;

oo) 750 nm−950 nm;

pp) 800 nm−950 nm;

qq) 850 nm−950 nm;

rr) 900 nm−950 nm;

ss) 700 nm−900 nm;

tt) 750 nm−900 nm;

uu) 800 nm−900 nm;

vv) 850 nm−900 nm;

ww) 700 nm−850 nm;

xx) 750 nm−850 nm;

yy) 800 nm−850 nm;

zz) 700 nm−800 nm;

aaa) 750 nm−800 nm;

bbb) 700 nm−750 nm;

ccc) between 650 nm and 1144 nm;

ddd) between 800 nm and 820 nm;

eee) 700 nm; and

fff) 800 nm.

8. The apparatus according to claim 1 , wherein the electronic processor is configured to:

a) compare the level of autofluorescence to a threshold; and

b) determine the fluorescence indicator using the results of the comparison.

9. The apparatus according to claim 1 , wherein the electronic processor is configured to:

a) determine an at risk level of autofluorescence sensed by the sensor at the second infrared wavelength in response to exposure of an at risk part of the artery to radiation at the first infrared wavelength, the at risk part being an area at risk of having an unstable plaque;

b) determine a healthy level of autofluorescence sensed by the sensor at the second infrared wavelength in response to exposure of a healthy part of the artery to radiation at the first infrared wavelength; and

c) determine the fluorescence indicator using the at risk level and the healthy level.

10. The apparatus according to claim 9 , wherein the electronic processor is configured to:

a) compare the at risk level to the healthy level; and

b) determine the fluorescence indicator using the results of the comparison.

11. The apparatus according to claim 9 , comprising determining if the at risk level of autofluorescence is greater than the healthy level of autofluorescence by a threshold factor of:

a) at least 2;

b) 3 or more;

c) 5 or more;

d) 10 or more; and/or

e) 15 or more.

12. The apparatus according to claim 1 , wherein the level of autofluorescence is based on an intensity of radiation emitted by the at least one part.

13. The apparatus according to claim 1 , wherein the apparatus is for detecting the vulnerability of atherosclerotic plaque, and wherein the fluorescence indicator is indicative of the vulnerability of an atherosclerotic plaque.

14. The apparatus according to claim 1 , wherein the apparatus is configured to provide representation comprising:

a) a numerical value indicative of the fluorescence indicator;

b) a symbolic value indicative of the fluorescence indicator;

c) a graphical indicator indicative of the fluorescence indicator; and/or

d) an indicator of at least one threshold.

15. The apparatus according to claim 1 , wherein the electronic processor is configured to:

a) determine a detected marker associated with a pathological condition by introducing an agent that detects the marker into the at least part of the artery; and

b) determine the fluorescence indicator at least partially using the at least one detected marker.

16. An apparatus for detecting a vulnerability of atherosclerotic plaques, the apparatus comprising:

a) a radiation source for generating radiation to thereby expose at least part of an artery to radiation at a first infrared wavelength, wherein the first infrared wavelength is in a range from 600 nm to 900 nm;

b) a sensor for sensing radiation emitted from at least part of the artery at a second infrared wavelength;

c) an electronic processor coupled to the sensor configured to:

i) determine a level of autofluorescence sensed by the sensor; and

ii) determine a fluorescence indicator using the level of autofluorescence, the fluorescence indicator being indicative of the vulnerability of an atherosclerotic plaque.

17. The apparatus according to claim 16 , wherein the apparatus comprises a catheter comprising one or more optical fibers extending between proximal and distal ends, the distal end being for insertion into the artery, and the radiation source and sensor being coupled to the proximal end.

18. The apparatus according to claim 1 , wherein the fluorescence indicator is indicative of one or more of:

a) intraplaque hemorrhage;

b) intraluminal thrombosis;

c) neovascularization;

d) one or more characteristics of plaque instability/rupture;

e) a high risk of plaque rupture;

f) a rupture prone plaque;

g) a presence of heme-degradation products;

h) a presence of heme;

i) a presence of metheme; or

j) a presence of protoporphyrin IX.

19. The apparatus according to claim 1 , wherein the apparatus is configured to:

a) determine levels of autofluorescence sensed by the sensor at one or more second infrared wavelengths in response to exposure of at least part of the artery to radiation at a plurality of first infrared wavelengths; and,

b) determine a fluorescence indicator using the levels of autofluorescence.

20. A method for detecting atherosclerotic plaques, the method comprising:

a) providing

i) a radiation source for generating radiation to thereby expose at least part of an artery to radiation at a first infrared wavelength, wherein the first infrared wavelength is in a range from 600 nm to 900 nm,

ii) a sensor for sensing radiation emitted from at least part of the artery at a second infrared wavelength, and

iii) an electronic processor

b) exposing at least part of the artery to radiation at the first infrared wavelength with the radiation source;

c) determining, with the electronic processor, a level of autofluorescence sensed by the sensor at the second infrared wavelength in response to exposure of at least part of the artery to radiation at the first infrared wavelength; and

d) determining, with the electronic processor, a fluorescence indicator using the level of autofluorescence, the fluorescence indicator being indicative of a presence, absence, degree or vulnerability of atherosclerotic plaques.

Assignments (1)
CHANGE OF NAME Recorded Jun 28, 2021
From: BAKER IDI HEART & DIABETES INSTITUTE HOLDINGS LIMITED
To: BAKER HEART AND DIABETES INSTITUTE
Reel/Frame 057291/0304 →
Priority Claims (1)
AU 2012901476 · Apr 13, 2012 · national
Continuity (2)
Continuation 14394057
Related Publication 20200405153A1 · Dec 31, 2020
References Cited (139)
US 4648892A · Kittrell et al. · 1987 [cited by applicant]
US 4718417A · Kittrell et al. · 1988 [cited by applicant]
US 4785806A · Deckelbaum · 1988 [cited by applicant]
US 4981138A · Deckelbaum et al. · 1991 [cited by applicant]
US 5046501A · Crilly · 1991 [cited by examiner]
US 5275594A · Baker et al. · 1994 [cited by applicant]
US 5507287A · Palcic et al. · 1996 [cited by applicant]
US 5590660A · Macaulay et al. · 1997 [cited by applicant]
US 6095982A · Richards-Kortum et al. · 2000 [cited by applicant]
US 6186780B1 · Hibst · 2001 [cited by applicant]
US 6258576B1 · Richards-Kortum et al. · 2001 [cited by applicant]
US 6365912B1 · Booth et al. · 2002 [cited by applicant]
US 6485300B1 · Muller · 2002 [cited by examiner]
US 6913743B2 · Licha et al. · 2005 [cited by applicant]
US 7108692B2 · Frenz et al. · 2006 [cited by applicant]
US 7328058B2 · Iwanczyk et al. · 2008 [cited by applicant]
US 7486985B2 · Marshik-Geurts et al. · 2009 [cited by applicant]
US 7539530B2 · Caplan et al. · 2009 [cited by applicant]
US 7603166B2 · Casscells et al. · 2009 [cited by applicant]
US 7865231B2 · Tearney et al. · 2011 [cited by applicant]
US 8050747B2 · Tearney et al. · 2011 [cited by applicant]
US 8060187B2 · Marshik-Geurts et al. · 2011 [cited by applicant]
US 8958867B2 · Madden et al. · 2015 [cited by applicant]
US 8971997B2 · Oral et al. · 2015 [cited by applicant]
US 9351702B2 · Wang et al. · 2016 [cited by applicant]
US 9513276B2 · Tearney et al. · 2016 [cited by applicant]
US 9693826B2 · Neuberger · 2017 [cited by applicant]
US 9918643B2 · Madden et al. · 2018 [cited by applicant]
US 10085802B2 · Neuberger · 2018 [cited by applicant]
US 10390708B2 · Nozaki · 2019 [cited by applicant]
US 10517669B2 · Peled et al. · 2019 [cited by applicant]
US 10835127B2 · Peter et al. · 2020 [cited by applicant]
US 20030044353A1 · Weissleder et al. · 2003 [cited by applicant]
US 20030055307A1 · Elmaleh et al. · 2003 [cited by applicant]
US 20040186383A1 · Rava et al. · 2004 [cited by applicant]
US 20040243022A1 · Carney et al. · 2004 [cited by applicant]
US 20050251116A1 · Steinke et al. · 2005 [cited by applicant]
US 20050260677A1 · Saaski · 2005 [cited by applicant]
US 20060041199A1 · Elmaleh et al. · 2006 [cited by applicant]
US 20070073162A1 · Tearney et al. · 2007 [cited by applicant]
US 20070078348A1 · Holman · 2007 [cited by applicant]
US 20070167836A1 · Scepanovic et al. · 2007 [cited by applicant]
US 20080058587A1 · Boyden · 2008 [cited by applicant]
US 20080059070A1 · Boyden · 2008 [cited by examiner]
US 20080103355A1 · Boyden et al. · 2008 [cited by applicant]
US 20080129993A1 · Brennan et al. · 2008 [cited by applicant]
US 20080193376A1 · Tawakol et al. · 2008 [cited by applicant]
US 20080221457A1 · Zeng et al. · 2008 [cited by applicant]
US 20090036770A1 · Tearney et al. · 2009 [cited by applicant]
US 20090073439A1 · Tearney et al. · 2009 [cited by applicant]
US 20090175576A1 · Tang · 2009 [cited by applicant]
US 20090192358A1 · Jaffer et al. · 2009 [cited by applicant]
US 20090231578A1 · Ling · 2009 [cited by applicant]
US 20100094138A1 · Gharib et al. · 2010 [cited by applicant]
US 20100272651A1 · Georgakoudi et al. · 2010 [cited by applicant]
US 20100315632A1 · Brennan, III · 2010 [cited by applicant]
US 20110275899A1 · Tearney et al. · 2011 [cited by applicant]
US 20120022338A1 · Subramaniam et al. · 2012 [cited by applicant]
US 20150080686A1 · Karlheinz et al. · 2015 [cited by applicant]
US 20160267360A1 · Madden et al. · 2016 [cited by applicant]
US 20170027427A1 · Salsman et al. · 2017 [cited by applicant]
US 20170209049A1 · Wang et al. · 2017 [cited by applicant]
US 20180040935A1 · Sliwa et al. · 2018 [cited by applicant]
US 20190008376A1 · Wortelboer et al. · 2019 [cited by applicant]
US 20190059734A1 · Yamada · 2019 [cited by applicant]
US 20190076005A1 · Song et al. · 2019 [cited by applicant]
US 20210041366A1 · Mamun et al. · 2021 [cited by applicant]
US 20230355105A1 · Peter et al. · 2023 [cited by applicant]
CA 1279901C · 1991 [cited by applicant]
CN 109381167A · 2019 [cited by applicant]
DK 2620119T3 · 2015 [cited by applicant]
EP 1153280A2 · 2001 [cited by applicant]
EP 1538968B1 · 2008 [cited by applicant]
EP 1357849B1 · 2009 [cited by applicant]
EP 2836128A1 · 2015 [cited by applicant]
EP 2620119B1 · 2015 [cited by applicant]
EP 2244626B1 · 2017 [cited by applicant]
EP 3267182A1 · 2018 [cited by applicant]
EP 3334321B1 · 2019 [cited by applicant]
EP 2974687B1 · 2019 [cited by applicant]
EP 3685783A1 · 2020 [cited by applicant]
ES 2555146T3 · 2015 [cited by applicant]
ES 2771673T3 · 2020 [cited by applicant]
HU E025580T2 · 2016 [cited by applicant]
JP 61257638A · 1986 [cited by applicant]
JP 2009183459A · 2009 [cited by applicant]
JP 2013505468A · 2013 [cited by applicant]
JP 2016506270A · 2016 [cited by applicant]
JP 2017519542A · 2017 [cited by applicant]
PT 2620119E · 2015 [cited by applicant]
PT 2974687T · 2020 [cited by applicant]
WO WO2005052558A · 2005 [cited by applicant]
WO WO2009029216A · 2009 [cited by applicant]
WO WO2011038006A1 · 2011 [cited by applicant]
WO WO2017147845A1 · 2017 [cited by applicant]
WO WO2019195881A1 · 2019 [cited by applicant]
WO WO2022027094A1 · 2022 [cited by applicant]
Jo, J.A. et al. “Diagnosis of Vulnerable Atherosclerotic Plaques by Time-Resolved Fluorescence Spectroscopy and Ultrasound Imaging.” Proceedings of the 28th IEEE EMBS Annual International Conference, p. 2663-2666 (Year:… [cited by examiner]
Calfon, M.A. et al. “Intravascular near-infrared fluorescence molecular imaging of atherosclerosis: toward coronary arterial visualization of biologically high-risk plaques.” Journal of Biomedical Optics 15(1), 011107 (… [cited by examiner]
Uchida, Y. et al. “Visualization of Lipid Components in Human Coronary Plaques Using Color Fluorescence Angioscopy.” Ciruclation Journal, vol. 74, 2181-2186 (2010) (Year: 2010). [cited by examiner]
Jaffer, F.A. et al. “Real-Time Catheter Molecular Sensing of Inflammation in Proteolytically Active Atherosclerosis.” Circulation, 118, 1802-1809 (2008) (Year: 2008). [cited by examiner]
Paras, C. et al. “Near-infrared autofluorescence for the detection of parathyroid glands.” Journal of Biomedical Optics 16(6), 067012 (2011) (Year: 2011). [cited by examiner]
Advisory Action and Interview Summary Dated Feb. 7, 2019 in U.S. Appl. No. 14/394,057. [cited by applicant]
Advisory Action and Interview Summary Dated Jan. 22, 2020 in U.S. Appl. No. 14/394,057. [cited by applicant]
Advisory Action and Interview Summary Dated Oct. 19, 2017 in U.S. Appl. No. 14/394,057. [cited by applicant]
Calfon, M.A., et al., In vivo Near Infrared Fluorescence (NIRF) Intravascular Molecular Imaging of Inflammatory Plaque, a Multimodal Approach to Imaging of Atherosclerosis, Journal of Visualized Experiments, 54, e2257, … [cited by applicant]
Fang, “Diagnosis of Vulnerable Atherosclerotic Plaques by Time-Resolved Fluorescence Spectroscopy and Ultrasound Imaging”, IEEE (Year: 2006). [cited by applicant]
Final Office Action Dated Feb. 8, 2016 in U.S. Appl. No. 14/394,057. [cited by applicant]
Final Office Action Dated Jul. 27, 2017 in U.S. Appl. No. 14/394,057. [cited by applicant]
Final Office Action Dated Nov. 21, 2018 in U.S. Appl. No. 14/394,057. [cited by applicant]
Final Office Action Dated Nov. 6, 2019 in U.S. Appl. No. 14/394,057. [cited by applicant]
Gillenwater, “Noninvasice Diagnosis of Oral Neoplasia Based on Fluorescence Spectroscopy and Native Tissue Autofluroescence”, JAMA Otolaryngology-Head and Neck Surgery, 124(11) pp. 1251-1258 (Year: 1998). [cited by applicant]
International Search Report issued in PCT/AU2013/000373 dated Jun. 11, 2013. [cited by applicant]
Japanese Office Action, dated Jan. 30, 2017, in Japanese Patent Application No. 2015-504818 X (with English translation). [cited by applicant]
Marcu, “Detection of rupture-prone atherosclerotic plaques by time-resolved laser-induced fluorescence spectroscopy”, Atherosclerosis, 204, pp. 156-164 (Year: 2009). [cited by applicant]
Notice of Allowance Dated Aug. 17, 2020 in U.S. Appl. No. 14/394,057. [cited by applicant]
Notice of Allowance Dated Jul. 2, 2020 in U.S. Appl. No. 14/394,057. [cited by applicant]
Office Action Dated Apr. 5, 2018 in U.S. Appl. No. 14/394,057. [cited by applicant]
Office Action Dated Feb. 9, 2017 in U.S. Appl. No. 14/394,057. [cited by applicant]
Office Action Dated Jun. 1, 2015 in U.S. Appl. No. 14/394,057. [cited by applicant]
Office Action Dated May 28, 2019 in U.S. Appl. No. 14/394,057. [cited by applicant]
Park, “Biochemical characterization of atherosclerotic plaques by endogenous multispectral fluorescence lifetime imaging microscopy”, Atherosclerosis, 220(2), pp. 394-401 (Year: 2012). [cited by applicant]
Piotrowski et al., Evidence For Lipid Peroxidation In Atherosclerosis, Life Sciences, vol. 46, pp. 715-721, 1990. [cited by applicant]
Piotrowski et al., Mature Human Atherosclerotic Plaque Contains Peroxidized Phosphatidylcholine As A Major Lipid Peroxide, Life Sciences, vol. 58, No. 9, pp. 735-737 40, 1996. [cited by applicant]
Weissleder, R., et al., In vivo imaging of tumors with protease-activated near-infrared fluorescent probes, Nature Biotechnology, vol. 17, pp. 375-378, Apr. 1999. [cited by applicant]
Zhu et al., Development Of A Near Infrared Fluorescence Catheter: Operating Characteristics And Feasibility For Atherosclerotic Plaque Detection, Journal Of Physics D: Applied Physics, vol. 38, pp. 2701-2707, 2005. [cited by applicant]
Calfon, et al., Intravascular near-infrared fluorescence molecular imaging of atherosclerosis: toward coronary arterial visualization of biologically high-risk plaques, Journal of Biomedical Optics 15(1), 011107 Jan./Fe… [cited by applicant]
Extended European Search Report dated Jan. 2, 2025 issued in European Patent Application No. 22758630.2, in 11 pages. [cited by applicant]
Htun et al., Near-infrared autofluorescence induced by intraplaque hemorrhage and heme degradation as marker for high-risk atherosclerotic plaques, Nature Communications, 8:75, DOI: 10.1038/s41467-017-00138-x, 2017. [cited by applicant]
International Preliminary Report On Patentability And Written Opinion in International Application No. PCT/AU2021/050845 dated Oct. 11, 2021 in 6 pages. [cited by applicant]
International Search Report and Written Opinion for PCT/AU2021/050845 mailed on Oct. 11, 2021. [cited by applicant]
Komachi et al., Micro-optical fiber probe for use in an intravascular Raman endoscope, Applied Optics, vol. 44, No. 22, pp. 2942-2944, 2005. [cited by applicant]
Komachi et al., Raman probe using a single hollow waveguide, Optics Letters, vol. 30, No. 21, pp. 2942-2944, 2005. [cited by applicant]
Le Grand et al., Superconductive tunnel junctions for X-ray spectroscopy, IEEE Transactions on Applied Superconductivity, vol. 3, No. 1, Part 4, pp. 2070-2075, 1993. [cited by applicant]
Liang et al., Intravascular atherosclerotic imaging with combined fluorescence and optical coherence tomography probe based on a double-clad fiber combiner, Journal of Biomedical Optics, vol. 17, No. 7, pp. 07050-1-0705… [cited by applicant]
Mavadia et al., An all-fiber-optic endoscopy platform for simultaneous OCT and fluorescence imaging, Biomedical Optics Express, vol. 3, No. 11, pp. 2851-2859, 2012. [cited by applicant]
Pekola et al., Trapping of quasiparticles of a nonequilibrium superconductor, Applied Physics Letters, vol. 76, No. 19, pp. 2782-2784, 2000. [cited by applicant]
Waxman et al., Near infrared spectroscopy for plaque characterization, Journal Interventional Cardiology, vol. 21, No. 6, pp. 452-458, 2008. [cited by applicant]
Office Action dated Apr. 16, 2025 issued in Japanese Patent Application No. 2023-507438, in 10 pages. [cited by applicant]