US 12,228,582 B2
Method and apparatus for testing near infrared-photoimmunotherapy treatment
Hisataka Kobayashi, Bethesda, MD (US); and Masayuki Nishimura, Columbia, MD (US)
Assigned to SHIMADZU CORPORATION, Kyoto (JP); and The United States of America as Represented By The Secretary of the Department of Health and Human, Bethesda, MD (US)
Appl. No. 17/253,671
Filed by SHIMADZU CORPORATION, Kyoto (JP); and THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES, Bethesda, MD (US)
PCT Filed Jun. 20, 2019, PCT No. PCT/US2019/038097
§ 371(c)(1), (2) Date Dec. 18, 2020,
PCT Pub. No. WO2019/246322, PCT Pub. Date Dec. 26, 2019.
Claims priority of provisional application 62/688,031, filed on Jun. 21, 2018.
Prior Publication US 2021/0263054 A1, Aug. 26, 2021
Int. Cl. G01N 33/94 (2006.01); A61K 41/00 (2020.01); A61K 47/68 (2017.01); C07K 16/28 (2006.01); G01N 33/68 (2006.01)
CPC G01N 33/94 (2013.01) [A61K 41/0042 (2013.01); A61K 41/0071 (2013.01); A61K 47/6849 (2017.08); A61K 47/6855 (2017.08); C07K 16/2863 (2013.01); G01N 33/6848 (2013.01)] 8 Claims
 
1. A method for testing efficiency and effectiveness of a near infrared photoimmunotherapy treatment, the method comprising:
injecting an antibody photosensitizer conjugate into a patient, wherein the antibody photosensitizer conjugate comprises an antibody conjugated to a C74H96N12Na4O27S6Si3 phthalocyanine dye;
applying radiation to the patient, thereby causing the antibody photosensitizer conjugate to release a C14H33NO10S3Si ligand, which is excreted in the patient's urine;
detecting the presence of the C14H33NO10S3Si ligand with liquid chromatography-mass spectrometry; and
measuring and quantifying an amount of the C14H33NO10S3Si ligand present in the patient's urine based on analytical results of the liquid chromatography-mass spectrometry to determine the efficiency and effectiveness of the near infrared photo-immunotherapy treatment,
wherein the amount of the C14H33NO10S3Si ligand present in the patient's urine inversely corresponds to an amount of an antibody photosensitizer conjugate remaining in the patient, and
wherein the amount of the C14H33NO10S3Si ligand present in the patient's urine positively corresponds with the efficiency and effectiveness of the near infrared photoimmunotherapy treatment.