US2008279772A1PendingUtilityA1
Methods for detecting pathological sites
Assignee: ACTINIUM PHARMACEUTICALS INCPriority: Feb 19, 1991Filed: May 9, 2008Published: Nov 13, 2008
Est. expiryFeb 19, 2011(expired)· nominal 20-yr term from priority
Inventors:Maurits Willem Geerlings
A61K 51/1045A61K 51/1093
68
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Claims
Abstract
The present invention relates to the field of site directed therapy. More specifically the invention relates to site directed radio therapy, and provides a method for production of radioconjugates and an apparatus for radioimmunotherapy. The method, conjugates and apparatus can be practicalized without the need for radioactive shielding and/or airtight facilities. Without these restrictions the invention provides a simple and efficient means of therapy at the bed-side of the patient.
Claims
exact text as granted — not AI-modified1 - 29 . (canceled)
30 . A method for detecting a pathological site in a mammal, said pathological site comprising a target moiety, said method comprising providing a radioconjugate of a targeting moiety bound, directly or indirectly, to an alpha-particle emitting radioisotope, said target moiety and said targeting moiety constituting a specific binding pair, administering said conjugate to said mammal to effectuate specific binding of said conjugate to said target moiety and detecting alpha-particles emitted by said bound conjugate.
31 . A method as claimed in claim 30 , wherein said pathological site comprises diseased cells.
32 . A method as claimed in claim 31 , wherein said alpha-particle emitting radioisotope is 213 Bi.
33 . A method as claimed in claim 32 , wherein said targeting moiety is a ligand having binding specificity for a cell surface receptor present on said diseased cells.
34 . A method as claimed in claim 33 , wherein said ligand is a peptide.
35 . A method as claimed in claim 30 , wherein said pathological site is an extracellular structure.
36 . A method as claimed in claim 35 , wherein said alpha-particle emitting radioisotope is 213 Bi.
37 . A method as claimed in claim 36 , wherein said targeting moiety is a ligand having binding specificity for a receptor present on said extracellular structure.
38 . A method as claimed in claim 37 , wherein said ligand is a peptide.
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