A composition useful as an imaging agent comprises a beta adrenergic receptor antagonist compound, preferably iodopindolol, to which is covalently attached an iodine radioisotope such as .sup.123 I or .sup.124 I. This composition is used in a method for radioimaging beta adrenergic receptors in a tissue, preferably brain. In particular, the method is useful with the radioimaging technique of single photon emission computed tomography (SPECT) or positron emission tomography (PET). The above compo...

The present invention provides vaccine compositions comprising an oil-in-water emulsion optionally with 3 De-O-acylated monophosphoryl lipid A and QS21. The vaccine compositions are potent induces of a range of immune responses.

2'-Deoxy-2'-[.sup.18F]-labeled and 3'-deoxy-3'-[.sup.18F]-labeled purine nucleoside analogs such as [.sup.18F]-FAA and [.sup.18F]-FXA have been found to have desirable properties for use as imaging agents. The analogs are particularly useful for in vivo imaging of biological material including organ tissues (e.g., heart, liver, brain and kidneys) and tumors. Methods for the preparation of the [.sup.18F]-FAA and [.sup.18F]-FXA are also provided.

Carbon powder, placed in a hermetically closed apparatus under vacuum together with radium ore, adsorbs radon gas emanating from the radium ore thus producing a radioactive carbonaceous material, the radioactivity of which is due to the presence of adsorbed radon. The radioactive carbon powder thus obtained has excellent therapeutical efficacy and is suitable for a variety of applications because of the mild radioactivity of radon. Radium ore permits substantially limitlessly repeated production...

A pharmaceutical preparation containing magnetic vesicular particles is disclosed, wherein the magnetic vesicular particles each include magnetic microparticles within a lipid membrane, an organic compound having at least two groups selected from the group consisting of a hydroxyl group, a carboxyl group, a carbamoyl group, an amino group, a mercapto group, a sulfo group, a dithio group, a thiocarboxyl group and a dithiocarboxyl group is bonded to the magnetic microparticle, and the magnetic ves...

A two-stage method of preparing essentially pure amino acid chelates, wherein the first stage comprises contacting a metal ion from a metal oxide or hydroxide with an amino acid thereby producing a metal hydroxyl amino acetate. The second stage comprises contacting the metal hydroxyl amino acetate from the first stage, with at least one amino-containing compound provided in excess thereby producing a reaction solution containing an amino acid chelate reaction product comprising a metal ion bound...

The present invention provides novel imaging agents for clinical diagnosis of injuries and diseases, in the form of a radionuclide in spatial proximity to a substantially pure stereoisomer of a fatty acid analog. The invention also provides methods for using the novel imaging agents, and kits containing one or more of the novel imaging agents of the invention.

This invention relates to radiodiagnostic agents and reagents for preparing such agents, and also methods for producing radiolabeled radiodiagnostic agents. Specifically, the invention relates to technetium-99m (.sup.99m Tc) labeled agents, methods and kits for making the agents, and methods for using the agents to image pathological sites, including sites of infection, inflammation, cancer and atherosclerosis in a mammalian body. Specifically the agents and reagents are derivatives of oligosacc...

The present invention is concerned with radiolabelled quinoline and quinolinone derivatives according Formula (I-A)* or (I-B)* showing metabotropic glutamate receptor antagonistic activity, in particular mGlu1 receptor activity, and their preparation; it further relates to compositions comprising them, as well as their use for marking and identifying metabotropic glutamate receptor sites and for imaging an organ. ##STR00001## In a preferable embodiment, X represents O; R.sup.1 represents C.sub.1...

The invention relates to a system for synthesizing radiopharmaceuticals employing one or more single-use integrated kits of materials, valves and vessels fitted to one or more stationary apparatus in the manner that the kit can be safely ejected and disposed of without manual operations. Fluidic connections on the kits are made with flexible tubing that can be inserted into the various components by hand. This, along with the use of flexible configuration rotary valves, makes it possible to conf...