IP Library Granted Patent US 8,980,185
Granted Patent B2
US 8,980,185 · App. 13/818,569 · Granted Mar 17, 2015

Microreactor and method for preparing a radiolabeled complex or a biomolecule conjugate

Inventors: David E. Reichert (St. Louis, MO); Paul J. A. Kenis (Champaign, IL); Tobias D. Wheeler (Alameda, CA); Amit V. Desai (Urbana, IL); Dexing Zeng (Pittsburgh, PA); Birce C. Önal (Champaign, IL)
Assignees: The Board of Trustees of the University of Illinois; Washington University
C07K1/13C07B59/00B01J19/0093C07B59/008C07K1/1077
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Quick Facts
Patent No.
US 8,980,185
App. No.
13/818,569
Granted
Mar 17, 2015
Kind
B2
Abstract

A microreactor for preparing a radiolabeled complex or a biomolecule conjugate comprises a microchannel for fluid flow, where the microchannel comprises a mixing portion comprising one or more passive mixing elements, and a reservoir for incubating a mixed fluid. The reservoir is in fluid communication with the microchannel and is disposed downstream of the mixing portion. A method of preparing a radiolabeled complex includes flowing a radiometal solution comprising a metallic radionuclide through a downstream mixing portion of a microchannel, where the downstream mixing portion includes one or more passive mixing elements, and flowing a ligand solution comprising a bifunctional chelator through the downstream mixing portion. The ligand solution and the radiometal solution are passively mixed while in the downstream mixing portion to initiate a chelation reaction between the metallic radionuclide and the bifunctional chelator. The chelation reaction is completed to form a radiolabeled complex.

Claims (18)

1. A method of preparing a radiolabeled complex, the method comprising:

flowing a precursor radiometal solution comprising a metallic radionuclide through an upstream mixing portion of a microchannel, the upstream mixing portion including one or more passive mixing elements, and the metallic radionuclide being selected from 60 Cu 2+ , Cu 61 Cu 2+ , 64 Cu 2+ , 67 Cu 2+, 66 Ga 3+ , 67 Ga 3+ , and 68 Ga 3+ ;

flowing a buffer solution through the upstream mixing portion;

passively mixing the buffer solution and the precursor radiometal solution while in the upstream mixing portion to form a radiometal solution comprising the metallic radionuclide, the radiometal solution further flowing through a downstream mixing portion of the microchannel, the downstream mixing portion including one or more passive mixing elements and being disposed downstream of the upstream mixing portion;

flowing a ligand solution comprising a bifunctional chelator through the downstream mixing portion, the bifunctional chelator being selected from DOTA and NOTA;

passively mixing the ligand solution and the radiometal solution while in the downstream mixing portion to form a mixed solution and to initiate a chelation reaction between the metallic radionuclide and the bifunctional chelator, a molar ratio of the metallic radionuclide to the bifunctional chelator being about 1:1, and the mixed solution comprising a concentration of >50 μm of the metallic radionuclide; and

completing the chelation reaction to form a radiolabeled complex,

wherein completing the chelation reaction comprises halting the flow of each solution and incubating the mixed solution for a residence time of at least 12 minutes, the incubation being carried out at a temperature of at least 37° C. in at least one microfluidic reservoir in fluid communication with the microchannel and disposed downstream of the downstream mixing portion, and

wherein the radiolabeled complex is obtained at a yield of at least about 80%.

2. The method of claim 1 , further comprising flowing a fluid into the microfluidic reservoir after the incubation to force the mixed solution through a reservoir outlet.

3. The method of claim 1 , wherein the flowing of each of the solutions occurs at a flow rate between about 0.1 μL/min and about 5 mL/min.

4. The method of claim 1 , wherein the bifunctional chelator is conjugated to a targeting biomolecule.

5. The method of claim 1 , further comprising:

flowing a chelator solution through a mixing portion of a second microchannel, the mixing portion including one or more passive mixing elements;

flowing a biomolecule solution through the mixing portion of the second microchannel;

passively mixing the chelator solution and the biomolecule solution to form a combined solution via a conjugation reaction; and

forming the ligand solution from the combined solution.

6. The method of claim 1 , wherein the width of the microchannel is between about 5 microns and about 500 microns.

Assignments (3)
CONFIRMATORY LICENSE Recorded Oct 7, 2015
From: BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS,THE
To: ENERGY, UNITED STATES DEPARTMENT OF
Reel/Frame 036816/0931 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2014
From: KENIS, PAUL J.A.; WHEELER, TOBIAS D.; DESAI, AMIT V.
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS
Reel/Frame 034025/0869 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 24, 2014
From: REICHERT, DAVID; ONAL, BIRCE; ZENG, DEXING
To: WASHINGTON UNIVERSITY
Reel/Frame 034025/0977 →
Continuity (2)
Provisional Application 61377364 · Aug 26, 2010
Related Publication 20130225791A1 · Aug 29, 2013