US2017030900A1PendingUtilityA1
Stimuli-responsive polymer diagnostic assay comprising magnetic nanoparticles and capture conjugates
Assignee: UNIV WASHINGTON THROUGH ITS CENTER FOR COMMERCIALIZATIONPriority: Nov 9, 2009Filed: Aug 4, 2016Published: Feb 2, 2017
Est. expiryNov 9, 2029(~3.3 yrs left)· nominal 20-yr term from priority
G01N 33/54333B82Y 25/00G01N 2001/4088G01N 33/545B03C 2201/26G01N 2446/84Y10T436/25G01N 27/745B03C 2201/18B03C 1/01Y10T436/255Y10T436/00C12Q 1/6834B03C 1/288G01N 33/54306G01N 2446/20G01N 2001/4038C12N 15/1013B01D 21/0009G01N 1/34G01N 33/54346
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Claims
Abstract
The present disclosure utilizes the aggregation of stimuli-responsive polymers to isolate a diagnostic target (e.g., an antigen) from a solution using magnetophoresis. Isolating the diagnostic target provides a route to identify the presence of the diagnostic target in the solution.
Claims
exact text as granted — not AI-modified1 - 5 . (canceled)
6 . The aggregate of claim 22 , wherein the target is an indicator for a disease or condition.
7 - 20 . (canceled)
21 . An aggregate, comprising
a stimuli-responsive magnetic nanoparticle comprising a first stimuli-responsive polymer attached to a magnetic core; and a stimuli-responsive capture conjugate comprising a second stimuli-responsive polymer attached to a capture moiety, wherein the capture moiety is capable of binding to a target; wherein the aggregate is formed through associative interactions between the first stimuli-responsive polymer and the second stimuli-responsive polymer.
22 . The aggregate of claim 21 , further comprising a target bound to the capture moiety.
23 . The aggregate of claim 22 , wherein the target is selected from the group consisting of an antibody, an antigen, a cell, a nucleic acid, an enzyme, a substrate for an enzyme, a protein, a peptide, a lipid, a carbohydrate, or other biomarker.
24 . The aggregate of claim 21 , wherein the associative interaction between the first stimuli-responsive polymer and the second stimuli-responsive polymer is responsive to a stimulus independently selected from the group consisting of temperature, pH, light, photo-irradiation, exposure to an electric field, ionic strength, and combinations thereof.
25 . The aggregate of claim 21 , wherein the associative interaction between the first stimuli-responsive polymer and the second stimuli-responsive polymer is responsive to a change in ionic strength.
26 . The aggregate of claim 21 , wherein the associative interaction between the first stimuli-responsive polymer and the second stimuli-responsive polymer is responsive to a change in pH.
27 . The aggregate of claim 21 , further comprising a second stimuli-responsive capture conjugate comprising a third stimuli-responsive polymer attached to a second capture moiety, wherein the second capture moiety is capable of capturing a second target, wherein the second target is different than the target.
28 . The aggregate of claim 27 , wherein the aggregate is formed through associative interactions between the first stimuli-responsive polymer, the second stimuli-responsive polymer, and the third stimuli-responsive polymer, and the associative interaction is responsive to a stimulus independently selected from the group consisting of temperature, pH, light, photo-irradiation, exposure to an electric field, ionic strength, and combinations thereof.
29 . The aggregate of claim 27 , wherein the aggregate is formed through associative interactions between the first stimuli-responsive polymer, the second stimuli-responsive polymer, and the third stimuli-responsive polymer, and the associative interaction is responsive to a change in ionic strength.
30 . The aggregate of claim 27 , wherein the aggregate is formed through associative interactions between the first stimuli-responsive polymer, the second stimuli-responsive polymer, and the third stimuli-responsive polymer, and the associative interaction is responsive to a change in pH.
31 . A target-capturing composition, comprising
a stimuli-responsive magnetic nanoparticle comprising a N-isopropylacrylamide-containing polymer attached to an iron oxide magnetic core; and a stimuli-responsive capture conjugate comprising a polymer including N-isopropylacrylamide repeating units attached to a capture moiety, wherein the capture moiety is capable of binding to a target; wherein the stimuli-responsive magnetic nanoparticle and the stimuli-responsive capture conjugate are capable of forming an aggregate through associative interaction between the N-isopropylacrylamide-containing polymer and the polymer including N-isopropylacrylamide repeat units.
32 . The target-capturing composition of claim 31 , wherein the associative interaction between the N-isopropylacrylamide-containing polymer and the polymer including N-isopropylacrylamide repeat units is responsive to a change in ionic strength.
33 . The target-capturing composition of claim 31 , wherein the associative interaction between the N-isopropylacrylamide-containing polymer and the polymer including N-isopropylacrylamide repeat units is responsive to a change in pH.
34 . The target-capturing composition of claim 31 , further comprising a target.
35 . The target-capturing composition of claim 34 , wherein the target is an indicator for a disease or condition.
36 . The target-capturing composition of claim 34 , wherein the target is selected from the group consisting of an antibody, an antigen, a cell, a nucleic acid, an enzyme, a substrate for an enzyme, a protein, a peptide, a lipid, a carbohydrate, or other biomarker.
37 . The target-capturing composition of claim 34 , wherein the target is a cell membrane receptor.Join the waitlist — get patent alerts
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