US2014346113A1PendingUtilityA1
Bioseparation compositions and methods for making and using same
Assignee: 3M INNOVATIVE PROPERTIES COPriority: Dec 21, 2011Filed: Dec 17, 2012Published: Nov 27, 2014
Est. expiryDec 21, 2031(~5.4 yrs left)· nominal 20-yr term from priority
Inventors:Masayuki NakamuraNaota SugiyamaCynthia D. ZookStephen E. AmosJerald K. RasmussenNicole M. Gryska
B01D 15/3804B01J 20/281B01J 20/289B01J 20/3291C12N 15/101B01J 2220/82C07K 1/16B01J 20/3204B01J 20/3219B01J 20/3261B01J 20/3248B01J 20/28021B01J 20/28004C12N 15/1006G01N 1/405
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Claims
Abstract
A composition for use in bioseparation. The composition includes a plurality of hollow particles having a siliceous surface. The composition further includes a surface-modifying agent bonded to the hollow particles. The surface-modifying agent includes a binding segment and a reactive segment. The binding segment includes a silyl group and the reactive segment includes a reactive nitrogen group.
Claims
exact text as granted — not AI-modified1 . A composition for use in bioseparation, the composition comprising:
a plurality of hollow particles, the hollow particles comprising a siliceous surface; and a surface-modifying agent bonded to the hollow particles, wherein the surface-modifying agent comprises a binding segment and a reactive segment, wherein the binding segment comprises a silyl group, and wherein the reactive segment comprises a reactive nitrogen group; wherein the plurality of hollow particles have an average density between about 0.05 and 0.4 g/ml.
2 . The composition according to claim 1 , wherein the hollow particles comprise glass bubbles.
3 . The composition according to claim 1 , wherein a size distribution of the plurality of hollow particles has a span of less than 1.0.
4 . The composition of claim 1 , wherein a mean particle size of the plurality of hollow particles ranges from about 10 micrometers to about 100 micrometers.
5 . The composition of claim 1 , wherein the binding segment has a formula:
—Si(R 1 ) 3-x (R 2 ) x ;
wherein x=0, 1, or 2; wherein each group R 1 comprises independently OH − or a hydrolyzable group from among halo, alkoxy, aryloxy, aralkyoxy, and acyloxy; and wherein each group R 2 comprises independently a non-hydrolyzable group from among alkyl, aryl, and aralkyl.
6 . The composition of claim 1 , wherein the surface-modifying agent further comprises a linking segment, the linking segment comprising alkylene, arylene, or both, and optionally further comprising —NH— or alkyleneoxy, or both.
7 . The composition of claim 1 , wherein the reactive segment has a formula:
—N(R 3 ) 2 , or salts thereof;
wherein each group R 3 comprises independently hydrogen, alkyl, aryl, or aralkyl.
8 . A method for making a bioseparation composition, the method comprising:
size fractionating a first plurality of hollow particles having a first particle size distribution with a first span to form a second plurality of hollow particles having a second particle size distribution with a second span that is less than the first span; and surface-modifying either or both of the first and second plurality of hollow particles with a surface modifying agent to form surface-modified hollow particles, wherein the surface-modifying agent comprises a binding segment and a reactive segment, wherein the binding segment comprises a silyl group, and wherein the reactive segment comprises a reactive nitrogen group.
9 . The method of claim 8 , wherein the first and second plurality of hollow particles comprise glass bubbles.
10 . The method of claim 8 , wherein the second span is less than 1.0.
11 . The method of claim 8 , wherein a mean particle size of the second plurality of hollow particles ranges from about 10 micrometers to about 100 micrometers.
12 . The method of claim 8 , wherein the binding segment has a formula:
—Si(R 1 ) 3-x (R 2 ) x ;
wherein x=0, 1, or 2; wherein each group R 1 comprises independently OH − or a hydrolyzable group from among halo, alkoxy, aryloxy, aralkyoxy, and acyloxy; and wherein each group R 2 comprises independently a non-hydrolyzable group from among alkyl, aryl, and aralkyl.
13 . The method of claim 8 , wherein the surface-modifying agent further comprises a linking segment, the linking segment comprising alkylene, arylene, or both, and optionally further comprising —NH— or alkyleneoxy, or both.
14 . The method of claim 8 , wherein the reactive segment has a formula:
—N(R 3 ) 2 , or salts thereof;
wherein each group R 3 comprises independently hydrogen, alkyl, aryl, or aralkyl.
15 . A method for capturing an analyte the method comprising:
providing a bioseparation composition comprising: a plurality of hollow particles; and a surface-modifying agent bonded to the hollow particles, wherein the surface-modifying agent comprises a binding segment and a reactive segment, wherein the binding segment comprises a silyl group, and wherein the reactive segment comprises a reactive nitrogen group; wherein the plurality of hollow particles have an average density between about 0.05 and 0.4 g/ml; and contacting the bioseparation composition with a solution comprising an analyte, wherein the surface-modifying agent is capable of coupling to the analyte.
16 . The method of claim 15 , further comprising separating the bioseparation composition from the solution.
17 . The method of claim 16 , wherein separating the bioseparation composition from the solution comprises allowing the bioseparation composition to float to an upper surface of the solution.
18 . The method of claim 15 , wherein the hollow particles comprise glass bubbles.
19 . The method of claim 15 , wherein a size distribution of the plurality of hollow particles has a span of less than 1.0.Join the waitlist — get patent alerts
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