Device for capturing circulating cells
The present invention provides devices and methods for capturing rare cells. The devices and methods described herein can be used to facilitate the diagnosis and monitoring of metastatic cancers.
1. A microfluidic device for capturing biological cells, comprising:
a substrate comprising a nanostructured surface region;
a plurality of binding agents attached to said nanostructured surface region of said substrate; and
a flow layer attached to said substrate to form a microfluidic channel such that at least a portion of said nanostructured surface region of said substrate is in contact with fluid that flows through said microfluidic channel while in operation,
wherein said nanostructured surface region comprises a plurality of nanostructures each having a longitudinal dimension and a lateral dimension, said longitudinal dimension being at least ten times greater than said lateral dimension,
wherein biological cells are selectively captured by said binding agents and said plurality of nanostructures acting in cooperation, and
wherein said flow layer comprises a textured surface that causes chaotic flow to increase the probability that said biological cells come into contact with said nanostructured surface region of said substrate to be captured.
2. A microfluidic device according to claim 1 , wherein said substrate is a silicon substrate and said plurality of nanostructures are silicon nanowires or nanofibers.
3. A microfluidic device for capturing biological cells according to claim 2 , wherein said longitudinal dimension of said nanostructures is at least 1 μm long, and said lateral dimension of said nanostructures is greater than 30 nm and less than 400 nm,
wherein said nanostructured surface region of said substrate is coated with streptavidin and said plurality of binding agents are biotinylated and attached to said nanostructured surface region of said substrate coated with streptavidin, and
wherein said plurality of binding agents is a plurality of anti-epithelial-cell adhesion molecule antibodies (anti-EpCAM).
4. A microfluidic device according to claim 1 , wherein said substrate is an inorganic oxide substrate comprising at least one of zinc oxide, silicon oxide, titanium oxide or aluminum oxide and said plurality of nanostructures are inorganic oxide nanowires or nanofibers.
5. A microfluidic device according to claim 1 , wherein said substrate is a polymer substrate comprising at least one of polymethylmethacrylate, polysaccharide, or polylactide and said plurality of nanostructures are polymer nanowires or nanofibers.
6. A microfluidic device according to claim 1 , wherein said longitudinal dimension is at least 1 μm long, and said lateral dimension is greater than 30 nm and less than 400 nm.
7. A microfluidic device according to claim 1 , wherein said nanostructured surface region of said substrate is coated with streptavidin and said binding agents are biotinylated and attached to said nanostructured surface region of said substrate coated with streptavidin.
8. A microfluidic device according to claim 1 , wherein said plurality of binding agents comprises one or more of DNA, peptides, aptamers, and antibodies.
9. A microfluidic device according to claim 1 , wherein said plurality of binding agents is a plurality of anti-epithelial-cell adhesion molecule antibodies (anti-EpCAM).
10. A microfluidic device for capturing biological cells, comprising:
a substrate comprising a nanostructured surface region;
a flow layer attached to said substrate to form a microfluidic channel such that at least a portion of said nanostructured surface region of said substrate is in contact with fluid that flows through said microfluidic channel while in operation; and
a plurality of binding agents attached to said nanostructured surface region of said substrate,
wherein said nanostructured surface region comprises a plurality of nanostructures each having a longitudinal dimension and a lateral dimension,
wherein biological cells are selectively captured by said binding agents and said plurality of nanostructures acting in cooperation, and
wherein said flow layer comprises a textured surface that causes chaotic flow to increase the probability that said biological cells come into contact with said nanostructured surface region of said substrate to be captured.
11. A microfluidic device according to claim 10 , wherein said substrate is a silicon substrate and said plurality of nanostructures are silicon nanowires or nanofibers.
12. A microfluidic device according to claim 10 , wherein said substrate is an inorganic oxide substrate comprising at least one of zinc oxide, silicon oxide, titanium oxide or aluminum oxide and said plurality of nanostructures are inorganic oxide nanowires or nanofibers.
13. A microfluidic device according to claim 10 , wherein said substrate is a polymer substrate comprising at least one of polymethylmethacrylate, polysaccharide, or polylactide and said plurality of nanostructures are polymer nanowires or nanofibers.
14. A microfluidic device according to claim 10 , wherein said longitudinal dimension is at least 1 μm long, and said lateral dimension is greater than 30 nm and less than 400 nm.
15. A microfluidic device according to claim 10 , wherein said nanostructured surface region of said substrate is coated with streptavidin and said binding agents are biotinylated and attached to said nanostructured surface region of said substrate coated with streptavidin.
16. A microfluidic device according to claim 10 , wherein said plurality of binding agents comprises one or more of DNA, peptides, aptamers, and antibodies.
17. A microfluidic device according to claim 10 , wherein said plurality of binding agents is a plurality of anti-epithelial-cell adhesion molecule antibodies (anti-EpCAM).
18. A microfluidic device according to claim 10 , wherein said textured surface comprises a plurality of structures orientated relative to a principle direction of fluid flow.
19. A microfluidic device according to claim 18 , wherein said plurality of structures is oriented in a herring-bone pattern.