Surfaces that selectively bind to moieties

• US 20040234954A1
• Filed: 03/03/2004
• Published: 11/25/2004
• Est. Priority Date: 03/03/2003
• Status: Abandoned Application

• Current Assignee: University Of Massachusetts
• Original Assignee: University Of Massachusetts
• Inventors: Das, Kanad, Nusslein, Klaus, Penelle, Jacques
• Application Number:
  US10/795,703
• Publication Number:
  US 20040234954A1
• Time in Patent Office: Days
• US Class Current: 435/5
• CPC Class Codes: C12N 11/087 Acrylic polymers
• CPC Class Codes: G01N 2600/00 Assays involving molecular imprinted polymers/polymers created around a molecular template
• CPC Class Codes: G01N 33/54373 involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
• CPC Class Codes: G01N 33/56911 Bacteria

Abstract

A thin film made of a stiff polymer and having indentations on its surface, and methods of making and using the thin film are disclosed. The surface includes a plurality of indentations, the shape of each indentation corresponding to an outer surface of an imprint moiety, such as an animal, bacterial, or plant cell. The thin film can be mounted on a detector, which can be used to selectively bind to and detect the imprint moiety in a sample, e.g., a biological or environmental sample, at a minimum concentration of as low as 500 to 1000 imprint moieties per milliliter of sample.

Claims

1. A thin film having a maximum thickness of 2 microns and comprising a polymer having a flexural modulus of at least 150,000 psi, wherein a surface of the film comprises a plurality of indentations, each indentation comprising a reverse impression of a portion of an outer surface of an imprint moiety, and wherein when the thin film is mounted on a quartz crystal microbalance (QCM), the QCM can detect the imprint moiety in a liquid sample at a minimum concentration of at least as low as 1000 imprint moieties per milliliter of sample.

2. The film of claim 1, wherein the imprint moiety is selected from the group consisting of bacteria, virus particles, animal cells, spores, plant cells, prokaryotic cells, and eukaryotic cells.

3. The film of claim 1, wherein the imprint moiety is selected from the group consisting of Escherichia coli, Staphylococcus aureus, and Bacillus megaterium.

4. The film of claim 1, wherein the maximum thickness is between about 100 nm and about 1500 nm.

5. The film of claim 1, wherein the flexural modulus is at least 200,000 psi.

6. The film of claim 1, wherein the flexural modulus is at least 250,000 psi.

7. The film of claim 1, wherein the QCM can detect the imprint moiety in a liquid sample at a minimum concentration of at least as low as 500 imprint moieties per milliliter of sample.

8. The film of claim 1, wherein the indentations have a maximum depth of from about 20% to about 40% of a largest dimension of the imprint moiety.

9. The film of claim 1, wherein the indentations on the surface number from about 40,000 to about 150,000 indentations/cm².

10. The film of claim 1, wherein the indentations on the surface number from about 60,000 to about 90,000 indentations/cm².

11. The film of claim 1, wherein the polymer comprises a bis-acrylate polymer.

12. The film of claim 1, wherein the polymer is selected from the group consisting of a methacrylate, an acrylate polymer, a nylon, a polyester, a polycarbonate, and mixtures thereof.

13. The film of claim 1, wherein the polymer is formed by polymerization of a mixture of 1,5-pentanediol bis(α

-acetamido acrylate), and benzyl methacrylate or benzyl acrylate.

14. The film of claim 1, wherein the polymer is formed by polymerization of a monomer selected from the group consisting of acrylic acid, methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethylhexyl acrylate, methacrylic acid, methylmethacrylate, isobutyl acrylate, tertiarybutyl acrylate, tertiarybutyl methacrylate, 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, butanediol monoacrylate, ethyldiglycol acrylate, lauryl acrylate, dimethylaminoethyl acrylate, dihydrodicyclopentadienyl acrylate, adipic acid, hexamethylene diamine, carolactam, bisphenol, an organic diacid, a cyclic amide, ethylene glycol, terephthalic acid, an aromatic diacid, and mixtures thereof.

15. An implantable medical device comprising the thin film of claim 1 attached to at least a portion of its surface.

16. The medical device of claim 15, wherein the imprint moiety is a mammalian cell.

17. The medical device of claim 16, wherein the mammalian cell is from a mammal into which the medical device is to be implanted.

18. The medical device of claim 16, wherein the mammalian cell is an endothelial cell.

19. The medical device of claim 16, wherein the mammalian cell is a cartilage cell.

20. A biosensor comprising:

a microbalance comprising a conducting element; and

the thin film of claim 1, attached to a surface of the conducting element.

21. The biosensor of claim 20, wherein the microbalance is a quartz crystal microbalance.

22. The biosensor of claim 20, wherein the thickness of the film is from about 100 nm to 1500 nm.

23. The biosensor of claim 20, wherein the thickness of the film is less than 500 nm.

24. The biosensor of claim 20, wherein the imprint moiety is selected from the group consisting of a bacterium, virus particles, a cell from an animal, a spore, a plant cell, a prokaryotic cell, and a eukaryotic cell.

25. A method of detecting a target imprint moiety in a sample, the method comprising:

obtaining a biosensor of claim 20, wherein the thin film comprises indentations that are reverse impressions of the target imprint moiety to be detected;

applying a sample to the thin film on the biosensor under conditions that enable the thin film to selectively bind to any target imprint moieties in the sample, wherein the detector can detect the target imprint moiety at a minimum concentration of at least as low as 1000 imprint moieties per milliliter of sample; and

detecting a change in mass of the thin film, wherein an increase in mass of the thin film indicates the presence of the imprint moiety in the sample.

26. The method of claim 25, wherein the microbalance is a quartz crystal microbalance.

27. The method of claim 25, wherein the sample is blood, sputum, saliva, urine, or serum.

28. The method of claim 25, wherein the sample is water.

29. The method of claim 25, wherein the target imprint moiety is selected from the group consisting of bacteria, virus particles, animal cells, spores, plant cells, prokaryotic cells, and eukaryotic cells.

30. A method of making a thin film, the method comprising

polymerizing one or more monomers in the presence of a plurality of imprint moieties to form a polymer having a flex modulus of at least 150,000 psi;

forming a sheet of the polymer having a maximum thickness of 2 microns; and

removing the imprint moieties from a surface of the polymer sheet leaving a plurality of indentations on the surface, each indentation comprising a reverse impression of a portion of an outer surface of an imprint moiety;

wherein when the thin film is mounted on a quartz crystal microbalance (QCM), the QCM can detect the imprint moiety in a liquid sample at a minimum concentration of at least as low as 1000 imprint moieties per milliliter of sample.

31. The method of claim 30, wherein all of the imprint moieties are of the same type.

32. The method of claim 30, wherein the imprint moieties are of two or more different types.